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Leading Manufacturer, Supplier & Retailer of Masterone, peptide hormone cjc 1295, Testosterone Phenylpropionate, Testosterone Undecanoate and Boldenone Propionate.

Masterone

74 /10 Gram
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  • Min. Order (MOQ) 10 Gram

Drostanolone propionate (trade name masteron) is an anabolicandrogenic steroid which is the propionate ester of drostanolone. It is known to be androgenic and anabolic. It is incapable of aromatization and has similar properties to dihydrotestosterone. It has been successfully used as a breast cancer drug, but because of the high risk of virilization, safer options are prescribed. Drostanolone propionate is used primarily by athletes who need to retain strength while losing mass. It is beneficial to runners and athletes who must remain in a certain weight class. It has gained popularity in the bodybuilding community as a diuretic and muscle defining drug. Individuals interested in using the drostanolone propionate are those that are looking to add muscle hardness and density to their physiques, nearly always for the purpose of bodybuilding competitions. Drostanolone propionate can increase muscle hardness and density, giving an individual a more complete appearance when competing on stage.however, an already rather low body-fat level is needed for it to take full effect.drostanolone propionate can promote increased strength while keeping body fat the same or even lowering it, something can help to prevent muscle loss while dieting. This can also allow strength athletes or those athletes in sports which have weight classes to increase performance without the risk of being raised into a higher weight class or add mass that may hinder performance.

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peptide hormone cjc 1295

74 /Gram
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  • Min. Order (MOQ) 10 Gram
  • Type Manufacutrer
  • Certification GBP, ISO9001, FDA
  • Color white
  • Properties White Powder
  • Place of Origin china
  • CAS 863288-34-0
  • MF C165H269N47O46
  • MW 3647.19
  • Puirty 98.71%
  • Appearance White Powder
  • Standard Enterprise standard
  • Usage Those looking for anti-aging benefits, improved physique and sense of well being.
  • Storage Store in cool and dry area and keep away from direct sunlight

Cjc-1295 is a derivative of human gh-releasing factor1-29(hgrf1-29). Hgrf1-29 is a naturally occurring peptide that is actually a truncated form of a larger peptide that binds to the growth hormone secretagogue receptor (ghs-r) and causes the release of growth hormone. Cjc-1295 has four amino acids substituted in its chain that result in strong binding to serum albumin and prolong its half-life in the body. Because of the way cjc-1295 is engineered its half life has been extended from ~7 minutes to greater than 7 days!. This is convenient as it means the product only needs to be injected 1-2 times per week for continuously elevated levels of human growth hormone (hgh) and igf-1. A single subcutaneous (sc) injection results in measurable quantities of cjc-1295 in the blood for up to 13 days. Additionally, a single dose of 60 ugkg of cjc-1295 results in elevated levels of growth hormone (125%) while the pulsatile secretion of gh is maintained. Furthermore, 60 ugkg of cjc-1295 elevated igf-1 levels to the upper limit of normal. A dose of 30 ugkg of cjc-1295 given weekly maintained its response with no evidence of desensitization.

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Payment Terms : L/C, D/A, D/P, T/T, Western Union, MoneyGram,

Packaging Details : Discreet packing ways as your requirement, 100% go through

Delivery Time : within 24 hours after your payment

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Testosterone Phenylpropionate

74 /10 Gram
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  • Min. Order (MOQ) 10 Gram
  • Type manfacturer
  • Brand Name JNJG
  • Material white crystalline powder
  • Certification GMP, ISO 9001, USP, BP
  • Properties white crystalline powder
  • Place of Origin China
  • CAS 1255-49-8
  • MF C28H36O3
  • MW 420.58
  • Purity >99%
  • Apperance white crystalline powder
  • Standard BP2003
  • Usage Pharmaceutical material, Steroid hormone, Anabolin. As a male hormone and anabolic hormones.

Testosterone phenylpropionate is a steroid hormone from the androgen and is found in mammals and other vertebrates, testosterone phenylpropionate is primarily secreted in the tests of mails and the ovaries of female, although small amount are also secreted by the adrenal glands, testosterone phenylpropionate is the principle male sex hormone and an anabolic steroid. Testosterone phenylpropionateis the name given to testosterone with the phenylproprionate ester. This particular ester is a medium length ester that falls squarely between testosterone long ester (cypionate) and short ester (propionate). Injections of two to three times per week are appropriate for this steroid.as with any testosterone, testosterone phenylpropionatewill give the user more mass to the muscle, burn fat in the body, enhance libido, increase immunity and increase energy. All the usual side effects of testosterone can also be expected conversion to estrogen and dht, gynocomastia and water-retention.

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Testosterone Undecanoate

74 /10 Gram
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  • Min. Order (MOQ) 10 Gram
  • Brand Name JNJG
  • Grade CP2000
  • CAS No. 5949-44-0
  • MF C30H48O3
  • State solid
  • Purity 97.0%~103.0%
  • Application A metabolite of Testosterone (T155000). It is a promising androgen for male hormonal contraception.
  • Purity 99%
  • Type manfacturer
  • Place of Origin China
  • Appearance white powder
  • CAS 5949-44-0
  • MW 456.70
  • Apperance white powder
  • Certification ISO 9001, USP, BP
  • Standard CP2000
  • Usgae A metabolite of Testosterone (T155000). It is a promising androgen for male hormonal contraception

Description: testosterone undecanoate or testosterone undecylate is an ester of testosterone which is used for the treatment of male hypogonadism, and is currently under research for use as a male contraceptive, testosterone undecanoate is sold and distributed under the brand names andriol, understor, nebido, pantestone, restandol. Andriol is a version of the anabolic steroid testosterone undecanoatedeveloped by the pharmaceutical company organon, testosterone is said to enter the body as a fat through the lymphatic system, experience from user indicates that in dose of less than 240mg per day, effects are negligible, except at every onset of use, while even in higher dose, effects are still minimal, testosterone undecanoate is therefor thought that most of the steroid is somehow not making it into the blood stream. Testosterone undecanoate or testosterone undecylate is an ester of testosterone. This hormone is used in androgen replacement therapy primarily for the treatment of male hypogonadism, and is currently under research for use as a male contraceptive. Application: testosterone undecanoate or testosterone undecylate is an ester which is used for the treatment of male hypogonadism, and is currently under research for use as a male contraceptive, testosterone undecanoate is sold and distributed under the brand names andriol, understor, nebido, pantestone, restandol. Andriol is a version of the anabolic steroid testosterone undecanoatedeveloped by the pharmaceutical company organon, experience from user indicates that in dose of less than 240mg per day, effects are negligible, except at every onset of use, while even in higher dose , effects are still minimal , testosterone undecanoate is therefor thought that most of the steroid is somehow not making it into the blood stream.

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Boldenone Propionate

74 /10 Gram
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  • Min. Order (MOQ) 10 Gram
  • Brand Name JNJG
  • Grade Enterprise Standard
  • CAS No. 13103-34-9
  • MF C22H30O3
  • State solid
  • Purity >98%
  • Application Hormones and Regulation of Endocrine Function of Drug, Steroid Powder for Bodybuilding
  • Application Pharmaceutical raw materials, the hormone
  • Type manfacturer
  • Place of Origin China
  • Appearance white powder
  • CAS 13103-34-9
  • MW 342.47
  • Puirty >98%
  • Apeprance white powder
  • Certification GMP, HSE, ISO 9001, USP, BP
  • Standard Enterprise standard

Boldenone propionate would be more intense to raises red blood cells, increase the appetite, and repair connective tissue which are also a huge plus for bodybuilders during training. Boldenone propionate is going to be a painful injection. This steroid is containing 25mgml of the hormone boldenone attached to the acetate ester and 75mgml of the hormone boldenone attached to the propionat ester. Having boldenone attached to these esters allows for it to raise blood levels rather quickly and for the effects to be faster than those seen with the slower ester of traditional eq. Boldenone will increase nitrogen retention, protein synthesis, increases appetite and stimulates the release of erythropoietin in the kidneys. Boldenone was synthesized in an attempt to create a long-acting injectable methandrostenolone (dianabol), for androgen deficiency disorders. Boldenone acts similar to methandrostenolone with less adverse androgenic effects. It has a very long half-life, and can show up on a steroid test for up to 5 months, due to the long undecylenate ester attached to the parent steroid. Trace amounts of the drug can easily be detected for months after discontinued use.

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Boldenone Cypionate

74 /10 Gram
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  • Min. Order (MOQ) 10 Gram
  • Certification GMP, ISO 9001, USP
  • Place of Origin China
  • CAS 106505-90-2
  • MF C26H38O3
  • MW 398.58
  • Purity 99%
  • Apperance white powder
  • Cetification GMP, ISO 9001, USP
  • Standard Enterprise standard
  • Usage pharmaceutical material, Steroid hormone, Anabolin. As a male hormone and anabolic hormones

Boldenone cypionate is an ester of boldenone and is recommended as an aid for the treatment of debilitated horses when an improvement in weight, hair coat or general physical condition is desired. Debilitation often follows disease or may occur following overwork and overexertion. Boldenone improves the general state of debilitated horses, thus aiding in correcting weight losses and improving appetite. It is not a substitute for a well-balanced diet. Optimal results can be expected only when good management and feeding practices are utilized. Boldenone should be considered only as adjunctive therapy to other specific and supportive therapy for diseases, surgical cases and traumatic injuries. Boldenone 200 usp injection provides boldenone cypionate, a long acting anabolic steroid used in veterinary medicine for the treatment of horses. Boldenone possess marked anabolic properties and a minimal amount of androgenic activity. Boldenone has a rapid onset of action; this is advantageous and is preferred over frequent oral dosing or even repeated injections. The esterification of the 17-beta-hydroxyl group increases the duration of the action of boldenone. Boldenone esters in oil injected intramuscularly are absorbed slowly from the lipid phase, thus boldenone 200 can be administered at intervals of every 2-3 weeks.

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Nandrolone Phenylpropionate

74 /10 Gram
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  • Min. Order (MOQ) 10 Gram
  • Purity >99%
  • CAS 62-90-8
  • MF C27H34O3
  • MW 406.56
  • Apeprance white or almost white crystalline powder
  • Certification GMP, ISO 9001, USP
  • Standard USP28;BP2003
  • Usage can be used as pharmaceutical material, Building Muscle, Burning Fat

Durabolin is an anabolic steroid that was created by organon in the late 1950's and is officially known as nandrolone phenylpropionate. This anabolic steroid is almost identical to organon's deca durabolin (nandrolone decanoate), the only difference being the ester attached. This makes durabolin or npp as it's commonly called a much faster acting version of nandrolone. Durabolin is also one of the oldest nandrolone compounds and was actually released a few years ahead of deca durabolin. However, it has been deca durabolin and the overall nandrolone decanoate mixture that has dominated the nandrolone market place throughout history. While organon still makes durabolin and there are many other pharmacies and underground labs that make npp, it is not as commonly available. However, in recent years it has seen its demand slightly increase due to performance enhancement use. Durabolin is one of the most beneficial anabolic steroids to ever hit the market. The benefits of this steroid can easily be seen in both therapeutic and performance based circles. In a medical setting, along with testosterone this is one of the most important anabolic steroids we have, and the advantages it can provide run extremely deep. Unfortunately, the full potential of this steroid has never been realized due to the tremendous amount of controversy that surrounds anabolic steroids, especially in the u.s. In fact, the u.s. Is far behind many parts of the world when it comes to nandrolone therapy. While tremendous for medicinal purposes, durabolin is also a premier lean mass promoting anabolic steroid. There are very few anabolic steroids that can pack on quality mass along side a high threshold of toleration like durabolin. It is also one of the best steroids for athletic enhancement due to the recovery and endurance enhancement it can provide.

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Nandrolone Laurate

74 /10 Gram
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  • Min. Order (MOQ) 10 Gram
  • CAS 26490-31-3
  • MF C30H48O3
  • MW 456.71
  • Puirty >99%
  • Apperance white or almost white crystalline powder
  • Certification GMP, ISO 9001, USP
  • Standard Enterprise Standard
  • Usage A synthetic , anabolic muscle growthsteroids . Used to promote muscle growth and combat involuntary

1.nandrolone laureate is the chemical name of active ingredient in laurabolin. Laurabolin is a registered trademark of intervet international in the united states andor other countries. 2.laurabolin (nandrolone laureate) is an injectable veterinary steroid containing the drug nandrolone laurate. Laurabolin is basically a long acting deca durabolin (nandrolone decanoate), staying active for up to a month in the body. If you have problems recovering natural testosterone production after using deca, you will definitely have problems using laurabolin. 3.athletes however generally inject this drug on a weekly basis. Being a nandrolone, laurabolin will exhibit noticeable anabolic effects with weaker androgenic side effects. 4.laurabolin has a strong anabolic action with minimal androgenic properties and was specifically designed to promote protein synthesis without the production of undesired (side) effects. This cellular protein synthesis allows the prevention of protein loss through the urea and promotes lean tissue build up. In animals this compound has also been used to correct metabolic deficiencies, malnutrition, anemia and slow maturation

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Nandrolone Cypionate

74 /10 Gram
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  • Min. Order (MOQ) 10 Gram
  • CAS 601-63-8
  • MF C26H38O3
  • MW 398.58
  • Puirty >99%
  • Apperance white powder
  • Certification GMP, HSE, ISO 9001, USP, BP
  • standard Enterprise Standard
  • Usage pharmaceutical material
  • Payment western union, T/T,Moneygrams, Bitcoin

Nandrolone-cypionate is one of the numerous nandrolone compounds on the market; however, it's not as common as the immensely popular and highly available nandrolone-decanoate (deca-durabolin). Deca-durabolin is carried by every supplier on earth and any pharmacy the world over, and after that we have nandrolone-phenylpropionate (durabolin or npp), and then we have nandrolone-cypionate; you may know it best as dynabol. Dynabol is not an inferior form of nandrolone compared to the other more popular forms; it's simply not as widely available and shares so many similarities with deca-durabolin that most suppliers do not feel the need to carry both. At any rate, as we move along with our discussion throughout these pages, you will find nandrolone-cypionate and nandrolone-decanoate to be for all intense purposes identical. Without question, this steroids primary mode of action is in the promotion of lean muscle mass, and it is for that very reason most will supplement. Yes, nandrolone-cypionate can be used in cutting cycles too for secondary purposes, but it is not recommended for most performance enhancers during this phase of use if other items are available. Beyond mass promotion, there are very few anabolic steroids that promote muscular endurance like dynabol, and when it comes to healing and recovery or simply total rejuvenation the nandrolone hormone cannot be beat. This is a steroid that is known for its ability to bring amazing relief to the joints, but it has also been shown to promote recovery in the tendons and ligaments; even in the muscle tissue itself; we're not talking about a masking effect, but direct rejuvenation.

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Nandrolone Propionate

74 /10 Gram
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  • Min. Order (MOQ) 10 Gram
  • Purity >98%
  • CAS 7207-92-3
  • MF C21H30O3
  • MW 330.46
  • Apperance White Crystalline Powder
  • Certification GMP, USP, BP
  • Standard Enterprise Standard
  • Usage It is an effective compound that produces quality, long-lasting muscle gains

Nandrolone propionate is an effective compound that produces quality, long-lasting muscle gains. This is because of the relatively long half-life of the drug (around 8 days). Users report mild side effects, with the biggest side effect being water retention.testosterone propionate is the shortest commonly ester attached to the testosterone hormone for bodybuilding and musclehencement. This means it takes your body the least amount of time to rid itself of the ester and release the parent hormone into the body. Due to its short active life, testosterone propionate typically needs to be injected every other day at a minimum.

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Trenbolone Hexahydrobenzylcarbonate

74 /10 Gram
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  • Min. Order (MOQ) 10 Gram
  • Type manfacturer
  • Brand Name JNJG
  • Packaging Type Discreet packing ways as your requirement, 100% go through.
  • Certification Enterprise Standard
  • Place of Origin China
  • CAS 23454-33-3
  • MF C26H34O4
  • MW 410.55
  • Purity Light Yellow Powder
  • Apperance GMP, ISO 9001, USP
  • Standard Enterprise Standard
  • Usage Parabolan is trenbolone cyclohexylmethylcarbonate
  • Payment western union, bitcoin, T/T, moneygram

Parabolan is trenbolone cyclohexylmethylcarbonate. The half-life of a steroid ester is mostly dependent on its ratio of fat solubility to water solubility: the longer chain the ester, the higher this ratio, and the longer the half-life. This particular carbonate could be most closely compared with an enanthate ester; the half-life is probably a little less than week. Parabolan or trenbolone cyclohexylmethylcarbonate is one of the most highly-rated anabolic steroids and performance enhancing drugs that are admired by one and all in the world of professional sports. The fact that the steroid is five times more potent than testosterone says it all. This means that this steroid can stimulate protein synthesis and muscle growth five times more than testosterone. Product features one of the most powerful (and hard and expensive to obtain) substances in the trenbolone family, parabolan is considered to be a superior product in many ways. Much like finaplix, parabolan can deliver very intense, lean gains without aromatizing in the body. Its half-life is very long, so injections can be spread out over the course of a week every two to three days should be sufficient. the biggest concern with parabolan is that it may be liver and kidney toxic at high doses, although most users report mild to no side effects associated with its use. on its own, parabolan won't aromatize, but when stacked with aromatizing compounds it may exaggerate gynocomastia. Adding nolvadex or winstrol will help counter this. Also, parabolan is a strong androgen receptor agonist, so using hcg at the end of a cycle is recommended.

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Cytadren

74 /10 Gram
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  • Min. Order (MOQ) 10 Gram
  • Brand Name JNJG
  • CAS No. 125-84-8
  • MF C13H16N2O2
  • EINECS No. 204-756-4
  • State solid
  • Purity 98%min
  • Application Inhibit Aromatase and Desmolase
  • Type manfacturer
  • Place of Origin China
  • Appearance White powder
  • CAS 125-84-8
  • MW 232.28
  • Puirty 98%min
  • Apperance White powder
  • Certification GMP, USP, BP
  • Standard Enterprise standard

Arimidex does not have the side effects of aminoglutethimide (Cytadren) and can achieve a high degree of estrogen blockade, much moreso than Cytadren. It is possible to reduce estrogen too much with Arimidex, and for this reason blood tests, or less preferably salivary tests, should be taken after the first week of use to determine if the dosing is correct. As an aromatase inhibitor, Arimidex's mechanism of action - blocking conversion of aromatizable steroids to estrogen - is in contrast to the mechanism of action of anti-estrogens such as clomiphene (Clomid) or tamoxifen (Nolvadex), which block estrogen receptors in some tissues, and activate estrogen receptors in others. During a cycle, if using Arimidex, there is generally no need to use Clomid as well, but (as mentioned in the section on Clomid) there may still be benefits to doing so. Arimidex at 0.5 mgday is usually sufficient for moderate dosages of testosterone and in some cases may be too much.

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femara letrozole

74 /10 Gram
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  • Min. Order (MOQ) 10 Gram
  • CAS 112809-51-5
  • MF C17H11N5
  • MW 285.31
  • Purity 99%
  • Apperance White or light yellow crystal
  • Certification GMP, ISO 9001, USP
  • Standard Enterprise standard
  • Usage Used as API in Treatment of breast disease

Femara is a type of hormone therapy drug used to treat breast cancer in women who have had their menopause. It is also called Femara. Femara lowers the levels of the female sex hormone oestrogen in the body. Oestrogen stimulates some breast cancers to grow. These breast cancers are called hormone sensitive or hormone receptor positive. Femara can stop or slow the growth of these cancers. It can also reduce the chance of a breast cancer coming back after surgery. Femara only works in women who have had their menopause. It is a type of drug called an aromatase inhibitor. After the menopause, women don't produce oestrogen from their ovaries. But they still produce a small amount by using an enzyme called aromatase which turns other sex hormones called androgens into oestrogen. This change happens mainly in fatty tissue, muscle and the skin. Aromatase inhibitors block aromatase so that it can't change the androgen into oestrogen.

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4-chlordehydromethyltestosterone

74 /10 Gram
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  • Min. Order (MOQ) 10 Gram
  • Brand Name JNJG
  • CAS No. 2446-23-3
  • MF C20H27ClO2
  • State solid
  • Purity >99%
  • Application Oral Turninabol is also known as Oral Turinabol (OT) or Pro Turinabol. Turinabol is a derivative of
  • Type manfacturer
  • Place of Origin China
  • Appearance White Powder
  • CAS 2446-23-3
  • MW 334.8854
  • Apperance White Powder
  • Certification GMP, ISO 9001, USP
  • Standard Enterprise Standard

Oral Turinabol is to some extent, enigmatic and prone to misunderstanding.It is not simply a tablet version of injectable Turinabol, or an alkylated version of it. Nor, despite claims, is it an anabolic steroid developed specifically for doping. That claim results from confusion with mestanolone.Structurally, it is Dianabol with an added chlorine at the -4 position, which has the predictable advantage of preventing aromatization. In the case of Oral Turinabol, due to the above structural relation to Dianabol it's commonly called a dry version of it. Now if this were true though, one could tell no difference between using OT alone and using Dianabol plus aromatase inhibitor. There is considerable difference in practice however.OT must be considered its own compound rather than simply as a dry Dianabol. That said, this popular description is not a bad first approximation. Simply be aware of its limitations. Background: Turinabol was developed in the 1960's when East German's were looking for an edge for their Olympic and competitive athletes. It is currently only obtainable through underground labs. Steroid Action: This is a slower acting steroid. When using Turinabol, weight, strength and muscle mass increases will not be overly dramatic; However, they will be of good quality. Turinabol also does not typically create risk for estrogenic side effects, so there is limited water retention or risk for gynecomastia. The user can obtain a hard look to their muscles due to limited water retention. If you really want to boost your natural , and receive all the benefits that come with it ie. Greater muscle mass and strength, improved endurance, enhanced recovery etc. It is the most important product you will ever use!

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Stanozolol Winstrol

74 /10 Gram
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  • Min. Order (MOQ) 10 Gram
  • CAS 10148-03-8
  • MF C21H32N2O
  • MW 328.49
  • Purity >99%
  • Apperance White or White Crystalline Powder
  • Certification ISO 9001, USP, BP
  • Standard USP28/BP2003
  • Usgae can be used as pharmaceutical material

Stanozolol Winstrol is a popular brand name for the anabolic steroid stanozolol. This compound is a derivative of dihydrotestosterone, although its activity is much milder than this androgen in nature. It is technically classified as an anabolic steroid, shown to exhibit a slightly greater tendency for muscle growth than androgenic activity in early studies. While dihydrotestosterone really only provides androgenic side effects when administered, stanozolol instead provides quality muscle growth. The anabolic properties of this substance are still mild in comparison to many stronger compounds, but it is still a ggod, reliable builder of muscle. Its anabolic properties could even be comparable to Dianabol, but Winstrol does not have the same tendency for water retention. Stanozolol also contains the same c17 methylation we see with Dianabol, an alteration used so that oral administration is possible. To spite this design however, there are many injectable versions of this steroid produced. Since stanozolol is not capable of converting into estrogen, an anti-estrogen is not necessary when using this steroid, gynecomastia is not a concern even among the most sensitive individuals. Since estrogen is also the cause of water retention, instead of bulk look, Winstrol produces a lean, quality look with no fear of excess subcutaneous fluid retention. This mkes it a great steroid to use during cutting cycles, when water and fat retention are a major concern. It is also very popular among athletes in combination strengthspeed sports such as Track and Field.

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Oxandrolone

74 /10 Gram
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  • Min. Order (MOQ) 10 Gram
  • CAS 53-39-4
  • MF C19H30O3
  • MW 306.4
  • Purity 99%
  • Apperance White or almost white crystalline powder
  • Certification ISO 9001, USP, BP
  • Standard USP28
  • Usage Oxandrol Anavar can be used as pharmaceutical material. Its main function is to Promote metabolism.

Anavar was the old u.s. Brand name for the oral steroid oxandrolone, first produced in 1964 by the drug manufacturer searle. It was designed as an extremely mild anabolic, one that could even be safely used as a growth stimulant in children. One immediately thinks of the standard worry, "steroids will stunt growth". But it is actually the excess estrogen produced by most steroids that is the culprit, just as it is the reason why women stop growing sooner and have a shorter average stature than men. Oxandrolone will not aromatize, and therefore the anabolic effect of the compound can actually promote linear growth. Women usually tolerate this drug well at low doses, and at one time it was prescribed for the treatment of osteoporosis. As the opinions surrounding steroids began to change in the 1980′s, prescriptions for oxandrolone began to drop. Lagging sales probably led searle to discontinue manufacture in 1989, and it had vanished from u.s. Pharmacies until recently. Oxandrolone tablets are again available inside the u.s. By btg, bearing the new brand name oxandrin. Btg purchased rights to the drug from searle and it is now manufactured for the new purpose of treating hivaids related wasting syndrome. Anavar is a mild anabolic with low androgenic activity. Its reduced androgenic activity is due to the fact that it is a derivative of dihydrotestosterone (dht).

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Oxymetholone

74 /10 Gram
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  • Min. Order (MOQ) 10 Gram
  • Brand Name JNJG
  • CAS No. 434-07-1
  • MF C21H32O3
  • State solid
  • Purity >99%
  • Application It is a corticosteroid, most often used after laser-based refractive surgery
  • Type manfacturer
  • Place of Origin China
  • Appearance white powder
  • CAS 434-07-1
  • MW 332.48
  • Apperance white powder
  • Certification GMP, ISO 9001, USP, BP
  • Standard USP28/BP2003

Anadrol is the strongset effective oral steroid and has an extremely androgenic which hand in hand with an extremely intense anabolic component, by taking the anadrol the athletes experiences an enormous"pump effect" during the workout in the exercised muscles.it self as an anabolic hormone drugs, can promote protein synthesis and inhibiting protein dysplasia, and can lower blood cholesterol, reduce calcium phosphorus excretion and reduce bone marrow suppression, promoting development, promote tissue freshmen and granulation. Caused by long-term use of adrenal cortical hormone have prevention and protection against the adrenal cortex hypofunction. Anadrol is the strongset effective oral steroid and has an extremely androgenic which hand in hand with an extremely intense anabolic component, by taking the anadrol the athletes experiences an enormous"pump effect" during the workout in the exercised muscles. It self as an anabolic hormone drugs, can promote protein synthesis and inhibiting protein dysplasia, and can lower blood cholesterol, reduce calcium phosphorus excretion and reduce bone marrow suppression, promoting development, promote tissue freshmen and granulation. Caused by long-term use of adrenal cortical hormone have prevention and protection against the adrenal cortex hypofunction.

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Ethynodiol Diacetate

74 /10 Gram
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  • Min. Order (MOQ) 10 Gram
  • Brand Name JNJG
  • CAS No. 297-76-7
  • MF C6H6O4
  • State solid
  • Purity 99%
  • Application Orally active progesteron with antiandrogenic activity; has been used in combinations as an oral con
  • Type manfacturer
  • Place of Origin China
  • Appearance white fine powder
  • CAS 297-76-7
  • MW 142.11
  • Apperance white fine powder
  • Cetification GMP, ISO 9001, USP, BP
  • Standard Enterprise standard

Ethinyl estradiol and ethynodiol diacetate is a combination drug that contains female hormones that prevent ovulation (the release of an egg from an ovary). This medication also causes changes in your cervical mucus and uterine lining, making it harder for sperm to reach the uterus and harder for a fertilized egg to attach to the uterus. Ethinyl estradiol and ethynodiol diacetate is used as contraception to prevent pregnancy. Ethinyl estradiol and ethynodiol diacetate may also be used for purposes not listed in this medication guide. Ethynodiol diacetate , or ethynodiol diacetate , is a steroidal progestin which is used as a hormonal contraceptive.relative to other 19-nortestosterone derivatives, it has relatively little or no potency as an androgen, and also unlike most progestins in general, has significant estrogenic effects. Ethynodiol diacetate (inn; sold as continuin, femulen, luteonorm, luto-metrodiol, and metrodiol), orethynodiol diacetate (usan, ban), is a steroidal progestin which is used as a hormonal contraceptive. Relative to other 19-nortestosterone derivatives, it has relatively little or no potency as an androgen and also unlike most progestins in general, has significant estrogenic effects.

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Estradiol

74 /10 Gram
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  • Min. Order (MOQ) 10 Gram
  • Brand Name JNJG
  • CAS No. 50-28-2
  • MF C18H24O2
  • State solid
  • Purity 99%
  • Application It is used to treat low levels of estrogen caused by certain conditions.
  • Type manfacturer
  • Place of Origin China
  • Appearance white powder
  • CAS 50-28-2
  • MW 272.38
  • Apperance white crystalline powder
  • Certification GMP, ISO 9001, USP, BP
  • Standard Enterprise standard

Estradiol, or more precisely, 17β-estradiol, is a human sex hormone and steroid, and the primary female sex hormone. It is named for and is important in the regulation of the estrous and menstrual female reproductive cycles. Estradiol is essential for the development and maintenance of female reproductive tissues[1] but it also has important effects in many other tissues including bone. While estrogen levels in men are lower compared to women, estrogens have essential functions in men as well. Estradiol is found in most vertebrates as well as many crustaceans, insects, fish, and other animal species. Estradiol is produced especially within the follicles of female ovaries, but also in other endocrine (i.e., hormone-producing) and non-endocrine tissues. Estradiol is biosynthesized fromprogesterone (arrived at in two steps from cholesterol, via intermediate pregnenolone). One principle pathway then converts progesterone to its 17-hydroxy-derivative, and then to androstenedione via sequential cytochrome p450-catalyzed oxidations. Action of aromatase on this dione generates estrone, and action of a dehydrogenase on this gives the title compound, 17β-estradiol.

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Progesterone

74 /10 Gram
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  • Min. Order (MOQ) 10 Gram
  • Purity 99%
  • Brand Name JNJG
  • Place of Origin China
  • Appearance White or almost white crystalline powder
  • Function Progesterone is implicated in the etiology of breast cancer
  • CAS 57-83-0
  • MF C21H30O2
  • MW 314.46
  • Apperance White or almost white crystalline powder
  • Certification GMP, ISO 9001, USP, BP
  • Standard USP, EP, BP and IP.
  • Usage It is reasonably anticipated to be a human carcinogen

Progesterone is a female Progesterone Hormones important for the regulation of ovulation and menstruation. Women take progesterone by mouth for inducing menstrual periods who have not yet reached menopause but are not having periods due to a lack of progesterone in the body; And treating abnormal uterine bleeding associated with hormonal imbalance, and severe symptoms of premenstrual syndrome (PMS). Progesterone is also used to prevent overgrowth in the lining of the uterus in postmenopausal women who are receiving estrogen hormone replacement therapy. Progesterone is also used in combination with the hormone estrogen to "oppose estrogen" as part of hormone replacement therapy. If estrogen is given without progesterone, estrogen increases the risk of uterine cancer.

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Corticosteroids

74 /10 Gram
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  • Min. Order (MOQ) 10 Gram
  • CAS 50-22-6
  • MF C21H30O4
  • MW 346.46
  • Purity 99%
  • Apperance White to light yellow powder
  • Certification Enterprise Standard
  • Standard Enterprise Standard

Synthetic pharmaceutical drugs with corticosteroid-like effects are used in a variety of conditions, ranging from brain tumors to skin diseases. Its derivatives are almost pure glucocorticoids, while and its derivatives have some mineralocorticoid action in addition to the glucocorticoid effect. (florinef) is a synthetic mineralocorticoid. Hydrocortisone (cortisol) is available for replacement therapy, e. G. In adrenal insufficiency and congenital adrenal hyperplasia. Synthetic glucocorticoids are used in the treatment of joint pain or inflammation (arthritis), temporal arteritis, dermatitis, allergic reactions, asthma, hepatitis, systemic lupus erythematosus, inflammatory bowel disease (ulcerative colitis and crohn's disease), sarcoidosis and for glucocorticoid replacement in addison's disease or other forms of adrenal insufficiency. Topical formulations are also available for the skin, eyes (uveitis), lungs (asthma), nose (rhinitis), and bowels. Corticosteroids are also used supportively to prevent nausea, often in combination with 5-ht3 antagonists (e. G. Ondansetron). Typical undesired effects of glucocorticoids present quite uniformly as drug-induced cushing's syndrome. Typical mineralocorticoid side-effects are hypertension (abnormally high blood pressure), hypokalemia (low potassium levels in the blood), hypernatremia (high sodium levels in the blood) without causing peripheral edema, metabolic alkalosis and connective tissue weakness. There may also be impaired wound healing or ulcer formation because of the immunosuppressive effects. Clinical and experimental evidence indicates that corticosteroids can cause permanent eye damage by inducing central serous retinopathy (csr, also known as central serous chorioretinopathy, csc). A variety of steroid medications, from anti-allergy nasal sprays (nasonex, flonase) to topical skin creams, to eye drops (tobradex), to have been implicated in the development of csr.

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Oxandrolone

74 /10 Gram
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  • Min. Order (MOQ) 10 Gram

Anavar was the old u.s. Brand name for the oral steroid oxandrolone, first produced in 1964 by the drug manufacturer searle. It was designed as an extremely mild anabolic, one that could even be safely used as a growth stimulant in children. One immediately thinks of the standard worry, "steroids will stunt growth". But it is actually the excess estrogen produced by most steroids that is the culprit, just as it is the reason why women stop growing sooner and have a shorter average stature than men. Oxandrolone will not aromatize, and therefore the anabolic effect of the compound can actually promote linear growth. Women usually tolerate this drug well at low doses, and at one time it was prescribed for the treatment of osteoporosis. As the opinions surrounding steroids began to change in the 1980′s, prescriptions for oxandrolone began to drop. Lagging sales probably led searle to discontinue manufacture in 1989, and it had vanished from u.s. Pharmacies until recently. Oxandrolone tablets are again available inside the u.s. By btg, bearing the new brand name oxandrin. Btg purchased rights to the drug from searle and it is now manufactured for the new purpose of treating hivaids related wasting syndrome. Anavar is a mild anabolic with low androgenic activity. Its reduced androgenic activity is due to the fact that it is a derivative of dihydrotestosterone (dht).

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Drostanolone Enanthate

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  • Min. Order (MOQ) 10 Gram

Drostanolone enanthate is an ester of drostanolone. Drostanolone is indicated in postmenopausal women with recurrent breast cancer, in combined hormone therapy.drostanolone causes retention of nitrogen, potassium, and phosphorus; increases protein anabolism; and decreases amino acid catabolism. The antitumor activity of drostanolone appears related to reduction or competitive inhibition of prolactin receptors or estrogen receptors or production. Drostanolone enanthate 100 usp injection provides drostanolone enanthate, a potent androgenic steroid that has similar characteristics of dihydrotestosterone. Drostanolone is incapable of aromization and therefore it doesn’t convert into oestrogen. Both drostanolone’ anabolic and androgenic activity is far greater than methyl testosterone. The esterification of the 17-beta-hydroxyl group increases the duration of the action of drostanolone. Drostanolone esters in oil injected intramuscularly are absorbed slowly from the lipid phase, thus drostanolone enanthate 100e can be administered at intervals of every 1-2 weeks. Drostanolone enanthate 100 contains drostanolone enanthate in a 10ml solution for injection (100mg drostanolone enanthate ml). Drostanolone enanthate 100 is a yellowish oily solution for intramuscular injection. This is a compound very near and dear to my heart, as I was actually one of the first people in the world to ever use masteron enanthate! I was contacted by the owner of dpharm after writing my original article on masteron, and asked a bunch of questions concerning making this drug with the enanthate ester. It seems that another lab had tried to produce this drug and people were getting sick from it. The attempt to get it right is really a very cool example of an underground lab pushing the frontier of developing anabolic steroids beyond those of the major pharmaceutical houses.

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Fluoxymesterone

74 /10 Gram
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  • Min. Order (MOQ) 10 Gram

1.fluoxymesterone is a man-made form of testosterone, a naturally occurring sex hormone that is produced in a man's testicles. Small amounts of testosterone are also produced in a woman's ovaries and adrenal system. 2.fluoxymesterone is used in men and boys to treat conditions caused by a lack of this hormone, such as delayed puberty or other hormonal imbalances. 3.fluoxymesterone is also used in women to treat breast cancer that has spread to other parts of the body. Fluoxymesterone treats only the symptoms of metastatic breast cancer but does not treat the cancer itself. 4.fluoxymesterone may be taken with or without food. If stomach upset occurs, take with food to reduce stomach irritation. If you miss a dose of fluoxymesterone, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.dosage is based on your medical condition, testosterone blood levels, and response to treatment. We are a comprehensive and high-tech enterprise special in chemical synthetic drug, pharmaceutical intermediates, chemical raw materials, chemical antisepsis, flavor & essence, and food additive, integrating r&d, manufacturing, operating and marketing into an organic whole.

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Cabergoline

74 /10 Gram
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  • Min. Order (MOQ) 10 Gram

Cabergoline is a dopamine agonist designed to reduce prolactin. In medical circles it is commonly used to combat prolactinomas, a benign tumor of the pituitary gland that may cause an excess production of prolactin. It is also used by athletes who supplement with anabolic steroids that may increase prolactin levels cabergoline, most commonly sold under the brand name dostinex, is not a new drug as it was first developed in 1981 by the italian drug manufacture farmitalia-carlo erba spa. the biggest reason why cabergoline is admired by amateur and professional athletes is because it helps them reduce or eliminate the risks associated with excess prolactin that is common with use of harsh and aromatizable steroids like trenbolone and deca durabolin. Furthermore, this drug is also useful for treating sexual dysfunction caused by excess prolactin besides gaining an erection between orgasms and reducing recovery time after intense workouts or weight training and strength training exercises. In addition to these advantages, the use of dostinex is equally beneficial to combat estrogenic side effects such as oily skin, acne, gynecomastia, and bloating and treating health complications like galactorrhea and sexual dysfunction. It is also routinely indicated to patients with parkinson's disease as it has the potential to work on information pathways and nervous system of the body. Dostinex is also admired for its ability to make athletes feel 'full' that helps in minimizing food cravings without dieting discomfort. Cabergoline is an ergot medication and works by blocking the release of prolactin from the pituitary gland. Dostinex is used to treat parkinson's disease, to prevent women producing milk when they want to stop breast feeding(hyperprolactinemia), cabergoline can lower prolactin levels in patients with a pituitary tumor. Cabergoline is also sometimes used to help men with sexual dysfunction.

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Local anesthetic Tetracaine

74 /10 Gram
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  • Min. Order (MOQ) 10 Gram

Tetracaine cas:94-24-6 synonyms:amethocaine;anetain molecular formula:c15h24n2o2 molecular weight:264.36 purity:99% apperance:white crystalline powder state:solid certification:uspiso9001 usage:tetracaine is a topical local anesthetic for the eyes. Tetracaine works by interfering with entry of sodium ions into nerve cells. This reduces the ability of nerves to generate an impulse and send pain sensations. Description: (1) in biomedical research, tetracaine is used to alter the function of calcium release channels (ryanodine receptors) that control the release of calcium from intracellular stores. Tetracaine is an allosteric blocker of channel function. At low concentrations, tetracaine causes an initial inhibition of spontaneous calcium release events, while at high concentrations, tetracaine blocks release completely. (2) tetracaine is the t in tac, a mixture of 5 to 12 per cent tetracaine, 5m(per myriad), a half per mille (0.5‰), or .05 per cent (1 part in 2000) , and 4 or 10 per cent hydrochloride used in ear, nose & throat surgery and in the emergemcy department where numbing of the surface is needed rapidly, especially when children have been injured in the eye, ear, or other sensitive locations. (3) tetracaine is synthesized from 4-butylaminobenzoic acid. The ethyl ester is formed through an acid-catalyzed esterification reaction. Base-catalyzed transesterification is achieved by boiling the ethyl ester of 4-butylaminobenzoic acid with excess 2-dimethylaminoethanol in the presence of a small amount of sodium ethoxide.

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Procaine

74 /10 Gram
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  • Min. Order (MOQ) 10 Gram

Procaine is a local anesthetic drug of the amino ester group. It is used primarily to reduce the pain of intramuscular injection of penicillin, and it is also used in dentistry. Owing to the ubiquity of the trade name novocain, in some regions procaine is referred to generically as procaine. It acts mainly by being a sodium channel blocker.today it is used therapeutically in some countries due to its sympatholytic, anti-inflammatory, perfusion enhancing, and mood enhancing effects. Procaine was first synthesized in 1905, shortly after amylocaine. It was created by the german chemist alfred einhorn who gave the chemical the trade name procaine, from the latin nov- (meaning new) and -caine, a common ending for alkaloids used as anesthetics. It was introduced into medical use by surgeon heinrich braun. Prior to the discovery of amylocaine and procaine, was the most commonly used local anesthetic.[citation needed] einhorn wished his new discovery to be used for amputations, but surgeons preferred general anesthetic. Dentists, however, found it very useful. Einhorn was displeased by this[why?] and spent many years touring dental schools to advise them not to use it.

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Xylocaine

74 /10 Gram
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  • Min. Order (MOQ) 10 Gram

Lidocaine, xylocaine, or lignocaine is a common local anesthetic and class-1b antiarrhythmic drug. Lidocaine is used topically to relieve itching, burning, and pain from skin inflammations, injected as a dental anesthetic, or as a local anesthetic for minor surgery. It is on the world health organization's list of essential medicines, a list of the most important medications needed in a basic healthcare system. Lidocaine is the most important class-1b antiarrhythmic drug; it is used intravenously for the treatment of ventricular arrhythmias (for acute myocardial infarction, digoxin poisoning, cardioversion, or cardiac catheterization) if amiodarone is not available or contraindicated. Lidocaine should be given for this indication after defibrillation, cpr, and vasopressors have been initiated. A routine prophylactic administration is no longer recommended for acute cardiac infarction; the overall benefit of this measure is not convincing.

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Mechano Growth Factor

74 /10 Gram
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  • Min. Order (MOQ) 10 Gram

Pegylated mechano growth is a new and innovative form of mgf that outperforms natural mgf many times over. Mgf is a splice variant of the igf gene which increases stem cell count in the muscle and allows for muscle fibers to fuse and mature. This is a process required for growth of adult muscle. Natural mgf is made locally and does not travel into the bloodstream. Synthetic mgf is water based and when administered intramuscularly, travels into the bloodstream. Mgf is only stable in the blood stream for only a few minutes. Pegylation is the act of attaching a polyethylene glycol (peg) structure to another larger molecule(in this case, mgf). The peg acts as a protective coating and the theory here is that this will allow the mgf to be carried through the blood stream without being broken down.

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Bremelanotide

74 /10 Gram
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  • Min. Order (MOQ) 10 Gram

Bremelanotide, also known as pt-141, is a melanocortin peptide hormone. Bremelanotide (pt-141) was developed from melanotan ii (mt-2) and can be regarded as a derivate from mt-2. Bremelanotide (pt-141) is regarded as the only synthetic aphrodisiac. Studies have shown bremelanotide to be effective in treating sexual dysfunction in both men (erectile dysfunction or impotence) and women (sexual arousal disorder). Unlike and other related medications (pde5s), pt-141 does not act upon the vascular system, but directly through the nervous system (hypothalamus) to increase desire. , cials and levitra are not considered aphrodisiacs as they do not have any direct effect on the libido. However, treatment with pde5 inhibitors and pt-141 are known to have a synergistic effect.

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pentadecapeptide BPC 157

74 /10 Gram
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  • Min. Order (MOQ) 1 Gram

Pentadecapeptide bpc 157, composed of 15 amino acids, is a partial sequence of body protection compound (bpc) that is discovered in and isolated from human gastric juice. Experimentally it has been demonstrated to accelerate the healing of many different wounds, including transected rat achilles tendon. This study was designed to investigate the potential mechanism of bpc 157 to enhance healing of injured tendon. The outgrowth of tendon fibroblasts from tendon explants cultured with or without bpc 157 was examined. Results showed that bpc 157 significantly accelerated the outgrowth of tendon explants. Cell proliferation of cultured tendon fibroblasts derived from rat achilles tendon was not directly affected by bpc 157 as evaluated by mtt assay. However, the survival of bpc 157-treated cells was significantly increased under the h(2)o(2) stress.

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Peptide Ipamorelin

74 /10 Gram
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  • Min. Order (MOQ) 1 Gram

Ipamorelin is a penta-peptide and the strength it displays may very well make regular old gh obsolete. But what athletes and bodybuilders really want to know is what is this wonder peptide capable of doing, how is it used, and how does it compare to the other ghrp peptides. Ipamorelin is a fascinating new muscle building discovery that is getting a lot of attention in the bodybuilding world. It is a synthetic peptide that has powerful growth hormone releasing properties. And these gh releasing properties are what is of interest to athletes and bodybuilders since they can make a tremendous difference in the amount of muscle you can grow and how quickly you burn fat.

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peptide melanotan

74 /10 Gram
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  • Min. Order (MOQ) 1 Gram

Mt-1 (or melanotan i, or afamelanotide, or cuv-1647) is a synthetic analog of peptides nature of endogenous melanocortin peptide alpha-melanocyte stimulating hormone. It has hormones nature as well as common proteins features, its molecular weightmass is 1646.88 and its molecular formula is c78h111n21o19. Afamelanotide was specifically developed by american scientists led by v. Hruby in 1991 as a possible research compound that can be used against skin cancer by stimulating tanning system which in own turn would generate protective natural tan during melanogenesis. So that synthetic analog was created to determine if it can show the same effect and stimulate melanocytes to produce and release melanin to protect skin from uv. Most of studies and trials were conducted in united states and australia.

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peptide follistatin

74 /10 Gram
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  • Min. Order (MOQ) 1 Gram

Follistatin is fascinating protein that can increase muscle mass beyond natural potential by suppressing myostatin. Scientists first identified follistatin while examining porcine (re: pig) follicular fluid in the ovaries. Follistatin is naturally found in the skeletal muscle of almost all mammals with advanced or developed characteristics, such as humans, rodents, and cows. Follistatin is high in the non-essential amino acid cystine but unlike most proteins discussed in the fitness world, follistatin has carbohydrates attached to it. follistatin, specifically follistatin 344 (fs344), quickly gained popularity in the bodybuilding community as a potential supplement to rapidly increase lean tissue mass. Another protein, follistatin-related gene (flrg) acts on similar pathways as fs344 regarding its muscle building properties. Increased lean tissue mass could give a bodybuilder an advantage in a competitive setting and be the differentiating factor between first and second place.

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peptide Oxytocin

74 /10 Gram
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  • Min. Order (MOQ) 1 Gram

Oxytocin is a neurohypophysial mammalian hormone that primarily acts as a neuromodulator in your brain.it is a generic medication that induces labor in females with rh problems preeclampsia, diabetes or in the fetus or the mother best interest.as a medication, it is used to cause contraction of the uterus in order to start labor or increase the speed of labor, and to stop bleeding following delivery.for this purpose, it is given either by injection into a muscle or into a vein.oxytocin is normally produced in the hypothalamus.it plays a role in social bonding, sexual reproduction in both sexes and during or after childbirth.oxytocin is released into the bloodstream as a hormone in response to stretching of the cervix and uterus during labor and with stimulation of the nipples from breastfeeding.it helps with birth, bonding with the baby and milk production.

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17-alpha-Methyl Testosterone steroid powder

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17-alpha-Methyl Testosterone Alias: 17beta-hydroxy-17alpha-methylandrost-4-en-3-one; Mesterone; Andrometh; 17-Methyl Testosterone; Nu-man; Testoviron CAS No: 58-18-4 Molecular formula: C20H30O2 Molecular weight: 302.45 Purity: >99% Appearance: white crystalline powder State: Powder and Liquid Certification: GMP, ISO 9001, USP, BP Suitable for: Adult Packing: 1kgFoil Bag or Tin or as Require, Foil Bag Use: It is used as a feed additive to produce predominately male populations of tilapia Description: Methyltesto-sterone is a 17-alpha-alkylated anabolic steroid used to treat men with a testosterone deficiency. It is also used in women to treat breast cancer, breast pain, swelling due to pregnancy, and with the addition of estrogen it can treat symptoms of menopause. Methyltesto-sterone can promote the male sex organs and used in seedling stage sex change. Methyltesto-sterone is a steroid hormone from the androgen and is found in mammals and other vertebrates, Methyltesto-sterone is primarily secreted in the tests of mails and the ovaries of female, although small amount are also secreted by the adrenal glands, Methyltesto-sterone is the principle male sex hormone and an anabolic steroid. Methyltesto-sterone plays a key role in the development of male reproductive tissue such as the testis and prostates. In addition, Methyltesto-sterone is essential for health and well-being as well as the prevention of osteoporosis, Methyltesto-sterone is conserved through most vertebrates, although fish make a slightly difference from called 11-ketotesto-sterone.

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Nandrolone Laurate Steroid

74 /10 Gram
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Nandrolone laurate Chemical Name: 4-estren-17beta-ol-3-one laurate CAS NO: 26490-31-3 Molecular Formula: C30H48O3 Molecular weight: 456.71 Puirty: >99% Appearance: white or almost white crystalline powder Suitable for: Adult Certification: GMP, ISO 9001, USP Standard: Enterprise Standard Usage: A synthetic , anabolic muscle growthsteroids . Used to promote muscle growth and combat involuntary weight loss . It has also been used to treat cases of osteoporosis . Description: Nandrolone Laurate (Laurabolin), The upside of nandrolone laurate is its remarkable increase in protein synthesis among its users. Nitrogen is a compound needed to increase protein synthesis which in turn helps to build muscles . The muscles that develop when using nandrolone laurate are the lean muscles , meaning that you will gain strength but not necessarily bulkiness . Nandrolone Laurate (Laurabolin), will help to cut off the fat in your system as well so this is recommended for overweight people . For athletes concerned about increasing power in their bodies rather than bulking , nandrolone laurate is recommended . You need to keep in mind however that the protein supply in your body has to be upped by dieting . It increases the red blood cells in your system and promotes healing after strenuous exercises . It increases the strength in the bones by increasing calcium levels

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Steroid Powder Methenolone Enanthate for muscle gain

74 /10 Gram
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  • Min. Order (MOQ) 10 Gram
  • Certification USP, BP
  • CAS 303-42-4
  • MF C27H42O3
  • MW 414.6206
  • Purity >99%
  • Appearance white or off-white crystalline powder
  • Standard Enterprise standard
  • Usage Building Muscle, Burning Fat

Methenolone enanthate cas no: 303-42-4 synonyms: primobolan depot; 1(5a)-androsten-1beta-methyl-17beta-ol-3-one enanthate chemical name: 1(5alpha)-androsten-1beta-methyl-17beta-ol-3-one enanthate chemical formula: c27h42o3 molecular weight: 414.6206 purity: >99% apperance: white or off-white crystalline powder state: solid suitable for: adult certificatoion: usp, bp specification: enterprise standard usage: building muscle, burning fat description: methenolone enanthate is the injectable version of methenolone with a long ester attached to slow absorption of a the active methenolone compound and provide steady blood concentrations. The oral version of this compound is practically identical with the difference being the attached ether (the oral version has a shorter acetate ester attached). Both versions of methenolone are good choices for cutting cycles for men andor women and have shown to maintain muscle while on a low-calorie diet. Methenolone enanthate provides a less frequent administration mode for methenolone and anecdotally appears to require a lower overall dose in order to be as effective as the oral acetate version.

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High quality anti estrogen steroid powder Nolvadex Tamoxifen Citrate

74 /10 Gram
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  • Min. Order (MOQ) 10 Gram
  • CAS 10148-03-8
  • MF C21H32N2O
  • MW 328.49
  • Purity >99%
  • Appearance White or White Crystalline Powder
  • Certification ISO 9001, USP, BP
  • Standard USP28/BP2003
  • Usage can be used as pharmaceutical material

Chemical name: (z)-2-[4-(1, 2-diphenyl-1-butenyl)phenoxyl]-n, n-dimethyl-ethanamine-citrate; 1-p-beta-dimethylaminoethoxyphenyl-trans-1, 2-diphenylbut-1-ene citrate alias:nolvadex, steranabol;turinabol, kessar;noltam;tamofen cas no: 54965-24-1 molecular formula: c26h29no.c6h8o7 molecular weight: 563.64 purity: 99% appearance: white crystalline powder certification: gmp, iso 9001, usp standard: cp2000; usp26 usage:the goods to anti-estrogen fertility inducer, the objects in dysfunctional uterine bleeding, polycystic ovary, menstrual disorders and drug-induced amenorrhea and other gynecologic diseases;it is used as a first line defense against breast cancer. Description: nolvadex (tamoxifen citrate) is very comparable to clomid, behaves in the same manner in all tissues, and is a mixed estrogen agonistantagonist of the same type as clomid. The two molecules are also very similar in structure. It is not correct that nolvadex reduces levels of estrogen: rather, it blocks estrogen from estrogen receptors and, in those tissues where it is an antagonist, causes the receptor to do nothing. The claim that nolvadex reduces gains should not be taken too seriously. The fact is that any number of bodybuilders have made excellent gains while using nolvadex. The belief that it reduces gains seems to stem from the fact that the scientific literature reports a slight reduction (individuals using anabolic steroids were not studied though) from use of nolvadex.

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High quality injectable steriod powder Stanozolol winstrol

74 /10 Gram
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  • Min. Order (MOQ) 10 Gram
  • CAS 434-07-1
  • MF C21H32O3
  • MW 332.48
  • Purity >99%
  • Appearance white powder
  • Certification GMP, ISO 9001, USP, BP
  • Standard USP28/BP2003
  • Usage It is a corticosteroid, most often used after laser-based refractive surgery

Chemical name: 5alpha-androstan-17alpha methyl-17beta ol-[3, 2-c] pyrazole cas no.: 10148-03-8 molecular formula: c21h32n2o molecular weight: 328.49 purity: >99% appearance: white or white crystalline powder state: powder suitable for: adult certification: iso 9001, usp, bp standard: usp28bp2003 usage: can be used as pharmaceutical material description: stanozolol winstrol is a popular brand name for the anabolic steroid stanozolol. This compound is a derivative of dihydrotestosterone, although its activity is much milder than this androgen in nature. It is technically classified as an anabolic steroid, shown to exhibit a slightly greater tendency for muscle growth than androgenic activity in early studies. While dihydrotestosterone really only provides androgenic side effects when administered, stanozolol instead provides quality muscle growth. The anabolic properties of this substance are still mild in comparison to many stronger compounds, but it is still a ggod, reliable builder of muscle. Its anabolic properties could even be comparable to dianabol, but winstrol does not have the same tendency for water retention. Stanozolol also contains the same c17 methylation we see with dianabol, an alteration used so that oral administration is possible. To spite this design however, there are many injectable versions of this steroid produced.

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Lidocaine Anesthetic

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lidocaine Xylocaine CAS: 137-58-6 Synonyms: 2-(Diethylamino)-2', 6'-acetoxylidide;2-(diethylamino)-2, 6'-acetoxylidide;2-(diethylamino)-n-(2, 6-dimethylphenyl)-acetamid;2', 6'-Acetoxylidide, 2-(diethylamino)-;6'-acetoxylidide, 2-(diethylamino)-2;Acetamide, 2-(diethylamino)-N-(2, 6-dimethylphenyl)-;Acetamide, 2-(diethylamino)-N-(2, 6-dimethylphenyl)-;a-Diethylamino-2, 6-acetoxylidide MF: C14H22N2O MW: 234.34 EINECS: 205-302-8 Melting point: 66-69°C storage temp: Store at RT solubility ethanol: 4 mgmL form: powder Water Solubility : practically insoluble Stability: Stable. Incompatible with strong oxidizing agents. Description: Lidocaine is a local anesthetic, also known as Xylocaine, in recent years it has been replaced procaine, widely used in local infiltration anesthesia in cosmetic plastic surgery, it can block the nerve excitability and conduction by inhibiting the sodium channels of nerve cell membrane. The fat soluble and protein binding rate of lidocaine is higher than procaine, its cell penetrating ability is strong, fast onset, long duration of action, the interaction strength is 4 times of procaine. Lidocaine is used in infiltration anesthesia, epidural anesthesia, topical anesthesia (including thoracoscopy or abdominal surgery for mucosal anesthesia) and nerve block. In order to extend the time of anesthesia, reduce the poisoning of lidocaine and other side effects, can be added in the anesthetic epinephrine.

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Procaine anesthetic

74 /10 Gram
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Procaine Synonyms: 2-(Diethylamino)ethyl 4-aminobenzoate;2-(Diethylamino)ethyl p-aminobenzoate;2-(diethylamino)ethylp-aminobenzoate;2-diethylaminoethyl4-aminobenzoate;2-Diethylaminoethylester kyseliny p-aminobenzoove;2-diethylaminoethylesterkyselinyp-aminobenzoove;2-diethylaminoethylp-aminobenzoate;4-Aminobenzoic acid diethylaminoethyl ester CAS: 59-46-1 MF: C13H20N2O2 MW: 236.31 Assay: More than 99% Character: White crystalline powder Certification: GMP, ISO 9001, USP, BP Packing: Foil bag or as requirments Usage: inhibitor of sodium channel Description: Procaine is a kind of local anesthetics. With low toxicity but quick and safe effects, procaine is suitable for local anesthesia, applied to the eye, ear, nose, teeth and other department operation, used for infiltration anesthesia, anesthesia and closed therapy supervisor. Procaine is also used in the production of procaine penicillin.

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Tetracaine anesthetic powder

74 /10 Gram
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Tetracaine cas:94-24-6 synonyms:amethocaine;anetain molecular formula:c15h24n2o2 molecular weight:264.36 purity:99% apperance: white crystalline powder state: solid certification: uspiso9001 usage: tetracaine is a topical local anesthetic for the eyes. Tetracaine works by interfering with entry of sodium ions into nerve cells. This reduces the ability of nerves to generate an impulse and send pain sensations. description: (1) in biomedical research, tetracaine is used to alter the function of calcium release channels (ryanodine receptors) that control the release of calcium from intracellular stores. Tetracaine is an allosteric blocker of channel function. At low concentrations, tetracaine causes an initial inhibition of spontaneous calcium release events, while at high concentrations, tetracaine blocks release completely. (2) tetracaine is the t in tac, a mixture of 5 to 12 per cent tetracaine, 5m(per myriad), a half per mille (0.5‰), or .05 per cent (1 part in 2000) , and 4 or 10 per cent hydrochloride used in ear, nose & throat surgery and in the emergemcy department where numbing of the surface is needed rapidly, especially when children have been injured in the eye, ear, or other sensitive locations.

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Pramoxine hydrochloride anesthetic

74 /10 Gram
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Pramoxine hydrochloride Synonyms: proctofoam; Pramoxine HCL;Praxomine Hydrochloride;Tronothane Hydrochloride;pramocaine Hydrochloride; CAS NO: 637-58-1 Molecular formula: C17H28ClNO3 Molecular weight: 329.8621 Purity: 99% State: powder Apperance: white or almost white crystalline powder Certification: GMP, ISO 9001, USP Suitable for: adult, edlerly Usage: Local anesthetics Description: Pharmacologic study revealed it to be potent and of low acute and subacute toxicity, well tolerated by most mucous membranes and of a low sensitizing index in man. Like other local anesthetics, paramoxine decreases the permeability of neuronal membranes to sodium ions, blocking both initiation and conduction of nerve impulses. Depolarization and repolarization of excitable neural membranes is thus inhibited, leading to numbness.

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Tetracain hydrochloride anesthetic

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Tetracain hydrochloride synonyms: tetracaine hydrochloride;tetracainehcl;pontocaine;tetracaine hcl cas no: 136-47-0 molecualr formula: c15h25cln2o2 molecular weight:300.82 purity:99% apperance:white powder melting point:149°c certification: ups bp usage: local anesthetic; mainly used in mucosa anesthetic. The function is stronger than procaine and lidocaine. Description: tetracaine hcl is synthesized from 4-butylaminobenzoic acid. The ethyl ester is formed through an acid-catalyzed esterification reaction. Base-catalyzed transesterification is achieved by boiling the ethyl ester of 4-butylaminobenzoic acid with excess 2-dimethylaminoethanol in the presence of a small amount of sodium ethoxide. Applciation: tetracaine (inn, also known as amethocaine; trade name pontocaine. Ametop and dicaine) is a potent local anesthetic of the ester group. It is mainly used topically in ophthalmology and as an antipruritic, and it has been used in spinal anesthesia. In biomedical research, tetracaine is used to alter the function of calcium release channels (ryanodine receptors) that control the release of calcium from intracellular stores. Tetracaine is an allosteric blocker of channel function. At low concentrations, tetracaine causes an initial inhibition of spontaneous calcium release events, while at high concentrations, tetracaine blocks release completely.

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Propitocaine hydrochloride anesthetic

74 /10 Gram
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Propitocaine hydrochloride synonyms:prilocainechloride;xylonest cas no:1786-81-8 molecular formula:c13h21cln2o molecular weight:256.77 purity:99% apperance:white powder certification: gmp, hse, iso 9001, usp standard: usp usage:anesthetic (local), pharmaceutical raw materials description: propitocaine hydrochloride is a local anesthetic of the amino amide type first prepared by claes tegner and nils l? fgren. In its injectable form, it is often used in dentistry. It is also often combined with lidocaine as a preparation for dermal anesthesia (lidocaineprilocaine or emla), for treatment of conditions like paresthesia. As it has low cardiac toxicity, it is commonly used forintravenous regional anaesthesia. In some patients, a metabolite of prilocaine may cause the unusual side effect of methemoglobinemia, which may be treated with methylene blue. Application: prilocaine is a local anesthetic of the amino amide type. Prilocaine is often used in dentistry. Prilocaine is also often combined with lidocaine as a preparation for dermal anesthesia (lidocainepril ocaine or emla), for treatment of conditions like paresthesia. W e also supply other hot sell:male sex enhancement hormone, body-building steroids.muscle building steroids;oral anabolic steroids;injectable anabolic steroids;weight loss steroids, etc.

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Procaine hydrochloride anesthetic

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Procaine hydrochloride alias: procaine hydrochloride;aminocaine;anadolor;atoxicocaine; cas no:51-05-8 einecs:200-077-2 molecular formula:c13h21cln2o2 molecular weight:272.77 assay:99% appearance:white crystalline powder melting point: 155-156 °c grade: pharmaceutical grade storage:shading, confined preservation usage: procaine hydrochloride is a kind of local anesthetics, for local anesthesia, nerve block etc, can block the conduction of nerve fibers with anesthetic effect, strong function, low toxicity, and no addiction, but the skin, mucous membrane penetration force is weak, not suitable for surface anesthesia, clinically used to infiltration, spine and conduction anesthesia. Description: procaine hydrochloride is a local anesthetic that can temporarily block the conduction of nerve fibers and has a narcotic effect, the role of strong, low toxicity, and no addiction, but the skin, mucous membranes penetrate weak, suitable for surface anesthesia, patients are used for infiltration, spine and conduction anesthesia.

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Bupivacaine anesthethic

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Bupivacaine synonyms:marcaine;bupivacaine;bupivacaine base;(.+-.)-1-butyl-2', 6'-pipecoloxylidide;1-butyl-2-(2, 6-xylycarbamoyl)piperidine;1-butyl-2', 6'-pipecoloxylidide;1-butyl-2, 6-pipecoloxylidide;1-butyl-n-(2, 6-dimethylphenyl)-2-piperidinecarboxamid cas:2180-92-9 mf:c18h28n2o mw:288.43 assay: 99% appearance: white powder certificaiton: gmp, hse, iso 9001, usp, bp standard: enterprise standard usage: bupivacaine hydrochloride usp is 2-piperidinecarboxamide, monohydrochloride, monohydrate, a white, odorless, crystalline powder that is freely soluble in 95 percent ethanol, soluble in water, and slightly soluble in chloroform or acetone. Description: bupivacaine hydrochloride injection, usp is available in sterile isotonic solution for injection via local infiltration, peripheral nerve block, and caudal and lumbar epidural blocks. Solution of bupivacaine hydrochloride injection, usp may be autoclaved. Solution is clear and colorless.

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Bupivacaine hydrochloride anesthetic

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Bupivacaine hydrochloride synonyms:bupivocoine hcl;bupivacaine hcl;marcaina;bupivacaine hydrochloride anhydrous cas: 14252-80-3 einecs number: 241-917-8 mf: c18h31cln2o2 mw: 342.9039 appearance:white crystalline powder. Assay:99% molecular structure: raw steroid powder local anesthetic usp standard bupivacaine hydrochloride bupivacaine hcl boiling point: 423.4°c at 760 mmhg flash point: 209.9°c vapor pressure: 2.24e-07mmhg at 25°c uses: after local anesthesia for surgery and postoperative analgesia description: bupivacaine hydrochloride injection, usp is available in sterile isotonic solution for injection via local infiltration, peripheral nerve block, and caudal and lumbar epidural blocks. Solution of bupivacaine hydrochloride injection, usp may be autoclaved. Solution is clear and colorless. Application: bupivacaine is related chemically and pharmacologically to the aminoacyl local anesthetics. It is a homologue of mepivacaine and is chemically related to lidocaine. All three of these anesthetics contain an amide linkage between the aromatic nucleus and the amino. They differ in this respect from the procaine-type local anesthetics, which have an ester linkage.

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Proparacaine hydrochloride Anesthetic powder

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Proparacaine hydrochloride Synonyms:chibro-heracaine CAS: 5875-06-9 MF: C16H27ClN2O3 MW: 330.85 EINECS: 227-541-7 Assay: 99% Appearance: White crystalline powder. Certification: ISO9001, ISO14000, KOSHER Standard: Pharma Grade Usage: API Description: Anesthesia, local- Proparacaine and tetracaine are indicated to produce local anesthesia of short duration for ophthalmic procedures including measurement of intraocular pressure, removal of foreign bodies and sutures, and conjunctival and corneal scraping in diagnosis and gonioscopy. Application: Proparacaine hydrochloride and tetracaine are also indicated to produce local anesthesia prior to surgical procedures such as cataract extraction and pterygium excision, usually as an adjunct to locally injected anesthetics.

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