Ravi Chemicals

Gota, Ahmedabad, Gujarat

• Moles5
• HLB9.1

Nonyl phenol ethoxylate glycol ether producer and the only plant in India to use a continuous process with world-renowned Sulzer Chemtech technology.

• HLB3.66
• Moles1

• HLB8.0
• Moles3

Fatty acid Ethoxylate produced by the reaction of ethylene oxide with Fatty acid i.e. Coconut oil fatty acid, Stearic acid, oleic acid. IGL offer a wide range of Lauric acid, Coconut oil fatty acid, Stearic acid and oleic acid ethoxylates in the brand name of stexel with various moles of ethylene oxide. These products find application in textile formulation and the manufacture of spin finishes.

• Purity99%
• CAS No224785-91-5
• APPERANCEWHITE POWDER
• PLACE OF ORIGININDIA
• GRADEMEDICINAL

We are offering 99% high purity vardenafil hydrochloride powder. It is used to manufacture "bulk drugs" in the form of tablet, capsule etc. Specification of vardenafil hcl trihydrate ihs sr. No. test specification 1. description - white to off-white crystalline powder. 2. solubility- soluble in water, ethanol. 3. identification - a. Ir spectrum ir spectrum of test sample should be concordant with that of the standard. b. Hplc the retention time of the major peak for vardenafil in the chromatogram of the assay preparation corresponds to that in the chromatogram of the standard preparation, as obtained in the assay 4. melting point - 227°c to 235°c 5. heavy metals - not more than 20 ppm 6. residue on ignition - not more than 0.1 % 7. water - 8.0 % to 10.0% 8. related substances i) single max. Impurity not more than 0.5% ii) total maximum impurities not more than 2.0 % 9. residual solvents - methanol nmt 3000 ppm, acetone nmt 5000 ppm 10. assay - not less than 98.0 % to not more than 102 % on anhydrous basis comments on specification: the material conforms to ihs.

• Purity99%
• GradeMEDICINAL
• APPERANCEWHITE POWDER
• Country of OriginIndia
• CAS NO129938-20-1

We are offering dapoxetine hcl. 99% high purity dapoxetine hydrochloride powder. It is used to manufacture "bulk drugs" in the form of tablet, capsule etc SPECIFICATIONS :- SR. NO. TEST SPECIFICATION 1. Appearance White to off white, crystalline powder. 2. Solubility - Soluble in methanol. 3. Identification - The retention time of the Dapoxetine Hydrochloride peak in the chromatogram of the test preparation should correspond to that in the chromatogram of the standard preparation as obtained in the Assay. 4. Loss on drying - Not More than 1.0 per cent 5. Residue on ignition - Not More than 0.1 per cent 6. Heavy metals - Not More than 10 ppm 7. Related Substance By HPLC - The area of any secondary peak in the chromatogram is not more than 0.5% and the sum of all secondary peaks is not more than 1.0%, calculated by area normalization. 8. Assay - 99.0 per cent to 101.0 per cent (dried substance) Comments on specification: The material conforms to IHS.

• MOQ NEGOTIABLE Box
• PurityNLT 98% TO NMT 102%
• Number Of FlowerANTIDIABETIC
• CAS No.83480-29-9
• Country of OriginIndia

we offer voglibose. antidiabetic. used in bulk drug formulation. specification of voglibose ip sr. no. test specification 1. description a white to off white crystalline powder. 2. solubility soluble in water and slightly soluble in methanol. 3. identification by ir the ir absorption spectrum of the sample is concordant with that of voglibose reference standard. 4. ph 9.0 to 10.4 5. specific optical rotation [α]d20 +450 to +480 6. related substances any other impurity, total impurity (by hplc) not more than 0.5% not more than 1.0% 7. heavy metals not more than 10 ppm. 8. water content - not more than 1.0% ww. 9. sulphated ash - not more than 0.1% ww. 10. assay nlt 98.0 % to nmt 102.0 % calculated on the anhydrous bases. comments on specification: the material conforms to ihs.

• CAS No52-49-3

We are offering trihexyphenidyl hcl/ benzhexol hcl. Antiparkinsonian, anticholinergic. Used in bulk drug formulation specification of trihexyphenidyl hcl (benzhexol hcl)ip sr. No. test specification 1. description a white or almost white, crystalline powder. 2. solubility slightly soluble in water, sparingly soluble in ethanol and in methylene chloride. 3. melting point about 2500c, with decompisition 4. identification a) infrared absorption spectrophotometry ir spectrum of the sample should be concordant with standard b) by melting point the precipitate is produced which after recrystallization from methanol melts at about 1130c to 1150c c) it give reaction (a) of chlorides to comply the test 5. ph 5.2 to 6.2 6. sulphated ash not more than 0.1 %. 7. loss on drying not more than 0.5 % 8. related substances impurities a :nmt 0.5% , unspecified impurities :nmt 0.10% total impurities nmt 0.5 % 9. optical rotation -0.100 to +0.10° 10. assay not less than 98.0 % and not more than 101.0 % ; on dried bases comments on specification: the material conforms to ip.

• MOQ NEGOTIABLE Kilogram
• CAS No.171596-29-5
• Purity99%
• Country of OriginIndia
• Number Of FlowerMALE ERECTILE DYSFUNCTION

we are offering Tadalafil. Male erectile dysfunction. Used in bulk drug formulation. Specification of tadalafil ihs sr. No. test specification 1. description a white or off-white crystalline powder. Odourless. 2. solubility practically insoluble in water. Freely soluble in dimethyl sulfoxide (dmso) .slightly soluble in methylene chloride. 3. identification (a) infrared absorption specrophotometry - the infrared absorption spectrum of substance being examined must be concordant with the ir spectrum obtained from tadalafil working standard. (b) by hplc - the retention time of the major peak for sample corresponds to that of the identification solution as obtained in the test for assay. (c) specific optical rotation +78.00 to +84.00. 4. loss on drying not more than 0.5% 5. sulphated ash not more than 0.1% 6. related substance by hplc-total impurities not more than 3 times the area of the principal peak in the chromatogram obtained with reference solution (a) (0.3 per cent) 7. impurities a, b and c  — impurity a: not more than 1.5 times the area of the principal peak in the chromatogram obtained with reference solution (b) (0.15 per cent);  — unspecified impurities: for each impurity, not more than the area of the principal peak in the chromatogram obtained with reference solution (b) (0.10 per cent). 8. assay not less than 99.0% and not more than 101.0% of c22h19n3o4, calculated on the dried basis. Comments on specification: the material conforms to ihs.

• MOQ NEGOTIABLE Kilogram

we are offering Ivermectin. ANTHELMINTIC. USED IN BULK DRUG FORMULATION

• MOQ NEGOTIABLE Box
• Number Of FlowerAPI FOR BULK DRUG FORMULATION
• CAS NO71675-85-9

We are offering amisulpride, antipsychotic. Used in bulk drug formulation specifications :-