Cetirizine Dihydrochloride

Listing ID #3142609

2,400 - 3,500 / Kilogram

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MOQ 25 Kilogram
TypeCetrizine Dihydrochloride Tablet,Bulk Drugs
Supply Type Manufacturer, Exporter, Supplier

Preferred Buyer From : All over the world

Cetirizine is a second-generation antihistamineused in the treatment of hay fever, allergies, angioedema, and urticaria. It is a major metabolite of hydroxyzine, and aracemicselective....

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Product Details

Cetirizine is a second-generation antihistamineused in the treatment of hay fever, allergies, angioedema, and urticaria. It is a major metabolite of hydroxyzine, and aracemicselective receptorantagonist.

MOLECULAR STRUCTURE:

Molecular formula : C₂₁H₂₅ClN₂O_{3_.}2HCl

Molecular weight : 461.8
CAS Number : 83881-52-1
Application : Anti-histamine, Anti allergic
Specification : As per IP/BP/EP/USP
Chemical Name [IUPAC Name]: (RS)-2-[2-[4-[(4-Chlorophenyl)phenylmethyl]piperazin-1-yl]ethoxy]acetic acid dihydrochloride.

Details :

Therapeutic Activity :Anti-histamine, Anti allergic
Standards :IP / BP / EP
CAS. No. :83881-52-1

Specifications

Description	A white or almost white crystalline powder.
Solubility	Freely soluble in water, practically insoluble in acetone, and in methylene chloride.
Appearance of Solution	5%solution is clear and not more intensely colored than reference solution BY7 .
Identifications	Test A,B,C & D as per IP/BP/EP/USP
PH(1 gm in 20 ml water)	1.2 to 1.8
Loss On Drying	Not more than 0.5% w/w.
Sulphated Ash	Not more than 0.2% w/w.
Related Substance ( By HPLC )	Any Individual Impurity : NMT 0.1% Impurity A : NMT 0.1% Impurity B : NMT 0.1% Impurity C : NMT 0.1% Impurity D : NMT 0.1% Impurity E : NMT 0.1% Impurity F : NMT 0.1% Total Impurity : NMT 0.3%
Assay ( On Dried Basis )	99% to 100.5% w/w as C21 H27O3N2Cl3.
Heavy Metals	Not more than 10 ppm

Additional Information

Payment Terms L/C, T/T
Port of Dispatch EX. FACTORY, PANOLI GIDC
Packaging Details We pack material in Fiber Board Drum or HDPE Drum in Double liner Bag with Proper Sealing .
Delivery Time Availability of Product & Confirmation with Customer

Company Details

We, karunesh remedies gmp, glp & iso 9001:2008 certified company established in 2007 and located at gidc industrial estate panoli, near ankleshwar , gujarat, india.
we are manufacturer and exporter of active pharmaceutical ingredients (apis) and pharmaceutical intermediates with standard grade as per pharmacopoeia and customer specification.
We continuously engaged in the developing advanced apis through
r&d using innovative technologies, taking full advantage of our core competencies, equipment, and facilities.