Pharmaceutical Cetirizine Hydrochloride Raw Material Cetirizine Hydrochloride Anti-Allergic Cetirizine HCl

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Xi`an Disheng Health Biotechnology Co., Ltd.

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D-sung Cetirizine Hcl/Cetirizine Hydrochloride
Yes
Customized
GMP, HSE, ISO 9001, USP, BP
Elderly, Children, Adult
Solid
>99%
2
C21h27cl3n2o3
461.81
83881-52-1
222-225-5
Easily Soluble
1.237 G/Cm³
281.6 ºC
S26;S36
Xn
3249
53.01000
3.82600
AG0977500
D-sung
Negotiable
99%
Shaanxi Xi'an
2933599090
Product Description
Pharmaceutical Cetirizine Hydrochloride Raw Material Cetirizine Hydrochloride Anti-Allergic Cetirizine Hcl
Product Description

Product Details

Product Name:Cetirizine hydrochloride
Synonyms:(2-(4-((4-chlorophenyl)phenylmethyl)-1-piperazinyl)ethoxy)aceticaciddihydro;2-[2-[4-[(4-chlorophenyl)-phenyl-methyl]piperazin-1-yl]ethoxy]acetic acid dihydrochloride;Cetirizine Hydrochloride (250 mg);Alercet;Alerid;Cesta;Cetiriz;Cetrak
CAS:83881-52-1
MF:C21H26Cl2N2O3
MW:425.35
EINECS:620-533-8
Cetirizine hydrochloride is an antiallergic drug, a new generation H1 receptor antagonist, and a second generation H1 antihistamine.
Application&Function

Function
Cetirizine is indicated for respiratory, skin and ocular allergic diseases, including perennial allergic diseases such as allergic skin diseases, hives, allergic rhinitis, itchy eyes, conjunctivitis and asthma. This product is also used to treat various types of dermatological allergic diseases. Such as for chronic, artificial, cold, delayed stress, solar measles and atopic dermatitis. This product is also an effective drug for rapid whealing and rapid-onset nucleus and itching caused by mosquito bites.
Application

Cetirizine Hydrochloride is a second-generation H1 antihistamine that is a long-acting, selective oral potent antiallergic drug. H1 receptor antagonists have good anti-allergic reactions and are commonly used in allergic rhinitis, allergic skin itching, conjunctivitis and the like. Compared with its similar drugs such as diphenhydramine, promethazine and chlorpheniramine, cetirizine hydrochloride has a polar polarity and rarely crosses the blood-brain barrier, thus greatly reducing the central sedative effect and selective action. At the H1 receptor, there is little effect on the muscarinic choline receptor and the 5-HT receptor, so there are few side effects associated with anticholinergic activity.

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