Cetirizine EP impurity B

Product Name Cetirizine EP impurity B
Alternate Names Cetirizine Impurities, Impurities of Cetirizine
CAT No. CS-T-14604
CAS No. 113740-61-7
Category Impurities
Stock IN-Stock
Mol. Wt. 344.84 g/mol
Mol. For. C₁₉H₂₁ClN₂O₂
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Cetirizine
Purity 95%
Therapeutic Antihistamine
Smileys ClC1=CC=C(C=C1)C(C2=CC=CC=C2)N3CCN(CC(O)=O)CC3
Canonical Smiles C1CN(CCN1CC(=O)O)C(C2=CC=CC=C2)C3=CC=C(C=C3)Cl
InchIKey NBQBQRKLQXVPIS-UHFFFAOYSA-N
Inchl InChI=1S/C19H21ClN2O2/c20-17-8-6-16(7-9-17)19(15-4-2-1-3-5-15)22-12-10-21(11-13-22)14-18(23)24/h1-9,19H,10-14H2,(H,23,24)
IUPAC 2-[4-[(4-chlorophenyl)-phenylmethyl]piperazin-1-yl]acetic acid
Controlled No
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Cetirizine EP impurity B is a chemical compound that is commonly used as a reference standard in analytical laboratories to assist in the identification and quantification of cetirizine impurities in drug formulations. It is also used in research and development to study the pharmacological effects and metabolism of cetirizine. Chemically, Cetirizine EP impurity B is known as 2-[4-(biphenyl-4-ylmethyl)piperazin-1-yl]acetic acid. This compound is a derivative of cetirizine, which is a second-generation antihistamine drug used to treat symptoms of allergies such as sneezing, runny nose, and itching. Cetirizine EP impurity B is a white crystalline powder that is soluble in water and organic solvents like methanol and ethanol. The usage of Cetirizine EP impurity B is of great importance in the pharmaceutical industry because it helps to ensure the safety and efficacy of drug formulations containing cetirizine. Impurities can affect the quality of drugs, and thus, it is necessary to monitor their presence and levels in drug formulations. The availability of Cetirizine EP impurity B as a reference standard makes it easier for analytical laboratories to accurately identify and quantify cetirizine impurities in drug formulations. In conclusion, Cetirizine EP impurity B is a useful compound in the pharmaceutical industry, assisting in the identification and quantification of cetirizine impurities in drug formulations. Its chemical properties make it a suitable reference standard for analytical laboratories, and it plays a critical role in ensuring the safety and efficacy of cetirizine-containing drugs.

Related Compounds

Cetirizine S-Isomer di HCl | Levocetirizine Ethyl ester impurity | Cetirizine Impurity G | Cetirizine EP Impurity C | Cetirizine EP Impurity D Dihydrochloride | Cetirizine EP Impurity E Di Hydrochloride | Cetirizine EP Impurity F | Cetirizine 3-Chloro Impurity | tert-Butyl Cetirizine | Cetirizine Amide | Cetirizine EP Impurity B Ethyl Ester | Cetirizine Amide Dihydrochloride | Cetirizine Lactose Ester(Technical Grade) (α/β-mixture, mixture of diastereomers) | Deschloro Cetirizine Dihydrochloride | Cetirizine Impurity BHA | Cetirizine S-Isomer | Cetirizine Sorbitol Ester Impurity Hydrochloride | Levocetirizine Lactose ester | Cetirizine Impurity C Dihydrochloride | Cetirizine Impurity BHT | Cetirizine Glycerol Ester Impurity Hydrochloride | Cetirizine impurity B di Hydrochloride | Levocetirizine benzyl | Cetirizine EP Impurity E | Cetirizine USP Related Compound A | Cetirizine Lactose Ester HCl salt | Cetirizine 3-Chloro | Levocetirizine Impurity 1 | Cetirizine Polyethylene Glycol (PEG) Ester | Cetirizine 1-​[(4-​Chlorophenyl)​phenylmethyl]​piperazine Amide | N-Tosyl Cetirizine EP impurity A | Cetirizine Impurity G | Cetirizine Dimer dihydrochloride | Cetirizine Impurity 7 | Cetirizine Methyl Ester Dihydrochloride | Cetirizine Impurity D | Cetirizine EP impurity A | Cetirizine USP Related Compund A (2HCl salt) | Cetirizine Impurity 15 DiHCl | Cetirizine Glycerol Ester | Cetirizine Impurity E Sodium Salt |

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