Cetirizine EP Impurity C

Product Name Cetirizine EP Impurity C
Alternate Names Cetirizine Impurities, Impurities of Cetirizine
CAT No. CS-O-07601
CAS No. 83881-59-8
Category Impurities
Stock IN-Stock
Mol. Wt. 461.81 g/mol
Mol. For. C₂₁H₂₇Cl₃N₂O₃
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Cetirizine
Purity Not less than 90 %
Therapeutic Antihistamine
Smileys O=C(O)COCCN1CCN(C(C2=CC=CC=C2Cl)C3=CC=CC=C3)CC1.[H]Cl.[H]Cl
Canonical Smiles C1CN(CCN1CCOCC(=O)O)C(C2=CC=CC=C2)C3=CC=CC=C3Cl
InchIKey AMWZYEYIOPBLEO-UHFFFAOYSA-N
Inchl InChI=1S/C21H25ClN2O3/c22-19-9-5-4-8-18(19)21(17-6-2-1-3-7-17)24-12-10-23(11-13-24)14-15-27-16-20(25)26/h1-9,21H,10-16H2,(H,25,26)
IUPAC 2-[2-[4-[(2-chlorophenyl)-phenylmethyl]piperazin-1-yl]ethoxy]acetic acid
Controlled No
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Cetirizine EP Impurity C is a chemical compound that is used as a reference standard in the analysis of cetirizine, which is an antihistamine drug used to treat allergies. This impurity is also known as 1,2,3,4-tetrahydro-4-oxoquinazoline, and its molecular formula is C8H7N3O. It is a white to off-white crystalline powder that is soluble in organic solvents like methanol and acetonitrile. The chemical structure of Cetirizine EP Impurity C contains a quinazoline ring, which is also present in cetirizine. This impurity is formed during the synthesis of cetirizine, and its presence can affect the purity and potency of the drug. Therefore, it is important to monitor the levels of this impurity in the drug during its manufacture and storage. Cetirizine EP Impurity C is typically used as a reference standard in analytical methods like high-performance liquid chromatography (HPLC) and gas chromatography (GC). These methods are used to determine the purity and content of cetirizine in drug formulations and raw materials. The impurity can be quantified by comparing the peak areas or heights of the impurity and the drug in the chromatogram. Overall, Cetirizine EP Impurity C is an important chemical reference standard that is used in the analysis of cetirizine. Its chemical properties and usage make it an essential tool in the quality control of cetirizine and its related products.

Related Compounds

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

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