Azelastine EP Impurity C

Product Name Azelastine EP Impurity C
CAT No. CS-T-12256
CAS No. 53242-76-5
Category Impurities
Stock IN-Stock
Mol. Wt. 274.7 g/mol
Mol. For. C₁₅H₁₁ClO₃
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Purity 95%
Therapeutic Antihistamine
Smileys C1=CC=C(C(=C1)C(=O)CC2=CC=C(C=C2)Cl)C(=O)O
Canonical Smiles C1=CC=C(C(=C1)C(=O)CC2=CC=C(C=C2)Cl)C(=O)O
InchIKey BDSINYHJZLINDJ-UHFFFAOYSA-N
Inchl InChI=1S/C15H11ClO3/c16-11-7-5-10(6-8-11)9-14(17)12-3-1-2-4-13(12)15(18)19/h1-8H,9H2,(H,18,19)
IUPAC 2-[2-(4-chlorophenyl)acetyl]benzoic acid
Controlled No
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Azelastine EP Impurity C is a chemical compound that is used as an impurity reference standard in the pharmaceutical industry. It is commonly used in the manufacturing of Azelastine hydrochloride, which is a type of antihistamine medication used to treat allergic rhinitis and other allergic conditions. Chemically, Azelastine EP Impurity C is known as (E)-1-(2-((4-(4-chlorobenzyl)-2-(1H-tetrazol-5-yl)-1H-imidazol-1-yl)methyl)phenyl)-3-phenylprop-2-en-1-one. It is a white to off-white powder that is sparingly soluble in water but soluble in organic solvents such as methanol, ethanol, and DMSO. As an impurity reference standard, Azelastine EP Impurity C is used to ensure the quality and purity of Azelastine hydrochloride. It is important to monitor impurities in pharmaceutical products as they can affect the safety and efficacy of the medication. Azelastine EP Impurity C is also used as a standard for analytical testing methods, such as high-performance liquid chromatography (HPLC) and gas chromatography-mass spectrometry (GC-MS). In conclusion, Azelastine EP Impurity C is a chemical compound that plays an important role in the quality control and manufacturing of Azelastine hydrochloride. Its usage as an impurity reference standard ensures that the medication is safe and effective for patients suffering from allergies.

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