Ebastine EP Impurity A

Product Name Ebastine EP Impurity A
Alternate Names Ebastine Impurities, Impurities of Ebastine
CAT No. CS-T-48645
CAS No. 91-01-0
Category Impurities
Stock IN-Stock
Mol. Wt. 184.23 g/mol
Mol. For. C₁₃H₁₂O
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Ebastine
Therapeutic Antihistamine
Smileys C1=CC=C(C=C1)C(C2=CC=CC=C2)O
Canonical Smiles C1=CC=C(C=C1)C(C2=CC=CC=C2)O
InchIKey QILSFLSDHQAZET-UHFFFAOYSA-N
Inchl InChI=1S/C13H12O/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10,13-14H
IUPAC diphenylmethanol
Controlled No
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Ebastine EP Impurity A is a chemical compound that is commonly used as a reference standard or impurity in the pharmaceutical industry. It is a known impurity in the synthesis of Ebastine, which is an antihistamine drug used to treat various allergic conditions. The chemical name of Ebastine EP Impurity A is 1,3-dihydro-5-(1-piperidinyl)-2H-benzimidazole-2-one. Ebastine EP Impurity A is typically used during the development and testing of Ebastine to ensure that the drug is pure and meets the required specifications. It is also used for quality control purposes during the production of Ebastine to ensure that the final product is safe and effective for patient use. In terms of its chemical properties, Ebastine EP Impurity A is a white to off-white crystalline powder with a molecular weight of 241.31 g/mol. It is sparingly soluble in water but soluble in methanol, ethanol, and DMSO. Overall, Ebastine EP Impurity A plays a crucial role in the pharmaceutical industry as a reference standard and impurity. Its usage and chemical information are important for ensuring the quality and safety of Ebastine and other related drugs.

Related Compounds

Ebastine EP Impurity F | tert-Amyl Ebastine | Ebastine Impurity E fumaric acid | Ebastine EP Impurity B | Ebastine EP Impurity G | Ebastine EP Impurity D |

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