Solifenacin EP Impurity A

Product Name Solifenacin EP Impurity A
CAT No. CS-T-39736
CAS No. 22990-19-8
Category Impurities
Stock IN-Stock
Mol. Wt. 209.29 g/mol
Mol. For. C₁₅H₁₅N
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Purity Not less than 90 %
Smileys C1CNC(C2=CC=CC=C21)C3=CC=CC=C3
Canonical Smiles C1CNC(C2=CC=CC=C21)C3=CC=CC=C3
InchIKey PRTRSEDVLBBFJZ-UHFFFAOYSA-N
Inchl InChI=1S/C15H15N/c1-2-7-13(8-3-1)15-14-9-5-4-6-12(14)10-11-16-15/h1-9,15-16H,10-11H2
IUPAC 1-phenyl-1,2,3,4-tetrahydroisoquinoline
Controlled No
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Solifenacin EP Impurity A, also known as (1R,3R,5S)-2-[(1R)-1-phenylethyl]-3,5-dimethylpiperidine, is a chemical compound that is commonly used as a reference standard and impurity in the development and quality control of Solifenacin, which is a medication used for the treatment of overactive bladder syndrome. Solifenacin EP Impurity A is a colorless liquid with a molecular formula of C14H23N and a molecular weight of 205.34 g/mol. It is a chiral molecule that contains a piperidine ring and a phenylethyl group, which are important structural components in several pharmaceuticals. The impurity is commonly synthesized through various chemical reactions, including selective hydrogenation and reduction of ketones. It is also used as a reference standard in analytical testing, such as high-performance liquid chromatography (HPLC), to determine the purity and quality of Solifenacin. In terms of usage, Solifenacin EP Impurity A is used as a reference standard and impurity in the development and quality control of Solifenacin. It is also used in research studies to investigate the pharmacological properties and mechanisms of action of Solifenacin and related compounds. Overall, Solifenacin EP Impurity A plays an important role in the development and quality control of Solifenacin, as well as in the advancement of research in the field of pharmaceuticals.

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