Paroxetine hydrochloride Final API
(-)-(3S,4R)-4-(4-FLUOROPHENYL)-3-[[(3,4-METHYLENEDIOXY)PHENOXY]METHYL]-N-PHENOXYCARBONYLPIPERIDINE (PAROXETINE CARBAMATE)
| Chemical Name | (-)-(3S,4R)-4-(4-FLUOROPHENYL)-3-[[(3,4-METHYLENEDIOXY)PHENOXY]METHYL]-N-PHENOXYCARBONYLPIPERIDINE (PAROXETINE CARBAMATE) |
|---|---|
| CAS No. | 253768-88-6 |
| Molecular Formula | C19H21ClFNO3 |
| Molecular Weight | 365.83 |
| Chemical Structure |
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Paroxetine hydrochloride Final API
(-)-(3S,4R)-4-(4-FLUOROPHENYL)-3-[[(3,4-METHYLENEDIOXY)PHENOXY]METHYL]-N-PHENOXYCARBONYLPIPERIDINE (PAROXETINE CARBAMATE) (CAS Number 253768-88-6) is the final active pharmaceutical ingredient (API) produced at the end of the synthetic route for Paroxetine hydrochloride. It has the molecular formula C19H21ClFNO3 and a molecular weight of 365.83 g/mol. It is supplied as a high-purity reference material to support process development, route verification, and regulatory documentation for Paroxetine hydrochloride manufacturing.
Paroxetine hydrochloride intermediates reference standards are useful in pharmaceutical research. They are useful in product development, ANDA and DMF filing, Quality control (QC), method validation, and stability studies. It is also useful in the identification of unknown intermediates and the assessment of genotoxic potential.
We are the BHAVANISH LIFE SCIENCES specializes in manufacturing and supplying of Paroxetine hydrochloride intermediates that meet specific pharmacopeial standards (USP/EP/BP/IP) as well as process-related intermediates.
This related products or intermediates are thoroughly characterized. Supplied with detailed COA & analytical data Like NMR / MASS / HPLC / GC / IR / TGA / Potency / Structure elucidation data (SER Report) meeting regulatory compliance.
BHAVANISH LIFE SCIENCES provides this compound for research and development and Analytical testing use only, and is not meant for human consumption. With product information including CAS number, molecular formula, molecular weight details.
BHAVANISH LIFE SCIENCES in providing high-quality impurity standards to support pharmaceutical companies in maintaining drug safety and efficacy.
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