share

Paroxetine Hydrochloride CAS NO 78246-49-8


Unit Price:

CAS No.:78246-49-8

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Paroxetine Hydrochloride CAS NO 78246-49-8 is the hydrochloride salt of paroxetine, a potent and selective serotonin reuptake inhibitor (SSRI). This active pharmaceutical ingredient (API) is critical for the formulation of antidepressant and anti-anxiety medications, offering high pharmacological efficacy. It is primarily required by pharmaceutical manufacturers and research institutions engaged in the development and production of central nervous system (CNS) therapeutics.

Application

  • Pharmaceutical API: Primary active ingredient in the manufacture of antidepressant tablets, capsules, and controlled-release formulations.
  • Generic Drug Production: Serves as the key component for generic versions of branded SSRI medications.
  • Clinical Research: Used in preclinical and clinical studies for investigating new therapeutic applications or dosage forms.
  • Reference Standard: Employed as a high-purity standard in analytical laboratories for quality control and method validation.
  • Drug Development: Utilized in R&D for formulating new combination therapies or improving drug delivery systems.

Basic Information

Product Name Paroxetine Hydrochloride
CAS No. 78246-49-8
Molecular Formula C19H21ClFNO3 • HCl
Molecular Weight 374.29 g/mol (as free base hydrochloride)
Synonyms Paroxetine HCl; (-)-trans-4-(4'-Fluorophenyl)-3-[(3',4'-methylenedioxy)phenoxy]methyl]piperidine Hydrochloride; BRL 29060A; FG 7051; Aropax 20; Paxil; Seroxat; (3S,4R)-3-[(1,3-Benzodioxol-5-yloxy)methyl]-4-(4-fluorophenyl)piperidine Hydrochloride
EINECS Contact for details

Quality Control

Our Paroxetine Hydrochloride is manufactured under strict quality management systems. It undergoes comprehensive analytical testing to ensure it meets high-purity pharmacopeial standards, including identification, assay, impurity profile, and residual solvent analysis. A Certificate of Analysis (COA) documenting compliance with relevant specifications (e.g., USP, EP, or in-house pharmaceutical grade) is provided with each batch.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed in a low-humidity environment to prevent moisture absorption.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to standard
Identification (HPLC) Retention time corresponds to reference standard
Assay (HPLC) 98.0% - 102.0% (on anhydrous basis)
Water Content (KF) ≤ 1.0%
Residue on Ignition ≤ 0.1%
Related Substances (HPLC) Total impurities ≤ 1.0% Any individual impurity ≤ 0.5%
Heavy Metals ≤ 20 ppm

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.

Complete Your RFQ

0/ 2000

Why choose US

Trusted Manufacturer

With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.

Rigorous Quality Assurance

Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

Advanced R&D Expertise

Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.