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HomecompanyParoxetine Hydrochloride powder
Paroxetine Hydrochloride

Paroxetine Hydrochloride powder

Price Get Latest Price
Packge 25Kg/Bag
  • Min. Order:2Kg/Bag
  • Supply Ability:20 tons
  • Time:2022-06-10

Product Details

  • Product NameParoxetine Hydrochloride
  • CAS No.78246-49-8
  • EINECS No.616-601-1
  • MFC19H21ClFNO3
  • MW365.83
  • Appearanceneat
  • Melting point 129-131°C
  • storage temp. 2-8°C

Product Information

Product NameParoxetine Hydrochloride
CAS No.78246-49-8
Synomyms(3s,4r)-orid;(3s-trans)-id;3-((1,3-benzodioxol-5-yloxy)methyl)-4-(4-fluorophenyl)-,hydrochloride,(3s-trans)-piperidin;3-((1,3-benzodioxol-5-yloxy)methyl)-4-(4-fluorophenyl)-piperidinhydrochl;3-((1,3-benzodioxol-5-yloxy)methyl)-4-(4-fluorophenyl)-piperidinhydrochlor;brl29060a;brl29060hydrochloride;BRL-29060
Molecular FormulaC19H21ClFNO3
Molecular Weight365.83
Melting Point129-131°C
Purity>99%
Physical StateWhite Powder
Usage1.This product is a new type of antidepressant that can be used in all types of depression.
2.Treat various types of depression. Includes depression with depression and reactive depression. Common depressive symptoms: fatigue, sleep disorders, lack of interest and pleasure in daily activities, loss of appetite. After the treatment is satisfactory, continue taking the product to prevent recurrence of depression.

COA 

ContentsSpecification: EP7.0Results of analysis
Appearance
 
White or almost white crystalline powderAlmost white crystalline powder
Identification
 
Comparing with the spectrum obtained with CRSConform 

The principal peak obtained with the test solution is similar in retention and size to that obtained with the reference solutionConform 

Water (by KF) Conform 

Reaction of chlorides Conform
Impurity D
 
≤0.2%Did not check out
Related substancesImpurity A: not more than 0.3%0.03%

Unspecified impurities: For each impurity, not more than 0.10 %0.06%

Total impurities: not more than 0.5%0.1%
Heavy metals≤0.002%<0.002%
Water
 
2.2%~2.7%2.46%
Sulfated ash≤0.1%<0.1%
Assay(anhydrous substance)97.5%~102.0%100.2%
Residual solventsMeets the requirementsConform 
Conclusion: Conforming to EP7.0. 

Company Informatio






Company Profile Introduction

Sinoway Industrial co., ltd. was established in 1987 in Xiamen, China, and now has been a leading group specialized in research, development, custom manufacturing and trading of pharmaceutical intermediates, APIs, health and food supplements, cosmetic raw materials, herbal extracts, polypeptides and prostaglandin derivatives, etc.. We have passed ISO9001:2015. With qualified products, competitive price and excellent service, we have received great reputation of our customers from all over the world, including Southeast Asia, Europe, North America, South America, Middle East and other countries. We have over 20 years good partners in Japan、Korea and Switzerland. Sinoway has a professional R&D team. We have built close cooperative relationships with many research institutes and universities in China. Moreover, Sinoway combines market analysis with technology, providing new business trends to our clients. In addition, we have very close cooperation relationships with many Chinese pharmaceutical factories. These pharmaceutical manufacturers have GMP regulated workshops, advanced production and testing equipments, first-class QC labs and a production team with rich experience. We can supply various Active Pharmaceutical Ingredients and finished products which meet EP/USP/BP standards. Chinese GMP, EU-GMP, COS/CEP certificates with DMF documents are available, and many products have been approved by FDA. We believe that quality and innovation are vital for an enterprise. Adhering to the business philosophy of integrity and win-win cooperation, Sinoway is looking forward to have a bright future with you together.
  • Since:1996-07-16
  • Address: Fujian China ,16F, Huicheng Comm. Complex, 839 Xiahe RD.
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