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Postion:Product Catalog >API>Synthetic Anti-infective Drugs>Antiviral drugs>NELFINAVIR
NELFINAVIR
  • NELFINAVIR
  • NELFINAVIR
  • NELFINAVIR
  • NELFINAVIR
  • NELFINAVIR

NELFINAVIR

Price Get Latest Price
Package 1Kg/Bag 25Kg/Bag 100Kg/Bag
Min. Order: 0.1Kg/Bag
Supply Ability: 20 tons
Update Time: 2024-07-22

Product Details

Product Name: NELFINAVIR CAS No.: 159989-64-7
EC-No.: 1533716-785-6 Min. Order: 0.1Kg/Bag
Purity: 99% up, High Density Supply Ability: 20 tons
Release date: 2024/07/22

Product Information


Product Name:NELFINAVIR
Synonyms:Nelfinavir Regeoisomer;N-tert-butyl-2-[2-hydroxy-3-[[(3-hydroxy-2-methylphenyl)-oxomethyl]amino]-4-(phenylthio)butyl]-3,4,4a,5,6,7,8,8a-octahydro-1H-isoquinoline-3-carboxamide;AG 1341; AG-1341; AG1341;3-isoquinolinecarboxamide,n-(1,1-dimethylethyl)decahydro-2-(2-hydroxy-3-((3-hy;8a-beta))-a-bet;nefinavir;NELFINAVIR;(3S,4aS,8aS)-N-(1,1-Dimethylethyl)decahydro-2-[(2R,3R)-2-hydroxy-3-[(3-hydroxy-2-methylbenzoyl)amino]-4-(phenylthio)butyl]-3-isoquinolinecarboxamide
CAS:159989-64-7
MF:C32H45N3O4S
MW:567.78
EINECS:1533716-785-6
Product Categories:peptides

COA

Item

Standard

Test Results

Identification

A.H-NMR:Comply with the structure

Complies

B.LC-MS:Comply with the structure

Complies

C.The IR spectrum of sample should be identical with that of reference standard.

Complies

D.HPLC-ESI-MSThe retention time of the major peak in the chromatogram of the Assay preparation corresponds to that in the chromatogram of the Standard preparation, as obtained in the Assay.

Complies

Crystallinity

meets the requirements.

Complies

Loss on drying

≤2.0%

0.19%

Heavy metals

≤10 ppm

<10ppm

Water

≤1.0%

0.1%

Sulphated ash

≤0.5% determined on 1.0 g.

0.009%

Residue on ignition

≤0.1%

0.03%

Related Substances

Unspecified impurities: for each impurity ≤0.10%

<0.10%

Total Impurity ≤0.5%

0.18%

Purity

≥99.0%

99.7%

Assay

99.0%~101.0% (anhydrous substance).

99.8%

 

 

Microbiological Analysis

Total plate count ≤1000cfu/g

Complies

Yeast & Moulds ≤100cfu/g

Complies

E. Coli.  Absent

Negative

Salmonella  Absent

Negative

S.aureus  Absent

Negative

Storage

Preserve in well-closed,light-resistant and airtight containers.

Complies

Article illustration


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.

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