Pharmaceutical Grade 1190307-88-0 Sofosbuvir For Treatment of Hepatitis C

Short Description:

Purity: ≧98%, White or off-white crystallize powder

Quality Standard: in-house or as required

Certificate: COA, MOA, MSDS, etc

Capacity: 50Kg/Month

Shelf Life: 2 Years

Application: A medication used to treat hepatitis C

Team Advantage: Experienced export sales team with professional training in factory

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Product Detail

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Product Tags

Product name	Sofosbuvir
Synonyms	N-[[P(S),2'R]-2′-Deoxy-2′-fluoro-2′-methyl-P-phenyl-5′-uridylyl]-L-alanine 1-methylethyl ester; PSI 7977
CAS No.	1190307-88-0
Appearance	White or off-white crystallize powder
Molecular Formula	C₂₂H₂₉FN₃O₉P
Molecular Weight	529.45
Usage	Research purpose
Packing	As per your request
Storage	Preserve in tight,light-resistant containers in a cool place

Sofosbuvir Cas: 1190307-88-0
Items	Standard	Results
Appearance	White or off-white crystallize powder	Complies
Identification	The retention time of the principal peak of the sample solution corresponds to that of the standard solution, as obtained in the test for Assay	Complies
Melting point	118.0℃-128.0℃	121.9℃-123℃
Loss on drying	N.M.T. 0.5%	0.16%
Residual on ignition	N.M.T. 0.2%	0.16%
Water	N.M.T. 0.5%	0.10%
Chiral purity	The Rp-isomer: N.M.T. 0.2%	0.01%
Related substance	Impurity A: N.M.T. 0.2%Impurity B: N.M.T. 0.1% Impurity C: N.M.T. 0.1% Any other impurity: N.M.T. 0.2% Total impurities: N.M.T. 1.0%	0.03%Not detected Not detected 0.04% 0.16%
Assay	98.0%~102.0%	98.78%
Residual Solvent	Tetrahydrofuran: N.M.T. 720ppmDichloromethane: N.M.T. 600ppm	0ppm0ppm
Conclusion: complies with the in-house standards.

Company Information

√ Management layer’s full experience in factory and skilled technicians followers;
√ Quality is always our top consideration, Strict QC system;
√ 11 years experienced exporting sales team;
√ Independent R&D lab;
√ Two signed long term GMP workshops;
√ Rich resources of plenty idle factories for customized project;
√ High Efficiency working team with consistent path.
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