Category
Cefotaxime
CAS Number
66340-33-8
Molecular Formula
C₁₄H₁₃N₅O₅S₂
Molecular Weight
395.41 g/mol
Catalogue Number
MLS-CFT-RC-E
Synonym

 (Z)-2-(2-aminothiazol-4-yl)-N-{(5aR,6R)-1,7-dioxo-1,3,4,5a,6,7- hexahydroazeto[2,1-b]furo[3,4-d][1,3]thiazin-6-yl}-2-(methoxyimino)acetamide;3-Desacetyl Cefotaxime Lactone; (5aR,6R)-6-[[(2Z)-2-(2-Aminothiazol-4-yl)-2-(methoxyimino)acetyl]amino]-5a,6-dihydro-3H,7H-azeto[2,1-b]furo[3,4-d][1,3]thiazine-1,7(4H)-dione;(Z)-2-(2-Aminothiazol-4-yl)-N-[(5aR ,6R )-1,7-dioxo-1,3,4,5a,6,7-hexahydroazeto[2,1-b]furo[3,4-d][1,3]thiazin-6-yl]-2-(methoxyimino)acetamide; Cefotaxime Related Compound E (USP); 

Keywords
Amines
sulphur and selenium compounds
Impurities
Heterocycles
Intermediates
Pharmaceutical Standards
Fine Chemicals
Impurities Manufacturer in India
Impurities manufacturer and Suppliers in Hyderabad india
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Purity:

Above - 95.0%

Technical Data:

We will provide complete documentation support for every Standard Material. All analytical reports such as ¹H NMR, ¹³C NMR, Mass, FT-IR, HPLC Purity/GC Purity/QNMR Purity, Water content by KF/ Loss on Drying/TGA (Thermo-gravimetric Analysis). Certificate of Analysis with potency report. Each Standard Material SER (Structure Elucidation Report) with NMR, Mass, IR spectral interpretation. This whole analytical document can be included in eCTD, ANDA, DMF submissions to regulatory agencies.

Cefotaxime Related Compound E (CAS No. 66340-33-8), with the molecular formula C₁₄H₁₃N₅O₅S₂ and a molecular weight of 395.41 g/mol, is offered by Manasa Life Sciences, a trusted manufacturer and supplier in India. Our services support pharmaceutical manufacturers, analytical laboratories, and research organizations requiring analytical testing, quality control, impurity profiling, synthesis, research and development (R&D), analytical method development, and pharmaceutical characterization.

Manasa Life Sciences provides a comprehensive range of analytical and regulatory documentation, including HPLC, LC-MS/MS, ¹H NMR, ¹³C NMR, FTIR, GC, QNMR, TGA, Potency testing, and Certificate of Analysis (COA). We can also provide Structural Elucidation Reports (SER), MSDS/SDS, regulatory submission documents, and other technical documentation based on customer requirements. Our analytical and documentation services are designed to support applicable ICH, USP, and EP guidelines, helping customers meet requirements for impurity identification, quality control, regulatory submissions, and pharmaceutical research and development.