Catégorie
Cefepime
Numéro CAS
65872-41-5
Formule moléculaire
C₆H₇N₃O₃S
Masse moléculaire
201.20 g/mol
Numéro de catéologue
MLS-CFP-RC-D
Synonyme

((Z)-2-(2-aminothiazol-4-yl)-2-(methoxyimino)acetic acid) ; syn-Thiazoximic Acid; (Z)-2-Amino-alpha-methoxyimino-4-thiazoleacetic acid; 2-amino-a-(methoxyimino)-4-thiazoleacetic acid; 2-(2-amino-1,3-thiazol-4-yl)-2-(methoxyimino)acetic acid ; Thiazolylglyoxalic Methyloxime (Cefepime Related Compound D) ;(2Z)-(2-aminothiazol-4-yl)(methoxyimino)acetic acid ; Cefepime EP Impurity D ; Cefepime Impurity D;

Mots-clés
Organic Acids
Amines
Intermediates
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.

Cefepime Related Compound D (CAS No. 65872-41-5), with the molecular formula C₆H₇N₃O₃S and a molecular weight of 201.20 g/mol, is offered by Manasa Life Sciences, a trusted manufacturer and supplier in India. We support pharmaceutical and research organizations with high-quality solutions for analytical testing, quality control, impurity profiling, synthesis, research and development (R&D), method development, and pharmaceutical characterization.

Manasa Life Sciences provides comprehensive analytical and regulatory documentation for Cefepime Related Compound D, including HPLC, LC-MS/MS, ¹H NMR, ¹³C NMR, FTIR, GC, QNMR, TGA, Potency testing, and Certificate of Analysis (COA). Based on customer requirements, we can also provide Structural Elucidation Reports (SER), MSDS/SDS, regulatory submission documentation, and other supporting technical documents.

Our services are designed to support ICH, USP, and EP regulatory guidelines, helping customers meet their requirements for quality control, impurity identification, analytical method development, regulatory submissions, and pharmaceutical research and development.