باب
Cefepime
رقم CAS
66340-33-8
الصيغة الجزيئية
C₁₉H₂₈Cl₂N₆O₆S₂
وزن جزيئي
571.50 g/mol
رقم كاتلوج
MLS-CFP-STD
مرادف

(6R,7R)-7-[[(2Z)-(2-Aminothiazol-4-yl)(methoxyimino)acetyl]amino]-3-[(1-methylpyrrolidinio)methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate Chloride hydrochloride monohydrate ; Pyrrolidinium, 1-[(7-{[(2-amino-4-thiazolyl)(methoxyimino)acetyl]amino}-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl]-1-methyl-, chloride, monohydrochloride, monohydrate, [6R-[6α,7β(Z)]]-; (6R,7R)-7-((Z)-2-(2-aminothiazol-4-yl)-2-(methoxyimino)acetamido)-3-((1-methylpyrrolidin-1-ium-1-yl)methyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate hydrate

الكلمات الرئيسية
Chiral standards
Heterocycles
Pharmaceutical Standards
Intermediates
Fine Chemicals
sulphur and selenium compounds
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 Hydrochloride (CAS No. 123171-59-5), molecular formula C₁₉H₂₈Cl₂N₆O₆S₂, and molecular weight 571.50 g/mol, is available from Manasa Life Sciences, a trusted manufacturer and supplier in India, serving the needs of pharmaceutical and analytical industries for quality control, analytical testing, impurity profiling, synthesis, method development, research, and development (R&D). We offer comprehensive characterization and regulatory documentation, including HPLC, LC-MS/MS, ¹H NMR, ¹³C NMR, FTIR, GC, QNMR, TGA, Potency testing, and COA, along with Structural Elucidation Reports (SER), MSDS/SDS, regulatory submission documents, and other customized technical documentation. Our services are aligned with relevant ICH, USP, and EP guidelines, supporting pharmaceutical characterization, impurity identification, analytical method development, regulatory compliance, quality assessment, and research and development activities.