Description

Ceftioxide CAS NO 71048-88-9 is a high-purity chemical intermediate primarily used in the synthesis of advanced pharmaceutical compounds. Its significance lies in its role as a key building block for third-generation cephalosporin antibiotics, which are critical for treating a wide range of bacterial infections. This product is essential for pharmaceutical manufacturers, research institutions, and fine chemical producers focused on developing and producing potent antimicrobial agents.

Application

• Pharmaceutical Intermediate: A crucial precursor in the synthesis of third-generation cephalosporin antibiotics such as Cefotaxime and Ceftriaxone.
• Active Pharmaceutical Ingredient (API) Synthesis: Used in multi-step chemical processes to construct the core β-lactam structure of advanced antibiotics.
• Research & Development: Serves as a standard reference compound and starting material in medicinal chemistry research for novel antibacterial agents.
• Fine Chemical Production: Employed in the manufacture of specialized, high-value chemical entities for the life sciences industry.
• Veterinary Medicine: Used in the development of antibacterial treatments for veterinary applications.

Basic Information

Product Name	Ceftioxide
CAS No.	71048-88-9
Molecular Formula	C16H16N5O7S2
Molecular Weight	454.46 g/mol
Synonyms	(6R,7R)-7-[[(2Z)-2-(2-Amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-3-[[(1-methyl-1H-tetrazol-5-yl)sulfanyl]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid; Cefotaxime Impurity C; Cefotaxime EP Impurity C; Ceftriaxone Intermediate; 7-ACA Derivative; 7-ACT; (6R,7R)-7-[2-(2-Aminothiazol-4-yl)-2-(methoxyimino)acetamido]-3-[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid
EINECS	Contact for details

Quality Control

Our Ceftioxide is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. The product undergoes rigorous analytical testing, including HPLC, NMR, and IR spectroscopy, to confirm identity and purity. Certificates of Analysis (COA) are provided with each shipment, detailing all relevant specifications. Production can be aligned with cGMP guidelines for pharmaceutical applications upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed to prevent moisture absorption, which can affect stability and purity. Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	≥ 98.5%
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.2%
Related Substances (HPLC)	Total impurities ≤ 1.5% Any single impurity ≤ 0.5%
Heavy Metals	≤ 20 ppm

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.