Description

Cefcanel is a synthetic cephalosporin antibiotic intermediate of significant importance in pharmaceutical manufacturing. Its primary value lies in its role as a key building block for the synthesis of advanced antibiotic compounds, ensuring high-purity inputs for critical drug production processes. This product is essential for research institutions, pharmaceutical companies, and fine chemical suppliers engaged in the development and production of next-generation antibacterial agents. We supply Cefcanel CAS NO 41952-52-7 to the global market with a commitment to consistent quality and reliable supply chain logistics.

Application

Cefcanel serves as a crucial intermediate in several high-value pharmaceutical and research applications:

• Active Pharmaceutical Ingredient (API) Synthesis: Core building block in the manufacturing of cephalosporin-class antibiotics.
• Pharmaceutical Research & Development: Used in medicinal chemistry for the design and testing of novel antibacterial compounds.
• Fine Chemical Production: Intermediate for producing more complex, specialized chemical entities in controlled synthesis.
• Reference Standard: Serves as a high-purity standard for analytical method development and quality control in pharmaceutical labs.

Basic Information

Product Name	Cefcanel
CAS No.	41952-52-7
Molecular Formula	C20H21N5O7S2
Molecular Weight	507.54 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; Cefcanelum; FK 037; FR 21818; (6R,7R)-7-[(Z)-2-(2-Aminothiazol-4-yl)-2-methoxyiminoacetamido]-3-[(1-methyl-1H-tetrazol-5-yl)thiomethyl]-3-cephem-4-carboxylic acid
EINECS	Contact for details

Quality Control

Our Cefcanel is produced and tested under a strict quality management system. Each batch undergoes rigorous analytical testing to ensure it meets the high-purity standards required for pharmaceutical intermediate applications. Certificates of Analysis (COA) documenting identity, purity, and impurity profiles are available upon request to support your quality assurance and regulatory compliance needs.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (typically 15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after each use to prevent degradation from atmospheric moisture.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to structure
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.5%

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