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Cefoxitin sodium

pharmaceutical raw materials
Cefoxitin sodium structure

Cefoxitin sodium 

structure
  • CAS No:

    33564-30-6

  • Formula:

    C16H17N3O7S2.Na

  • Chemical Name:

    Cefoxitin sodium

  • Synonyms:

    5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid,3-[[(aminocarbonyl)oxy]methyl]-7-methoxy-8-oxo-7-[(2-thienylacetyl)amino]-,sodium salt (1:1),(6R,7S)-;5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid,3-[[(aminocarbonyl)oxy]methyl]-7-methoxy-8-oxo-7-[(2-thienylacetyl)amino]-,monosodium salt,(6R-cis)-;5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid,3-[[(aminocarbonyl)oxy]methyl]-7-methoxy-8-oxo-7-[(2-thienylacetyl)amino]-,monosodium salt,(6R,7S)-;Cefoxitin sodium salt;Cefoxitin sodium;Cenomycin;Monosodium cefoxitin;Mefoxin;Merxin;Mefoxithin;Mefoxitin;MK 306;Farmoxin;Betacef;Cefaxilin sodium;Sodium cefoxitin;41224-60-6;51829-86-8

  • Categories:

    Active Pharmaceutical Ingredients  >  Antibiotics

Description

Cefoxitin sodium (MK-306) is a cephamycin antibiotic, often grouped with the second generation cephalosporins, acts by interfering with cell wall synthesis, its activity spectrum includes a broad range of gram-negative and gram-positive bacteria.

Cefoxitin sodium Basic Attributes

449.43

449.032745

252-641-2

29419000

Characteristics

205

-0.20700

White to almost white powder

>160°C

843℃

>110°(230°F)

soluble in water or methanol

2-8°C

Intravenous-rat LD50: 8580 mg/kg; Intravenous-mouse LD50: 4970 mg/kg

Thermal decomposition releases toxic nitrogen oxides, sulfur oxides, sodium oxide fumes

25589nm +210° (c = 1 in methanol)

Safety Information

III

9

3077

3

36/37/38-42/43

22-26-36/37-36/37/39

XI0330500

Xn,Xi

The warehouse is low-temperature, ventilated and dry

P280

H317

Toxicity

practically nontoxic

Cefoxitin sodium Use and Manufacturing

Methods of Manufacturing

Compound IV287.1 lg, THF was added to a three-necked reaction flask, cooled, Add 158.97 g of pre-cooled chlorosulfonyl isocyanate in portions and stir until fully reacted. The reaction solution was poured into precooled distilled water, stirred for 2 h, ethyl acetate was added, the insoluble material was filtered and a 10percent sodium chloride solution was added to the filtrate. Stir for 1 Omin. The organic layer was washed with 10percent sodium chloride solution and adjusted to pH 2.0 with 2 mol / L hydrochloric acid. The white crystals were allowed to stand overnight and filtered. The filter cake was washed with ethyl acetate and dried in vacuo. Obatined Cefoxitin acid. Add acetone solution at 30 ° C, add sodium lactate 2.0g, stirring lOmin, then add acetone, the resulting solid filtration drying in vacuum to give cefoxitin sodium 319.59g (yield 95percent, purity 99.5percent).

Uses

An antibiotic derived from Cephamycin C.

Price Analysis

Make your Cefoxitin sodium purchase based on the price and market insights! ECHEMI provides professional market insights with prices for you to make a better choice. Learn more on Cefoxitin sodium prices .

Drug Function and Efficacy

It kills bacteria by inhibiting bacterial cell wall synthesis and has high resistance to β-lactamase produced by bacteria. Some common Gram-positive, Gram-negative aerobic and anaerobic pathogens are highly sensitive to this product. It is resistant to Pseudomonas aeruginosa, most strains of enterococci, and Escherichia coli.

This ingredient has been used in drugs with the following functions (note: it does not mean that the ingredient itself has the following health functions)

Related Drugs

Registered Holders

  • Guangzhou HC Pharmaceutical Co., Ltd.

    China China
    Active
  • China UNION Chempharma (SUZHOU) Co., Ltd.

    China China
    Active
  • Suzhou Wanqing Pharmaceutical Co., Ltd.

    China China
    Active

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