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| CEFTIOFUR SODIUM | ||
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PRODUCT IDENTIFICATION |
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| CAS NO. | 80370-57-6 |
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| EINECS NO. | ||
| FORMULA | C19H16N5O7S3·Na | |
| MOL WT. | 544.53 | |
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H.S. CODE |
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| DERIVATION |
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TOXICITY |
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| CLASSIFICATION |
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| SYNONYMS | Naxcel; Excenel; | |
| [6r-[6a,7b(z)]]-7-[[(2-amino-4- thiazolyl)(methoxyimino)acetyl]amino]- 3-[[2-furanylcarbonyl) thio] methyl]-8-oxo-5-thia- 1-azabicyclo [4.2.0] oct-2-ene-2- carboxylic acid; (6R-7R)-7- [[2-amino -4-thiazolyl)-z-(methoxyimino)acetyl]amino]-3- [[(2-furanylcarbonyl) thio] methyl]- 8-oxo-5-thia-1-azabicyclo [4.2.0]oct-2-ene-carboxylic acid | ||
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PHYSICAL AND CHEMICAL PROPERTIES |
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| PHYSICAL STATE | White to off-white powder | |
| MELTING POINT | ||
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| SPECIFIC GRAVITY | ||
| SOLUBILITY IN WATER | ||
| pH | ||
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AUTOIGNITION |
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NFPA RATINGS |
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REFRACTIVE INDEX |
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| FLASH POINT |
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| STABILITY | Stable under ordinary conditions. | |
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GENERAL DESCRIPTION & APPLICATIONS |
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| Ceftiofur, a semisynthetic cephalosporin, is a broad-spectrum antibiotic against both Gram-positive and Gram-negative bacteria including beta-lactamase-producing bacterial strains and anaerobes. Its antibacterial activity results from the inhibition of mucopeptide synthesis in the cell wall in a similar fashion to other cephalosporins. Ceftiofur is used in the treatment of respiratory infections in cattle and pigs. The chemical designation is [6r-[6a,7b(z)]]-7-[[(2-amino-4- thiazolyl)(methoxyimino)acetyl]amino]- 3-[[2-furanylcarbonyl)thio] methyl]-8-oxo-5-thia- 1-azabicyclo [4.2.0] oct-2-ene-2- carboxylic acid. The sodium and hydrochloride salts are administered intramuscularly and intravenously. | ||
| SALES SPECIFICATION | ||
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APPEARANCE |
White to off-white powder | |
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ASSAY |
98.0% | |
| WATER | 4.0% max | |
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RELATED SUBSTANCE |
2.0% max | |
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HEAVY METALS |
20ppm max |
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| TRANSPORTATION | ||
| PACKING | 5kgs - 25kgs | |
| HAZARD CLASS | ||
| UN NO. | ||
| OTHER INFORMATION | ||
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