| Identification | Back Directory | [Name]
chloramphenicol 3-acetate | [CAS]
10318-16-8 | [Synonyms]
ChloraMphenicol acetate
chloramphenicol 3-acetate
Chloramphenicol Impurity 9
3-O-AcetylchloraMphenicol, ChloraMphenicol 3-acetate
N-[(1R,2R)-1-[(Acetyloxy)methyl]-2-hydroxy-2-(4-nitrophenyl)ethyl]-2,2-dichloroacetamide | [Molecular Formula]
C13H14Cl2N2O6 | [MDL Number]
MFCD28898459 | [MOL File]
10318-16-8.mol | [Molecular Weight]
365.17 |
| Chemical Properties | Back Directory | [Melting point ]
89-91oC | [Boiling point ]
589.0±50.0 °C(Predicted) | [density ]
1.473±0.06 g/cm3(Predicted) | [storage temp. ]
-20°C Freezer | [solubility ]
Chloroform (Slightly), Methanol (Slightly) | [form ]
Solid | [pka]
10.85±0.46(Predicted) | [color ]
White to Off-White |
| Hazard Information | Back Directory | [Description]
Chloramphenicol acetate is an acetylated and inactive version of chloramphenicol. It is formed in E. coli and S. aureus by the inducible enzyme chloramphenicol acetyltransferase in the presence of acetyl coenzyme A (acetyl-CoA; ) to confer chloramphenicol resistance. Chloramphenicol acetate has no antibiotic activity against S. sonnei in a turbidimetric assay. | [Uses]
Chloramphenicol 3-Acetate is an Chloramphenicol (C325030) derivative found in metabolic decomposition of Chloramphenicol by Alcaligenes faecalis. | [Uses]
Chloramphenicol acetate is a naturally-occurring co-metabolite of chloramphenicol in Streptomyces venezuelae with albeit significantly lower potency. Chloramphenicol acetate is the major product of chloramphenicol acetyltransferase, the major resistance mechanism to chloramphenicol. | [Definition]
ChEBI: Chloramphenicol 3-acetate is an acetate ester. It is functionally related to a chloramphenicol. | [References]
[1] W V SHAW R F B. Characterization of chloramphenicol acetyltransferase from chloramphenicol-resistant Staphylococcus aureus.[J]. Journal of Bacteriology, 1968, 95 1: 28-36. DOI: 10.1128/jb.95.1.28-36.1968 |
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