Chloramphenicol Acetate

Chloramphenicol Acetate
Item number Size Datasheet Manual SDS Delivery time Quantity Price
Cay23811-5 5 mg -

6 - 10 business days*

166.00€
Cay23811-25 25 mg -

6 - 10 business days*

742.00€
 
Chloramphenicol acetate is an acetylated and inactive version of chloramphenicol. It is formed in... more
Product information "Chloramphenicol Acetate"
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, Cay-16160) to confer chloramphenicol resistance. Chloramphenicol acetate has no antibiotic activity against S. sonnei in a turbidimetric assay.Formal Name: N-[(1R,2R)-1-[(acetyloxy)methyl]-2-hydroxy-2-(4-nitrophenyl)ethyl]-2,2-dichloro-acetamide. CAS Number: 10318-16-8. Molecular Formula: C13H14Cl2N2O6. Formula Weight: 365.2. Purity: >97%. Formulation: (Request formulation change), A solid. Solubility: DMF: Soluble, DMSO: Soluble, Ethanol: Soluble, Methanol: Soluble. SMILES: O=C(C)OC[C@@H](NC(C(Cl)Cl)=O)[C@H](O)C1=CC=C([N+]([O-])=O)C=C1. InChi Code: InChI=1S/C13H14Cl2N2O6/c1-7(18)23-6-10(16-13(20)12(14)15)11(19)8-2-4-9(5-3-8)17(21)22/h2-5,10-12,19H,6H2,1H3,(H,16,20)/t10-,11-/m1/s1. InChi Key: VVOIFRARHIZCJD-GHMZBOCLSA-N. Origin: Bacterium/Streptomyces.
Keywords: N-[(1R,2R)-1-[(acetyloxy)methyl]-2-hydroxy-2-(4-nitrophenyl)ethyl]-2,2-dichloro-acetamide
Supplier: Cayman Chemical
Supplier-Nr: 23811

Properties

Application: Chloramphenicol acetyltransferase reaction product
MW: 365.2 D
Formula: C13H14Cl2N2O6
Purity: >97%
Format: Solid

Database Information

CAS : 10318-16-8| Matching products
KEGG ID : K19271 | Matching products

Handling & Safety

Storage: -20°C
Shipping: +20°C (International: -20°C)
Caution
Our products are for laboratory research use only: Not for administration to humans!
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