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Thermo Scientific Chemicals (R,R)-Chloramphenicol, 98%

Catalog Number AAB2084114
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Quantity:
25 g
100 g
56-75-7
C11H12Cl2N2O5
323.126
MFCD00078159
WIIZWVCIJKGZOK-RKDXNWHRSA-N
5959
CHEBI:17698
2,2-dichloro-N-[(1R,2R)-1,3-dihydroxy-1-(4-nitrophenyl)propan-2-yl]acetamide
C1=CC(=CC=C1C(C(CO)NC(=O)C(Cl)Cl)O)[N+](=O)[O-]
56-75-7
C11H12Cl2N2O5
323.126
MFCD00078159
WIIZWVCIJKGZOK-RKDXNWHRSA-N
5959
CHEBI:17698
2,2-dichloro-N-[(1R,2R)-1,3-dihydroxy-1-(4-nitrophenyl)propan-2-yl]acetamide
C1=CC(=CC=C1C(C(CO)NC(=O)C(Cl)Cl)O)[N+](=O)[O-]

(R,R)-Chloramphenicol, CAS # 56-75-7, also known as chloromycetin, is a compound with broad-spectrum antibiotic and bacteriostatic activities.

Inhibitor of translation on the 50S subunit at the peptidyltransferase step. (R,R)-Chloramphenicol is widely utilized as an antibiotic, which is used for the treatment of number of bacterial infections and also act as a bacteriostatic. It is often used for bacterial selection in molecular biology applications. It also finds an application in ophthalmic and veterinary purposes. It also protects the mitochondrial and chloroplast protein synthesis and ribosomal formation of (p)ppGpp, de-pressing rRNA transcription.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

General Description

  • (R,R)-chloramphenicol is a compound with antibiotic and bacteriostatic activity and is derived from Streptomyces venequelae
  • It that can block the translation on the 50S subunit at the peptidyltransferase step. The binding affects the peptidyl transferase activity, preventing the transfer of amino acids to the growing peptide chains and inhibiting peptide bond formation. The resulting inhibition of the bacterial protein synthesis impedes bacterial cell proliferation

Application

  • (R,R)-chloramphenicol has been used for several molecular biology approaches, mainly for bacterial selection. It can be used to select transformed cells containing chloramphenicol resistance genes
  • This compound can also promote mitochondrial and chloroplast protein synthesis and the ribosomal formation of (p)ppGpp, depressing the rRNA transcription process
  • In vitro results demonstrate that (R,R)-chloramphenicol shows activity against several vancomycin-resistant E. faecium strains
TRUSTED_SUSTAINABILITY
Type Chloramphenicol
Physical Form Crystalline Powder
Melting Point 149°C to 152°C
Assay Percent Range 0.99
Beilstein 2225532
Merck Index 14,2077
Solubility Information Soluble in alcohol,propylene,glycol,acetone and ethyl acetate. Slightly soluble in water.
Formula Weight 323.14
Percent Purity ≥99%
Quantity 25 g
Chemical Name or Material Chloramphenicol
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Hazard Category H350
Hazard Statement GHS H Statement
H350-H361
Precautionary Statement P201-P202-P281-P308+P313-P501c
EINECSNumber 200-287-4
RTECSNumber AB6825000
TSCA Yes

RUO – Research Use Only

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