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

(R,R)-Chloramphenicol, CAS # 56-75-7, also known as chloromycetin, is a compound with broad-spectrum antibiotic and bacteriostatic activities. | CAS: 56-75-7 | C11H12Cl2N2O5 | 323.126 g/mol

$118.64 - $329.30

Chemical Identifiers

CAS 56-75-7
Molecular Formula C11H12Cl2N2O5
Molecular Weight (g/mol) 323.126
MDL Number MFCD00078159
InChI Key WIIZWVCIJKGZOK-RKDXNWHRSA-N
Synonym Chloromycetin
PubChem CID 5959
ChEBI CHEBI:17698
IUPAC Name 2,2-dichloro-N-[(1R,2R)-1,3-dihydroxy-1-(4-nitrophenyl)propan-2-yl]acetamide
SMILES C1=CC(=CC=C1C(C(CO)NC(=O)C(Cl)Cl)O)[N+](=O)[O-]
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AAB2084114
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Thermo Scientific Chemicals
B2084114
25 g
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AAB2084122
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Thermo Scientific Chemicals
B2084122
100 g
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Description

Description

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
Specifications

Chemical Identifiers

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

Specifications

Chloramphenicol
56-75-7
25 g
C11H12Cl2N2O5
2225532
Soluble in alcohol,propylene,glycol,acetone and ethyl acetate. Slightly soluble in water.
C1=CC(=CC=C1C(C(CO)NC(=O)C(Cl)Cl)O)[N+](=O)[O-]
323.126
CHEBI:17698
≥99%
Crystalline Powder
149°C to 152°C
0.99
MFCD00078159
14,2077
WIIZWVCIJKGZOK-RKDXNWHRSA-N
2,2-dichloro-N-[(1R,2R)-1,3-dihydroxy-1-(4-nitrophenyl)propan-2-yl]acetamide
5959
323.14
Chloramphenicol
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Safety and Handling

Safety and Handling

GHS H Statement
H350-H361
May cause cancer.
Suspected of damaging fertility or the unborn child.

P201-P202-P281-P308+P313-P501c

H350

EINECSNumber : 200-287-4

RTECSNumber : AB6825000

TSCA : Yes

SDS
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RUO – Research Use Only