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Thermo Scientific™ (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.
47.20 EUR - 150.00 EUR
Chemical Identifiers
| CAS | 56-75-7 |
|---|---|
| Molecular Formula | C11H12Cl2N2O5 |
| Molecular Weight (g/mol) | 323.126 |
| MDL Number | MFCD00078159 |
| InChI Key | WIIZWVCIJKGZOK-RKDXNWHRSA-N |
| 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-] |
| Product Code | Brand | Quantity | Price | Quantity & Availability | |||||
|---|---|---|---|---|---|---|---|---|---|
| Product Code | Brand | Quantity | Price | Quantity & Availability | |||||
|
11445786
|
Thermo Scientific™
B20841.14 |
25g |
47.20 EUR
25g |
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|
11455786
|
Thermo Scientific™
B20841.22 |
100g |
150.00 EUR
100g |
Please sign in to purchase this item. Need a web account? Register with us today! | |||||
Description
This Thermo Scientific 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.
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
Chemical Identifiers
| 56-75-7 | |
| 323.126 | |
| WIIZWVCIJKGZOK-RKDXNWHRSA-N | |
| CHEBI:17698 | |
| C1=CC(=CC=C1C(C(CO)NC(=O)C(Cl)Cl)O)[N+](=O)[O-] |
| C11H12Cl2N2O5 | |
| MFCD00078159 | |
| 5959 | |
| 2,2-dichloro-N-[(1R,2R)-1,3-dihydroxy-1-(4-nitrophenyl)propan-2-yl]acetamide |
Specifications
| 56-75-7 | |
| 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% |
| 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 |
Safety and Handling
GHS H Statement
H350-H361
P201-P202-P281-P308+P313-P501c
H350
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missing translation for 'rtecsNumber' : AB6825000
missing translation for 'tsca' : Yes
Product Identifier
Signal Word
Hazard Category
Hazard Statement
Precautionary Statement
Supplemental information
- (R,R)-Chloramphenicol
Signal Word
- Danger
Hazard Category
- Carcinogenicity Category 1B
Hazard Statement
- H350-May cause cancer.
Precautionary Statement
- P201-Obtain special instructions before use.
- P308+P313-IF exposed or concerned: Get medical advice/attention.
Supplemental information
- MIXTURE LIST-Contains : Chloramphenicol
RUO – Research Use Only
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