| Identification | More | [Name]
Chloramphenicol sodium succinate | [CAS]
982-57-0 | [Synonyms]
CHLORAMPHENICOL ALPHA-SUCCINATE SODIUM SALT
CHLORAMPHENICOL SODIUM SUCCINATE
CHLORAMPHENICOL SUCCINATE SODIUM
CHLORAMPHENICOL SUCCINATE SODIUM SALT
alpha-esterwithsodiumsuccinate
chloramphenicolmonosuccinatesodiumsalt
chloramphenicolsodiummonosuccinate
chloramphenicolsuccinatesodium*minimum80%(hpl
chloramphenicol-sukzinat-natrium
protophenicol
sodiumchloramphenicolsuccinate
CHLORAMPHENICOL SUCCINATE SODIUMMINIMUM 80% (HPLC)
Betamicetin
Butanedioic acid, mono[(2R,3R)-2-[(dichloroacetyl)amino]-3-hydroxy-3-(4-nitrophenyl)propyl] ester, monosodium salt
Butanedioic acid, mono[2-[(dichloroacetyl)amino]-3-hydroxy-3-(4-nitrophenyl)propyl] ester, monosodium salt, [R-(R*,R*)]-
Chloramphenicol sodium hemisuccinate
Chloromycetin sodium succinate
Clorofenicina
Cloromoin
D-Chloramphenicol sodium succinate | [EINECS(EC#)]
213-568-1 | [Molecular Formula]
C26H28Cl4N4Na2O14 | [MDL Number]
MFCD00083598 | [Molecular Weight]
808.31 | [MOL File]
982-57-0.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
R40:Limited evidence of a carcinogenic effect. | [Safety Statements ]
S22:Do not breathe dust .
S36:Wear suitable protective clothing . | [WGK Germany ]
3
| [RTECS ]
AB6905000
|
| Hazard Information | Back Directory | [General Description]
White powder. | [Air & Water Reactions]
Freely soluble in water. | [Fire Hazard]
Flash point data for this chemical are not available, but CHLORAMPHENICOL SODIUM SUCCINATE is probably combustible. | [Chemical Properties]
White or yellowish-white powder, hygroscopic | [Uses]
antibacterial, antirickettsial, inhibits protein synthesis | [Uses]
Chloramphenicol succinate sodium is the salt prepared from chloramphenicol succinate using the free carboxylic acid of the succinate which ionises and readily forms in weakly sodium hydroxide solutions. The sodium salt is the preferred formulation for pharmaceutical applications, providing a more readily soluble product. Chloramphenicol succinate is significantly less active than chloramphenicol but acts as a prodrug, forming chloramphenicol in the presence of succinate dehydrogenase. | [storage]
-20°C, protect from light, stored under argon |
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