| Identification | Back Directory | [Name]
Sultamicillin | [CAS]
76497-13-7 | [Synonyms]
VD 1827
Baeimex
CP 49952
Unacid PD
SULTAMICILLIN
Bethadl Orale
Sultamiccillin
SultaMcillin Base
SULTAMICILLIN BASE
Sultancillin alkali
Unacid PD Oral：UnacimOrale
Sultamicillin (base and/or unspecified derivatives)
Hydroxymethyl (+)-(2S,5R,6R)-6-[(R)-(2-amino-2-phenylacetamido)]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo [3.2.0] heptan-2-carboxylate,(2S,5R)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptan-2-carboxyalate (ester) S,S-dioxide
4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[(aminophenylacetyl)amino]-3,3-dimethyl-7-oxo-, [[(3,3-dimethyl-4,4-dioxido-7-oxo-4-thia-1-azabicyclo[3.2.0]hept-2-yl)carbonyl]oxy]methyl ester, [2S-[2a(2R*,5S*),5a,6b(S*)]]-
4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[(aminophenylacetyl)amino]-3,3-dimethyl-7-oxo-, [[(3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]hept-2-yl)carbonyl]oxy]methyl ester, S,S-dioxide, [2S-[2a(2R*,5S*),5a,6b(S*)]]-
4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[(2R)-aminophenylacetyl]amino]-3,3-dimethyl-7-oxo-, [[[(2S,5R)-3,3-dimethyl-4,4-dioxido-7-oxo-4-thia-1-azabicyclo[3.2.0]hept-2-yl]carbonyl]oxy]methyl ester, (2S,5R,6R)- (9CI) | [EINECS(EC#)]
1312995-182-4 | [Molecular Formula]
C25H30N4O9S2 | [MDL Number]
MFCD00864948 | [MOL File]
76497-13-7.mol | [Molecular Weight]
594.66 |
| Chemical Properties | Back Directory | [Appearance]
White or almost white, slightly hygroscopic, crystalline powder. | [Melting point ]
190° | [Boiling point ]
907.7±65.0 °C(Predicted) | [density ]
1.55±0.1 g/cm3(Predicted) | [storage temp. ]
2-8°C | [solubility ]
Practically insoluble in water, very slightly soluble in methanol, practically insoluble in ethanol (96 per cent). | [form ]
neat | [pka]
12.15±0.60(Predicted) | [color ]
White to off-white |
| Hazard Information | Back Directory | [Chemical Properties]
White or almost white, slightly hygroscopic, crystalline powder. | [Uses]
Antibacterial. | [Definition]
ChEBI: Sultamicillin is a penicillanic acid ester. It is functionally related to an ampicillin and a sulbactam. |
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