| Name | Sulbactam sodium |
|---|---|
| Synonyms |
4-thia-1-azabicyclo(3.2.0)htane-2-cboxylicacid,3,3-dimethyl-7-oxo-,4,4-d
SULBACTAM SODIUM SODIUM SULBACTAM SulbactaM SodiuM API penicillanicacid1,1-dioxidesodiumsalt Sterile Sulbactum Sodium Powder sodiumsalt,(2s-cis)-ioxid sodium (2s-cis)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]htane-2-cboxylate 4,4-dioxide 45899sodiumsalt l^{6}-thia-1-azabicyclo[3.2.0]htane-2-cboxylate 3,3-dimethyl-7-oxo-4,4-dioxide-4-thia-1-azabicyclo[3.2.0]htane-2-cboxylic acid, sodium salt (1:1) Sodium Sodium sulbacyam sodium Shu ba sodium Sulbactam sodium salt, beta-lactamase inhibitor penicillanicacidsulfonesodiumsalt sodium1,1-dioxopenicillanate (2S,5R) Sulbactam sodium CRS SULBACTAM SODIUM (NON-STERILE BULK) AMPICILLIN SODIUM AND SULBACTAM SODIUM 2:1 sodiumpenicillanate1,1-dioxide sodium Penicillanate 1,1-Dioxide Sulbactam sodium //BP sodium (2S,5R)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]htane-2-cboxylate 4,4-dioxide 4-Thia-1-azabicyclo[3.2.0]htane-2-cboxylicacid, 3,3-dimethyl-7-oxo-, 4,4-dioxide, sodium salt, (2S,5R)- (9CI) Sterile Sulbactam sodium Antibiotic medicine veteriny sulbactam sodium sodium 3,3-dimethyl-4,4,7-trioxo-4 Sulbactam sodium - 45899 sodium SULBACTAM SODIUM SALT (2S,5R)-3,3-Dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]htane-2-cboxylicacidsodiumsalt4,4-dioxide SulbactaM SodiuM,USP Sulbactam sodiumQ: What is Sulbactam sodium Q: What is the CAS Number of Sulbactam sodium Q: What is the storage condition of Sulbactam sodium Q: What e the applications of Sulbactam sodium penicillanic acid 1,1-dioxide sodium salt EINECS 273-984-4 penicillanicaciddioxidesodiumsalt 45899-2 Sulbactam sodium, 10 mM in DMSO Sulbatam Sodium Penicillanic acid 4,4-dioxide sodium salt MFCD01750374 Natrium-(2S-cis)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]htan-2-cboxylat-4,4-dioxid (2S-cis)-3,3-Dimethyl-7-oxo-4-thia-1-azabicyclo[3,2,0]htane-2-cboxylic acid 4,4-dioxide sodium salt |
| Description | Sulbactam (CP45899) sodium is a competitive, irreversible beta-lactamase inhibitor. Sulbactam sodium shows antimicrobial activity against multidrug-resistant (MDR) acinetobacter calcoaceticus--Acinetobacter baumannii (Acb) complex[1][2]. |
|---|---|
| Related Catalog | |
| In Vitro | Ampicillin-Sulbactam has a wide range of antibacterial activity that includes Gram-positive and Gram-negative aerobic and anaerobic bacteria[3]. |
| References |
[1]. Noguchi JK, et al. Sulbactam: a beta-lactamase inhibitor. Clin Pharm. 1988;7(1):37-51. |
| Boiling Point | 567.7ºC at 760 mmHg |
|---|---|
| Melting Point | 121-123 °C(lit.) |
| Molecular Formula | C8H10NNaO5S |
| Molecular Weight | 255.223 |
| Flash Point | 297.1ºC |
| Exact Mass | 255.017731 |
| PSA | 102.96000 |
| Storage condition | -20°C Freezer, Under Inert Atmosphere |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
|
| Hazard Codes | Xn: Harmful; |
|---|---|
| Risk Phrases | R42/43 |
| Safety Phrases | S26-S37/39 |
| WGK Germany | 3 |
| HS Code | 2941109900 |
|
~92%
69388-84-7 |
| Literature: SANDOZ AG Patent: WO2009/53256 A2, 2009 ; Location in patent: Example 1 ; |
|
~77%
69388-84-7 |
| Literature: Leo Pharmaceutical Products Ltd. A/S Patent: US4816580 A1, 1989 ; |
| Precursor 3 | |
|---|---|
| DownStream 4 | |
| HS Code | 2941109900 |
|---|