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Sulbactam sodium

Product Name
Sulbactam sodium
CAS No.
69388-84-7
Chemical Name
Sulbactam sodium
Synonyms
Sodium Sodium;Sulbatam Sodium;SODIUM SULBACTAM;Sterile Sulbactam sodium;(2S,5R);CP-45899-2;Shu ba sodium;sulbacyam sodium;SULBACTAM SODIUM;cp45899sodiumsalt
CBNumber
CB0370356
Molecular Formula
C8H12NNaO5S
Formula Weight
257.24
MOL File
69388-84-7.mol
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Sulbactam sodium Property

Melting point:
>230°C (dec.)
storage temp. 
-20°C Freezer, Under Inert Atmosphere
solubility 
Freely soluble in water, sparingly soluble in ethyl acetate, very slightly soluble in ethanol (96 per cent). It is freely soluble in dilute acids.
form 
Solid
color 
White
InChIKey
NKZMPZCWBSWAOX-IBTYICNHSA-M
CAS DataBase Reference
69388-84-7(CAS DataBase Reference)
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Safety

Hazard Codes 
Xn
Risk Statements 
42/43
Safety Statements 
22-24-36/37-45-24/25
HS Code 
29349990
Toxicity
LD50 ivn-rat: 6500 mg/kg NKRZAZ 32(Suppl 4),97,84
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P330Rinse mouth.

P332+P313IF SKIN irritation occurs: Get medical advice/attention.

P337+P313IF eye irritation persists: Get medical advice/attention.

P362Take off contaminated clothing and wash before reuse.

P403+P233Store in a well-ventilated place. Keep container tightly closed.

P405Store locked up.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
Y0000529
Product name
Sulbactam sodium
Purity
European Pharmacopoeia (EP) Reference Standard
Packaging
y0000529
Price
$220
Updated
2024/03/01
TRC
Product number
S699185
Product name
SulbactamSodiumSalt
Packaging
2g
Price
$180
Updated
2021/12/16
TRC
Product number
S699185
Product name
SulbactamSodiumSalt
Packaging
50mg
Price
$65
Updated
2021/12/16
Axon Medchem
Product number
Axon2041
Product name
Sulbactamsodium-CP45899sodium
Purity
98%
Packaging
25mg
Price
$77
Updated
2021/12/16
Apolloscientific
Product number
BIS0150
Product name
Sulbactam sodium
Packaging
1g
Price
$95
Updated
2021/12/16
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Sulbactam sodium Chemical Properties,Usage,Production

Description

Sulbactam sodium is a parenterally-active, β-lactamase inhibitor recently introduced as a 1: 1 combination product with cefoperazone. Like clavulanic acid, the first agent of this type to b e introduced, sulbactam enhances the effectiveness of β-lactam antibiotics against resistant strains.

Chemical Properties

White Solid

Originator

Pfizer (USA)

Uses

A semi-synthetic β-lactamase inhibitor. It is used in combination with β-lactam antibiotics as antibacterial.

Definition

ChEBI: Sulbactam sodium is an organooxygen compound and an organonitrogen compound. It is functionally related to an alpha-amino acid.

Manufacturing Process

Sulbactam sodium is semi-synthetic antibiotic of penicillinic group. Start material for it's synthesis is 6-aminopenicillanic acid. First 6-aminopenicillanic acid was isolated in 1957 year from benzylpenicilline as resalt of treating of it by penicillinaze. Benzylpenicilline is produced by microorganism of genus Streptomyces.
Further, 6-aminopenicillanic acid reacted with bromine, hydrochloric acid and NaNO2. As a result the 6,6-dibromopenicillanic acid was obtained.
6,6-Dibromopenicillanic acid was oxidized by KMnO4, to give 6,6-dibromo-1,1-The 6,6-dibromo-1,1-dioxopenicillanic acid in presence of Fe was converted to the 1,1-dioxopenicillanic acid (sulbactam acid). The sulbactam acid was treated by sodium 2-ethylhexanoate and crude sulbactam sodium was obtained.

brand name

SULPERAZONE

Therapeutic Function

Beta-lactamase inhibitor

General Description

Sulbactam was synthesized by Pfizer Research Laboratories in 1977 in the course of screening for β-lactamase inhibitors. It shows strong activity against penicillinase and moderate activity against cephalosporinase. Sulbactam itself shows activity against some gramnegative bacteria but no activity against most pathogenic bacteria. The use of sulbactam in combination with cefoperazone, which is partially hydrolyzed by penicillinase, is under study along with its use as an esterified complex with ampicillin (sultamicillin) for therapy of cefoperazone-ampicillin-resistant infections.

Safety Profile

Poison by intravenous route. Experimental reproductive effects. When heated to decomposition it emits toxic fumes of NOx and SOx

Sulbactam sodium Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from Sulbactam sodium manufacturers

Sinoway Industrial co., ltd.
Product
Sulbactam sodium 69388-84-7
Price
US $0.00-0.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
20tons
Release date
2024-04-03
WUHAN FORTUNA CHEMICAL CO., LTD
Product
Sulbactam sodium 69388-84-7
Price
US $0.00/KG/Tin
Min. Order
10KG
Purity
98%min, sterile or non-sterile, USP
Supply Ability
500kg
Release date
2021-10-20
shandong perfect biotechnology co.ltd
Product
Sulbactam sodium 69388-84-7
Price
US $0.00/g
Min. Order
1g
Purity
98% HPLC
Supply Ability
100kg
Release date
2023-08-08

69388-84-7, Sulbactam sodiumRelated Search:


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