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Tazobactam sodium

Product Name
Tazobactam sodium
CAS No.
89785-84-2
Chemical Name
Tazobactam sodium
Synonyms
TazobactuM SodiuM;TAZOBACTAM SODIUM SALT;Piperacillin sodium salt;D03707;ytr830;cl307579;CL-30757;TAZOBACTAM SODIUM;YTR-830H SODIUM SALT;TAZOBACTAMACID/SODIUM
CBNumber
CB3181854
Molecular Formula
C10H12N4NaO5S
Formula Weight
323.28
MOL File
89785-84-2.mol
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Tazobactam sodium Property

Melting point:
140-147°C
Boiling point:
77℃
Flash point:
>110°(230°F)
storage temp. 
Keep in dark place,Inert atmosphere,2-8°C
solubility 
H2O: 50 mg/mL, clear, colorless
form 
powder
color 
white
optical activity
[α]/D 144±4°, c = 0.1 in H2O
Water Solubility 
Soluble in water.Soluble in water and methanol.
Stability:
Hygroscopic
CAS DataBase Reference
89785-84-2(CAS DataBase Reference)
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
22-24/25-36-26
WGK Germany 
3
RTECS 
XI0191500
HS Code 
2941900000
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P271Use only outdoors or in a well-ventilated area.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
T2820
Product name
Tazobactam sodium salt
Purity
β-lactamase inhibitor
Packaging
10mg
Price
$97.5
Updated
2024/03/01
Sigma-Aldrich
Product number
68300
Product name
Tazobactam sodium salt
Purity
analytical standard
Packaging
5mg
Price
$88.8
Updated
2024/03/01
Alfa Aesar
Product number
J66226
Product name
Tazobactam sodium
Packaging
100mg
Price
$67.65
Updated
2024/03/01
Alfa Aesar
Product number
J66226
Product name
Tazobactam sodium
Packaging
1g
Price
$182
Updated
2024/03/01
Cayman Chemical
Product number
17185
Product name
Tazobactam (sodium salt)
Purity
≥95%
Packaging
100mg
Price
$32
Updated
2024/03/01
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Tazobactam sodium Chemical Properties,Usage,Production

Description

Tazobactam sodium is a new triazolylmethyl beta-lactamase inhibitor launched in combination with the antibiotic piperacillin as tazocilline. Tazobactam sodium is active against penicillinases and wide spectrum of beta-lactamases. The combination product tazobactdpiperacillin is effective against a broad range of both Gram-positive and -negative organisms and is indicated for the treatment of lower respiratory tract, urinary tract, intra-abdominal, biliary and skin and soft tissue infections. It is expected to compete against the combination product augmentin (amoxicillidclavulanate).

Chemical Properties

White to off-white powder

Originator

Taiho (Japan)

Uses

Lactamase inhibitor, used with ?lactam antibiotics to enhance their effect

Uses

β-Lactamase inhibitor, used with β-lactam antibiotics to enhance their effect.

Uses

A β-lactamase inhibitor and antibacterial agent

Uses

Tazobactam sodium is a beta-Lactamase inhibitor, which is used with penicillinase inhibition studies and beta-lactam antibiotics to enhance their effect. It serves as an antibacterial penicillin derivative, which inhibits the action of bacterial beta-lactamases.

Definition

ChEBI: Tazobactam sodium is an organic sodium salt having tazobactam(1-) as the counterion; used in combination with ceftolozane sulfate for treatment of complicated intra-abdominal infections and complicated urinary tract infections. It has a role as an antimicrobial agent, an antiinfective agent and an EC 3.5.2.6 (beta-lactamase) inhibitor. It contains a tazobactam(1-).

Manufacturing Process

A known β-lactam type antibiotic (for example, benzhydryl 2-β-chloromethyl- 2-α-methylpenam-3-α-carboxylate) was used for synthesis of new penicillinic derivatives.
A solution of 5.00 g of sodium azide in 53 ml of water was added to a solution of benzhydryl 2-β-chloromethyl-2-α-methylpenam-3-α-carboxylate (5.13 g) in dimethylformamide (155 ml). The mixture was stirred at room temperature for 4 h. The resulting reaction mixture was poured into cooled water and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried over magnesium sulfate and concentrated to provide 4.87 g of the benzhydryl 2-β-azidomethyl-2-α-methylpenam-3-α-carboxylate as oil in 93% yield.
To a solution of benzhydryl 2-β-azidomethyl-2-α-methylpenam-3-α- carboxylate (7.03 g) in a mixture of acetic acid (240 ml) and water (40 ml) was added potassium permanganate (6.02 g) over a period of more than 1 h. The mixture was stirred at room temperature for 2.5 h. The resulting reaction mixture was diluted with ice water. The precipitate was collected by filtration, and washed with water. The resulting product was dissolved in ethyl acetate and the solution was washed with an aqueous solution of sodium hydrogen carbonate and dried over magnesium sulfate. Concentration gave 5.48 g of the benzhydryl 2-β-azidomethyl-2-α-methylpenam-3-α-carboxylate-1,1-dioxide in 72% yield.
A 200 mg quantity of benzhydryl 2-β-azidomethyl-2-α-methylpenam-3-α- carboxylate-1,1-dioxide was reacted with 10 ml of vinyl acetate in a sealed reactor at 100° to 110°C for 30 h. The reaction mixture was concentrated at reduced pressure. The residue was crystallized with cooled chloroform. The white crystals of benzhydryl 2-α-methyl-2-β-(1,2,3-triazol-1-yl)methylpenam- 3-α-carboxylate-1,1-dioxide have a melting point 206°-208°C, dec.
Hydrogenation was conducted in 10 ml of ethyl acetate and 10 ml of water at room temperature for 30 min by using 45 mg of benzhydryl 2-α-methyl-2-β- (1,2,3-triazol-1-yl)methylpenam-3-α-carboxylate-1,1-dioxide, 15 mg of 10% palladium charcoal and 16 mg of sodium hydrogen carbonate. The aqueous layer was separated from the reaction mixture and washed once with ethyl acetate. The aqueous solution was then purified with an MCl gel, CHP-20P (product of Mitsubishi Kasei Co., Ltd., Japan). After freeze-drying, there was obtained an amorphous product of sodium 2-α-methyl-2-β-(1,2,3-triazol-1- yl)methylpenam-3-α-carboxylate-1,1-dioxide with a melting point 170°C, dec.

brand name

Tazocilline

Therapeutic Function

Antibiotic

Tazobactam sodium Preparation Products And Raw materials

Raw materials

Preparation Products

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Tazobactam sodium Suppliers

Alfa Aesar, Thermo Fisher Scientific
Tel
--
Fax
--
Email
es@alfa.com
Country
Germany
ProdList
5123
Advantage
58
CHEMOS GmbH & Co. KG
Tel
--
Fax
--
Email
chemos@chemos.de
Country
Germany
ProdList
6727
Advantage
58
ChemPur GmbH
Tel
--
Fax
--
Email
info@ChemPur.de
Country
Germany
ProdList
2737
Advantage
50
ABCR GmbH & CO. KG
Tel
--
Fax
--
Email
info@abcr.de
Country
Germany
ProdList
6831
Advantage
75
Service Chemical Inc.
Tel
--
Fax
--
Email
sales@chemos-group.com
Country
Germany
ProdList
6350
Advantage
71
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View Lastest Price from Tazobactam sodium manufacturers

Sinoway Industrial co., ltd.
Product
Tazobactam sodium 89785-84-2
Price
US $0.00-0.00/Kg/Bag
Min. Order
1Kg/Bag
Purity
99% up, High Density
Supply Ability
20 tons
Release date
2023-11-16
Hebei Weibang Biotechnology Co., Ltd
Product
Tazobactam sodium 89785-84-2
Price
US $9.90/KG
Min. Order
1KG
Purity
99%
Supply Ability
10 mt
Release date
2024-11-22
WUHAN FORTUNA CHEMICAL CO., LTD
Product
Tazobactam sodium 89785-84-2
Price
US $0.00/KG
Min. Order
1KG
Purity
98%min
Supply Ability
500kg
Release date
2021-11-02

89785-84-2, Tazobactam sodiumRelated Search:


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