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Ertapenem Disodium

Ertapenem Disodium Structure
CAS No.
153832-38-3
Chemical Name:
Ertapenem Disodium
Synonyms
ERTAPENEM NA;Ertapenen Sodium;Ertapenem disodium;Ertapenam disodium;Ertapenem Disodium 90%;ErtapeneM SodiuM(crude);Ertapenem (sodium salt);Ertapenem Disodium (85%);Ertapenem Disodium USP/EP/BP;1-Azabicyclo(3.2.0)hept-2-ene-2-carboxylic acid
CBNumber:
CB41261369
Molecular Formula:
C22H26N3NaO7S
Molecular Weight:
499.51
MOL File:
153832-38-3.mol
MSDS File:
SDS
Modify Date:
2023/8/17 18:11:45

Ertapenem Disodium Properties

Melting point 230-234°C (dec.)
storage temp. Sealed in dry,2-8°C
solubility Methanol (Slightly), Water (Slightly)
form Solid
color White to Off-White
Stability Unstable at room temperature!

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319
Precautionary statements  P264-P280-P302+P352-P305+P351+P338-P332+P313-P337+P313-P362
NFPA 704
0
2 0

Ertapenem Disodium Chemical Properties,Uses,Production

Description

Ertapenem sodium was introduced in the US as a once daily intravenous or intramuscular injection for the treatment of adult patients with moderate to severe bacterial infections. This new I-β-methyl carbapenem can be assembled from commercially available 4-nitrobenzyl protected β-methyl carbapenem enolphosphate and the appropriate thiol derivative. The last intermediate can be synthesized from a suitably N-protected 4- hydroxy proline derivative in a one pot operation involving bis activation of the carboxy and hydroxy groups, reaction with sodium sulfide yielding the corresponding thiolactone, aminolysis with 2-aminobenzoic acid and Kdeprotection. This bacterial cell wall synthesis inhibitor has broad spectrum antimicrobial activity including common Gram-positive and Gram-negative aerobic pathogens and restricted activity against nosocomial pathogens such as Pseudomonas aeruginosa, Acinetobacfer species, methicillin-resistant staphylococci and enterococci. Ertapenem is resistant to a broad and extended spectrum of β-lactamases (excluding metallo-beta-lactamase) and is also more resistant than imipenem to human renal dehydroxypeptidase-I-inactivation (DHP-I). In drug-resistant strains of P. aeruginosa, resistance to ertapenem and imipenem was common but almost all strains remain susceptible to at least one antipseudomal agent. In phase III studies, ertapenem showed efficacy in the treatment of obstetric and gyneacological infections, skin and soft tissues infections, community-acquired pneumonia, urinary tract infections and in intra abdominal infections. Ertapenem has improved pharmacokinetics over currently available carbapenems and cephalosporins with an extended serum half-life of 4h. The overall safety and tolerability profile of ertapenem was comparable to that seen with comparator antibacterials.

Chemical Properties

Pale Yellow Solid

Uses

Group 1 carbapenem antibiotic. An antibacterial.

Ertapenem Disodium Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 116)Suppliers
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SOLARA ACTIVE PHARMA SCIENCES LTD +91 44 4344 6700 New Delhi, India 89 58 Inquiry
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Hebei Mojin Biotechnology Co., Ltd +86 13288715578 +8613288715578 China 12446 58 Inquiry
career henan chemical co +86-0371-86658258 +8613203830695 China 29888 58 Inquiry

Ertapenem Disodium Spectrum

1-Azabicyclo(3.2.0)hept-2-ene-2-carboxylic acid ErtapeneM SodiuM(crude) disodium (4R,5R,6S)-3-[(3S,5S)-5-[(3-carboxylatophenyl)carbamoyl]pyrro lidin-3-yl]sulfanyl-6-(1-hydroxyethyl)-4-methyl-7-oxo-1-azabicyclo[3.2 .0]hept-2-ene-2-carboxylate Ertapenem disodium Ertapenem Disodium (85%) Ertapenem (sodium salt) Ertapenam disodium Ertapenem Disodium 90% ERTAPENEM NA Ertapenem Disodium USP/EP/BP sodium (4R,5S,6S)-3-(((3S,5S)-5-((3-carboxylatophenyl)carbamoyl)pyrrolidin-3-yl)thio)-6-((R)-1-hydroxyethyl)-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate sodium 3-((2S,4S)-4-(((4R,5S,6S)-2-carboxy-6-((R)-1-hydroxyethyl)-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-en-3-yl)thio)pyrrolidine-2-carboxamido)benzoate 1-Azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid, 3-[[(3S,5S)-5-[[(3-carboxyphenyl)amino]carbonyl]-3-pyrrolidinyl]thio]-6-[(1R)-1-hydroxyethyl]-4-methyl-7-oxo-, sodium salt (1:2), (4R,5S,6S)- Ertapenen Sodium 153832-38-3 C22H25N3O7S2Na C22H23N3Na2O7S C22H23N3O7S2Na Aromatics Chiral Reagents Heterocycles Intermediates & Fine Chemicals Pharmaceuticals Sulfur & Selenium Compounds API