Cefpirome Sulfate with Sodium Carbonate

Description

Cefpirome is a fourth generation cephalosporin antibiotic targeting gram-positive and gram-negative bacteria. Is it not effective against many Bacteroides, Enterococci, and Haemophili species due to the resistance they have developed. Cefpirome sulfate with sodium carbonate is a mixture of cefpirome sulfate and anhydrous sodium carbonate and is commonly used for the stabilization of pH.

Cephalosporins are a type of β-lactam antibiotic consisting of a four-membered β-lactam ring bound to a six-membered dihydrothiazine ring. This two-ring system causes distortion of the β-lactam amide bond, resulting in decreased resonance stabilization and increased reactivity. β-lactams inhibit the formation of peptidoglycan cross-links within bacterial cell walls by targeting penicillin-binding proteins or PBPs. Consequently, the bacterial cell wall becomes weak and cytolysis occurs. Cephalosporins are less susceptible to β-lactamases than the penicillin β-lactam antibiotics.


Product Specifications
Cefpirome Sulfate with Sodium Carbonate

MOLECULAR BIOLOGY GRADE

Formula: C22H22N6O5S2 • H2SO4 and Na2CO3

MW: 612.66 g/mol (cefpirome sulfate) + 105.99 g/mol (sodium bicarbonate)

Storage/Handling: Store at 2-8 °C.

Cefpirome Sulfate with Sodium Carbonate

View Sizes & Pricing

Catalog Number:
C-702-1
CAS Number:
98753-19-6; 497-19-8
$243.00

Availability:
2-3 Weeks
Shipping:
Shipping calculated at checkout

    Description

    Cefpirome is a fourth generation cephalosporin antibiotic targeting gram-positive and gram-negative bacteria. Is it not effective against many Bacteroides, Enterococci, and Haemophili species due to the resistance they have developed. Cefpirome sulfate with sodium carbonate is a mixture of cefpirome sulfate and anhydrous sodium carbonate and is commonly used for the stabilization of pH.

    Cephalosporins are a type of β-lactam antibiotic consisting of a four-membered β-lactam ring bound to a six-membered dihydrothiazine ring. This two-ring system causes distortion of the β-lactam amide bond, resulting in decreased resonance stabilization and increased reactivity. β-lactams inhibit the formation of peptidoglycan cross-links within bacterial cell walls by targeting penicillin-binding proteins or PBPs. Consequently, the bacterial cell wall becomes weak and cytolysis occurs. Cephalosporins are less susceptible to β-lactamases than the penicillin β-lactam antibiotics.


    Product Specifications
    Cefpirome Sulfate with Sodium Carbonate

    MOLECULAR BIOLOGY GRADE

    Formula: C22H22N6O5S2 • H2SO4 and Na2CO3

    MW: 612.66 g/mol (cefpirome sulfate) + 105.99 g/mol (sodium bicarbonate)

    Storage/Handling: Store at 2-8 °C.

    Product Specifications

    Catalog ID: C-702
    CAS #: 98753-19-6; 497-19-8
    MW: 612.66 g/mol
    Grade: MOLECULAR BIOLOGY GRADE
    Storage/handling: Store at 4°C.

    Login

    Forgot your password?

    Don't have an account yet?
    Create account