Amoxicillin Sodium Salt

Request Lot Specific COA

View Current Lot COA

Citation Search Tool

Description

Amoxicillin is an extended-spectrum ß-lactam antibiotic with a structure similar to that of ampicillin. It is effective against a variety of ß-lactamase negative bacteria including E. coli and various Streptococcus and Staphylococcus bacteria. It is also effective against a variety of other gram-negative and gram-positive bacteria. Amoxicillin sodium salt is freely soluble in aqueous solution.

Penicillins are a type of β-lactam antibiotic consisting of a four-membered β-lactam ring bound to a five-membered thiazolidine 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. Resistance to β-lactam antibiotics occurs in the presence of cells containing plasmid encoded extended spectrum β-lactamases or ESBLs.


Product Specifications
Amoxicillin Sodium Salt

MOLECULAR BIOLOGY GRADE

Formula: C16H18N3NaO5S

MW: 387.39 g/mol

Storage/Handling: Store at 2-8°C.

PubChem Chemical ID: 23663126

Amoxicillin Sodium Salt

View Sizes & Pricing

Catalog Number:
A-551-1
CAS Number:
34642-77-8
$69.00

For research use only. Not for food, drug, household, or cosmetic use.
Availability:
In stock
Shipping:
$14.99 Ground shipping (In continental US only.)

    Description

    Amoxicillin is an extended-spectrum ß-lactam antibiotic with a structure similar to that of ampicillin. It is effective against a variety of ß-lactamase negative bacteria including E. coli and various Streptococcus and Staphylococcus bacteria. It is also effective against a variety of other gram-negative and gram-positive bacteria. Amoxicillin sodium salt is freely soluble in aqueous solution.

    Penicillins are a type of β-lactam antibiotic consisting of a four-membered β-lactam ring bound to a five-membered thiazolidine 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. Resistance to β-lactam antibiotics occurs in the presence of cells containing plasmid encoded extended spectrum β-lactamases or ESBLs.


    Product Specifications
    Amoxicillin Sodium Salt

    MOLECULAR BIOLOGY GRADE

    Formula: C16H18N3NaO5S

    MW: 387.39 g/mol

    Storage/Handling: Store at 2-8°C.

    PubChem Chemical ID: 23663126

    Product Specifications

    Catalog ID: A-551
    CAS #: 34642-77-8
    MW: 387.39 g/mol
    Grade: MOLECULAR BIOLOGY GRADE
    Storage/handling: Store at 4°C.
    PubChem Chemical ID: 23663126
    IUPAC Name: sodium (2S,5R,6R)-6-[[(2R)-2-amino-2-(4-hydroxyphenyl)acetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate
    InChI: InChI=1S/C16H19N3O5S.Na/c1-16(2)11(15(23)24)19-13(22)10(14(19)25-16)18-12(21)9(17)7-3-5-8(20)6-4-7;/h3-6,9-11,14,20H,17H2,1-2H3,(H,18,21)(H,23,24);/q;+1/p-1/t9-,10-,11+,14-;/m1./s1
    InChIKey: BYHDFCISJXIVBV-YWUHCJSESA-M
    SMILES: CC1(C(N2C(S1)C(C2=O)NC(=O)C(C3=CC=C(C=C3)O)N)C(=O)[O-])C.[Na+]

    CITATIONS

    Featured Articles

      Login

      Forgot your password?

      Don't have an account yet?
      Create account