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MW 365.4 Da, Purity >98%. β-lactam antibiotic. 4-hydroxy analog of ampicillin. Shows antibacterial activity. Inhibits cross-linkage between linear peptidoglycan polymer chains of Gram-positive and Gram-negative bacterial cell walls.
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CAS number

26787-78-0

Purity

> 98%

Form

Solid

Molecular weight

365.4 Da

Molecular formula

C16H19N3O5S

PubChem identifier

33613

Nature

Synthetic

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United States

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MW 365.4 Da, Purity >98%. β-lactam antibiotic. 4-hydroxy analog of ampicillin. Shows antibacterial activity. Inhibits cross-linkage between linear peptidoglycan polymer chains of Gram-positive and Gram-negative bacterial cell walls.
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Key facts

Purity

> 98%

PubChem identifier

33613

Solubility

In water, 3.43X10+3 mg/L at 25 °C (est). 1 g sol in about 370 mL water, about 2000 mL alc, about 290 mL phosphate buffer (1%, ph 7), about 330 mL methanol.

Biochemical name

Amoxicillin

Biological description

β-lactam antibiotic. 4-hydroxy analog of ampicillin. Shows antibacterial activity. Inhibits cross-linkage between linear peptidoglycan polymer chains of Gram-positive and Gram-negative bacterial cell walls.

Canonical SMILES

CC1(C(N2C(S1)C(C2=O)NC(=O)C(C3=CC=C(C=C3)O)N)C(=O)O)C

Isomeric SMILES

CC1([C@@H](N2[C@H](S1)[C@@H](C2=O)NC(=O)[C@@H](C3=CC=C(C=C3)O)N)C(=O)O)C

InChI

InChI=1S/C16H19N3O5S/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)/t9-,10-,11+,14-/m1/s1

InChIKey

LSQZJLSUYDQPKJ-NJBDSQKTSA-N

IUPAC name

(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-carboxylic acid

Storage

Shipped at conditions

Ambient - Can Ship with Ice

Appropriate long-term storage conditions

+4°C

Storage information

Store under desiccating conditions, The product can be stored for up to 12 months

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Product protocols

For this product, it's our understanding that no specific protocols are required. You can:

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