Amoxicillin

Key Features and Details

Amoxicillin

SYNONYMS: 2S-[2a,5a,6b(S*)]]-6-[[Amino (4-hydroxyphenyl) acetyl]amino]-3,3- dimethyl-7- oxo- 4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid; (-)-6-[2-Amino-2- (p-hydroxyphenyl) acetamido]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo [3.2.0] heptane-2-carboxylic acid; 6-[D(-)- a-Amino-p- hydroxyphenylacetamido]penicillanic acid; a-Amino-p- hydroxybenzylpenicillin; 6-(p-Hydroxy-a-aminophenylacetamido) penicillanic acid; p-Hydroxyampicillin; Amoxycillin; AMPC;Amolin; Amoxi
CAS: # 26787-78-0
MOLECULAR FORMULA: C16H19N3O5S
MOLECULAR WEIGHT: 365.404 g/mol
BEILSTEIN REGISTRY No.: 7507120
EC No: 248-003-8
MDL No: MFCD00056860
SKU 02190145-CF Categories , , Tag

You need to register an account with us
to be able to place an order, Click to Register.

PRODUCT DESCRIPTION

Amoxicillin Application Notes Amoxicillin is a moderate-spectrum, ß-lactam antibiotic . Amoxicillin is one of the most common antibiotics prescribed for children. It is used to study the oxygen dependent antimicrobial systems of polymorphonuclear leukocytes (PMNLs), the risk of resistance development in Helicobacter pylorI, and various dosing strategies against Streptococcus pneumoniae and Pneumococcal pneumonia. It is also used to study the synthesis of bacterial cell walls at the level of peptidoglycan polymer chain cross-linking involving bacterial transpeptidase. Amoxicillin is used to study the synthesis of bacterial cell walls at the level of peptidoglycan polymer chain cross-linking involving bacterial transpeptidase. Usage Statement Unless specified otherwise, MP Biomedical's products are for research or further manufacturing use only, not for direct human use. For more information, please contact our customer service department. Key Applications Antibiotic
SPECIFICATIONS
SKU: 02190145-CF
Base Catalog Number: 190145
Alternate Names: 2S-[2a,5a,6b(S*)]]-6-[[Amino (4-hydroxyphenyl) acetyl]amino]-3,3- dimethyl-7- oxo- 4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid; (-)-6-[2-Amino-2- (p-hydroxyphenyl) acetamido]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo [3.2.0] heptane-2-carboxylic acid; 6-[D(-)- a-Amino-p- hydroxyphenylacetamido]penicillanic acid; a-Amino-p- hydroxybenzylpenicillin; 6-(p-Hydroxy-a-aminophenylacetamido) penicillanic acid; p-Hydroxyampicillin; Amoxycillin; AMPC;Amolin; Amoxi
Beilstein Registration No : 7507120
Biochemical Physiological Actions : Amoxicillin inhibits the synthesis of bacterial cell walls. It inhibits cross-linkage between the linear peptidoglycan polymer chains that make up a major component of the cell walls of both Gram-positive and Gram-negative bacteria.
CAS : # 26787-78-0
EC No : 248-003-8
Format : White Crystalline Powder
Hazard Statements : H317-H334
MDL No : MFCD00056860
Melting Point : 194 °C
Molecular Formula : C16H19N3O5S
Molecular Weight : 365.404 g/mol
PPE : Eyeshields, Faceshields, Gloves
RTECS No : XH8300000
Safety Symbol : GHS08
Solubility : 10.7 [ug/mL]
Typical Working Concentration : Typically used at a concentration of 100 ug/mL and is stable in media at 37 °C for approximately 3 days.
Vapor Pressure : 4.69X10-17 mm Hg at 25 deg C (est)

© All rights reserved byJuniperlifesciences.com 2021

All logos and Trademarks are names the property of their respective owners.

Shopping Cart
Scroll to Top

Enquire

Submit your details and receive all the download links in your email

Login to your account
Login to your account