Amoxicillin

Amoxicillin structural formula

CAS Number26787-78-0
Molecular FormulaC16H19N3O5S
Molecular Weight365.400
InChI KeyLSQZJLSUYDQPKJ-NJBDSQKTSA-N
LogP0.87
Synonyms
  • Amoxicillin
  • (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
  • 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[(2R)-2-amino-2-(4-hydroxyphenyl)acetyl]amino]-3,3-dimethyl-7-oxo-, (2S,5R,6R)-
  • 26787-78-0
  • p-Hydroxyampicillin
  • (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
  • 6-[D-(-)-2-Amino-2-(p-hydroxyphenyl)acetamido]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
  • 6-[D-α-Amino-α-(4-hydroxyphenyl)acetamido]penicillanic acid
  • 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[(2R)-amino(4-hydroxyphenyl)acetyl]amino]-3,3-dimethyl-7-oxo-, (2S,5R,6R)-
  • [2S-[2alpha,5alpha,6beta(S*)]]-6-[[Amino(4-hydroxyphenyl)acetyl amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptan-2-carboxylic acid
  • 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[(2R)-2-amino-2-(4-hydroxyphenyl)acetyl]amino]-3,3-dimethyl-7-oxo-, (2S,5R,6R)-
  • 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[amino(4-hydroxyphenyl)acetyl]amino]-3,3-dimethyl-7-oxo-, [2S-[2α,5α,6β(S*)]]-
  • 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[2-amino-2-(p-hydroxyphenyl)acetamido]-3,3-dimethyl-7-oxo-, D-
  • 6-[D-(-)-p-Hydroxy-α-aminobenzyl]penicillin
  • 6-[D(-)-α-Amino-p-hydroxyphenylacetamido]penicillanic acid
  • Abdimox
  • Actimoxi
  • Adbiotin
  • Agerpen
  • Alfamox
  • Almodan
  • Alphamox
  • Amagesen Solutab
  • Amocilline
  • Amoclen
  • Amo-flamsian
  • Amoflux
  • Amopenixin
  • Amosine
  • Amoxapen
  • Amoxaren
  • Amoxcillin
  • Amoxi-basan
  • Amoxibiotic
  • amoxicilina
  • Amoxicillin Chewable Tablets
  • Amoxicilline
  • Amoxidal
  • Amoxiden
  • Amoxidin
  • Amoxihexal
  • Amoxillin
  • Amoxi-Mast
  • Amoxipen
  • Amoxipenil
  • Amoxisol
  • Amoxivan
  • Amoxivet
  • Amoxtrex
  • Amoxycillin
  • Amoxy-diolan
  • Amoxypen
  • Ampidroxyl
  • Ampy-Penyl
  • Anemolin
  • Apitart
  • Apo-Amoxi
  • Aspenil
  • Audumic
  • Azillin
  • Bactamox
  • Betamox
  • Bintamox
  • Bioxidona
  • Bioxyllin
  • Bridopen
  • Bristamox
  • Cabermox
  • Cemoxin
  • Cilamox
  • Clamoxyl
  • Coamoxin
  • Comoxyl
  • D-(-)-α-Amino-p-hydroxybenzyl penicillin
  • D-(α-Amino-p-hydroxybenzyl)penicillin
  • D-2-Amino-2-(4-hydroxyphenyl)acetamidopenicillanic acid
  • Damoxicil
  • D-Amoxicillin
  • Delacillin
  • Draximox
  • Efpenix
  • Efpinex
  • Eupensol
  • Excillin
  • Farconcil
  • Fisamox
  • Flemoxin
  • Foxolin
  • Fullcilina
  • Gimalxina
  • Gomcillin
  • Gramidil
  • Grinsil
  • Grinsul
  • Grunamox
  • Helvamox
  • Hiconcil
  • Hidramox
  • Histocillin
  • Hosboral
  • Ibiamox
  • Ikamoxil
  • Imacillin
  • Imaxilin
  • Intermox
  • Isimoxin
  • Izoltil
  • Jerramcil
  • Kamoxin
  • Larocilin
  • Larotid
  • Majorpen
  • Matasedrin
  • Medimox
  • Metafarma capsules
  • Metifarma capsules
  • Morgenxil
  • Moxacin
  • Moxaline
  • Moxarin
  • Moxilen
  • Moxylin
  • Moxypen
  • Moxyvit
  • Novabritine
  • Novamoxin
  • Novenzymin
  • NSC 277174
  • Ospamox
  • Pamocil
  • Pamoxicillin
  • Pasetocin
  • Penamox
  • Penbiosyn
  • Penimox
  • Piramox
  • Polymox
  • Protexillin
  • Ranmoxy
  • Ranoxyl
  • Reloxyl
  • Rhamoxilina
  • Robamox
  • Rocillin
  • Ronemox
  • Saltermox
  • Samosillin
  • Samthongcillin
  • Sawacillin
  • Sawamezin
  • Sia-mox
  • Sigmopen
  • Sil-A-mox
  • Simoxil
  • Simplamox
  • Specillin
  • Superpeni
  • Suprapen
  • Suramox PM
  • Teramoxyl
  • Tolodina
  • Triafamox
  • Triamoxil
  • Trilaxin
  • Unicillin
  • Velamox
  • Vetomoxin
  • Vetramox
  • Virgoxillin
  • Widecillin
  • Yisulon
  • Zamocillin
  • Zamoxil
  • Zerrsox
  • D-(-)-alpha-Amino-p-hydroxybenzylpenicillin
  • (-)-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-(-)-alpha-Amino-p-hydroxyphenylacetamido)penicillanic acid
  • EINECS 248-003-8
  • 6-(D-(-)-p-Hydroxy-alpha-aminobenzyl)penicillin
  • Sawamox PM
  • DisperMox
  • Moxatag
  • Amoxicillin pediatric
  • Amoxicaps
  • Amoxicillinum
  • UNII-9EM05410Q9
  • 6-(p-hydroxy-alpha-aminophenylacetamido)penicillanic acid
  • AX
  • Amoxicillin
  • Amoxicillin anhydrous
  • alpha-amino-p-hydroxybenzylpenicillin
  • amoxycilin
  • 33911-69-2
  • 71447-36-4
  • 81030-75-3
  • 1236363-38-4

Applications:

HPLC MS Method for Analysis of Amoxicillin on Primesep 100 Column

February 26, 2024

HPLC MS Method for Analysis of Procainamide on Primesep 100 Column

Separation type: Liquid Chromatography Mixed-mode SIELC Technologies

HPLC MS Method for Analysis of Amoxicillin on Primesep 100 Column
HPLC Method for Analysis of Amoxicillin on Primesep 100 Column by SIELC Technologies


 High Performance Liquid Chromatography (HPLC) Method for Analysis of Amoxicillin

Amoxicillin is a widely used antibiotic belonging to the penicillin class. It is used to treat a variety of bacterial infections, including respiratory tract infections, ear infections, skin infections, urinary tract infections, and certain types of bacterial endocarditis.

  • Mechanism of Action: Amoxicillin works by inhibiting the synthesis of bacterial cell walls. It does this by interfering with the formation of peptidoglycan, an essential component of the bacterial cell wall.
  • Spectrum of Activity: Amoxicillin is effective against a broad spectrum of bacteria, including both Gram-positive and Gram-negative bacteria. However, its effectiveness may be limited against bacteria that produce beta-lactamase enzymes.
  • Administration: It is commonly available in oral formulations, such as capsules, tablets, and oral suspensions. There are also intravenous formulations for more severe infections.
  • Common Uses:
  • Respiratory Tract Infections: Amoxicillin is often prescribed for conditions like bronchitis and pneumonia.
  • Ear Infections: It is used to treat middle ear infections.
  • Skin Infections: Amoxicillin can be effective against various skin infections.
  • Urinary Tract Infections (UTIs): It is sometimes prescribed for uncomplicated UTIs.

Amoxicillin can be retained and analyzed using a Primesep 100 mixed-mode stationary phase column. The analysis employs an isocratic method with a simple mobile phase comprising water, acetonitrile (MeCN), and ammonium formate as a buffer. This method allows for detection using UV at 272 nm

ColumnPrimesep 100, 2.1 x 100 mm, 5 µm, 100 A
Mobile PhaseMeCN 20%
BufferAmFm pH 3.0  – 15 mM
Flow Rate0.2 ml/min
DetectionUV 272nm, SIM + 349, 366
Samples1 mg/ml
Injection volume5 µl
LOD*0.3 ppm
* LOD was determined for this combination of instrument, method, and analyte, and it can vary from one laboratory to another even when the same general type of analysis is being performed.

Class of Compounds
Drug
Analyzing CompoundsAmoxicillin

Application Column

Primesep 100

Column Diameter: 2.1 mm
Column Length: 100 mm
Particle Size: 5 µm
Pore Size: 100 A

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Application Analytes:
Amoxicillin

Application Detection:
UV Detection
LC MS Detection
SIELC Technologies usually develops more than one method for each compound. Therefore, this particular method may not be the best available method from our portfolio for your specific application. Before you decide to implement this method in your research, please send us an email to research@sielc.com so we can ensure you get optimal results for your compound/s of interest.

HPLC Separation of β-Lactam Antibiotics such as Amoxicillin and Cephalexin on Primesep 100 Column

March 18, 2021

Separation type: Liquid Chromatography Mixed-mode


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High Performance Liquid Chromatography (HPLC) Method for Analysis of Amoxicillin and Cephalexin.

Both amoxicillin and cephalexin are beta-lactam antibiotics. Beta-lactam antibiotics contain a beta-lactam ring in their molecular structure. As a group, these drugs are active against many gram-positive, gram-negative and anaerobic organisms. Both compounds can be retained and baseline separated with an isocratic method in 30/70 Acetonitrile (ACN) and water mobile phase with a Sulfuric acid (H2SO4) buffer. UV detection at 250 nm.

Condition

Column Primesep 100, 4.6×100 mm, 5 µm, 100A
Mobile Phase MeCN/H2O
Buffer TFA, H2SO4
Flow Rate 1.0 ml/min
Detection UV, 250 nm

 

Description

Class of Compounds
Drug, Antibiotics, Hydrophobic, Ionizable
Analyzing Compounds Cephalexin,  Amoxicillin

 

Application Column

Primesep 100

The Primesep family of mixed-mode columns offers a wide variety of stationary phases, boasting unprecedented selectivity in the separation of a broad array of chemical compounds across multiple applications. Corresponding Primesep guard columns, available with all stationary phases, do not require holders. SIELC provides a method development service available to all customers. Inquire about our specially-tailored custom LC-phases for specific separations.

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Application Analytes:
Amoxicillin
Amoxicillin hydrate (1:3)
Cephalexin
SIELC Technologies usually develops more than one method for each compound. Therefore, this particular method may not be the best available method from our portfolio for your specific application. Before you decide to implement this method in your research, please send us an email to research@sielc.com so we can ensure you get optimal results for your compound/s of interest.

HPLC Separation of Albuterol and Amoxicillin

March 27, 2015

Primesep 100 separates albuterol and amoxicillin with baseline resolution by a combination of cation-exchange, hydrophobic, and polar interactions. The mass spec (LC/MS) compatible separation uses a mobile phase mixture of water, acetonitrile (MeCN, ACN) and trifluoroacetic acid (TFA) with UV detection at 210 nm.

 

Condition

Column Primesep 100, 4.6×150 mm, 5 µm, 100A
Mobile Phase MeCN/H2O – 30/70%
Buffer TFA – 0.15%
Flow Rate 1.0 ml/min
Detection UV, 210 nm

 

Description

Class of Compounds
Drug, Antibiotics, Hydrophobic, Ionizable
Analyzing Compounds Albuterol,  Amoxicillin

 

Application Column

Primesep 100

The Primesep family of mixed-mode columns offers a wide variety of stationary phases, boasting unprecedented selectivity in the separation of a broad array of chemical compounds across multiple applications. Corresponding Primesep guard columns, available with all stationary phases, do not require holders. SIELC provides a method development service available to all customers. Inquire about our specially-tailored custom LC-phases for specific separations.

Select options
Application Analytes:
Albuterol
Amoxicillin

Application Detection:
UV Detection
SIELC Technologies usually develops more than one method for each compound. Therefore, this particular method may not be the best available method from our portfolio for your specific application. Before you decide to implement this method in your research, please send us an email to research@sielc.com so we can ensure you get optimal results for your compound/s of interest.

USP Method for the Analysis of Amoxicillin using the Legacy L1 Column

June 21, 2012

 

Application Notes: Amoxicillin is one of the most commonly prescribed antibiotics. It is often used for treating strep throat. According to USP methods, amoxicillin should not contain less than 900ug and no more than 1050ug of amoxicillin per mg.  The USP HPLC method for the separation of amitriptyline was developed on Legacy L1 column according to the US Pharmacopeia methodology. L1 classification is assigned to reversed-phase HPLC column containing C18 ligand. Support for the material is spherical silica gel with particles size 3-10 um and pore size of 100-120A. Resolution between critical pairs corresponds to rules and specifications of UPS.

Application Columns: Legacy L1 C18 HPLC column

Application compounds: Amoxicillin

Mobile phase: MeCN/50 mM dibasic sodium phosphate

Detection technique: UV

Source: USP35: NF30 

Condition

Column Legacy L1, 4.6×150 mm, 5 µm, 100A
Mobile Phase MeCN/50 mM NaH2PO4  pH 5.0 (4/96)
Buffer NaH2PO4
Flow Rate 1.0 ml/min
Detection UV, 230 nm

 

Description

Class of Compounds
Drug, Antibiotics, Hydrophobic, Ionizable
Analyzing Compounds Amoxicillin

 

Application Column

SIELC Legacy L1 HPLC column

Legacy L1

SIELC's family of Legacy columns is based on the United States Pharmacopeia's (USP) published chromatographic methods and procedures. Numerous brands have columns used in USP reference standards and methods. USP has created various designations to group together columns with similar types of packing and properties in the solid phase. SIELC's Legacy columns adhere to these strict requirements and properties, allowing you to easily replace older columns that are no longer available without needing to significantly modify your method or SOPs.

Select options
Application Analytes:
Amoxicillin

Application Detection:
UV Detection
SIELC Technologies usually develops more than one method for each compound. Therefore, this particular method may not be the best available method from our portfolio for your specific application. Before you decide to implement this method in your research, please send us an email to research@sielc.com so we can ensure you get optimal results for your compound/s of interest.