3-Fluorophenylacetic acid

CAS Number331-25-9
Molecular Formula C8H7FO2
Molecular Weight154.14
InChI KeyYEAUYVGUXSZCFI-UHFFFAOYSA-N
LogP1.7
Synonyms
  • 3-Fluorophenylacetic acid
  • 331-25-9
  • 2-(3-fluorophenyl)acetic acid
  • Benzeneacetic acid, 3-fluoro-
  • m-Fluorophenylacetic acid
  • (3-fluorophenyl)acetic acid
  • 3-Fluorophenyl acetic acid
  • 3-Fluorophenlacetic acid
  • Acetic acid, (m-fluorophenyl)-
  • (m-Fluorophenyl)acetic acid
  • MFCD00004331
  • 3-Fluorophenylaceticacid
  • EINECS 206-360-7
  • NSC 88344
  • PubChem4167
  • ACMC-209hyk
  • m-Fluorophenyl acetic acid
  • SCHEMBL9113
  • 3-fluoro phenyl acetic acid
  • NCIOpen2_001447
  • CHEMBL136104
  • RARECHEM AL BO 0121
  • DTXSID0059821
  • 3-Fluorophenylacetic acid, 98%

Applications:

HPLC Method for 2-Fluorophenylacetic acid, 4-Fluorophenylacetic acid, 3-Fluorophenylacetic acid Compatible with Mass Spectrometry

October 1, 2021

Separation type: Liquid Chromatography Mixed-mode


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High Performance Liquid Chromatography (HPLC) Method for Analysis of 2-Fluorophenylacetic acid , 4-Fluorophenylacetic acid,  3-Fluorophenylacetic acid

2-Fluorophenylacetic acid is a popular chiral derivatizing agent used in 19F NMR spectroscopy. 3-Fluorophenylacetic acid is a common precursor for synthesizing various pentaamine and bis-heterocyclic compounds. 4-Fluorophenylacetic acid is a common intermediary compound used to produce fluorinated anesthetics. While these 3 compounds all have the same chemical formula, the position of the Fluoride group varies between them, changing slightly their retention and chromatographic characteristics.
All 3 isomers can be measured at low UV. Using a Primsep SB reverse-phase column and a mobile phase consisting of acetonitrile (MeCN) and water with either formic acid or acetic acid buffer, these fluorophenylacetic acid isomers can be retained, separated, and UV detected at 264 nm with precise resolution. This method is compatible with Mass Spectrometry.

 

Condition 1

Column Primesep SB, 4.6×250 mm, 5 µm, 100A
Mobile Phase MeCN/H2O – 40/60%
Buffer Formic Acid – 0.2%
Flow Rate 1.0 ml/min
Detection UV 264  nm

Condition 2

Column Primesep SB, 4.6×250 mm, 5 µm, 100A
Mobile Phase MeCN/H2O – 60/40%
Buffer Acetic Acid – 2.0%
Flow Rate 1.0 ml/min
Detection UV 264  nm

Description

Class of Compounds Acid
Analyzing Compounds 2-Fluorophenylacetic acid (2-FPAA), 4-Fluorophenylacetic acid (4-FPAA), 3-Fluorophenylacetic acid

 

Application Column

Primesep SB

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:
2-Fluorophenylacetic acid
3-Fluorophenylacetic acid
4-Fluorophenylacetic acid
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 2-Fluorophenylacetic acid, 4-Fluorophenylacetic acid, 3-Fluorophenylacetic acid on Primesep SB Column

September 29, 2021

Separation type: Liquid Chromatography Mixed-mode


HPLC.cloud
View on hplc.cloud

High Performance Liquid Chromatography (HPLC) Method for Analysis of 2-Fluorophenylacetic acid , 4-Fluorophenylacetic acid,  3-Fluorophenylacetic acid

2-Fluorophenylacetic acid is a popular chiral derivatizing agent used in 19F NMR spectroscopy. 3-Fluorophenylacetic acid is a common precursor for synthesizing various pentaamine and bis-heterocyclic compounds. 4-Fluorophenylacetic acid is a common intermediary compound used to produce fluorinated anesthetics. While these 3 compounds all have the same chemical formula, the position of the Fluoride group varies between them, changing slightly their retention and chromatographic characteristics.
All 3 isomers can be measured at low UV. Using a Primsep SB reverse-phase columns and a mobile phase consisting of acetonitrile (MeCN) and water with either formic acid or acetic acid buffer, these fluorophenylacetic acid isomers can be retained, separated, and UV detected at 210nm with precise resolution.

 
Column Newcrom BH, 4.6×250 mm, 3 µm, 100A
Mobile Phase MeCN/H2O – 30/70%
Buffer H3PO4 – 0.05%
Flow Rate 1.0 ml/min
Detection UV 210  nm

Condition 2

Column Primesep SB, 4.6×250 mm, 5 µm, 100A
Mobile Phase MeCN/H2O – 40/60%
Buffer H3PO4 – 0.1%
Flow Rate 1.0 ml/min
Detection UV 210  nm

Description

Class of Compounds Acid
Analyzing Compounds 2-Fluorophenylacetic acid (2-FPAA), 4-Fluorophenylacetic acid (4-FPAA), 3-Fluorophenylacetic acid

Application Column

Primesep SB

Column Diameter: 4.6 mm
Column Length: 250 mm
Particle Size: 5 µm
Pore Size: 100 A

Add to cart
Application Analytes:
2-Fluorophenylacetic acid
3-Fluorophenylacetic acid
4-Fluorophenylacetic acid
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 2-Fluorophenylacetic acid, 4-Fluorophenylacetic acid, 3-Fluorophenylacetic acid on Newcrom BH Column

June 5, 2021

Separation type: Liquid Chromatography Mixed-mode


HPLC.cloud
View on hplc.cloud

High Performance Liquid Chromatography (HPLC) Method for Analysis of 2-Fluorophenylacetic acid , 4-Fluorophenylacetic acid,  3-Fluorophenylacetic acid

2-Fluorophenylacetic acid is a popular chiral derivatizing agent used in 19F NMR spectroscopy. 3-Fluorophenylacetic acid is a common precursor for synthesizing various pentaamine and bis-heterocyclic compounds. 4-Fluorophenylacetic acid is a common intermediary compound used to produce fluorinated anesthetics. While these 3 compounds all have the same chemical formula, the position of the Fluoride group varies between them, changing slightly their retention and chromatographic characteristics.
All 3 isomers can be measured at low UV. Using a Newcrom BH reverse-phase columns and a mobile phase consisting of acetonitrile (MeCN) and water with either formic acid or acetic acid buffer, these fluorophenylacetic acid isomers can be retained, separated, and UV detected at 210 nm with precise resolution.

 
Column Newcrom BH, 4.6×250 mm, 3 µm, 100A
Mobile Phase MeCN/H2O – 30/70%
Buffer H3PO4 – 0.05%
Flow Rate 1.0 ml/min
Detection UV 210  nm

Description

Class of Compounds Acid
Analyzing Compounds 2-Fluorophenylacetic acid (2-FPAA), 4-Fluorophenylacetic acid (4-FPAA), 3-Fluorophenylacetic acid

Application Column

Newcrom BH

Column Diameter: 4.6 mm
Column Length: 250 mm
Particle Size: 3 µm
Pore Size: 100 A

Add to cart
Application Analytes:
2-Fluorophenylacetic acid
3-Fluorophenylacetic acid
4-Fluorophenylacetic acid

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.