Aniline

Aniline structural formula

CAS Number62-53-3
Molecular FormulaC6H7N
Molecular Weight93.129
InChI KeyPAYRUJLWNCNPSJ-UHFFFAOYSA-N
LogP0.9
Synonyms
  • Aniline
  • Benzenamine
  • 62-53-3
  • Benzenamine
  • 6253-3 Aniline
  • Aminobenzene
  • Aminophen
  • ANILIN, REIN
  • ANILIN, TECHNISCH
  • anilina
  • Benzene, amino-
  • Benzeneamine
  • Blue Oil
  • NCI 176889
  • Phenylamine
  • UN 1547
  • C.I. Oxidation Base 1
  • Aniline oil
  • Arylamine
  • Benzene, amino
  • Caswell No. 051C
  • CI Oxidation Base 1
  • EINECS 200-539-3
  • EPA Pesticide Chemical Code 251400
  • NCI-C03736
  • RCRA waste number U012
  • Huile d'aniline
  • UNII-SIR7XX2F1K
  • Anilin
  • Aniline hydrobromide
  • Aniline reagent
  • Anyvim
  • Benzidam
  • Cyanol
  • D'Aniline
  • Krystallin
  • kyanol
  • 146997-94-6
  • 37342-16-8

Applications:

HPLC Method for Analysis of Aniline on Primesep 100 Column

August 1, 2024

High Performance Liquid Chromatography (HPLC) Method for Analysis of Aniline on Primesep 100 by SIELC Technologies

Separation type: Liquid Chromatography Mixed-mode SIELC Technologies

HPLC Method for Analysis of Aniline on Primesep 100 Column


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

Aniline is an organic compound consists of a phenyl group attached to an amino group.

Chemical Properties: Aniline is a primary aromatic amine. It is a colorless to slightly yellow liquid with a characteristic odor.

Production: Aniline is produced by the reduction of nitrobenzene or by the catalytic hydrogenation of nitrobenzene.

Uses: Aniline is a precursor to many industrial chemicals. It is used in the manufacture of polyurethane foam, rubber chemicals, dyes, agricultural chemicals, and pharmaceuticals. Aniline derivatives are also used as intermediates in the production of pigments and perfumes.

Toxicity: Aniline is toxic and can be absorbed through the skin, inhaled, or ingested. It can cause methemoglobinemia, a condition where hemoglobin is converted to methemoglobin, which cannot carry oxygen efficiently.

Aniline 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 sulfuric acid as a buffer. This method allows for detection using UV 200 nm

ColumnPrimesep 100, 4.6 x 150 mm, 5 µm, 100 A
Mobile PhaseMeCN – 45%
BufferH2SO4 -0.05%
Flow Rate1.0 ml/min
DetectionUV 200 nm
Samples1.2 mg/ml in MeCN/H2O – 50/50%
Injection volume1 µl
LOD*10 ppb (200 nm)
* 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
Aromatic amines
Analyzing CompoundsAniline

Application Column

Primesep 100

Column Diameter: 4.6 mm
Column Length: 150 mm
Particle Size: 5 µm
Pore Size: 100 A

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Application Analytes:
Aniline

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.

Separation of Aniline on Newcrom R1 HPLC column

May 16, 2018
Separation of Aniline on Newcrom R1 HPLC column

Aniline is a compound made up of a benzene ring attached to an amino group. It is a precursor to many chemical compounds and used in rubber processing agents, dyes, and herbicides. Aniline can be analyzed by this reverse phase (RP) HPLC method with simple conditions. The mobile phase contains acetonitrile (MeCN), water, and phosphoric acid. For Mass-Spec (MS) compatible applications the phosphoric acid needs to be replaced with formic acid. Smaller 3 µm particle columns are available for fast UPLC applications. This liquid chromatography method is scalable and can be used for isolation of impurities in preparative separation. It also suitable for pharmacokinetics.

Application Column

Newcrom R1

The Newcrom columns are a family of reverse-phase-based columns. Newcrom A, AH, B, and BH are all mixed-mode columns with either positive or negative ion-pairing groups attached to either short (25 Å) or long (100 Å) ligand chains. Newcrom R1 is a special reverse-phase column with low silanol activity.

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Application Analytes:
Aniline
The result was obtained by a proprietary SIELC algorithm. It may deviate from the actual experimental data. The experimental data are available upon request. Contact us by e-mail: support@sielc.com or by phone: 847-229-2629.

HPLC Method for Analysis of Pesticides: Thiamphenicol, Aniline, Simazine, Alachlor, Thiabendazole, Diazinon, Trifluralin on Primesep B2 Column

July 11, 2017

 

Condition 

Column Primesep B2, 3.2×100 mm, 5 µm, 100A
Mobile Phase Gradient MeCN – 35-85%, 6 min , 4 min hold
Buffer Gradient H2SO4 – 0.05- 0.15%, 6 min, 4 min hold
Flow Rate 0.6 ml/min
Detection UV, 230 nm

 

Description

Class of Compounds
Drug, Acid, Hydrophilic, Ionizable, Vitamin, Supplements
Analyzing Compounds Thiamphenicol, Aniline, Simazine, Alachlor, Thiabendazole, Diazinon, Trifluralin

 

Application Column

Primesep B2

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:
Alachlor
Aniline
Diazinon
Simazine
Thiabendazole
Thiamphenicol
Trifluralin
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.