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Home » Bolg » Detection methods for p-bromoaniline

Detection methods for p-bromoaniline

Publish Time: 2024-10-10     Origin: Site

Basic Information:

Alias: 4-Bromoaniline, p-Bromoaniline

CAS No: 106-40-1

Molecular Formula: C6H6BrN

Molecular Weight: 172.02

Physical State:White to light yellow to light orange solid

Melting Point:56-62°C (lit.)

Boiling Point:230-250°C

Uses:Used in the manufacturing of azo dyes and organic synthesis

Employed in the preparation of dihydroquinazoline


4-Bromoanilineis an important organic compound widely used in fields such as pharmaceuticals, dyes, and pesticides. Due to its toxicity and potential environmental hazards, effective detection methods are crucial. This article introduces several commonly used methods for detecting 4-Bromoaniline, including gas chromatography (GC), high-performance liquid chromatography (HPLC), UV-visible spectrophotometry, and mass spectrometry (MS).


Gas Chromatography (GC)

Gas chromatography is an efficient and sensitive method commonly used for detecting 4-Bromoaniline. The basic principle involves separating the sample using a gas chromatograph and quantitatively analyzing the separated compounds with a detector. The specific steps are as follows:

Sample Preparation: Dissolve the sample in an appropriate solvent, such as ethanol or methanol.

Column Selection: Choose a suitable column, such as a non-polar column.

Detector: Typically, a flame ionization detector (FID) or mass spectrometry detector (MS) is used.

Data Processing: Analyze the retention time and peak area of 4-Bromoaniline from the chromatogram for qualitative and quantitative analysis.


High-Performance Liquid Chromatography (HPLC)

HPLC is a commonly used liquid phase separation technique suitable for detecting 4-Bromoaniline. The principle involves separating the compounds in the sample using a liquid chromatograph, followed by analysis with a detector. The specific steps are as follows:

Sample Preparation: Dissolve the sample in an appropriate solvent.

Column Selection: Choose a suitable reversed-phase column (e.g., C18 column).

Mobile Phase: Select an appropriate mobile phase, such as a water-acetonitrile mixture.

Detector: Typically, a UV detector or mass spectrometry detector (MS) is used.

Data Processing: Analyze the retention time and peak area of 4-Bromoanilinefrom the chromatogram for qualitative and quantitative analysis.


Ultraviolet-Visible Spectrophotometry (UV-Vis)

UV-Vis spectrophotometry is a simple and rapid method for the quantitative analysis of 4-Bromoaniline. The principle is based on measuring the absorbance of 4-Bromoaniline at a specific wavelength. The procedure includes the following steps:

Sample Preparation: Dissolve the sample in an appropriate solvent.

Wavelength Selection: Choose the characteristic absorption wavelength of 4-Bromoaniline, typically measured at its λ_max.

Absorbance Measurement: Use a spectrophotometer to measure the absorbance of the sample at the selected wavelength.

Quantitative Analysis: Perform quantitative analysis by using a standard curve method to calculate the concentration of 4-Bromoaniline.


Mass Spectrometry (MS)

Mass spectrometry is a highly sensitive analytical technique suitable for the precise analysis of 4-Bromoaniline. The method operates by ionizing the sample, separating the ions using a mass analyzer, and detecting them based on their mass-to-charge ratio (m/z). The steps include:

Sample Preparation: Dissolve the sample in an appropriate solvent.

Ionization Method: Select a suitable ionization technique, such as Electron Ionization (EI) or Electrospray Ionization (ESI).

Mass Analyzer: Use an appropriate mass analyzer, such as a quadrupole mass spectrometer or time-of-flight (TOF) mass spectrometer.

Data Processing: Analyze the mass spectrum to determine the mass-to-charge ratio of 4-Bromoaniline for qualitative and quantitative analysis.


There are various methods for detecting 4-Bromoaniline, including gas chromatography (GC), high-performance liquid chromatography (HPLC), ultraviolet-visible spectrophotometry (UV-Vis), and mass spectrometry (MS). Each method has its own advantages and disadvantages, and the appropriate method should be chosen based on specific detection requirements and sample characteristics. The proper application of these detection methods can not only improve detection efficiency but also ensure the accuracy and reliability of the results.


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