Ethyl red

Ethyl_red

CAS Number76058-33-8
Molecular FormulaC17H19N3O2
Molecular Weight297.358
InChI KeyHBRCDTRQDHMTDA-UHFFFAOYSA-N
LogP4.1
Synonyms
  • Ethyl red
  • 76058-33-8
  • UNII-FTV19WGM7I
  • DIETHYL RED
  • FTV19WGM7I
  • 4-Diethylaminoazobenzene-2'-carboxylic acid
  • HBRCDTRQDHMTDA-UHFFFAOYSA-N
  • Benzoic acid, 2-[[4-(diethylamino)phenyl]azo]-
  • 2-{2-[4-(diethylamino)phenyl]diazen-1-yl}benzoic acid
  • 2-[[4-(diethylamino)phenyl]diazenyl]benzoic acid
  • 2-{[4-(diethylamino)phenyl]diazenyl}benzoic acid
  • Benzoic acid, 2-((4-(diethylamino)phenyl)azo)-
  • Ethyl Red Indicator

Applications:

UV-Vis Spectrum of Ethyl Red

July 16, 2024

Access the UV-Vis Spectrum SIELC Library

 

UV-Vis Spectrum of Ethyl Red. Absorption Maxima: 218 nm, 292 nm, 520 nm.

If you are looking for optimized HPLC method to analyze Ethyl red check our HPLC Applications library

For optimal results in HPLC analysis, it is recommended to measure absorbance at a wavelength that matches the absorption maximum of the compound(s) being analyzed. The UV spectrum shown can assist in selecting an appropriate wavelength for your analysis. Please note that certain mobile phases and buffers may block wavelengths below 230 nm, rendering absorbance measurement at these wavelengths ineffective. If detection below 230 nm is required, it is recommended to use acetonitrile and water as low UV-transparent mobile phases, with phosphoric acid and its salts, sulfuric acid, and TFA as buffers.
For some compounds, the UV-Vis Spectrum is affected by the pH of the mobile phase. The spectra presented here are measured with an acidic mobile phase that has a pH of 3 or lower.

Application Analytes:
Ethyl red
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 Method for Separation of Methyl Red and Ethyl Red on Primesep 100 Column

December 22, 2022

High Performance Liquid Chromatography (HPLC) Method for Separation of Methyl Red, Ethyl red on Primesep 100 by SIELC Technologies.

HPLC Method for Separation of Меthyl Red and Ethyl Red on Primesep 100 Column
HPLC Method for Separation of Methyl Red, Ethyl red on Primesep 100 Column by SIELC Technologies

Methyl Red, also known as C.I. Acid Red 2, is a dark-red, single-charged basic dye that turns a deep red in acidic (low pH) solutions and yellow at solution with pH above 6.2. It has the chemical formula C15H15N3O2. You can find detailed UV spectra of Methyl Red and information about its various lambda maxima by visiting the following link.

Ethyl red is a pH indicator with C17H19N3O2 as its molecular structure. When the pH transitions from acidic to neutral, Ethyl red turns from yellow to red, hence the name. Outside of experiments, it is occasionally used as a dye in textiles and foods. You can find detailed UV spectra of Ethyl Red and information about its various lambda maxima by visiting the following link.

Methyl Red, Ethyl red can be separated, retained, and analyzed on a Primesep 100 mixed-mode stationary phase column using an isocratic analytical method with a simple mobile phase of water, Acetonitrile (MeCN), and a sulfuric acid (H2SO4) buffer. This analysis method can be detected in the Visible spectrum at 520 nm.

Condition

ColumnPrimesep 100, 4.6 x 150 mm, 5 µm, 100 A, dual ended
Mobile PhaseMeCN/H2O – 60/40%
BufferH3PO4 – 0.2%
Flow Rate1.0 ml/min
DetectionVis, 520 nm
Peak Retention Time6.19, 7.28 min

Description

Class of CompoundsDyes
Analyzing CompoundsMethyl Red, Ethyl red

Application Column

Primesep 100

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

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Application Analytes:
Ethyl red
Methyl Red

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.

HPLC Method for Analysis of Pararosaniline and Ethyl Red on Primesep 100 Column

December 7, 2022

High Performance Liquid Chromatography (HPLC) Method for Analysis of Pararosaniline and Ethyl Red on Primesep 100 by SIELC Technologies.

HPLC Method for Analysis of Pararosaniline and Ethyl Red on Primesep 100 Column
HPLC Method for Analysis of Pararosaniline Hydrochloride, Ethyl red on Primesep 100 Column by SIELC Technologies

Pararosaniline (Basic Red 9) is a popular basic magenta dye and part of the triarylmethane family of dyes with the chemical formula C19H17N3. It is a free base version of pararosaniline hydrochloride. Primarily, it is used to dye synthetic materials, to detect sulfur dioxide, and as an antischistosomal. You can find detailed UV spectra of Pararosaniline and information about its various lambda maxima by visiting the following link.

Ethyl Red is a pH indicator with C₁₇H₁₉N₃O₂ as its molecular structure. When the pH transitions from acidic to neutral, Ethyl red turns from yellow to red, hence the name. Outside of experiments, it is occasionally used as a dye in textiles and foods. You can find detailed UV spectra of Pararosaniline Hydrochloride, Ethyl red and information about its various lambda maxima by visiting the following link.

These two basic dyes can be separated, retained, and analyzed on a Primesep 100 mixed-mode stationary phase column using an isocratic analytical method with a simple mobile phase of water, Acetonitrile (MeCN), and a sulfuric acid (H2SO4) buffer. This analysis method can be detected in the visible regime at 520 nm.

Condition

ColumnPrimesep 100, 4.6 x 150 mm, 5 µm, 100 A, dual ended
Mobile PhaseMeCN/H2O – 50/50%
BufferH3PO4 – 0.2%
Flow Rate1.0 ml/min
DetectionUV, 520 nm
Peak Retention Time10.82 min

Description

Class of CompoundsDyes
Analyzing CompoundsPararosaniline Hydrochloride, Ethyl red

Application Column

Primesep 100

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

Add to cart
Application Analytes:
Ethyl red
Pararosaniline Hydrochloride

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.

HPLC Method for Analysis of Ethyl Red on Primesep 100 Column

December 7, 2022

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

HPLC Method for Analysis of Ethyl Red on Primesep 100 Column
HPLC Method for Analysis of Ethyl red on Primesep 100 Column by SIELC Technologies

Ethyl Red is a pH indicator with C₁₇H₁₉N₃O₂ as its molecular structure. When the pH transitions from acidic to neutral, Ethyl red turns from yellow to red, hence the name. Outside of experiments, it is occasionally used as a dye in textiles and foods. You can find detailed UV spectra of Ethyl red and information about its various lambda maxima by visiting the following link.

Ethyl red can be retained and analyzed on a Primesep 100 mixed-mode stationary phase column using an isocratic analytical method with a simple isocratic mobile phase of water, Acetonitrile (MeCN), and a sulfuric acid (H2SO4) buffer.  This analysis method can be UV detected at 600 nm with high resolution and peak symmetry.

Condition

ColumnPrimesep 100, 4.6 x 150 mm, 5 µm, 100 A, dual ended
Mobile PhaseMeCN/H2O – 80/20%
BufferH3PO4 – 0.2%
Flow Rate1.0 ml/min
DetectionUV, 550 nm
Peak Retention Time3.82 min

Description

Class of CompoundsDyes
Analyzing CompoundsEthyl red

Application Column

Primesep 100

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

Add to cart
Application Analytes:
Ethyl red

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.

HPLC Method for Analysis of Ethyl Red

June 1, 2018

HPLC Method for Ethyl red on Newcrom R1 by SIELC Technologies

HPLC Method for Analysis of Ethyl red

High Performance Liquid Chromatography (HPLC) Method for Analysis of Ethyl red 

Ethyl red is a pH indicator with C₁₇H₁₉N₃O₂ as its molecular structure. When the pH transitions from acidic to neutral, Ethyl red turns from yellow to red, hence the name. Outside of experiments, it is occasionally used as a dye in textiles and foods. You can find detailed UV spectra of Ethyl red and information about its various lambda maxima by visiting the following link.

Ethyl red can be retained and analyzed using the Newcrom R1 stationary phase column. The analysis utilizes an isocratic method with a simple mobile phase consisting of water and acetonitrile (MeCN) with a phosphoric acid buffer. Detection is performed using UV.

ColumnNewcrom R1, 3.2 x 100 mm, 5 µm, 100 A, dual ended
Mobile PhaseMeCN/H2O – 60/10%
BufferH3PO4 – 0.1%
Flow Rate0.5 ml/min
DetectionUV, 250 nm
Class of Compounds
Dye, Hydrophobic
Analyzing CompoundsEthyl red

Application Column

Newcrom R1

Column Diameter: 3.2 mm
Column Length: 100 mm
Particle Size: 5 µm
Pore Size: 100 A
Column options: dual ended

Add to cart
Application Analytes:
Ethyl red

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.