Methyl Red

Methyl Red is one of the most widely used pH indicators in chemistry, recognized for its distinct color changes and its utility in acid-base titrations. It plays a critical role in various fields, including analytical chemistry, microbiology, and environmental testing. In this detailed guide, we provide an exhaustive overview of methyl red, covering its chemical properties, uses, applications, and much more.

Introduction to Methyl Red

Methyl Red (chemical formula: C15H15N3O2) is a synthetic azo dye used as a pH indicator in laboratory analysis. This compound changes color depending on the acidity or basicity of the solution, a characteristic that makes it highly valuable in titrimetric analyses.

  • IUPAC Name: 2-(N,N-Dimethyl-4-aminophenylazo)benzoic acid
  • Molar Mass: 269.30 g/mol
  • Solubility: Slightly soluble in water; more soluble in ethanol and acetone
  • Appearance: Orange-red powder

pH Range and Color Change

One of methyl red’s most important attributes is its distinct pH transition range:

  • pH Range: 4.4 to 6.2
  • Color in Acidic Solution (pH < 4.4): Red
  • Color in Neutral to Basic Solution (pH > 6.2): Yellow

Between these two points, the color of the solution changes through various shades of orange, making it an ideal indicator for strong acid to weak base titrations.

Chemical Structure and Properties

Methyl Red

Methyl red belongs to the azo dye class of compounds, characterized by the presence of the functional group R-N=N-R’. Its conjugated double bonds give it its vibrant color, and its pH sensitivity arises from protonation and deprotonation of the azo and carboxyl groups under different pH conditions.

Key Chemical Properties:

  • Melting Point: 179–182 °C
  • pKa: Approximately 5.1
  • UV-Visible Absorption Maxima:
    • Acidic form: 520 nm (red)
    • Basic form: 430 nm (yellow)

Preparation and Synthesis of Methyl Red

The synthesis of methyl red is a classic example of diazotization followed by azo coupling, typically performed in organic chemistry laboratories.

  1. Diazotization:
    • p-Aminodimethylaniline is treated with sodium nitrite and hydrochloric acid at low temperature to form a diazonium salt.
  2. Coupling Reaction:
    • The diazonium salt is then reacted with anthranilic acid, resulting in the formation of methyl red.

This method showcases foundational chemical reactions used in azo dye synthesis, making methyl red a popular compound in educational labs.

Applications of Methyl Red

Methyl Red

1. Acid-Base Titrations

Methyl red is extensively used in analytical chemistry as an indicator for titrations involving strong acids and weak bases. Its sharp and distinct color change near the mid-acidic pH range makes it ideal for precise endpoint determination.

2. Microbiology: Methyl Red Test

In microbiology, the Methyl Red (MR) test is a key component of the IMViC tests used to differentiate Enterobacteriaceae species.

  • Purpose: Determines whether the organism produces stable acid end products from glucose fermentation.
  • Procedure: After incubation in a buffered glucose broth, methyl red is added.
    • Red color = Positive result (acidic end products)
    • Yellow color = Negative result

This test is commonly used to distinguish Escherichia coli (MR positive) from Enterobacter aerogenes (MR negative).

3. Environmental and Wastewater Analysis

Methyl red is employed in monitoring wastewater treatment processes, where pH levels need to be strictly controlled. The indicator helps in real-time pH assessment, aiding in maintaining optimal conditions for microbial digestion.

Storage and Handling Precautions

As with many laboratory reagents, methyl red requires careful handling:

Advantages of Using Methyl Red

  • Clear visual transition makes it easy to determine pH changes.
  • Stable and reliable in a variety of titration environments.
  • Useful in both chemical and biological experimental settings.
  • Cost-effective and readily available in multiple forms (powder, solution).

Limitations of Methyl Red

Despite its usefulness, methyl red does have limitations:

  • Narrow pH range restricts its use to specific titration types.
  • Not suitable for strong base titrations due to its acidic transition zone.
  • It can be toxic to aquatic environments if not disposed of correctly.

Alternatives to Methyl Red

Methyl Red

In cases where methyl red is not suitable, several alternative indicators may be used:

  • Phenolphthalein: pH range 8.2–10.0; colorless to pink
  • Methyl Orange: pH range 3.1–4.4; red to yellow
  • Bromothymol Blue: pH range 6.0–7.6; yellow to blue

The choice depends on the specific acid-base strength involved in the reaction.

Methyl Red in Educational Settings

Methyl red is commonly used in educational laboratories to teach concepts related to acid-base reactions, colorimetry, and organic synthesis. Its vivid color transitions help students visualize chemical changes effectively, fostering deeper understanding.

Conclusion

Methyl red remains a fundamental tool in the chemist’s arsenal due to its well-defined pH transition, stability, and versatility across various scientific disciplines. Whether for routine titrations, microbial differentiation, or pH monitoring in environmental samples, its relevance endures.

Proper usage, storage, and disposal ensure that methyl red continues to serve as a safe and effective indicator across a range of applications. Understanding its properties not only enhances analytical accuracy but also strengthens foundational scientific knowledge.

What is Methyl red?


Methyl Red is one of the most widely used pH indicators in chemistry, recognized for its distinct color changes and its utility in acid-base titrations. It plays a critical role in various fields, including analytical chemistry, microbiology, and environmental testing. In this detailed guide, we provide an exhaustive overview of methyl red, covering its chemical properties, uses, applications, and much more.
Introduction
Methyl (chemical formula: C15H15N3O2) is a synthetic azo dye used as a pH indicator in laboratory analysis. This compound changes color depending on the acidity or basicity of the solution, a characteristic that makes it highly valuable in titrimetric analyses.
IUPAC Name: 2-(N,N-Dimethyl-4-aminophenylazo) benzoic acid
Molar Mass: 269.30 g/mol
Solubility: Slightly soluble in water; more soluble in ethanol and acetone
Appearance: Orange-red powder
pH Range and Color Change
One of methyl red’s most important attributes is its distinct pH transition range:
pH Range: 4.4 to 6.2
Color in Acidic Solution (pH < 4.4): Red
Color in Neutral to Basic Solution (pH > 6.2): Yellow
Between these two points, the color of the solution changes through various shades of orange, making it an ideal indicator for strong acid to weak base titrations.
Chemical Structure and Properties
Methyl belongs to the azo dye class of compounds, characterized by the presence of the functional group R-N=N-R’. Its conjugated double bonds give it its vibrant color, and its pH sensitivity arises from protonation and deprotonation of the azo and carboxyl groups under different pH conditions.
Key Chemical Properties:
Melting Point: 179–182 °C
pKa: Approximately 5.1
UV-Visible Absorption Maxima: Acidic form: 520 nm (red)
Basic form: 430 nm (yellow)
Preparation and Synthesis
The synthesis of methyl red is a classic example of diazotization followed by azo coupling, typically performed in organic chemistry laboratories.
Diazotization: p-Aminodimethylaniline is treated with sodium nitrite and hydrochloric acid at a low temperature to form a diazonium salt.
Coupling Reaction: The diazonium salt is then reacted with anthranilic acid, resulting in the formation of methyl red.
This method showcases foundational chemical reactions used in azo dye synthesis, making it a popular compound in educational labs.
Applications
1. Acid-Base Titrations
It is extensively used in analytical chemistry as an indicator for titrations involving strong acids and weak bases. Its sharp and distinct color change near the mid-acidic pH range makes it ideal for precise endpoint determination.
2. Microbiology: Test
In microbiology, the (MR) test is a key component of the IMViC tests used to differentiate Enterobacteriaceae species.
Purpose: Determines whether the organism produces stable acid end products from glucose fermentation.
Procedure: After incubation in a buffered glucose broth, methyl red is added. Red color = Positive result (acidic end products)
Yellow color = Negative result
This test is commonly used to distinguish Escherichia coli (MR positive) from Enterobacter aerogenes (MR negative).
3. Environmental and Wastewater Analysis
It is employed in monitoring wastewater treatment processes, where pH levels need to be strictly controlled. The indicator helps in real-time pH assessment, aiding in maintaining optimal conditions for microbial digestion.
Storage and Handling Precautions
As with many laboratory reagents, methyl red requires careful handling:
Advantages of Using
A clear visual transition makes it easy to determine pH changes.
Stable and reliable in a variety of titration environments.
Useful in both chemical and biological experimental settings.
Cost-effective and readily available in multiple forms (powder, solution).
Limitations
Despite its usefulness, methyl red does have limitations:
Narrow pH range restricts its use to specific titration types.
Not suitable for strong base titrations due to its acidic transition zone.
It can be toxic to aquatic environments if not disposed of correctly.
Alternatives
In cases where methyl red is not suitable, several alternative indicators may be used:
Phenolphthalein: pH range 8.2–10.0; colorless to pink
Methyl Orange: pH range 3.1–4.4; red to yellow
Bromothymol Blue: pH range 6.0–7.6; yellow to blue
The choice depends on the specific acid-base strength involved in the reaction.
In Educational Settings
It is commonly used in educational laboratories to teach concepts related to acid-base reactions, colorimetry, and organic synthesis. Its vivid color transitions help students visualize chemical changes effectively, fostering deeper understanding.
Conclusion
It remains a fundamental tool in the chemist’s arsenal due to its well-defined pH transition, stability, and versatility across various scientific disciplines. Whether for routine titrations, microbial differentiation, or pH monitoring in environmental samples, its relevance endures.
Proper usage, storage, and disposal ensure that it continues to serve as a safe and effective indicator across a range of applications. Understanding its properties not only enhances analytical accuracy but also strengthens foundational scientific knowledge.

How does methyl red work as an indicator?


Methyl Red is one of the most widely used pH indicators in chemistry, recognized for its distinct color changes and its utility in acid-base titrations. It plays a critical role in various fields, including analytical chemistry, microbiology, and environmental testing. In this detailed guide, we provide an exhaustive overview of methyl red, covering its chemical properties, uses, applications, and much more.
Introduction
Methyl (chemical formula: C15H15N3O2) is a synthetic azo dye used as a pH indicator in laboratory analysis. This compound changes color depending on the acidity or basicity of the solution, a characteristic that makes it highly valuable in titrimetric analyses.
IUPAC Name: 2-(N,N-Dimethyl-4-aminophenylazo) benzoic acid
Molar Mass: 269.30 g/mol
Solubility: Slightly soluble in water; more soluble in ethanol and acetone
Appearance: Orange-red powder
pH Range and Color Change
One of methyl red’s most important attributes is its distinct pH transition range:
pH Range: 4.4 to 6.2
Color in Acidic Solution (pH < 4.4): Red
Color in Neutral to Basic Solution (pH > 6.2): Yellow
Between these two points, the color of the solution changes through various shades of orange, making it an ideal indicator for strong acid to weak base titrations.
Chemical Structure and Properties
Methyl belongs to the azo dye class of compounds, characterized by the presence of the functional group R-N=N-R’. Its conjugated double bonds give it its vibrant color, and its pH sensitivity arises from protonation and deprotonation of the azo and carboxyl groups under different pH conditions.
Key Chemical Properties:
Melting Point: 179–182 °C
pKa: Approximately 5.1
UV-Visible Absorption Maxima: Acidic form: 520 nm (red)
Basic form: 430 nm (yellow)
Preparation and Synthesis
The synthesis of methyl red is a classic example of diazotization followed by azo coupling, typically performed in organic chemistry laboratories.
Diazotization: p-Aminodimethylaniline is treated with sodium nitrite and hydrochloric acid at a low temperature to form a diazonium salt.
Coupling Reaction: The diazonium salt is then reacted with anthranilic acid, resulting in the formation of methyl red.
This method showcases foundational chemical reactions used in azo dye synthesis, making it a popular compound in educational labs.
Applications
1. Acid-Base Titrations
It is extensively used in analytical chemistry as an indicator for titrations involving strong acids and weak bases. Its sharp and distinct color change near the mid-acidic pH range makes it ideal for precise endpoint determination.
2. Microbiology: Test
In microbiology, the (MR) test is a key component of the IMViC tests used to differentiate Enterobacteriaceae species.
Purpose: Determines whether the organism produces stable acid end products from glucose fermentation.
Procedure: After incubation in a buffered glucose broth, methyl red is added. Red color = Positive result (acidic end products)
Yellow color = Negative result
This test is commonly used to distinguish Escherichia coli (MR positive) from Enterobacter aerogenes (MR negative).
3. Environmental and Wastewater Analysis
It is employed in monitoring wastewater treatment processes, where pH levels need to be strictly controlled. The indicator helps in real-time pH assessment, aiding in maintaining optimal conditions for microbial digestion.
Storage and Handling Precautions
As with many laboratory reagents, methyl red requires careful handling:
Advantages of Using
A clear visual transition makes it easy to determine pH changes.
Stable and reliable in a variety of titration environments.
Useful in both chemical and biological experimental settings.
Cost-effective and readily available in multiple forms (powder, solution).
Limitations
Despite its usefulness, methyl red does have limitations:
Narrow pH range restricts its use to specific titration types.
Not suitable for strong base titrations due to its acidic transition zone.
It can be toxic to aquatic environments if not disposed of correctly.
Alternatives
In cases where methyl red is not suitable, several alternative indicators may be used:
Phenolphthalein: pH range 8.2–10.0; colorless to pink
Methyl Orange: pH range 3.1–4.4; red to yellow
Bromothymol Blue: pH range 6.0–7.6; yellow to blue
The choice depends on the specific acid-base strength involved in the reaction.
In Educational Settings
It is commonly used in educational laboratories to teach concepts related to acid-base reactions, colorimetry, and organic synthesis. Its vivid color transitions help students visualize chemical changes effectively, fostering deeper understanding.
Conclusion
It remains a fundamental tool in the chemist’s arsenal due to its well-defined pH transition, stability, and versatility across various scientific disciplines. Whether for routine titrations, microbial differentiation, or pH monitoring in environmental samples, its relevance endures.
Proper usage, storage, and disposal ensure that it continues to serve as a safe and effective indicator across a range of applications. Understanding its properties not only enhances analytical accuracy but also strengthens foundational scientific knowledge.

What are the advantages of Methyl red?

Advantages of Using Methyl Red
A clear visual transition makes it easy to determine pH changes.
Stable and reliable in a variety of titration environments.
Useful in both chemical and biological experimental settings.
Cost-effective and readily available in multiple forms (powder, solution).
Limitations of Methyl Red
Despite its usefulness, methyl red does have limitations:
Narrow pH range restricts its use to specific titration types.
Not suitable for strong base titrations due to its acidic transition zone.
It can be toxic to aquatic environments if not disposed of correctly.
Alternatives to Methyl Red
In cases where methyl red is not suitable, several alternative indicators may be used:
Phenolphthalein: pH range 8.2–10.0; colorless to pink
Methyl Orange: pH range 3.1–4.4; red to yellow
Bromothymol Blue: pH range 6.0–7.6; yellow to blue
The choice depends on the specific acid-base strength involved in the reaction.
Methyl Red in Educational Settings
Methyl red is commonly used in educational laboratories to teach concepts related to acid-base reactions, colorimetry, and organic synthesis. Its vivid color transitions help students visualize chemical changes effectively, fostering deeper understanding.

What are the applications of Methyl red?

Applications of Methyl Red
1. Acid-Base Titrations
Methyl red is extensively used in analytical chemistry as an indicator for titrations involving strong acids and weak bases. Its sharp and distinct color change near the mid-acidic pH range makes it ideal for precise endpoint determination.
2. Microbiology: Methyl Red Test
In microbiology, the Methyl Red (MR) test is a key component of the IMViC tests used to differentiate Enterobacteriaceae species.
Purpose: Determines whether the organism produces stable acid end products from glucose fermentation.
Procedure: After incubation in a buffered glucose broth, methyl red is added. Red color = Positive result (acidic end products)
Yellow color = Negative result
This test is commonly used to distinguish Escherichia coli (MR positive) from Enterobacter aerogenes (MR negative).
3. Environmental and Wastewater Analysis
Methyl red is employed in monitoring wastewater treatment processes, where pH levels need to be strictly controlled. The indicator helps in real-time pH assessment, aiding in maintaining optimal conditions for microbial digestion.

Leave a Comment