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3-methyl-4-nitrosophenol

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Identification
Molecular formula
C7H7NO2
CAS number
2042-14-4
IUPAC name
3-methyl-4-nitroso-phenol
State
State

At room temperature, 3-methyl-4-nitrosophenol is in a solid state.

Melting point (Celsius)
101.00
Melting point (Kelvin)
374.15
Boiling point (Celsius)
276.00
Boiling point (Kelvin)
549.00
General information
Molecular weight
137.14g/mol
Molar mass
137.1250g/mol
Density
1.2190g/cm3
Appearence

3-Methyl-4-nitrosophenol typically appears as a crystalline solid. Its color can range from pale yellow to a deeper shade of yellow depending on the purity and specific conditions of observation.

Comment on solubility

Solubility of 3-methyl-4-nitroso-phenol

3-methyl-4-nitroso-phenol, known for its unique structure, exhibits some interesting properties when it comes to solubility. This compound belongs to a group of nitroso compounds that often display limited solubility in water. Here are some key points regarding its solubility:

  • Aqueous Solubility: 3-methyl-4-nitroso-phenol is generally considered to have low solubility in water, which means it does not dissolve well.
  • Organic Solvents: However, it tends to be more soluble in organic solvents such as ethanol, methanol, and acetone. This can be attributed to its hydrophobic aromatic ring structure.
  • pH Dependence: The solubility can also be affected by the pH of the solution. In acidic conditions, the solubility may alter due to protonation effects.

Understanding the solubility properties of this compound is key for its applications in various chemical processes and formulations. As with many organic compounds, the intermolecular interactions play a crucial role in determining its solubility characteristics.

Interesting facts

Interesting Facts about 3-methyl-4-nitroso-phenol

3-methyl-4-nitroso-phenol, often referred to in scientific literature, is a fascinating compound with a variety of applications and properties. Here are some notable points about this compound:

  • Nitroso Group Influence: The presence of the nitroso group (–NO) significantly impacts the compound's reactivity and stability. It is crucial in the formation of various derivatives and can lead to interesting chemical behavior.
  • Phenolic Nature: As a phenol derivative, 3-methyl-4-nitroso-phenol exhibits some properties typical of phenolic compounds, such as acting as a weak acid and participating in various substitution reactions.
  • Colorimetric Applications: This compound is particularly useful in colorimetric analysis, where it acts as a reagent for detecting nitrites in various samples. The vivid color change can be utilized in both qualitative and quantitative analyses.
  • Biological Activity: Research has indicated that various nitroso compounds exhibit biological activities, which may be explored for pharmacological applications. 3-methyl-4-nitroso-phenol is no exception and is worth investigating further.
  • Industrial Relevance: Due to its functional groups, this compound serves as an intermediate in the synthesis of dyes and other organic compounds, making it valuable in the dye and chemical manufacturing industries.

To sum up, 3-methyl-4-nitroso-phenol is a compound that brings together the intriguing world of organic chemistry and practical applications. Its distinctive structural features allow it to participate in various chemical interactions, making it a subject of interest in both academic research and industrial processes.

Synonyms
3-Methyl-4-nitrosophenol
p-Nitroso-m-cresol
615-01-0
4-Nitroso-m-cresol
m-CRESOL, 4-NITROSO-
Phenol, 3-methyl-4-nitroso-
4-Nitroso-3-cresol
4-Nitroso-3-methylphenol
AV0MPT9XZE
EINECS 210-405-6
NSC 21470
BRN 2206014
AI3-18991
NSC-21470
NSC-677513
DTXSID40210464
DTXCID40132955
210-405-6
NSC677513
(4E)-4-(HYDROXYIMINO)-3-METHYLCYCLOHEXA-2,5-DIEN-1-ONE
NSC21470
UNII-AV0MPT9XZE
3-methyl-4-nitroso-phenol
WLN: QR C1 DNO
SCHEMBL766049
SCHEMBL5164437
2-methylbenzoquinone 1-monoxime
MSDYBZSZDFKGIH-UHFFFAOYSA-N
2-methyl-[1,4]-benzoquinone oxime
3-Methyl-1,4-benzoquinone-4-oxime
MFCD00020126
AKOS006272884
AKOS021984328
1,4-Benzoquinone, 1-oxime, 2-methyl-
NS00034708