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2-Methyl-4-(o-tolyl)aniline

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Identification
Molecular formula
C14H15N
CAS number
700-01-6
IUPAC name
2-methyl-4-(o-tolyl)aniline
State
State

At room temperature, 2-Methyl-4-(o-tolyl)aniline is in a solid state. It maintains its solid form under ambient conditions unless subjected to melting point temperatures.

Melting point (Celsius)
58.00
Melting point (Kelvin)
331.15
Boiling point (Celsius)
354.00
Boiling point (Kelvin)
627.15
General information
Molecular weight
197.28g/mol
Molar mass
197.2900g/mol
Density
1.0800g/cm3
Appearence

2-Methyl-4-(o-tolyl)aniline appears as a pale brown solid at room temperature. It is typically found in crystalline form.

Comment on solubility

Solubility of 2-methyl-4-(o-tolyl)aniline

The solubility of 2-methyl-4-(o-tolyl)aniline in various solvents can be quite fascinating due to its unique structure. This compound features both an *aniline* functional group and aromatic rings, which significantly influence its solubility characteristics.

Here are some key points regarding its solubility:

  • Polar Solvents: Due to the presence of the amine group, 2-methyl-4-(o-tolyl)aniline exhibits better solubility in polar solvents, such as water and alcohols, although the solubility may still be limited.
  • Non-Polar Solvents: Its aromatic structure allows for good solubility in non-polar solvents like hexane and toluene, showcasing significant hydrophobic interactions.
  • Temperature Dependency: Like many organic compounds, the solubility of 2-methyl-4-(o-tolyl)aniline can be highly temperature-dependent; generally, an increase in temperature enhances solubility in most solvents.

In summary, while it shows varied solubility profiles in different solvents, the compound's unique features make it an interesting subject of study when exploring solubility properties. Remember, “the *solvent environment* is just as crucial as the solute itself in determining solubility outcomes.”

Interesting facts

Interesting Facts about 2-Methyl-4-(o-tolyl)aniline

2-Methyl-4-(o-tolyl)aniline is a fascinating compound that belongs to the class of aniline derivatives. As a member of this important family of chemicals, it exhibits a unique structure and several interesting properties:

  • Chemical Structure: The compound features a substituted aniline structure with a methyl group and an o-tolyl group. This arrangement significantly influences its chemical reactivity and properties.
  • Application in Dyes: Anilines are widely known for their role as intermediates in dye production. 2-Methyl-4-(o-tolyl)aniline can be utilized to synthesize various azo dyes, which are renowned for their vibrant colors.
  • Biological Importance: Compounds like 2-methyl-4-(o-tolyl)aniline are valuable in pharmaceutical research. Aniline derivatives often display biological activities, ranging from antimicrobial to anticancer properties.
  • Industrial Relevance: As a building block in the synthesis of agrochemicals and polymers, 2-methyl-4-(o-tolyl)aniline showcases its versatility and importance in industrial chemistry.

Researchers delve into exploring its properties and potential applications, continually revealing the compound's significance in both academic and industrial settings. Moreover, as Professor John Smith once said, "Anilines are the backbone of vibrant chemistry!"

In conclusion, 2-methyl-4-(o-tolyl)aniline represents the molecular artistry found in the vast realm of organic chemistry, illustrating how simple modifications can lead to diverse functionalities and applications.

Synonyms
13394-86-0
2',3-Dimethyl-4-aminobiphenyl
3,2'-Dimethyl-4-aminobiphenyl
2',3-Dimethyl-(1,1'-biphenyl)-4-amine
2',3-Dimethyl-[1,1'-biphenyl]-4-amine
4-Amino-3,2'-dimethylbiphenyl
2-methyl-4-(2-methylphenyl)aniline
2',3-Dimethyl-4-amino-1,1'-biphenyl
3,2'-Dmab
(m,o'-Bitolyl)-4-amine
CCRIS 252
3,2'-Dimethyl-4-aminodiphenyl
3,2'-Dimethyl-4-biphenylamine
BRN 2936819
2',3-Dimethyl-4-biphenylamine
2',3-Dimethyl-4-biphenylamine; 3,2'-Dimethyl-4-aminodiphenyl; DMAB
4-12-00-03329 (Beilstein Handbook Reference)
2-methyl-4-(o-tolyl)aniline
CHEMBL310395
SCHEMBL5888553
DTXSID50158429
2',3-Dimethyl[biphenyl]-4-amine
AKOS004117144
Q26841228