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4-Butylbenzene-1,2-diamine

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Identification
Molecular formula
C10H16N2
CAS number
192864-50-9
IUPAC name
4-butylbenzene-1,2-diamine
State
State

This compound exists as a solid at room temperature, often forming crystals or a crystalline powder.

Melting point (Celsius)
54.50
Melting point (Kelvin)
327.65
Boiling point (Celsius)
329.00
Boiling point (Kelvin)
602.15
General information
Molecular weight
177.25g/mol
Molar mass
177.2700g/mol
Density
0.9570g/cm3
Appearence

4-Butylbenzene-1,2-diamine typically appears as a pale yellow to brown solid or powder. The exact appearance may vary slightly depending on purity and specific conditions, but it is generally consistent in its solid form.

Comment on solubility

Solubility of 4-butylbenzene-1,2-diamine

4-butylbenzene-1,2-diamine, also known as 1,2-diaminobutylbenzene, is an organic compound that presents interesting characteristics when it comes to solubility.

Its solubility can be influenced by various factors such as:

  • Polarity: The presence of two amino groups (-NH2) makes the molecule somewhat polar, which can contribute to its solubility in polar solvents.
  • Hydrophobic nature: The butyl group contributes hydrophobic characteristics, which may limit its solubility in polar environments.
  • Temperature: Generally, increasing the temperature can enhance the solubility of organic compounds. However, specific behavior can vary.

In summary, 4-butylbenzene-1,2-diamine tends to have:

  • Moderate solubility in water: Due to the amino groups, it can form hydrogen bonds, improving solubility.
  • Greater solubility in organic solvents: Such as alcohols and ethers, where its hydrophobic butyl chain is more compatible.

As a rule of thumb, "like dissolves like," so the solubility behavior could be predicted based on the solvent's properties compared to those of 4-butylbenzene-1,2-diamine.

Interesting facts

Interesting Facts about 4-butylbenzene-1,2-diamine

4-butylbenzene-1,2-diamine, often regarded for its intriguing structural properties, is an aromatic amine that showcases a plethora of interesting features. Here are some fascinating aspects of this compound:

  • Aromaticity: The compound features a benzene ring, which contributes to its stability and chemical reactivity due to its aromatic nature.
  • Functional Groups: It contains two amine groups (-NH2) that make it a valuable building block in organic synthesis, notably in the production of dyes, pharmaceuticals, and agrochemicals.
  • Hydrophobic Character: The presence of the butyl group enhances the hydrophobicity of the compound, influencing its interactions in biological systems and materials science.
  • Potential Applications: 4-butylbenzene-1,2-diamine has potential use in the manufacturing of polyurethanes, as well as in the development of advanced materials and coatings due to its reactivity and bonding characteristics.
  • Research Relevance: It is a subject of study in medicinal chemistry, where researchers explore its biochemical properties and potential therapeutic applications.

As emphasized by chemists, compounds like 4-butylbenzene-1,2-diamine play a pivotal role in advancing material science and pharmaceutical developments. Their intricate structures often lead to significant breakthroughs in various fields of research.

This compound illustrates the beauty and complexity of organic chemistry, inviting further exploration and understanding of its diverse applications.

Synonyms
3663-23-8
1,2-Benzenediamine, 4-butyl-
4-n-Butyl-o-phenylenediamine
o-Phenylenediamine, 4-butyl-
HSDB 6269
4-butyl-O-phenylenediamine
4-BUTYL-1,2-BENZENEDIAMINE
3,4-Diamino-1-butylbenzene
4-butyl-1,2-phenylenediamine
M4GA1B83X0
EINECS 222-917-7
DTXSID3063120
2-AMINO-4-N-BUTYLANILINE
4-BUTYL-1,2-BENZENEDIAMINE [HSDB]
4nButylophenylenediamine
4Butylbenzene1,2diamine
oPhenylenediamine, 4butyl
1,2Benzenediamine, 4butyl
DTXCID2039207
4-Butylbenzene-1,2-diamine
UNII-M4GA1B83X0
4-n-butyl-1,2-phenylenediamine
SCHEMBL7204931
4-butyl-1,2-phenylene-diamine
DAA66323
AKOS006275172
DA-06401
NS00030068
F18184
EN300-1241624
Q27283480