2-phenylbutane-1,2-diamine | Solubility of Things

Identification

Molecular formula

C₁₀H₁₆N₂

CAS number

1459-41-6

IUPAC name

2-phenylbutane-1,2-diamine

State

At room temperature, 2-phenylbutane-1,2-diamine is a liquid. It is not very volatile, owing to its relatively high boiling point.

Melting point (Celsius)

9.00

Melting point (Kelvin)

282.15

Boiling point (Celsius)

262.00

Boiling point (Kelvin)

535.15

General information

Molecular weight

164.26g/mol

Molar mass

164.2630g/mol

Density

0.9875g/cm³

Appearence

2-Phenylbutane-1,2-diamine typically appears as a colorless to pale yellow liquid. It is often used in chemical synthesis and can be identified by its distinct aromatic odor due to the presence of the phenyl group.

Comment on solubility

Solubility of 2-phenylbutane-1,2-diamine

2-phenylbutane-1,2-diamine, a compound characterized by its amine functional groups, exhibits some noteworthy solubility properties. The solubility of this compound is influenced by several factors:

Polarity: The presence of two amine groups provides the molecule with polar characteristics, which enhances its ability to interact with polar solvents like water.
Hydrogen Bonding: The amine groups can form hydrogen bonds with water molecules, facilitating dissolution.
Chain Length: The hydrophobic butane chain can limit solubility in polar solvents, meaning there is a delicate balance between hydrophobic and hydrophilic interactions.

Generally, 2-phenylbutane-1,2-diamine tends to have moderate solubility in water, but it is more soluble in organic solvents due to its hydrophobic segments. In practice, it can be noted that:

It is likely to dissolve well in alcohols and ethers.
Solubility decreases in non-polar solvents like hexane.

In summary, while 2-phenylbutane-1,2-diamine shows potential for solubility in various solvents, its specific solubility profile is significantly determined by its chemical structure and the nature of the solvents being used.

Interesting facts

Interesting Facts About 2-phenylbutane-1,2-diamine

2-phenylbutane-1,2-diamine is an intriguing chemical compound that has garnered interest in various fields such as organic chemistry and pharmacology. This compound features a unique structure that contributes to its potential applications. Here are some fascinating insights:

Amine Functionality: The presence of two amine (-NH₂) groups in its structure makes 2-phenylbutane-1,2-diamine a versatile building block in organic synthesis and a key component in the production of various pharmaceuticals.
Chirality: This compound can exhibit chirality due to the two stereogenic centers in its backbone, allowing it to exist as enantiomers that may have different biological activities.
Potential Therapeutic Uses: Compounds containing amine groups are often studied for their potential as drug candidates. This compound could provide insight into the design of new therapeutic agents, especially in the areas of neurochemistry and anti-cancer research.
Synthetic Pathways: The synthesis of 2-phenylbutane-1,2-diamine serves as an excellent example of strategies used in organic synthesis, where chemists can explore various methods to create this compound efficiently.
Role in Biological Systems: Due to its diamine nature, it can mimic the behavior of natural amino compounds, providing a model for understanding interactions at a molecular level in biological systems.

In conclusion, 2-phenylbutane-1,2-diamine not only exemplifies the rich tapestry of organic compounds but also continues to inspire research aimed at unlocking new applications in pharmaceuticals. As scientists explore its properties and potential, this compound stands as a reminder of the possibilities that chemistry holds in enhancing our understanding of the molecular world.

Synonyms

2-Phenyl-1,2-butanediamine

2-phenylbutane-1,2-diamine

5062-64-6

Phenyl-2 butanediamine-1,2

BRN 2084566

1,2-Diaminobutane, 2-phenyl-

1,2-BUTANEDIAMINE, 2-PHENYL-

SCHEMBL7004942

DTXSID20964857

CBBWBITZUIWDJB-UHFFFAOYSA-N

AKOS015890272