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6-Aminohexanoic acid

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Identification
Molecular formula
C6H13NO2
CAS number
3698-99-9
IUPAC name
6-aminohexylcarbamic acid
State
State

At room temperature, 6-aminohexanoic acid is typically in a solid state.

Melting point (Celsius)
205.00
Melting point (Kelvin)
478.15
Boiling point (Celsius)
282.00
Boiling point (Kelvin)
555.15
General information
Molecular weight
145.19g/mol
Molar mass
145.1900g/mol
Density
1.0960g/cm3
Appearence

6-Aminohexanoic acid generally appears as a white crystalline solid. It tends to have a powdery texture and is usually odorless. This compound is commonly used in various chemical and pharmaceutical applications.

Comment on solubility

Solubility of 6-Aminohexylcarbamic Acid

6-aminohexylcarbamic acid, with the chemical formula C7H16N2O2, exhibits notable solubility characteristics that are worth discussing. This compound is primarily recognized as a polar molecule due to the presence of both amino and carbamic functional groups which significantly influence its interaction with solvents.

Generally, the solubility of 6-aminohexylcarbamic acid can be summarized as follows:

  • Water Solubility: The compound is soluble in water, largely attributed to its hydrophilic nature from the amino group, which can form hydrogen bonds with water molecules.
  • Polar Organic Solvents: It also shows good solubility in polar organic solvents such as alcohols due to similar interactions as seen with water.
  • Non-Polar Solvents: Conversely, 6-aminohexylcarbamic acid is poorly soluble in non-polar solvents, reflecting the typical behavior of polar substances in non-polar environments.

As such, the solubility of 6-aminohexylcarbamic acid can be described as:

  1. Highly soluble in water and other polar solvents.
  2. Poorly soluble in non-polar solvents.

In conclusion, the dual presence of hydrophilic sites within its structure makes 6-aminohexylcarbamic acid a polar compound with unique solubility properties, making it versatile for various applications in chemical and biological contexts.

Interesting facts

6-Aminohexylcarbamic Acid

6-Aminohexylcarbamic acid is a fascinating compound that belongs to the class of amino acids and is recognized for its unique structural features and potential applications. This compound has gained attention in various fields, particularly in biochemistry and medicinal chemistry, due to its ability to influence biological pathways.

Interesting Facts

  • Structural Versatility: The compound's long hexyl chain provides exceptional structural versatility, allowing it to interact with other biomolecules, making it a subject of interest in drug design.
  • Biological Significance: As a derivative of carbamic acid, it plays a crucial role in enzyme interactions and can influence the activity of certain neurotransmitters, providing insights into neurobiological functions.
  • Potential Therapeutic Applications: Research is ongoing to explore its potential use in treating disorders related to neurotransmission and could lead to novel treatments for conditions like anxiety or depression.
  • Research Insights: Various studies are investigating its functionalities as a drug delivery system due to its ability to enhance the solubility and stability of therapeutic agents.
  • Benefits of Amino Group: The presence of the amino group allows for the formation of peptides, expanding its applications in protein synthesis and biotechnology.

This compound not only showcases the intricacies of chemical synthesis but also the potential for real-world applications that can arise from simple molecular constructs. As research continues to unfold, 6-aminohexylcarbamic acid may yield new insights that can significantly impact medicinal chemistry.

Synonyms
(6-Aminohexyl)carbamic acid
143-06-6
6-aminohexylcarbamic acid
HEXAMETHYLENEDIAMINE CARBAMATE
Diak 1
Carbamic acid, (6-aminohexyl)-
UNII-1W993R5ORT
1W993R5ORT
HSDB 2585
Carbamic acid, N-(6-aminohexyl)-
CHEMINOX AC 6
EINECS 205-581-6
DTXSID2059726
HEXAMETHYLENEDIAMINE CARBAMATE [HSDB]
(6Aminohexyl)carbamic acid
Carbamic acid, (6aminohexyl)
SCHEMBL944344
DTXCID9034658
HDIHOAXFFROQHR-UHFFFAOYSA-N
AKOS022171978
FH173271
DB-020018
NS00019779
F87618
Q27252986
205-581-6