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Aceglutamide

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Identification
Molecular formula
C11H20N2O4
CAS number
2222-15-9
IUPAC name
3-(1-aminoethyl)nonanedioic acid
State
State

At room temperature, Aceglutamide is a solid.

Melting point (Celsius)
140.00
Melting point (Kelvin)
413.15
Boiling point (Celsius)
351.00
Boiling point (Kelvin)
624.15
General information
Molecular weight
246.29g/mol
Molar mass
246.2720g/mol
Density
1.3000g/cm3
Appearence

Aceglutamide appears as a white crystalline powder that is odorless. It is soluble in water and has a slightly bitter taste.

Comment on solubility

Solubility of 3-(1-aminoethyl)nonanedioic acid

The solubility of 3-(1-aminoethyl)nonanedioic acid, with the chemical formula C11H20N2O4, can be influenced by several factors including temperature, pH, and the solvent used. As a carboxylic acid derivative, this compound features two carboxylic acid groups that can significantly impact its solubility profile.

In general, the solubility characteristics can be summarized as follows:

  • Polarity: The presence of polar functional groups, such as -COOH, contributes to the solubility in water.
  • Hydrophobic segments: The nonanedioic acid part of the molecule has a long hydrophobic hydrocarbon chain that may hinder full solubility in polar solvents.
  • Temperature sensitivity: Like many acids, its solubility is likely to increase with rising temperatures, allowing for greater dissolution in aqueous solutions.
  • pH dependency: At higher pH levels, the carboxylic acid groups can deprotonate, leading to increased solubility in a basic medium.

Moreover, it is important to note that the solubility of this compound may also vary depending on the specific salt forms or derivatives present in solutions. Therefore, while it may be soluble to some extent in water, its solubility in organic solvents or different media can be quite different.

In summary, while 3-(1-aminoethyl)nonanedioic acid is expected to exhibit varied solubility depending on the circumstances, the impact of its carboxylic acid groups and overall molecular structure plays a crucial role in determining how well it dissolves in various solvents.

Interesting facts

Interesting Facts about 3-(1-aminoethyl)nonanedioic acid

3-(1-aminoethyl)nonanedioic acid is an intriguing compound that belongs to the family of amino acids and dicarboxylic acids. Here are some fascinating insights into this unique chemical:

  • Structure and Significance: The compound features a nonanedioic acid backbone with an aminoethyl side chain, which plays a vital role in various biochemical processes. Its structure contributes to its functionality in biological systems.
  • Biochemical Relevance: Amino acids, including 3-(1-aminoethyl)nonanedioic acid, are crucial building blocks of proteins. They are involved in multiple metabolic pathways, including energy production and cellular repair.
  • Potential Applications: This compound could have various applications in fields like pharmaceuticals or biotechnology. As a precursor for synthesizing other important molecules, it might play a role in drug development or as a supplement in nutritional products.
  • Research Interest: Scientists are exploring the mechanisms of amino acids in the body, and compounds like 3-(1-aminoethyl)nonanedioic acid could offer insight into amino acid metabolism and interactions.
  • Synthesis Methods: The synthesis of this compound can involve several innovative methods, often requiring careful manipulation of reaction conditions to achieve the desired product. Knowledge of organic synthesis techniques is essential for chemists working with such compounds.

In conclusion, 3-(1-aminoethyl)nonanedioic acid is not just a simple chemical entity; it represents a complex interplay of chemistry and biology, highlighting the importance of amino acids in various scientific domains. As research progresses, this compound may unlock further understanding of biological processes and lead to new discoveries.

Synonyms
SCHEMBL4316691
PD042439
(RS*, RS*)-3-(1-aminoethyl)nonanedioic acid