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isopropyl 7-aminoheptanoate

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Identification
Molecular formula
C10H21NO2
CAS number
64002-45-3
IUPAC name
isopropyl 7-aminoheptanoate
State
State

Isopropyl 7-aminoheptanoate is typically in a liquid state at room temperature.

Melting point (Celsius)
-73.30
Melting point (Kelvin)
199.90
Boiling point (Celsius)
221.50
Boiling point (Kelvin)
494.70
General information
Molecular weight
187.30g/mol
Molar mass
187.2960g/mol
Density
0.8790g/cm3
Appearence

Isopropyl 7-aminoheptanoate is a colorless to light yellow liquid.

Comment on solubility

Solubility of Isopropyl 7-Aminoheptanoate

Isopropyl 7-aminoheptanoate, with its chemical formula, presents interesting characteristics when evaluated for solubility. Understanding its solubility is crucial for its applications in various chemical and pharmaceutical processes. Here are some key points regarding its solubility:

  • Polarity: The presence of both an isopropyl group and an amino functional group affects the overall polarity of the molecule. Typically, compounds with significant polar groups, such as amino (-NH2) groups, tend to have increased solubility in polar solvents.
  • Solvent Compatibility: Isopropyl 7-aminoheptanoate is likely to be more soluble in polar solvents like water and alcohols. However, it may exhibit limited solubility in non-polar solvents due to the hydrophilic nature of the amino group.
  • Temperature Effects: As with many organic compounds, increasing temperature can enhance solubility. Therefore, elevated temperatures could lead to greater dissolution of isopropyl 7-aminoheptanoate in suitable solvents.
  • Concentration Considerations: The solubility may vary based on the concentration of the compound in the solvent. It is essential to consider saturation levels when working with this compound.

In summary, the solubility of isopropyl 7-aminoheptanoate is significantly influenced by its molecular structure, polarity, and interaction with various solvents. Proper understanding of these factors can aid in maximizing its effectiveness in different applications.

Interesting facts

Interesting Facts About Isopropyl 7-Aminoheptanoate

Isopropyl 7-aminoheptanoate is a fascinating chemical compound that belongs to the family of amino acids and esters. Here are some intriguing aspects of this compound:

  • Biochemical Importance: This compound serves as an important intermediate in the synthesis of various biologically active molecules. Amino acid derivatives, such as isopropyl 7-aminoheptanoate, are often involved in metabolic pathways that are essential to cellular functions.
  • Applications in Pharmaceuticals: With its unique structure, isopropyl 7-aminoheptanoate shows promise in the development of new pharmaceuticals. Its ability to interact with biological systems can lead to innovative treatments in areas like pain management and metabolic disorders.
  • Role in Peptide Synthesis: Isopropyl 7-aminoheptanoate is utilized in peptide synthesis, which is crucial for creating proteins and enzymes. This compound can function as a building block for larger, complex peptides, making it valuable in both research and industrial applications.
  • Potential as a Surfactant: The amphiphilic nature of isopropyl 7-aminoheptanoate may enable its use as a surfactant. Surfactants are important in various formulations, including detergents and emulsifiers, due to their ability to lower surface tension between liquids.

Furthermore, the exploration of isopropyl 7-aminoheptanoate can lead to exciting discoveries in organic synthesis and medicinal chemistry. As we continue expanding our understanding of such compounds, we march forward into a future where these small molecules could have a significant impact on health and technology.

Synonyms
propan-2-yl 7-aminoheptanoate
T3S8PBT8B8
HEPTANOIC ACID, 7-AMINO-, ISOPROPYL ESTER
DTXSID70228532
ISOPROPYL 7-AMINOHEPTANOATE
1-METHYLETHYL 7-AMINOHEPTANOATE
4-04-00-02792 (Beilstein Handbook Reference)
HEPTANOIC ACID, 7-AMINO-, 1-METHYLETHYL ESTER
DTXCID20151023
7790-12-7
7-Aminoheptanoic acid, isopropyl ester
BRN 1765284
UNII-T3S8PBT8B8