2-Ethyl-N-propyl-1-hexanamine

2-Ethyl-N-propyl-1-hexanamine is a type of branched-chain amine, which means its molecular structure features branches rather than a straight chain. This particular compound is characterized by the presence of both ethyl and propyl substituents attached to its backbone. An ethyl substituent consists of an ethane molecule minus one hydrogen atom, while a propyl substituent is derived from propane with one hydrogen atom removed. This chemical substance typically presents itself as a colorless or pale yellow liquid, indicating its state at room temperature. Its visual appearance can vary slightly depending on the purity and storage conditions. The most notable feature of 2-Ethyl-N-propyl-1-hexanamine is its distinctive amine odor, which is a common characteristic of compounds containing amino functional groups. Amines are known for their strong, often pungent smell, which can be quite pronounced in this compound. The odor serves as a warning property, alerting individuals to the presence of the chemical, especially in industrial or laboratory settings where such substances are commonly handled.

2-Ethyl-N-Propyl-1-Hexanamine, a versatile chemical compound, finds extensive application in the creation of surfactants, which are substances that significantly reduce the surface tension of liquids, thereby facilitating the mixing of otherwise immiscible substances. This compound is also utilized in the production of corrosion inhibitors, agents that protect materials from deterioration caused by chemical reactions with their environment. Beyond these applications, 2-Ethyl-N-Propyl-1-Hexanamine serves as a crucial reagent in numerous chemical reactions, playing a pivotal role in the synthesis of various compounds. The unique properties of this compound make it an indispensable component in the formulation of agrochemicals, which are essential for enhancing crop yields and protecting plants from pests and diseases. Additionally, 2-Ethyl-N-Propyl-1-Hexanamine is employed in the development of specialty chemicals, where its specific characteristics are leveraged to create products with tailored functionalities. These applications underscore the compound's importance in both industrial and agricultural sectors, highlighting its versatility and value in modern chemical processes.

Molecular Weight:171.32
XLogP3:3.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:8
Exact Mass:171.198699802
Monoisotopic Mass:171.198699802
Topological Polar Surface Area:12
Heavy Atom Count:12
Complexity:81.1
Undefined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes