3241-23-4

Usage

Uses

Used in Detergent Industry:
Nonadecan-10-amine is used as a surfactant and emulsifier for its ability to improve the spreading and wetting properties of detergents, making them more effective in cleaning applications.
Used in Wetting Agents:
In the production of wetting agents, nonadecan-10-amine serves as a key component that helps in reducing the surface tension of liquids, thus facilitating better wetting and spreading.
Used in Corrosion Inhibitors:
Nonadecan-10-amine is utilized as a corrosion inhibitor in various industrial applications, where its surfactant properties help in preventing the corrosion of metals.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, nonadecan-10-amine is used as a building block in the synthesis of various pharmaceuticals, contributing to the development of new drugs.
Used in Agrochemicals:
Nonadecan-10-amine is also employed in the synthesis of agrochemicals, where it plays a role in the formulation of effective pesticides and other agricultural products.
It is important to handle nonadecan-10-amine with care, as it is considered to be harmful if ingested, inhaled, or in contact with the skin, and may cause irritation to the eyes and respiratory tract.

InChI:InChI=1/C19H41N/c1-3-5-7-9-11-13-15-17-19(20)18-16-14-12-10-8-6-4-2/h19H,3-18,20H2,1-2H3

Upstream product

• 504-57-4 10-Nonadecanon 
• 77287-34-4 formamide 
• 86325-38-4 10-nonadecanone oxime 
• 943545-41-3 (C₉H₁₉)2CHOSO₂CH₃ 
• 943545-46-8 10-azidononadecane 
• 16840-84-9 nonadecan-10-ol 
• 693-58-3 1-Bromononane 

Downstream Products

• 1224962-64-4 N-(1-nonyldecyl)-9-(di-p-tert-octylphenyl)amino-perylene-3,4-dicarboximide 
• 1369426-79-8 C₆₂H₇₆N₂O₄Si 
• 1369426-81-2 C₅₃H₅₆N₂O₄ 
• 1369426-74-3 C₅₁H₅₅IN₂O₄ 

Relevant academic research and scientific papers

Synthesis and characterization of new electron acceptor perylene diimide molecules for photovoltaic applications

Two new perylene diimide molecules, 1, 7-bis(1-naphtyl)-N,N′-bis-(10- nonadecyl)-perylene-3,4,9,10-bis (dicarboximide) PDI-2 and 1,7-bis(5- acenaphtenyl)-N,N′-bis-(10-nonadecyl)-perylene-3,4,9,10-bis(dicarboximide) PDI-3 have been synthesized and used as acceptor components in P3HT/PDI bulk heterojunction solar cells. The introduction of fused aromatic rings into the bay positions of the perylene core creates a stong steric hindrance, twisting the perylene plane with a direct consequence on the π-π intramolecular interactions between the adjacent PDIs. All these features contribute to the reduction of molecular aggregation in the solid state, with a strong influence on the performances of P3HT/PDI photovoltaic devices.

Synthesis and antimicrobial activity of symmetrical two-tailed dendritic tricarboxylato amphiphiles

Two series of water-soluble, symmetrical two-tailed homologous dendritic amphiphiles-R2NCONHC((CH2)2COOH)3, 2(n,n), and R2CHNHCONHC((CH2)2COOH)3, 3(n,n), where R = n-CnH2n+1-were synthesized and compared to R″NHCONHC((CH2)2COOH)3, 1(n), R″ = n-CnH2n+1, to determine whether antimicrobial activity was influenced by total or individual alkyl chain lengths, and whether antimicrobial activity depends on hydrophobicity or tail topology (one or two). In a broad screen of 11 microorganisms, 2(n,n) and 3(n,n) generally displayed higher minimal inhibitory concentrations (MICs) than 1(n) against growth as measured by broth microdilution assays. Chain-length specificity was observed against Candida albicans as 1(16), 2(8,8), and 3(8,8) showed the lowest MIC in their respective series. The one case where two-tailed compounds displayed the lowest MICs-3(10,10), 15 μM; 3(11,11), 7.2 μM; and 3(12,12), 6.9 μM-was against Cryptococcus neoformans.

Donor-σ-Acceptor Molecules Incorporating a Nonadecyl-Swallowtailed Perylenediimide Acceptor

Donor-σ-acceptor-lipid molecules were prepared by using perylenetetracarboxylic diimide as the acceptor, starting from perylenetetracarboxylic dianhydride. One imide nitrogen was attached to a "swallowtail" lipid (a long alkyl tail connected at midchain), which imparts enough solubility to make the system tractable and provides a lipophilic region suitable for promoting Langmuir-Blodgett monolayer formation. The other imide link was to a donor group (pyrene, ferrocene, tetramethylphenylenediamine, phenyl) through a short alkyl σ bridge. Features of the 1H and 13C NMR spectra of swallowtailed perylenediimides are interpreted as resulting from restricted rotation about the imide C-N bond; the 13C NMR spectra and stereochemistry of these molecules are contrasted with the case of the related bis-(2,5-di-tert-butylphenyl)perylenetetracarboxylic diimide.