18618-64-9

Usage

Uses

Used in Surfactant Production:
Pentadecan-8-amine is used as an intermediate for the production of surfactants, which are essential in industries such as cosmetics, cleaning products, and detergents, due to their ability to reduce surface tension and stabilize emulsions.
Used in Emulsifier Production:
In the emulsifier industry, pentadecan-8-amine is utilized as a component in creating emulsifying agents that help mix immiscible liquids, such as oil and water, commonly used in food, pharmaceutical, and cosmetic products.
Used in Corrosion Inhibitor Production:
Pentadecan-8-amine is used as an intermediate in the manufacturing of corrosion inhibitors, which are crucial in protecting metal surfaces from corrosion in various industrial applications.
Used in Lubricant Production:
pentadecan-8-aMine is also used in the production of lubricants, enhancing the performance and longevity of machinery by reducing friction and wear.
Used in Specialty Chemicals Synthesis:
Pentadecan-8-amine is employed in the synthesis of specialty chemicals, which have specific applications in various industries, including plastics, coatings, and adhesives.
Used in Pharmaceutical Synthesis:
It is used as a building block in the synthesis of pharmaceuticals, contributing to the development of new drugs and medications.
Used in Agricultural Product Production:
Pentadecan-8-amine is utilized in the production of agricultural products, potentially enhancing crop protection and yield.
Used in Hair Care Products:
As a conditioning agent in hair care products, pentadecan-8-amine helps to improve the texture and manageability of hair.
Used in Powdered Food Products:
It is used as an anti-caking agent in powdered food products to maintain their free-flowing properties and prevent clumping.
Used in Quaternary Ammonium Compounds Production:
Pentadecan-8-amine is used in the manufacturing of quaternary ammonium compounds, which are employed in fabric softeners, antimicrobial agents, and textile treatments for their antimicrobial and softening properties.

InChI:InChI=1/C15H33N/c1-3-5-7-9-11-13-15-16-14-12-10-8-6-4-2/h16H,3-15H2,1-2H3

Upstream product

• 818-23-5 8-Pentadecanon 
• 77287-34-4 formamide 
• 943545-44-6 8-azidopentadecane 
• 1653-35-6 pentadecan-8-ol 
• 111-25-1 1-bromo-hexane 
• 629-04-9 1-Bromoheptane 
• 943545-39-9 (C₇H₁₅)2CHOSO₂CH₃ 
• 26077-65-6 pentadecan-8-one oxime 

Downstream Products

• 1402905-31-0 8,9-dibromo-5,6,11,12-tetrachloro-2-(pentadecan-8-yl)-1H-benzo[5,10]anthra[2,1,9-def]isoquinoline-1,3(2H)-dione 
• 1224962-63-3 N-(1-heptyloctyl)-9-(di-p-tert-octylphenyl)amino-perylene-3,4-dicarboximide 
• 909191-87-3 N-(1-heptyloctyl)-9-bromoperylene-3,4-dicarboximide 
• 909191-86-2 N-(1-heptyloctyl)-perylene-3,4-dicarboxylic acid monoimide 
• 130296-47-8 2,9-bis(1-heptyloctyl)-anthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10-tetrone 

Relevant academic research and scientific papers

Carborane-perylene diimide derivative and synthesis method thereof, sensing array based on derivative and preparation method and application of sensor array

The invention discloses a carborane-perylene diimide derivative and a synthesis method thereof, a sensing array based on the derivative and a preparation method and an application of the sensor array,and belongs to the technical field of small-molecular fluorescent sensing thin film materials. The carborane-perylene diimide derivative is placed in a solution, is assembled into a fiber structure with relatively large specific surface, and then is transferred to different substrate surfaces, so as to obtain the sensing array composed of a variety of fluorescent thin films; the sensing array canbe sensitive to sense six important drug gases, and drug samples have no need of any treatment; at the same time, through array combination, the interference of common interferents is eliminated thoroughly. The operation is simple, and the reaction conditions are mild. The prepared fluorescent sensing thin film has good stability and long service life, and is an excellent drug gas sensing thin film array. With combination use of the thin film and commercial fluorescent instruments, the drug gases can be sensitively detected. In addition, the drug gas special detection instrument can be developed through the device of the sensing thin film.

Synthesis and characterization of mesogenic triphenylene-perylene dyads with phenoxy-alkoxy linkers

Three novel triphenylene-perylene dyads with phenoxy-alkoxy linkers (PDI-OPhO-Cn-O- TP6, n = 6, 8, 10) have been synthesized and characterized by FT-IR, MS, 13C, and 1H NMR. The mesomorphic properties of these compounds were investigated by polarizing optical microscopy (POM) and differential scanning calorimetry (DSC). It was found that the dyads (PDI-OPhO-Cn-O-TP6, n = 6, 8) only showed thermotropic columnar mesophase in the heating process, while the dyad (PDI-OPhO-C10-O-TP6) showed enantiotropic columnar mesophase in both heating and cooling processes.

Chemical engineering of donor-acceptor liquid crystalline dyads and triads for the controlled nanostructuration of organic semiconductors

Multi-segregated columnar structures provide a geometrically ideal scheme for ambipolar organic semiconductors, but are not easy to design. A set of novel materials with dyad and triad architectures based on 2 different discotic cores is reported and the conditions of emergence of such complex structures are investigated. The designed molecules associate together electron-donor triphenylene cores (D) and perylene or naphthalene diimides as acceptor moieties (A), both entities being linked via alkyl chain spacers. The evaluation in solution of their HOMO/LUMO energy levels by cyclic voltammetry demonstrates the preservation of the individual features of the D and A units. Their thermal and self-organization behaviors were studied by polarized-light optical microscopy, differential scanning calorimetry, temperature-dependent small-angle X-ray scattering and dilatometry, which permitted detailed investigation of the self-organization behaviour. These D-A compounds turned out to spontaneously self-organize into columnar mesophases at room temperature, with the D and A moieties segregated into either alternated stacks within mixed columns or in distinct columns, the latter providing an ideal configuration for 1D hole and electron transport pathways. In view of potential applications of the triad/dyad template, thin films of these self-organized materials were also probed by atomic force microscopy and grazing incidence X-ray scattering.

Triphenylene-flexible bridge-perylene diimide binary compound and preparation method and application thereof

The invention discloses a triphenylene-flexible bridge-perylene diimide binary compound and a preparation method thereof and application of the compound serving as an organic solar cell active layer. Compared with the prior art, the triphenylene-flexible bridge-perylene diimide binary compound has the advantage of easily adjusting the liquid crystalline phase transformation temperature and temperature interval, and the compound has the application in photology, electrooptics and electronics, and particularly has the application in serving as the organic solar cell active layer. Please see the formula in the description.

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.