41755-58-2

Basic information

• Product Name: TRIACONTYL ACETATE
• Synonyms: TRIACONTYL ACETATE
• CAS NO: 41755-58-2
• Molecular Formula: C₃₂H₆₄O₂
• Molecular Weight: 494.88
• Product Categories: Alcohol Acetates;Esters;Saturated fatty acids and derivatives
• Mol File: 41755-58-2.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 436.4 °C at 760 mmHg
• Flash Point: 191.2 °C
• Appearance: /
• Density: 0.858 g/cm³
• Vapor Pressure: 8.11E-08mmHg at 25°C
• Refractive Index: 1.455
• Storage Temp.: 2-8°C
• CAS DataBase Reference: TRIACONTYL ACETATE(CAS DataBase Reference)
• NIST Chemistry Reference: TRIACONTYL ACETATE(41755-58-2)
• EPA Substance Registry System: TRIACONTYL ACETATE(41755-58-2)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 41755-58-2(Hazardous Substances Data)

Usage

General Description

Triactonyl acetate, also known as triacontanyl acetate, is a chemical compound commonly found in insects, particularly in their pheromones. It is a long-chain acetate ester comprising of 30 carbon atoms, and is believed to play a role in the communication and mating behaviors of insects. Triactonyl acetate is also used in the formulation of perfumes and other fragrances due to its pleasant scent and ability to imitate insect pheromones, making it a valuable component in the production of insect attractants and repellents. Additionally, it has potential applications in agriculture as a biopesticide, serving as a natural alternative to synthetic insecticides.

InChI:InChI=1/C32H64O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-28-29-30-31-34-32(2)33/h3-31H2,1-2H3

Upstream product

• 593-50-0 melissyl alcohol 
• 108-24-7 acetic anhydride 
• 629-73-2 1-Hexadecene 
• 7505-12-6 Ethyl tricontanoate 
• 506-50-3 melissic acid 
• 1501-82-2 cyclododecene 
• 22147-38-2 (E)-9-octadecenyl acetate 
• 87418-99-3 Acetic acid (9E,21E)-triaconta-9,21-dienyl ester 
• 72443-19-7 15-triacontene 

Downstream Products

• 593-50-0 melissyl alcohol 

Relevant articles and documents

Ovipositional responses of the pulse beetle, Bruchus chinensis (Coleoptera: Bruchidae) to extracts and compounds of Capparis decidua

Extracts of Capparis decidua stems and flowers showed insecticidal and oviposition inhibitory activities against Bruchus chinensis. The LC50 values of these extracts were found to increase with the increase in the polarity of the extract at different exposure periods. For instance, after 96 h, the LC50 values were found to be 3.619, 7.319, and 10.151 μg for CD1, CD2, and CD3, respectively. Extract CD7 was effective only at higher doses. The toxicity was found to be dose- and time-dependent. The females laid lesser number of eggs, when exposed to sublethal doses of different extracts and pure compounds, as compared to control. The maximum oviposition deterrence index was found for extract CD1 followed in decreasing order by CD2, CD3, and CD7. From extract CD1, two compounds were isolated and characterized as triacontanol (C1) and 2-carboxy-1,1-dimethylpyrrolidine (C2). When the females were exposed to sublethal doses of these compounds, they laid lesser number of eggs as compared to the control. C2 was found to have a slightly greater oviposition inhibition effect than C1. From fraction CD7, one novel compound labeled as CDF1 has been isolated and identified as 6-(1-hydroxy-non-3-enyl)tetrahydropyran-2-one. CDF1 has also shown insecticidal and oviposition inhibitory activities against B. chinensis at low concentrations.

Chemical Components of Cassia didymobotrya Fresem.

-

Constituents from Salmalia malabaricum

The phytochemical investigation of the root of Salmalia malabaricum has resulted in the isolation and identification of n-triacontanol, β-sitosterol, and a new glycoside which was characterized as 5,7,3',4'-tetrahydroxy-6-methoxyflavan-3-O-β-D-glucopyranosyl-α-D-xylopyranoside on the basis of spectral and degradative studies.