1072-33-9

Basic information

• Product Name: TRIDECYL ACETATE
• Synonyms: TRIDECANYL ACETATE;TRIDECYL ACETATE;1-tridecanol,acetate;ACETIC ACID N-TRYDECYL ESTER;tridecyl ethanoate;ACETIC ACID N-TRIDECYL ESTER;ACETIC ACID TRIDECYL ESTER
• CAS NO: 1072-33-9
• Molecular Formula: C₁₅H₃₀O₂
• Molecular Weight: 242.4
• Product Categories: Alcohol Acetates;Esters;Saturated fatty acids and derivatives
• Mol File: 1072-33-9.mol
• Article Data: 7

Chemical Properties

• Melting Point: 8.4°C
• Boiling Point: 143 °C / 5mmHg
• Flash Point: 126.6 °C
• Appearance: /liquid
• Density: 0.86
• Vapor Pressure: 0.00251mmHg at 25°C
• Refractive Index: 1.4330-1.4360
• Storage Temp.: 2-8°C
• CAS DataBase Reference: TRIDECYL ACETATE(CAS DataBase Reference)
• NIST Chemistry Reference: TRIDECYL ACETATE(1072-33-9)
• EPA Substance Registry System: TRIDECYL ACETATE(1072-33-9)

Safety Data

• WGK Germany: 3
• RTECS: YD4300000
• Hazardous Substances Data: 1072-33-9(Hazardous Substances Data)

Usage

General Description

Tridecyl acetate is a chemical compound that belongs to the class of organic compounds known as fatty acid esters. It is derived from tridecyl alcohol and acetic acid. Tridecyl acetate is commonly used as a fragrance ingredient in various cosmetic and personal care products such as shampoos, soaps, and perfumes due to its pleasant fruity and floral odor. It is also used as a solvent and emollient in cosmetic formulations. Tridecyl acetate is known for its low toxicity and is considered safe for use in consumer products when used at appropriate concentrations.

InChI:InChI=1/C15H30O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-17-15(2)16/h3-14H2,1-2H3

Upstream product

• 629-27-6 1-Iodooctane 
• 65921-65-5 5-iodopentyl acetate 
• 112-70-9 tridecan-1-ol 
• 108-24-7 acetic anhydride 
• 112-41-4 1-dodecene 
• 201230-82-2 carbon monoxide 
• 64-19-7 acetic acid 
• 546-67-8 lead(IV) tetraacetate 
• 544-63-8 n-tetradecanoic acid 
• 71-43-2 benzene 
• 604-69-3 β-D-glucose pentaacetate 

Downstream Products

• 1713-31-1 (+/-)-1,2-epoxytridecane 
• 2437-56-1 1-tridecene 

Related news

Subchronic toxicity evaluation of TRIDECYL ACETATE (cas 1072-33-9) in rats07/26/2019

Tridecyl acetate was administered to male and female Sprague-Dawley rats by oral gavage, 5 days per week for 13 weeks (90 days). Treated rats received daily doses of 0.1, 0.5, or 1.0 g/kg/day and control rats received distilled water at a dose of 1.0 g/kg/day. After 45 days an interim terminatio...detailed

Relevant articles and documents

Geographic variation in sex pheromone of asian corn borer, Ostrinia furnacalis, in Japan

Geographic variation in the sex pheromone of the Asian corn borer, Ostrinia furnacalis (Guenee), was surveyed in populations sampled at four locations ranging from 39.7°N to 32.9°N in Japan. The sex pheromone of the three northern populations was composed of (E)- and (Z)-12-tetradecenyl acetates with a mean E proportion of 36-39%. The southernmost population (Nishigoshi) had the same components but with a significantly higher E composition of 44%. The frequency distribution of the E ratio in the Nishigoshi population exhibited a small peak near 38% and a major peak near 46%. A family-wise analysis of the sex pheromone of this population confirmed that there were two distinct phenotypes regarding the E ratio. An '? 46% E strain' inhabits southern parts of Japan, in addition to an '? 38 % E strain,' which seems to be predominant in other regions of Japan.

Stabilization of long-chain intermediates in solution. octyl radicals and cations

The rearrangements of 1-octyl, 1-decyl and 1-tridecyl intermediates obtained from thermal lead(IV) acetate (LTA) decarboxylation of nonanoic, undecanoic and tetradecanoic acid were investigated experimentally through analysis and distribution of the products. The relationships between 1,5-, 1,6- and possibly existing 1,7-homolytic hydrogen transfer in 1-octyl-radical, as well as successive 1,2-hydride shift in corresponding cation have been computed via Monte-Carlo method. Taking into account that ratios of 1,5-/1,6-homolytic rearrangements in 1-octyl- and 1-tridecyl radical are approximately the same, the simulation shows very low involvement of 1,7-hydrogen rearrangement (1,5-/1,6-/1,7-hydrogen rearrangement = 85:31:1) in 1-octyl radical.

Reptilian chemistry: volatile compounds from paracloacal glands of the American crocodile (Crocodylus acutus).

The secretion of the paracloacal glands of the American crocodile (Crocodylus acutus) contains over 80 lipophilic compounds, including saturated and unsaturated long-chain alcohols along with their formic, acetic, and butyric acid esters, and several isoprenoids. Most of these compounds were identified on the basis of mass spectra, obtained by GC-MS. In addition, identification of the major components was supported by infrared spectra obtained by GC-FTIR. Major differences are indicated in the composition of the paracloacal gland secretion of C. acutus and that of another crocodylid, the African dwarf crocodile (Osteolaemus tetraspis).