16974-10-0

Basic information

• Product Name: (Z)-7-TETRADECEN-1-YL ACETATE
• Synonyms: CIS-7-TETRADECEN-1-YL ACETATE;(Z)-7-TETRADECEN-1-YL ACETATE;(7Z)-7-Tetradecenyl acetate;acetate,(z)-7-tetradecen-1-o;CIS-7-TETRADECENYL ACETATE;(Z)-7-Tetradecenylacetate;(Z)-Tetradecen-1-olacetate;(Z)-7-TDA, Z-7-TDA
• CAS NO: 16974-10-0
• Molecular Formula: C₁₆H₃₀O₂
• Molecular Weight: 254.41
• Mol File: 16974-10-0.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 333.5±21.0℃ (760 Torr)
• Flash Point: 144 °F
• Appearance: /
• Density: 0.878±0.06 g/cm3 (20 ºC 760 Torr)
• Vapor Pressure: 0.000136mmHg at 25°C
• Refractive Index: 1.45
• Storage Temp.: -20°C
• CAS DataBase Reference: (Z)-7-TETRADECEN-1-YL ACETATE(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-7-TETRADECEN-1-YL ACETATE(16974-10-0)
• EPA Substance Registry System: (Z)-7-TETRADECEN-1-YL ACETATE(16974-10-0)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36-26/36
• WGK Germany: 3
• Hazardous Substances Data: 16974-10-0(Hazardous Substances Data)

Usage

General Description

(Z)-7-Tetradecen-1-yl acetate is a chemical compound that belongs to the class of organic compounds known as fatty acid esters. It is derived from the combination of acetic acid and (Z)-7-tetradecen-1-ol, an alcohol. (Z)-7-TETRADECEN-1-YL ACETATE is commonly found in various fruits and flowers and is responsible for their distinct floral and fruity aroma. It is widely used in the production of perfumes, soaps, and other cosmetic products for its pleasant scent. Additionally, it is also used as a flavoring agent in food products. However, it is important to note that (Z)-7-tetradecen-1-yl acetate may cause skin and eye irritation and should be handled with caution.

InChI:InChI=1/C16H30O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-18-16(2)17/h8-9H,3-7,10-15H2,1-2H3/b9-8-

Upstream product

• 40642-43-1 (Z)-tetradec-7-en-1-ol 
• 108-24-7 acetic anhydride 
• 75-36-5 acetyl chloride 
• 6294-17-3 1-bromo-6-chlorohexane 
• 111-25-1 1-bromo-hexane 
• 92169-43-2 ethyl 7,7-diethoxyheptanoate 
• 2009-83-8 6-chloro-1-hexanol 
• 37011-94-2 7-tetradecyne-1-ol 
• 49592-98-5 (Z)-methyl tetradec-7-enoate 
• 41453-56-9 (Z)-2-nonen-1-ol 
• 5048-26-0 5-hexenyl acetate 
• 10160-25-5 7-bromo-1-(2-tetrahydropyranyloxy)heptane 
• 533-87-9 9,10,16-trihydroxyhexadecanoic acid 
• 77295-58-0 1-acetoxy-6-iodohexane 

Downstream Products

• 40642-43-1 (Z)-tetradec-7-en-1-ol 
• 76963-23-0 3-oxo-(Z)-9-hexadecenal 
• 65128-96-3 (Z)-7-tetradecenal 

Relevant articles and documents

Method for synthesizing cis-7-tetradecenol acetate which is main component of sex pheromone of holcocerus vicarius walker

The invention discloses a method for synthesizing cis-7- tetradecenol acetate which is a main component of sex pheromone of holcocerus vicarius walker. The method includes (1), preparing (7-bromo-heptyl-1-)-2-tetrahydropyran ether; (2), preparing (7-bromo

Syntheses of (Z)-7-Tetradecen-l-yl Acetate, (Z)-9-Tetradecen-l-ol and its Acetate from Aleuritic Acid

-

The Reactivity of the Highly Functionalized Copper, Zinc Reagents RCu(CN)ZnI Toward 1-Haloalkynes and Acetylenic Esters

The highly functionalized organometallics RCu(CN)ZnI 1 react efficiently with 1-haloalkynes providing polyfunctionalized alkynes in high yields.This method has been used to prepare a pheromone of the Amathes c-nigrum in 3 steps and 64percent overall yield.The reagents 1 also add in the presence of an excess of Me3SiCl to acetylenic esters to afford polyfunctionalized C-silylated ethylenic esters.In the case of ethyl propiolate, the reaction is highly stereoselective and affords 97percent pure (E)-2-trimethylsilyl ethylenic esters.