89353-62-8

Basic information

• Product Name: (3Z,6Z,9Z)-3,6,9-Nonadecatriene
• Synonyms: (3Z,6Z,9Z)-3,6,9-Nonadecatriene;(Z,Z,Z)-3,6,9-Nonadecatriene
• CAS NO: 89353-62-8
• Molecular Formula: C19H34
• Molecular Weight: 262.4733
• Mol File: 89353-62-8.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 342.2°Cat760mmHg
• Flash Point: 155.7°C
• Appearance: /
• Density: 0.812g/cm³
• Vapor Pressure: 0.000151mmHg at 25°C
• Refractive Index: 1.47
• CAS DataBase Reference: (3Z,6Z,9Z)-3,6,9-Nonadecatriene(CAS DataBase Reference)
• NIST Chemistry Reference: (3Z,6Z,9Z)-3,6,9-Nonadecatriene(89353-62-8)
• EPA Substance Registry System: (3Z,6Z,9Z)-3,6,9-Nonadecatriene(89353-62-8)

Safety Data

• Hazardous Substances Data: 89353-62-8(Hazardous Substances Data)

Usage

Description

(3Z,6Z,9Z)-3,6,9-Nonadecatriene, a long-chain hydrocarbon and a member of the polyunsaturated fatty acid family, is a chemical compound with 19 carbon atoms and three double bonds in the Z configuration at the 3rd, 6th, and 9th carbon positions. It is commonly found in plant oils, such as citrus fruits, and contributes to their characteristic aroma.

Uses

Used in the Food Industry:
(3Z,6Z,9Z)-3,6,9-Nonadecatriene is used as a natural flavor enhancer for its characteristic aroma derived from plant oils, particularly citrus fruits.
Used in the Fragrance Industry:
(3Z,6Z,9Z)-3,6,9-Nonadecatriene is used as a natural fragrance enhancer for its distinct aroma, adding a pleasant scent to various products.
Used in the Health and Wellness Industry:
(3Z,6Z,9Z)-3,6,9-Nonadecatriene is studied for its potential health benefits, including its anti-inflammatory and anti-cancer properties, making it a promising candidate for pharmaceutical applications.

InChI:InChI=1/C19H34/c1-3-5-7-9-11-13-15-17-19-18-16-14-12-10-8-6-4-2/h5,7,11,13,17,19H,3-4,6,8-10,12,14-16,18H2,1-2H3/b7-5-,13-11-,19-17-

Upstream product

• 112-31-2 caprinaldehyde 
• 764-62-5 1-Jod-4-methoxybut-2-in 
• 3739-97-7 (trimethylsilyl)methylenetriphenylphosphorane 
• 111-83-1 1-bromo-octane 
• 125285-14-5 1-bromo-(2Z,5Z,8Z)-2,5,8-undecatriene 
• 21944-83-2 (3Z,6Z)-nona-3,6-dienal 
• 32339-43-8 decyltriphenylphosphonium bromide 
• 1638153-00-0 (3Z,6Z)-9,9-dimethoxy-nona-3,6-dien-1-yl 4-methylbenzenesulfonate 
• 696-86-6 cis,cis,cis-1,4,7-cyclononatriene 
• 1638152-99-4 (3Z,6Z)-9,9-dimethoxynona-3,6-dien-1-ol 
• 75-16-1 methylmagnesium bromide 
• 129750-65-8 (1R,2R)-2-[(Z)-(R)-1-(tert-Butyl-dimethyl-silanyl)-hex-3-enyl]-1-methyl-3,6-dihydro-2H-pyridine 1-oxide 
• 129750-65-8 (R)-2-[(Z)-(R)-1-(tert-Butyl-dimethyl-silanyl)-hex-3-enyl]-1-methyl-3,6-dihydro-2H-pyridine 1-oxide 
• 129750-66-9 C₁₈H₃₅NOSi 

Relevant articles and documents

A nine carbon homologating system for skip-conjugated polyenes

Ozonolysis of Z,Z,Z-cylonona-1,4,7-triene leads to a 1,9-difunctionalised Z,Z-3,6-nonadiene which is readily converted into a range of polyunsaturated pheromones and fatty acids.

Facile and efficient syntheses of (3Z,6Z,9Z)-3,6,9-nonadecatriene and homologues: Pheromone and attractant components of lepidoptera

Facile and efficient chemical syntheses of (3Z,6Z,9Z)-3,6,9-nonadecatriene and homologues from commercially available α-linolenic acid [(9Z,12Z,15Z)-9,12,15-octadecatrienoic acid] are reported. These straight-chain homoconjugated trienes are common sex pheromone and attractant components for many lepidopterous insect pests. The metal-catalyzed cross-coupling reactions between (9Z,12Z,15Z)-9,12,15-octadecatrienyl triflate and the appropriate Grignard reagents proceed very rapidly under notable mild conditions using Li2CuCl4 as catalyst in diethyl ether, and the resulting (3Z,6Z,9Z)-3,6,9-trienes with retention of geometrical configuration were in >92% isolated yield.

Facile Synthesis of 1,4-Dienic Compounds from 4-Pentyn-1-ol: Synthesis of Pheromone Components of Boarmia Selenaria and B. Rhomboidaria

The bifunctionality of 4-pentyn-1-ol has been suitably exploited to prepare 1,4-dienic unit.This has been applied for the synthesis of two important sex pheromone components.