104188-11-6

Basic information

• Product Name: (4Z,7Z)-deca-4,7-dien-1-ol
• Synonyms: (4Z,7Z)-deca-4,7-dien-1-ol;(4Z,7Z)-deca-4,7-dienol;4,7-Decadien-1-ol, (Z,Z)-
• CAS NO: 104188-11-6
• Molecular Formula: C10H18O
• Molecular Weight: 154.24932
• EINECS: -0
• Mol File: 104188-11-6.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 240.8 °C at 760 mmHg
• Flash Point: 94.8 °C
• Appearance: /
• Density: 0.864 g/cm³
• PKA: 15.07±0.10(Predicted)
• CAS DataBase Reference: (4Z,7Z)-deca-4,7-dien-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (4Z,7Z)-deca-4,7-dien-1-ol(104188-11-6)
• EPA Substance Registry System: (4Z,7Z)-deca-4,7-dien-1-ol(104188-11-6)

Safety Data

• Hazardous Substances Data: 104188-11-6(Hazardous Substances Data)

Usage

General Description

"(4Z,7Z)-Deca-4,7-dien-1-ol" is a chemical compound with the molecular formula C10H18O. It belongs to the organic compound class of unsaturated aliphatic hydrocarbons and is characterized by a carbon chain backbone with a double bond and an alcohol group. (4Z,7Z)-deca-4,7-dien-1-ol exists as a yellow to light yellow clear liquid and is insoluble in water but soluble in ethanol and ether. With its pleasant aroma, it is used extensively in the flavor and fragrance industry. Its odor has been described as citrus, sweet, waxy, and floral, and it is a common ingredient in citrus and floral flavorings for food and drink products. It is also used in cosmetics and detergents for its aromatic properties.

InChI:InChI=1S/C10H18O/c1-2-3-4-5-6-7-8-9-10-11/h3-4,6-7,11H,2,5,8-10H2,1H3/b4-3-,7-6-

Upstream product

• 5390-04-5 pent-1-yn-5-ol 
• 185955-53-7 1-(methoxymethyloxy)pent-4-yne 
• 16400-32-1 1-bromo-pent-2-yne 
• 166901-10-6 1-(tetrahydropyran-2-yloxy)-4,7-decadiyne 
• 92666-05-2 toluene-4-sulfonic acid pent-2-ynyl ester 
• 6261-22-9 pent-2-yn-1-ol 

Downstream Products

• 163041-94-9 (3E,8Z,11Z)-3,8,11-tetradecatrien-1-yl acetate 

Relevant articles and documents

An Improved and Convenient New Synthesis of the Pheromone Components of the Tomato Leafminer Tuta absoluta

A convenient new synthesis of the two pheromone components of the tomato pest Tuta absoluta in high overall yields and high stereoselectivity (30% yield, E,Z,Z 97% for the major compound and 23% yield, E,Z 99% for the minor component) is reported. The approaches compare favorably with others previously described.

(3E,8Z,11Z)-3,8,11-tetradecatrienyl acetate, major sex pheromone component of the tomato pest Scrobipalpuloides absoluta (Lepidoptera: Gelechiidae)

The major sex attractant emitted by Scrobipalpuloides absoluta females is shown to be (3E,8Z,11Z)-3,8,11-tetradecatrien-1-yl acetate by a novel strategy involving the random reduction of double bonds, followed by methylthiolation of the reduced products. Each female sex gland contains ca. 1-5 ng of this pheromone. This triene ester, synthesized by a stereospecific procedure, shows spectral and gas chromatographic properties identical to those of the natural substance. In field tests and wind tunnel bioassays, the synthetic ester was found to be highly attractive to conspecific males. The male response to this pheromone, however, is restricted to the same early-morning time window during which females exhibit calling behavior.