1-OCTEN-3-OL

1-OCTEN-3-OL Structure
CAS No.
3191-86-4
Chemical Name:
1-OCTEN-3-OL
Synonyms
FEMA 2805;OCT-1-EN-3-OL;OCTANOL,3-(SG);1-OCTYLENE-3-OL;AMYL VINYL CARBINOL;VINYL PENTYL CARBINOL;PENTYL VINYL CARBINOL;5-Isobutyl-1-phenyl-1H-pyrazole;1H-Pyrazole, 5-(2-methylpropyl)-1-phenyl-
CBNumber:
CB2201397
Molecular Formula:
C13H16N2
Molecular Weight:
200.28
MOL File:
3191-86-4.mol
Modify Date:
2023/4/23 13:52:06

1-OCTEN-3-OL Properties

Boiling point 84-85 °C25 mm Hg(lit.)
Density 0.83 g/mL at 25 °C(lit.)
refractive index n20/D 1.437(lit.)
Flash point 142 °F
color A colourless liquid.
CAS DataBase Reference 3191-86-4(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Hazard Codes  Xn
Risk Statements  22-36/38
Safety Statements  26-36
WGK Germany  3
RTECS  RH3300000
Toxicity The acute oral LD50 in rats was reported as 0.34 g/kg and the acute dermal LD50 in rabbits as 3.3 g/kg.

1-OCTEN-3-OL Chemical Properties,Uses,Production

Chemical Properties

1-OCTEN-3-OL is a colorless liquid. B.P. 175° C. Sp.Gr. 0.84. Very powerful, sweet-earthy, almost buttery and fungus- or fermentation-like odor with a strong herbaceous note, -suggestive of Lavender-Lavandin-Rose and Hay. Somewhat acridchemical undertone which is hardly perceptible at proper (high) dilution. Almost insoluble in water, soluble in alcohol and oils. Sweet-herbaceous, haylike-earthy taste.

Occurrence

Originally reported to be found in the mushroom Armillaria matsutake, a parasite growing on the radical hairs of Pinus densiflora in the forests of Japan. It has been isolated also from the essential oils of Mentha pulegium L., lavender and M. timjia.

Uses

1-OCTEN-3-OL has been identified in Lavandin and many other important essential oils, it has become extremely popular in the art and science of preparing artificial or "reconstituted" essential oils. This is where the alcohol finds its main outlet. It also used in flavors (and in artificial Spearmint), such as Spice, Fruit, etc. usuall> in very low concentration: 0.2 to 6 ppm in the finished consumer product.

Preparation

By a vinyl Grignard reaction on hexaldehyde or from amyl magnesium bromide and acrolein.

Metabolism

In the animal body secondary alcohols can undergo either conjugation with glucuronic acid or oxidation to a ketone, which may be excreted in the urine or expired air or further oxidized or reduced back to the alcohol. Studies of secondary alcohols containing more than seven carbon atoms have been limited to octan-2-ol. The conjugation of this alcohol in rabbits is low and much of the alcohol may be excreted unchanged . A dilute solution of synthetic (dl)-locten-3-ol fed directly into the rumen of a cow produced after 2-4 hr a maximum concentration in the milk of 20 μg octenol/litre. This concentration did not give the milk an off-flavour, and was not reported to have any other effects.

1-OCTEN-3-OL Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 39)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
ABCR GmbH & CO. KG 49 721 95061 0 Germany 6846 75 Inquiry
Pushan Industry (Shaanxi) Co., Ltd. 029-81310890 13571859809 China 9999 58 Inquiry
Shaanxi Xihua Chemical Industry Co., Ltd 17691182729 15529505138 China 9966 58 Inquiry
Shanghai Haohong Pharmaceutical Co., Ltd. 4008210725 4008210725 China 55023 58 Inquiry
ChemSampCo, Inc. 609 656 2440 United States 3585 60 Inquiry
International Flavours & Fragrances I.F.F. (GB) Ltd. 0440 704 488 United Kingdom 1119 77 Inquiry
Oxford Chemicals +44 (0) 1429 863 555 United Kingdom 427 64 Inquiry
Penta Manufacturing Company 973 740 2300 United States 5077 65 Inquiry
ChemPacific Corporation 410 633 5771 United States 6902 51 Inquiry
Merck Schuchardt OHG +49 (0) 8102 802 0 Germany 5831 74 Inquiry
1-OCTYLENE-3-OL FEMA 2805 OCT-1-EN-3-OL PENTYL VINYL CARBINOL VINYL PENTYL CARBINOL OCTANOL,3-(SG) AMYL VINYL CARBINOL 1H-Pyrazole, 5-(2-methylpropyl)-1-phenyl- 5-Isobutyl-1-phenyl-1H-pyrazole 3191-86-4 Organic Building Blocks Building Blocks Acyclic Alkenes