6,7-dihydrolinalool

1-octen-3-ol, 3,7-dimethyl-

CAS: 18479-49-7 C10 H20 O MW: 156.26860000 woody

Identification

Name6,7-dihydrolinalool
IUPAC3,7-dimethyloct-1-en-3-ol
CAS Number18479-49-7
EINECS242-358-2
FDA UNII25VV2M2VR9
Molecular FormulaC10 H20 O
Molecular Weight156.26860000
Nikkaji NumberJ100.792K

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Boiling Point 183.00 to 185.00 °C. @ 760.00 mm Hg (est)
Vapor Pressure 0.212000 mmHg @ 25.00 °C. (est)
Flash Point 146.00 °F. TCC ( 63.30 °C. ) (est)
logP (o/w) 3.284 (est)
Soluble in alcohol
Insoluble in water

Cosmetic Information

CosIngcosmetic data
Cosmetic Usesperfuming agents

Organoleptic Properties

Odor Description at 100.00 %.

Safety Information

Preferred SDSView
Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categoryflavor and fragrance agents
RIFM Fragrance Material Safety AssessmentSearch
maximum skin levels for fine fragrances0.0200 % and are based on the assumption that the fragrance mixture is used at 20% in a consumer product (IFRA Use Level Survey).
Recommendation for 6,7-dihydrolinalool usage levels up to4.0000 % in the fragrance concentrate.
use level in formulae for use in cosmetics0.0200 %
Dermal Systemic Exposure in Cosmetic Products0.0005 mg/kg/day

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Potential Uses

None Found

Natural Occurrence

ham cured ham PMC

Synonyms

3,7- dimethyl oct-1-en-3-ol 3,7- dimethyl-1-octen-3-ol 3,7- dimethyloct-1-en-3-ol 1- octen-3-ol, 3,7-dimethyl- PubMed: Acaricidal activities of the active component of Lycopus lucidus oil and its derivatives against house dust and stored food mites (Arachnida: Acari). PubMed: Investigation of bound aroma constituents of yellow-fleshed nectarines (Prunus persica L. Cv. Springbright). changes in bound aroma profile during maturation. PubMed: Glycosides and xanthine oxidase inhibitors from Conyza bonariensis. PubMed: Mechanism of monoterpene cyclization: stereochemical aspects of the transformation of noncyclizable substrate analogs by recombinant (-)-limonene synthase, (+)-bornyl diphosphate synthase, and (-)-pinene synthase.