Epoxydihydrolinalool

Epoxydihydrolinalool Basic information
Product Name:Epoxydihydrolinalool
Synonyms:Epoxydihydrolinalool;LINALOOL OXIDE;(2S)-α,α,5-Trimethyl-5β-ethenyltetrahydrofuran-2α-methanol;(2S,5S)-α,α,5-Trimethyl-5β-vinyltetrahydrofuran-2α-methanol;5β-Ethenyltetrahydro-α,α,5-trimethyl-2α-furanmethanol;5β-Ethenyltetrahydro-α,α,5-trimethylfuran-2α-methanol;(2R,5R)-2-(1-Hydroxy-1-methylethyl)-5-methyl-5-vinyltetrahydrofuran;(2R,5R)-α,α,5-Trimethyl-5-vinyltetrahydrofuran-2-methanol
CAS:1365-19-1
MF:C10H18O2
MW:170.25
EINECS:215-723-9
Product Categories:
Mol File:1365-19-1.mol
Epoxydihydrolinalool Structure
Epoxydihydrolinalool Chemical Properties
Boiling point 188 ºC
density 0.935-0.950
refractive index 1.440-1.460
Fp 63 ºC
Odorat 100.00 %. floral herbal earthy green
Odor Typefloral
LogP2.15
EPA Substance Registry SystemLinalool oxide (1365-19-1)
Safety Information
HS Code 29329990
MSDS Information
Epoxydihydrolinalool Usage And Synthesis
DescriptionLinalool oxide has a powerful sweet woody, penetrating odor with floral, woody-earthy undertones.
Synthesis: From linalool by oxidation.
Chemical PropertiesLinalool oxide has a powerful, sweet, woody, penetrating odor with floral, woody-earthy undertones.
Chemical PropertiesLinalool Oxide has been identified in essential oils and in fruit aromas. Commercial linalool oxide is a mixture of the cis and trans forms, [5989-33-3] and [34995-77-2], respectively. It is a liquid with an earthy, floral, slightly bergamot-like odor.
OccurrenceReported found in apricot, apricot essence, bilberry, Mindanaese cinnamomum oil, citrus fruit blossom, cloud berry oil, cocoa, cocoa powder, coffee, roaster coffee, cranberry, black currant, grape, muscat grape juice, Vinifera grape, grapefruit blossoms, grapefruit essence, grapefruit juice, grapefruit oil, Japanese Ho leaf oil, hops, hop oil, lavender essence, lavandin oil, lime essence, lingonberry juice, mango, orange essence, orange juice, passion fruit and other natural sources.
PreparationLinalool oxide is prepared by oxidation of linalool, for example, with peracids. The isomeric compound 2,2,6-trimethyl-6-vinyltetrahydro-2H-pyran-3-ol [14049-11-7], which also occurs in nature, is formed as a by-product:
Aroma threshold valuesDetection: 320 ppb
Taste threshold valuesTaste characteristics at 50 ppm: green, floral, fatty, woody, fermented, herbal, fruity and berry.
SynthesisFrom linalool by oxidation.
Epoxydihydrolinalool Preparation Products And Raw materials
Gadolinium oxide Terbium Oxide Acetamidine hydrochloride DICHLOFLUANID Cinnamaldehyde Dicyandiamide Triethyl phosphate 4-tert-Butyltoluene 1-Nonanal 4'-tert-Butylacetophenone Polypropylenglycol diglycidyl ether Nitrite Phenethyl alcohol VANILLIN PROPYLENE GLYCOL ACETAL Food grade calcium chloride 1-Hexanol 1-Butanol Linalool

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