(E,E)-2,4-hexadien-1-ol

(E,E)-sorbyl alcohol

CAS: 17102-64-6 C6 H10 O MW: 98.14490000 green

Identification

Name(E,E)-2,4-hexadien-1-ol
IUPAC(2E,4E)-hexa-2,4-dien-1-ol
CAS Number17102-64-6
EINECS241-173-4
FDA UNII11CF2E3HNG
Molecular FormulaC6 H10 O
Molecular Weight98.14490000
MDL NumberMFCD00002925
Nikkaji NumberJ100.696G
Beilstein1719722

Regulatory

Physical Properties

Appearance white solid (est)
Assay 97.00 to 100.00
Food Chemicals Codex Listed No
Specific Gravity 0.87100 @ 25.00 °C.
Refractive Index 1.50000 @ 20.00 °C.
Melting Point 31.00 to 33.00 °C. @ 760.00 mm Hg
Boiling Point 80.00 °C. @ 12.00 mm Hg, 178.00 to 179.00 °C. @ 760.00 mm Hg
Vapor Pressure 0.281000 mmHg @ 25.00 °C. (est)
Flash Point 162.00 °F. TCC ( 72.22 °C. )
logP (o/w) 1.083 (est)
Soluble in alcohol

Organoleptic Properties

Odor Description at 100.00 %.

Safety Information

Preferred SDSView
European informationMost important hazard(s):
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

Categoryflavoring agents
IFRA Critical EffectInsufficient data
Recommendation for (E,E)-2,4-hexadien-1-ol usage levels up toPROHIBITED: Should not be used as a fragrance ingredient.

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Potential Uses

FR fresh and clean FR green FR herbal

Natural Occurrence

asparagus cooked asparagus asparagus raw asparagus naranjilla fruit

Synonyms

(2E,4E)- hexa-2,4-dien-1-ol (E,E)- hexa-2,4-dien-1-ol (E)-2,(E)-4- hexadien-1-ol E,E-2,4- hexadien-1-ol trans-2,trans-4- hexadien-1-ol trans,trans-2,4- hexadien-1-ol 2,4- hexadien-1-ol, (2E,4E)- 2,4- hexadien-1-ol, (E,E)- (2E,4E)-1- hydroxyhexa-2,4-diene (E,E)- sorbyl alcohol PubMed: The acyl nitroso Diels-Alder (ANDA) reaction of sorbate derivatives: an X-ray and 15N NMR study with an application to amino-acid synthesis. PubMed: Reactions of hydro(pero)xy derivatives of polyunsaturated fatty acids/esters with nitrite ions under acidic conditions. Unusual nitrosative breakdown of methyl 13-hydro(pero)xyoctadeca-9,11-dienoate to a novel 4-nitro-2-oximinoalk-3-enal product.