3,5-octadien-2-one

3,5-octadienone

CAS: 38284-27-4 C8 H12 O MW: 124.18284000 fatty

Identification

Name3,5-octadien-2-one
IUPACocta-3,5-dien-2-one
CAS Number38284-27-4
FDA UNIISearch
Molecular FormulaC8 H12 O
Molecular Weight124.18284000
Nikkaji NumberJ475.291K

Regulatory

Physical Properties

Appearance colorless to pale yellow clear liquid (est)
Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Specific Gravity 0.86700 to 0.87300 @ 25.00 °C.
Pounds per Gallon - (est). 7.214 to 7.264
Refractive Index 1.50900 to 1.51500 @ 20.00 °C.
Boiling Point 194.00 to 195.00 °C. @ 760.00 mm Hg (est)
Vapor Pressure 0.437000 mmHg @ 25.00 °C. (est)
Flash Point 156.00 °F. TCC ( 69.30 °C. ) (est)
logP (o/w) 1.640 (est)
Soluble in alcohol
Insoluble in water

Organoleptic Properties

Odor Description at 1.00 % in dipropylene glycol.

Safety Information

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
Recommendation for 3,5-octadien-2-one usage levels up tonot for fragrance use.
Maximised Survey-derived Daily Intakes (MSDI-EU)0.011 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA)3.00 (μg/capita/day)
Structure ClassII

Chemical sources Association Inc

Exchange of knowledge

Need This Item for Flavor? You can contact the Chemical Sources Association.

Potential Uses

FL anchovy

Natural Occurrence

coffee PMC

Synonyms

octa-3,5-dien-2-one 3,5- octadienone US Patents: 3,937,228 - Aromatic compositions PubMed: Odorant synergy effects as the cause of fishy malodors in algal marine oils. US Patents: Flavoring phenol or phenol derivative containing food or feed with cycloaliphatic derivatives PubMed: Pro-oxidant/antioxidant behaviours of ascorbic acid, tocopherol, and plant extracts in n-3 highly unsaturated fatty acid rich oil-in-water emulsions. PubMed: Studies on the aroma of maté (Ilex paraguariensis St. Hil.) using headspace solid-phase microextraction.