dihydro-beta-ionol

4-(2,6,6-trimethylcyclohex-1-en-1-yl)butan-2-ol

CAS: 3293-47-8 C13 H24 O MW: 196.33348000 woody

Identification

Namedihydro-beta-ionol
IUPAC4-(2,6,6-trimethyl-1-cyclohexenyl)butan-2-ol
CAS Number3293-47-8
EINECS221-957-2
FDA UNIIS3T0WG30TW
Molecular FormulaC13 H24 O
Molecular Weight196.33348000
Nikkaji NumberJ24.332I

Regulatory

JECFA Food Flavoring395 dihydro-beta-ionol
DG SANTE Food Flavourings02.107 dihydro-beta-ionol
FEMA Number3627
FDANo longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm (SATF)3293-47-8 ; DIHYDRO-BETA-IONOL

Physical Properties

Appearance white solid (est)
Assay 97.00 to 100.00
Food Chemicals Codex Listed No
Melting Point 38.00 to 40.00 °C. @ 760.00 mm Hg
Boiling Point 234.00 °C. @ 760.00 mm Hg
Vapor Pressure 0.001000 mmHg @ 25.00 °C. (est)
Flash Point > 200.00 °F. TCC ( > 93.33 °C. )
logP (o/w) 4.634 (est)
Soluble in alcohol
Insoluble in water

Cosmetic Information

CosIngcosmetic data
Cosmetic Usesperfuming agents

Organoleptic Properties

Odor Description at 100.00 %.

Safety Information

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

Categoryflavor and fragrance agents
RIFM Fragrance Material Safety AssessmentSearch
Recommendation for dihydro-beta-ionol usage levels up to2.0000 % in the fragrance concentrate.
baked goods-
beverages(nonalcoholic)-
beverages(alcoholic)-
breakfast cereal-
cheese-
chewing gum-
condiments / relishes-
confectionery froastings-
egg products-
fats / oils-
fish products-
frozen dairy-
fruit ices-
gelatins / puddings-
granulated sugar-
gravies-
hard candy-
imitation dairy-
instant coffee / tea-
jams / jellies-
meat products-
milk products-
nut products-
other grains-
poultry-
processed fruits-
processed vegetables-
reconstituted vegetables-
seasonings / flavors-
snack foods-
soft candy-
soups-
sugar substitutes-
sweet sauces-

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Potential Uses

FR amber FR balsam FR beeswax absolute replacer FR berry FR blueberry FR cassia FR chypre FR cranberry FR cyclamen diffusion FR fir needle oil replacer FR floral FR fruit FR genet FR herbal FR leather FR leather russian leather FR mimosa FR moss FR oriental FR patchouli FR prune FR raspberry FR rose FR violet FR woody

Natural Occurrence

champaca absolute @ 1.10% Data champaca concrete @ 0.40% Data

Synonyms

1- cyclohexene-1-propanol, a,2,6,6-tetramethyl- dihydro beta-ionol dihydro-beta-ionol beta- dihydroionol alpha,2,6,6- tetramethyl cyclohexene-1-propan-1-ol tetramethyl cyclohexene-1-propanol 4-(2,6,6- trimethyl-1-cyclohexen-1-yl)-2-butanol 4-2,6,6- trimethyl-1-cyclohexenyl butan-2-ol 4-(2,6,6- trimethyl-1-cyclohexenyl)butan-2-ol 4-(2,6,6- trimethyl-cyclohex-1-enyl)-butan-2-ol 4-(2,6,6- trimethylcyclohex-1-en-1-yl)butan-2-ol US Patents: 4,461,309 - Ionyl-alkyl and ionyl alkenyl ethers as flavorants for tobacco PubMed: Discovery of aromatic components with excellent fragrance properties and biological activities: β-ionols with antimelanogenetic effects and their asymmetric syntheses. PubMed: Glucose exerts a negative effect over a peroxidase from Trichosporon asahii, with carotenoid cleaving activity. PubMed: Bioactive apocarotenoids from Tectona grandis. PubMed: Bioconversion of lutein using a microbial mixture--maximizing the production of tobacco aroma compounds by manipulation of culture medium. PubMed: Investigation of bound aroma constituents of yellow-fleshed nectarines (Prunus persica L. Cv. Springbright). changes in bound aroma profile during maturation. PubMed: Aroma composition of Vitis vinifera Cv. tannat: the typical red wine from Uruguay. PubMed: Stereoselective synthesis of optically active 3-hydroxy-7,8-dihydro-beta-ionol-glucosides. PubMed: Production of tobacco aroma from lutein. Specific role of the microorganisms involved in the process. PubMed: Ionone, iridoid and phenylethanoid glycosides from Ajuga salicifolia. PubMed: Metabolism and CYP-inducer properties of astaxanthin in man and primary human hepatocytes. PubMed: Isolation of some glycosides as aroma precursors in young leaves of Japanese pepper (Xanthoxylum piperitum DC.). PubMed: The (3R,9R)-3-hydroxy-7,8-dihydro-beta-ionol disaccharide glycoside is an aroma precursor in tea leaves. PubMed: The efficiency of antioxidants delivered by liposomal transfer.