Identification

Namedihydrojasmone
IUPAC3-methyl-2-pentylcyclopent-2-en-1-one
CAS Number1128-08-1
EINECS214-434-5
FDA UNIIY953R7PP90
Molecular FormulaC11 H18 O
Molecular Weight166.26366000
MDL NumberMFCD00036480
Nikkaji NumberJ12.280G
Beilstein1906471

Regulatory

JECFA Food Flavoring1406 3-methyl-2-(N-pentanyl)-2-cyclopenten-1-one
DG SANTE Food Flavourings07.140 3-methyl-2-pentylcyclopent-2-en-1-one
FEMA Number3763
FDANo longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm (SATF)1128-08-1 ; 2-PENTYL-3-METHYL-2-CYCLOPENTEN-1-ONE

Physical Properties

Appearance pale yellow clear liquid (est)
Assay 99.00 to 100.00
Food Chemicals Codex Listed No
Specific Gravity 0.91100 to 0.91700 @ 25.00 °C., 0.91200 to 0.91700 @ 20.00 °C.
Pounds per Gallon - (est). 7.580 to 7.630
Pounds per Gallon - est. 7.598 to 7.639
Refractive Index 1.67600 to 1.68200 @ 20.00 °C.
Boiling Point 120.00 to 121.00 °C. @ 12.00 mm Hg, 112.00 °C. @ 7.00 mm Hg
Acid Value 1.00 max. KOH/g
Vapor Pressure 0.010000 mmHg @ 20.00 °C.
Flash Point 230.00 °F. TCC ( 110.00 °C. )
logP (o/w) 2.754 (est)
Soluble in alcohol
Insoluble in water
Stability alcoholic fine fragrance, good

Cosmetic Information

CosIngcosmetic data
Cosmetic Usesperfuming agents

Organoleptic Properties

Odor Strength medium
Substantivity 340 hour(s) at 100.00 %
Odor Description
at 100.00 %.
Fruity, sweet, floral, woody with a powdery nuance
A fresh, fruity, jasmine odor with woody and herbal undertones
deep jasmin type odour intensely floral vital celery myrrh aspects Intensely floral and fresh
Intensely floral green, jasmine odor with fresh and fruity undertones
Fresh, fruity, scented jasmine with woody and herbal hues
Odor sample from Takasago International Corp
Taste Description
at 10.00 ppm.
Creamy mouthfeel, lactonic

Safety Information

Preferred SDSView
European informationMost important hazard(s):
Oral/Parenteral Toxicityoral-rat LD50 2500 mg/kg
Dermal Toxicityskin-rabbit LD50 > 5000 mg/kg
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 dihydrojasmone usage levels up to5.0000 % in the fragrance concentrate.
Maximised Survey-derived Daily Intakes (MSDI-EU)0.34 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA)0.20 (μg/capita/day)
Structure ClassII
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-

ACS International GmbH

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PerfumersWorld Ltd.

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The John D. Walsh Company, Inc

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WholeChem, LLC

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Potential Uses

FR apricot FR bergamot FR celery FR chypre FR citrus FR coconut FR fern FR floral FR fresh outdoors FL fruit tropical fruit FR green FR herbal FR honey FR jasmin FR lavender FR lily of the valley FR maple modifier natural FR oriental FR peach seedy FR spice FL tropical waxy FR woody

Natural Occurrence

osmanthus absolute @ trace% Data

Synonyms

2- amyl-3-methyl-2-cyclopenten-1-one 2- cyclopenten-1-one, 3-methyl-2-pentyl- dihydro jasmone 3- methyl-2-(N-pentanyl)-2-cyclopenten-1-one 3- methyl-2-n-pentylcyclopent-2-en-1-one 3- methyl-2-pentyl cyclopent-2-en-1-one 3- methyl-2-pentyl cyclopent-2-enone 3- methyl-2-pentyl-2-cyclopenten-1-one 3- methyl-2-pentyl-cyclopent-2-en-1-one 3- methyl-2-pentyl-cyclopent-2-enone 3- methyl-2-pentylcyclopent-2-en-1-one 3- methyl-2-pentylcyclopent-2-enone 2- pentyl-3-methyl-2-cyclopenten-1-one US Patents: 3,981,920 - Method for preparing cyclopentenone derivatives PubMed: Unusual endoperoxide isomerizations: a convenient entry into 2-vinyl-2-cyclopentenones from saturated fulvene endoperoxides. PubMed: A three-component coupling approach to cyclopentanoids. PubMed: Conversion of nitroheptane to dihydrojasmone. PubMed: Synthesis of 2-alkylcyclopentenones. Jasmone, dihydrojasmone, and a prostaglandin precursor. PubMed: Synthetic studies on cyclopentane derivatives. Pt. 1. Alternative routes to dl-prostaglandin-B1 and dihydrojasmone.