isopinocamphone

3-pinanone

CAS: 18358-53-7 C10 H16 O MW: 152.23672000 woody

Identification

Nameisopinocamphone
IUPAC2,6,6-trimethylbicyclo[2.2.1]heptan-3-one
CAS Number18358-53-7
EINECS242-228-5
FDA UNIISearch
Molecular FormulaC10 H16 O
Molecular Weight152.23672000
Nikkaji NumberJ1.824.679A
CoE Number11125

Regulatory

JECFA Food Flavoring1868 3-pinanone
DG SANTE Food Flavourings07.171 isopinocamphone
FEMA Number4198
FDANo longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm (SATF)18358-53-7 ; 3-PINANONE

Physical Properties

Appearance colorless clear liquid (est)
Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Specific Gravity 0.96300 to 0.96900 @ 25.00 °C.
Pounds per Gallon - (est). 8.013 to 8.063
Refractive Index 1.47200 to 1.47800 @ 20.00 °C.
Boiling Point 207.00 to 209.00 °C. @ 760.00 mm Hg, 69.00 to 71.00 °C. @ 5.00 mm Hg
Vapor Pressure 0.213000 mmHg @ 25.00 °C. (est)
Flash Point 163.00 °F. TCC ( 72.78 °C. )
logP (o/w) 2.343 (est)
Soluble in alcohol

Organoleptic Properties

Odor Description at 100.00 %.

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

Categoryflavor and fragrance agents
RIFM Fragrance Material Safety AssessmentSearch
Recommendation for isopinocamphone usage levels up to2.0000 % in the fragrance concentrate.
Maximised Survey-derived Daily Intakes (MSDI-EU)0.024 (μg/capita/day)
Modified Theoretical Added Maximum Daily Intake (mTAMDI)1000 (μg/person/day)
Threshold of Concern540 (μg/person/day)
Structure ClassII
baked goods5.00000
beverages(nonalcoholic)-
beverages(alcoholic)-
breakfast cereal2.00000
cheese3.00000
chewing gum-
condiments / relishes2.00000
confectionery froastings4.00000
egg products-
fats / oils2.00000
fish products1.00000
frozen dairy3.00000
fruit ices3.00000
gelatins / puddings-
granulated sugar-
gravies-
hard candy5.00000
imitation dairy3.00000
instant coffee / tea-
jams / jellies-
meat products1.00000
milk products3.00000
nut products-
other grains-
poultry1.00000
processed fruits2.00000
processed vegetables-
reconstituted vegetables-
seasonings / flavors2.00000
snack foods-
soft candy5.00000
soups2.00000
sugar substitutes-
sweet sauces2.00000
Dairy products, excluding products of category 02.0 (01.0)3.00000
Fats and oils, and fat emulsions (type water-in-oil) (02.0)2.00000
Edible ices, including sherbet and sorbet (03.0)3.00000
Processed fruit (04.1)2.00000
Processed vegetables (incl. mushrooms & fungi, roots & tubers, pulses and legumes), and nuts & seeds (04.2)-
Confectionery (05.0)4.00000
Chewing gum (05.3)-
Cereals and cereal products, incl. flours & starches from roots & tubers, pulses & legumes, excluding bakery (06.0)2.00000
Bakery wares (07.0)5.00000
Meat and meat products, including poultry and game (08.0)1.00000
Fish and fish products, including molluscs, crustaceans and echinoderms (MCE) (09.0)1.00000
Eggs and egg products (10.0)-
Sweeteners, including honey (11.0)-
Salts, spices, soups, sauces, salads, protein products, etc. (12.0)2.00000
Foodstuffs intended for particular nutritional uses (13.0)3.00000
Non-alcoholic ("soft") beverages, excl. dairy products (14.1)-
Alcoholic beverages, incl. alcohol-free and low-alcoholic counterparts (14.2)4.00000
Ready-to-eat savouries (15.0)5.00000
Composite foods (e.g. casseroles, meat pies, mincemeat) - foods that could not be placed in categories 01.0 - 15.0 (16.0)2.00000

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Potential Uses

FR acacia FR amber FR ambergris FR ambreine FR amyris FL/FR angelica FR armoise FR ash mountain ash FR bark FR bayberry FL/FR beech FL/FR benzoin absolute replacer FL/FR birch tar FR boronia FR boxwood FL buchu leaf FR cabreuva wood FR cade oil replacer FR calamus oil replacer FR cardamom oil replacer FR cedar FR cedar FR cedar forest FR cedarwood FR cedarwood atlas FR celery FR cigar FL/FR cistus FR citronella FR clary sage oil replacer FR costus FL/FR croton eluteria bark FR cypress oil replacer FR dogwood FR elemi FR fern FR fir needle oil replacer FR forest FR frankincense FL/FR galangal root FR galbanum FR ginger FR gingergrass FL/FR guaiacwood FR gurjun balsam FR hay new mown hay FR heather FR herbal FR hinoki oil replacer FL/FR hyssop FR iris blossom FR juniper FR juniper berry FR labdanum FR mace FR mimosa FR oakwood FR opoponax FL/FR orange bitter orange peel FR oregano FR orris FR osmanthus FR patchouli FR pine forest FL/FR pine needle FL/FR pine scotch pine FR pinion FR redwood FR sage FR sandalwood FR spikenard oil replacer FR spruce FR sweet grass FL/FR tansy oil replacer FL/FR tarragon oil replacer FL tea black tea timber FR tolu balsam FL/FR valerian FR vetiver FR woody FR wormseed oil replacer

Natural Occurrence

apricot fruit - up to 2.2 mg/kg bergamot mint oil @ 0.0-0.2% Data castoreum PMC cistus oil @ 0.7% Data hyssop oil @ 17.4% Data hyssop oil CO2 extract @ 16.5% Data labdanum leaf oil @ 0.50% Data lime oil distilled peru @ 0.05% Data mandarin oil uruguay @ 0.01-0.02% Data nepeta denudata benth. oil iran @ 0.30% Data patchouli oil china @ 0.01% Data rosemary oil france @ 0.06-0.58% Data rosemary oil morocco @ 0.04-0.13% Data wormwood oil italy @ trace% Data

Synonyms

dihydropinocarvone 3- pinanone 2,6,6- trimethyl bicyclo(3.1.1)heptan-3-one 2,6,6- trimethylbicyclo[2.2.1]heptan-3-one PubMed: Mycotoxicogenic fungal inhibition by innovative cheese cover with aromatic plants. PubMed: Synthesis of 2-(pyridin-3-yl)-1-azabicyclo[3.2.2]nonane, 2-(pyridin-3-yl)-1-azabicyclo[2.2.2]octane, and 2-(pyridin-3-yl)-1-azabicyclo[3.2.1]octane, a class of potent nicotinic acetylcholine receptor-ligands. PubMed: A general, efficient and stereospecific route to sphingosine, sphinganines, phytosphingosines and their analogs. PubMed: A general procedure for the enantioselective synthesis of the minor tobacco alkaloids nornicotine, anabasine, and anatabine. PubMed: Synthesis, theoretical and structural analyses, and enantiopharmacology of 3-carboxy homologs of AMPA. PubMed: Identification of plant odours activating receptor neurones in the weevil Pissodes notatus F. (Coleoptera, Curculionidae). PubMed: Metabolism and mode of action of cis- and trans-3-pinanones (the active ingredients of hyssop oil). PubMed: Muscle relaxing activity of Hyssopus officinalis essential oil on isolated intestinal preparations. PubMed: A novel enantioselective synthesis of (S)-(-)- and (R)-(+)-nornicotine via alkylation of a chiral 2-hydroxy-3-pinanone ketimine template. PubMed: [Investigation of variation of the production of biological and chemical compounds of Hyssopus officinalis L]. PubMed: Neutral compounds from male castoreum of North American beaver,Castor canadensis. PubMed: Electroantennogram responses of the southern pine beetle parasitoidDinotiscus dendroctoni (Ashmead) (Hymenoptera: Pteromalidae) to potential semiochemicals. PubMed: Volatile Constituents of Dracocephalum nutans. PubMed: Composition of essential oil of Ledum palustre. PubMed: [Experimental study of the toxic convulsant properties of commercial preparations of essences of sage and hyssop (author's transl)]. PubMed: [Synthesis and properties of 4-hydroxymethylene(-)3-pinanone and various derivatives]. PubMed: [PREPARATION OF (-)4-HYDROXYMETHYLENE-3-PINANONE].