Category:flavor and fragrance agents
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Physical Properties:
Appearance: | colorless clear liquid (est) |
Assay: | 99.00 to 100.00 sum of isomers
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Food Chemicals Codex Listed: | No |
Boiling Point: | 170.00 to 171.00 °C. @ 760.00 mm Hg
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Vapor Pressure: | 1.904000 mmHg @ 25.00 °C. (est) |
Flash Point: | 136.00 °F. TCC ( 57.78 °C. )
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logP (o/w): | 3.020 (est) |
Soluble in: |
| alcohol | | water, 70.97 mg/L @ 25 °C (est) |
Insoluble in: |
| water |
Stability: |
| detergent | | soap |
Organoleptic Properties:
Odor Type: herbal |
Odor Strength:medium , recommend smelling in a 10.00 % solution or less |
Substantivity:4 hour(s) at 20.00 % |
fresh camphoreous herbal rosemary |
Odor Description:at 10.00 % in dipropylene glycol. fresh camphor herbal rosemary Luebke, William tgsc, (1985) |
Odor sample from: Roure Bertrand Dupont Inc. |
sweet floral citrus woody cooling minty camphoreous |
Odor Description:Sweet, floral, citrus with woody, cooling, minty and camphoreous nuances Mosciano, Gerard P&F 18, No. 3, 53, (1993) |
Flavor Type: camphoreous |
sweet camphoreous woody cooling floral |
Taste Description: at 20.00 ppm. Sweet, camphoreous, woody, cooling, with floral nuances Mosciano, Gerard P&F 18, No. 3, 53, (1993) |
Odor and/or flavor descriptions from others (if found). |
Bedoukian Research |
2,2,6-TRIMETHYL-6-VINYLTETRAHYDROPYRAN ≥95.0%, Kosher |
Odor Description:A fresh camphor, herbal, rosemary odor Blends well with marjoram and lavender; also can be used in bois de rose and geranium. |
Taste Description:herbal Used in berry, blueberry, tea and other floral flavors. |
Givaudan |
Limetol |
Odor Description:Fresh, Camphoraceous, Woody, Cineole-Lime Limetol is used where a lemon-woody note is desired. It also offers pine needle and lime nuances. |
Taste Description:sweet camphor woody cooling floral |
Indukern F&F |
LIMETOL |
Odor Description:CITRUS, FRESH, TERPENIC, MENTHOLATED |
Moellhausen |
LIMETOL |
Odor Description:Fresh, Camphoraceous, Woody, Cineole-Lime |
Taste Description:sweet camphor woody cooling floral |
Cosmetic Information:
Suppliers:
BOC Sciences |
For experimental / research use only. |
2,2,6-Trimethyl-6-vinyltetrahydropyran
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Givaudan |
Limetol
Odor: Fresh, Camphoraceous, Woody, Cineole-Lime Use: Limetol is used where a lemon-woody note is desired. It also offers pine needle and lime nuances. |
Indukern F&F |
LIMETOL
Odor: CITRUS, FRESH, TERPENIC, MENTHOLATED |
Lluch Essence |
LIMETOL
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Moellhausen |
LIMETOL
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Penta International |
2,2,6-TRIMETHYL-6-VINYLTETRAHYDROPYRAN NATURAL
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Penta International |
2,2,6-TRIMETHYL-6-VINYLTETRAHYDROPYRAN
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Santa Cruz Biotechnology |
For experimental / research use only. |
Limetol
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The Perfumers Apprentice |
Limetol (G)
Odor: Fresh, Camphoraceous, Woody, Cineole-Lime-like Use: Used where a lemon-woody note is desired. Also gives a pine needle and lime nuance |
Vigon International |
Limetol
Odor: Fresh, Camphoraceous, Woody, Cineole-Lime |
Safety Information:
European information : |
Most important hazard(s): | Xi - Irritant |
R 10 - Flammable. R 38 - Irritating to skin. S 02 - Keep out of the reach of children. S 24/25 - Avoid contact with skin and eyes. S 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S 36 - Wear suitable protective clothing.
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Hazards identification |
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Classification of the substance or mixture |
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS) |
None found. |
GHS Label elements, including precautionary statements |
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Pictogram | |
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Hazard statement(s) |
None found. |
Precautionary statement(s) |
None found. |
Oral/Parenteral Toxicity: |
oral-rat LD50 [sex: M,F] 2700 - 2800 mg/kg (Sauer-Freeman, 1980)
oral-mouse LD50 [sex: M,F] 4000 - 8000 mg/kg (Roure Bertrand Dupont, 1979)
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Dermal Toxicity: |
Not determined
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Inhalation Toxicity: |
Not determined
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Safety in Use Information:
Category: | flavor and fragrance agents |
RIFM Fragrance Material Safety Assessment: Search |
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice |
Recommendation for geranic oxide usage levels up to: | | 3.0000 % in the fragrance concentrate.
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Maximised Survey-derived Daily Intakes (MSDI-EU): | 0.024 (μg/capita/day) |
Maximised Survey-derived Daily Intakes (MSDI-USA): | 8.00 (μg/capita/day) |
Structure Class: | II |
Use levels for FEMA GRAS flavoring substances on which the FEMA Expert Panel based its judgments that the substances are generally recognized as safe (GRAS). |
The Expert Panel also publishes separate extensive reviews of scientific information on all FEMA GRAS flavoring substances and can be found at FEMA Flavor Ingredient Library |
publication number: 13. Update in publication number(s): 14 |
Click here to view publication 13 |
| average usual ppm | average maximum ppm |
baked goods: | - | - |
beverages(nonalcoholic): | - | 0.50000 |
beverages(alcoholic): | - | - |
breakfast cereal: | - | - |
cheese: | - | - |
chewing gum: | - | - |
condiments / relishes: | - | - |
confectionery froastings: | - | 1.00000 |
egg products: | - | - |
fats / oils: | - | - |
fish products: | - | - |
frozen dairy: | - | - |
fruit ices: | - | - |
gelatins / puddings: | - | 2.00000 |
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: | - | 0.50000 |
soups: | - | - |
sugar substitutes: | - | - |
sweet sauces: | - | - |
Safety References:
European Food Safety Athority(EFSA):Flavor usage levels; Subacute, Subchronic, Chronic and Carcinogenicity Studies; Developmental / Reproductive Toxicity Studies; Genotoxicity Studies...
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European Food Safety Authority (EFSA) reference(s):
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Opinion of the Scientific Panel on food additives, flavourings, processing aids and materials in contact with food (AFC) related to Flavouring Group Evaluation 23 (FGE.23): Aliphatic, alicyclic and aromatic ethers including anisole derivatives From chemical groups 15, 16 and 26 (Commission Regulation (EC) No 1565/2000 of 18 July 2000 View page or View pdf
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Flavouring Group Evaluation 59 (FGE.59): Consideration of aliphatic and aromatic ethers evaluated by JECFA (61st meeting) structurally related to aliphatic, alicyclic and aromatic ethers including anisole derivatives evaluated by EFSA in FGE.23 (2006) (Commission Regulation (EC) No 1565/2000 of 18 July 2000) - Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in contact with Food (AFC) View page or View pdf
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Flavouring Group Evaluation 23, Revision 1 (FGE.23Rev1): Aliphatic, alicyclic and aromatic ethers including anisole derivatives from chemical groups 15, 16, 26 and 30[1] - Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in Contact with Food View page or View pdf
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Flavouring Group Evaluation 33 (FGE.33)[1] - Six Tetrahydrofuran Derivatives from Chemical Groups 13, 14, 16 and 26 - Scientific Opinion of the Panel on Food Additives, Flavourings, Processing Aids and Materials in Contact with Food View page or View pdf
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Scientific Opinion on Flavouring Group Evaluation 59, Revision 1 (FGE.59Rev1): Consideration of aliphatic and aromatic ethers evaluated by JECFA (61st meeting and 63rd meeting) structurally related to aliphatic, alicyclic and aromatic ethers including anisole derivatives evaluated by EFSA in FGE.23 Rev2 (2010) View page or View pdf
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EPI System: View |
AIDS Citations:Search |
Cancer Citations:Search |
Toxicology Citations:Search |
EPA Substance Registry Services (TSCA):7392-19-0 |
EPA ACToR:Toxicology Data |
EPA Substance Registry Services (SRS):Registry |
Laboratory Chemical Safety Summary :522514 |
National Institute of Allergy and Infectious Diseases:Data |
WISER:UN 1993 |
WGK Germany:2 |
2-ethenyl-2,6,6-trimethyloxane |
Chemidplus:0007392190 |
References:
Other Information:
Potential Blenders and core components note
For Odor |
No odor group found for these |
fenchone FL/FR |
|
laurel leaf absolute FL/FR |
2- methyl-3-butanone FL/FR |
balsamic |
balsamic |
laevo- borneol FL/FR |
dextro,laevo-iso borneol FL/FR |
dextro,laevo- borneol FL/FR |
bornyl acetate FL/FR |
iso bornyl acetate FL/FR |
iso bornyl formate FL/FR |
iso bornyl methyl ether FL/FR |
iso bornyl propionate FL/FR |
dextro- fenchone FL/FR |
camphoreous |
3- benzylidene-2-butanone FL/FR |
bornyl isobutyrate FL/FR |
butyrophenone FL/FR |
dextro- camphor FL/FR |
(±)- camphor FL/FR |
camphor tree bark oil FL/FR |
beta-homo cyclocitral FL/FR |
2,6- dimethyl-3-oxatricyclo(4.2.1.0*2,4*)nonane FR |
fenchol FL/FR |
laevo- fenchone FL/FR |
herbal ethanone FR |
hinoki leaf oil FR |
thujyl alcohol FL/FR |
verbenone FL/FR |
citrus |
bergamot oil italy FL/FR |
bergamot oil ivory coast FL/FR |
bergamot oil terpeneless FL/FR |
(S)-(-)- citronellal FL/FR |
citrus ocimenol FR |
citrus woody floral fragrance FR |
ocimene quintoxide FL/FR |
tetrahydromyrcenyl acetate FR |
earthy |
(-)-alpha- fenchol FL/FR |
2- octanone FL/FR |
floral |
iso amyl salicylate FL/FR |
anise indene FR |
bigarade oxide FR |
bois de rose oil peru FL/FR |
cilantro herb oil egypt FL/FR |
citronellyl acetate FL/FR |
coriander oil fractions FL/FR |
cyclohexyl ethyl acetate FL/FR |
2- decalinol FR |
dihydrolinalool FL/FR |
dihydromyrcene FR |
gardenia amide FR |
geranium oil china FL/FR |
geranyl tiglate FL/FR |
ho leaf oil FR |
(Z)- jasmone FL/FR |
karo karounde absolute FR |
lavandula angustifolia flower oil FL/FR |
lavender oil france FL/FR |
menthadienyl formate FR |
(E)- nerolidol FL/FR |
nerolidol FL/FR |
nonisyl propionate FR |
petitgrain bigarade oil FL/FR |
prenyl salicylate FL/FR |
fruity |
3- allyl oxy-1,4-dimethyl bicyclo(3.2.1)octane FR |
3- benzyl-4-heptanone FL/FR |
linalyl isobutyrate FL/FR |
ocimen-1-yl acetate FR |
green |
agrumen aldehyde FR |
cilantro leaf oil FL/FR |
iso cyclocitral (IFF) FL/FR |
geranium absolute FL/FR |
3,6- ivy carbaldehyde FL/FR |
2,4- ivy carbaldehyde FL/FR |
3,5- ivy carbaldehyde FL/FR |
ivy carbaldehyde FL/FR |
para- methyl hydratropaldehyde FL/FR |
herbal |
6- acetoxydihydrotheaspirane FL/FR |
acorus calamus rhizome oil FR |
1- allyl-2,2,7,7-tetramethyl cycloheptanol FR |
bornyl butyrate FL/FR |
beta- bourbonene FL/FR |
alpha- cadinol FL/FR |
1,4- cineole FL/FR |
(R)-(+)- citronellal FL/FR |
citrus ocimenol acetate FR |
coriander oleoresin FL/FR |
iso dihydrolavandulol FR |
(Z)-iso dihydrolavandulyl acetate FR |
dihydroterpinyl acetate FL/FR |
dimethyl cyclormol (IFF) FR |
eucalyptus citriodora oil FR |
eucalyptus radiata leaf/stem oil FR |
freesia heptanol FL/FR |
guava leaf oil cuba FR |
cis- herbal cyclohexane FR |
herbal dioxane FR |
herbal undecanol FR |
herbal undecanone FR |
6- hydroxydihydrotheaspirane (mixture of isomers) FL/FR |
hyssop oil FL/FR |
immortelle flower oil FL/FR |
jambu oleoresin FL/FR |
laurus nobilis leaf oil FL/FR |
spike lavender oil FL/FR |
methyl cyclogeranate (Firmenich) FR |
origanum oil FL/FR |
origanum oil greece FL/FR |
curled parsley leaf oil FL/FR |
petitgrain heptane FR |
pine hexanol FR |
alpha- pinene FL/FR |
pinocarveol FL/FR |
piperitone FL/FR |
rosemary absolute FL/FR |
rosemary oil FL/FR |
rosemary oil africa FL/FR |
rosemary oil egypt FL/FR |
rosemary oil morocco FL/FR |
rosemary oil spain FL/FR |
rosemary oil tunisia FL/FR |
sabinene hydrate FL/FR |
saffron pyranone FR |
tea leaf absolute FL/FR |
oswego tea specialty FR |
terpinolene FL/FR |
thyme oil wild or creeping FL/FR |
tricyclodecenyl propionate FR |
yarrow oil FL/FR |
mentholic |
laevo- menthyl acetate FL/FR |
peppermint cyclohexanone FL/FR |
minty |
dextro- dihydrocarvone FL/FR |
pennyroyal oil FL/FR |
naphthyl |
para- methyl anisole FL/FR |
pine |
dipentene terpene hydrocarbon byproducts FR |
pine oil 85 FR |
spicy |
4- carvomenthenol FL/FR |
beta- caryophyllene FL/FR |
caryophyllene FL/FR |
cinnamon acrolein FL/FR |
cubeb oil CO2 extract (piper cubeba) FL/FR |
black currant bud absolute FL/FR |
galangal root oil FL/FR |
ginger oleoresin africa FL/FR |
ginger root oil cochin FL/FR |
4-iso propyl-2-cyclohexenone FL/FR |
white sassafras oil FL/FR |
sugandha kokila berry oil FR |
laevo- verbenone FL/FR |
terpenic |
para- cymene FL/FR |
gamma- terpinene FL/FR |
alpha- terpineol FL/FR |
thujonic |
armoise oil FR |
cedarleaf oil terpeneless FR |
common tansy leaf oil dutch FR |
woody ketone FL/FR |
waxy |
decanal dimethyl acetal FL/FR |
woody |
iso bornyl isovalerate FL/FR |
2-tert- butyl cyclohexanone FR |
(+)- camphene FL/FR |
camphene FL/FR |
cistus twig/leaf oil FL/FR |
6,7- dihydrolinalool FL/FR |
dragons blood fragrance FR |
alpha- farnesene FL/FR |
(E)-beta- farnesene FL/FR |
hinoki root oil FR |
juniper berry oil terpenes FR |
iso longifolene epoxide FR |
marine formate FR |
patchouli ethanol FR |
patchouli hexanol FR |
polylimonene FL/FR |
spruce needle oil canada FL/FR |
For Flavor |
No flavor group found for these |
6- acetoxydihydrotheaspirane FL/FR |
3- benzylidene-2-butanone FL/FR |
dextro,laevo- borneol FL/FR |
bornyl butyrate FL/FR |
bornyl isobutyrate FL/FR |
iso bornyl methyl ether FL/FR |
beta- bourbonene FL/FR |
butyrophenone FL/FR |
delta- cadinene FL |
alpha- cadinol FL/FR |
(+)- camphene FL/FR |
(S)-(-)- citronellal FL/FR |
(R)-(+)- citronellal FL/FR |
decanal dimethyl acetal FL/FR |
6,7- dihydrolinalool FL/FR |
dihydroterpinyl acetate FL/FR |
epoxyoxophorone FL |
(E)-beta- farnesene FL/FR |
fenchone FL/FR |
2- heptyl cyclopropane carboxylic acid FL |
ivy carbaldehyde FL/FR |
3,5- ivy carbaldehyde FL/FR |
3- methyl cyclohexanone FL |
1- methyl pyrrole FL |
2- methyl-3-butanone FL/FR |
3- octyl butyrate FL |
(Z,Z)- photocitral A FL |
piperitenone oxide FL |
polylimonene FL/FR |
4-iso propyl-2-cyclohexenone FL/FR |
white sassafras oil FL/FR |
(E)-4- undecenal FL |
laevo- verbenone FL/FR |
verbenone FL/FR |
woody ketone FL/FR |
|
laurel leaf absolute FL/FR |
thujyl alcohol FL/FR |
balsamic |
balsamic |
iso bornyl propionate FL/FR |
camphoreous |
dextro,laevo-iso borneol FL/FR |
laevo- borneol FL/FR |
bornyl acetate FL/FR |
camphene FL/FR |
(±)- camphor FL/FR |
camphor tree bark oil FL/FR |
fenchol FL/FR |
(-)-alpha- fenchol FL/FR |
laevo- fenchone FL/FR |
6- hydroxydihydrotheaspirane (mixture of isomers) FL/FR |
pinocarveol FL/FR |
rosemary oil tunisia FL/FR |
citrus |
bergamot oil italy FL/FR |
bergamot oil ivory coast FL/FR |
bergamot oil terpeneless FL/FR |
cilantro leaf oil FL/FR |
freesia heptanol FL/FR |
petitgrain bigarade oil FL/FR |
alpha- terpineol FL/FR |
cooling |
4- carvomenthenol FL/FR |
1,4- cineole FL/FR |
beta-homo cyclocitral FL/FR |
dextro- fenchone FL/FR |
jambu oleoresin FL/FR |
spike lavender oil FL/FR |
iso menthol FL |
sabinene hydrate FL/FR |
dairy |
2- octanone FL/FR |
floral |
bois de rose oil peru FL/FR |
citronellyl acetate FL/FR |
dihydrolinalool FL/FR |
geranium oil china FL/FR |
geranyl tiglate FL/FR |
linalyl isobutyrate FL/FR |
fruity |
3- benzyl-4-heptanone FL/FR |
green |
iso amyl salicylate FL/FR |
iso cyclocitral (IFF) FL/FR |
cyclohexyl ethyl acetate FL/FR |
dextro- dihydrocarvone FL/FR |
alpha- farnesene FL/FR |
geranium absolute FL/FR |
2,4- ivy carbaldehyde FL/FR |
3,6- ivy carbaldehyde FL/FR |
para- methyl hydratropaldehyde FL/FR |
(E)- nerolidol FL/FR |
nerolidol FL/FR |
ocimene quintoxide FL/FR |
iso phorone FL |
herbal |
cilantro herb oil egypt FL/FR |
coriander oil fractions FL/FR |
coriander oleoresin FL/FR |
hyssop oil FL/FR |
immortelle flower oil FL/FR |
laurus nobilis leaf oil FL/FR |
lavandula angustifolia flower oil FL/FR |
lavender oil france FL/FR |
origanum oil FL/FR |
origanum oil greece FL/FR |
curled parsley leaf oil FL/FR |
prenyl salicylate FL/FR |
rosemary absolute FL/FR |
rosemary oil FL/FR |
rosemary oil africa FL/FR |
rosemary oil egypt FL/FR |
rosemary oil morocco FL/FR |
rosemary oil spain FL/FR |
thyme oil wild or creeping FL/FR |
yarrow oil FL/FR |
medicinal |
dextro- camphor FL/FR |
mentholic |
peppermint cyclohexanone FL/FR |
minty |
laevo- menthyl acetate FL/FR |
pennyroyal oil FL/FR |
piperitone FL/FR |
naphthyl |
para- methyl anisole FL/FR |
spicy |
caryophyllene FL/FR |
beta- caryophyllene FL/FR |
cinnamon acrolein FL/FR |
cubeb oil CO2 extract (piper cubeba) FL/FR |
black currant bud absolute FL/FR |
galangal root oil FL/FR |
ginger oleoresin africa FL/FR |
ginger root oil cochin FL/FR |
tea |
tea leaf absolute FL/FR |
terpenic |
para- cymene FL/FR |
gamma- terpinene FL/FR |
woody |
iso bornyl acetate FL/FR |
iso bornyl formate FL/FR |
iso bornyl isovalerate FL/FR |
cistus twig/leaf oil FL/FR |
(Z)- jasmone FL/FR |
alpha- pinene FL/FR |
spruce needle oil canada FL/FR |
terpinolene FL/FR |
Potential Uses:
Occurrence (nature, food, other): note
Synonyms:
| bois de rose oxide | 2- | ethenyl tetrahydro-2,6,6-trimethyl-2H-pyran | 2- | ethenyl-2,6,6-trimethyloxane | 2- | ethenyl-2,6,6-trimethyltetrahydro-2H-pyran | 2- | ethenyltetrahydro-2,6,6-trimethyl-2H-pyran | | geranic oxide | | limetol (Givaudan) | | linaloyl oxide | 4H- | pyran, 2,6,6-trimethyl-2-vinyl- | 2H- | pyran, 2-ethenyltetrahydro-2,6,6-trimethyl- | 2H- | pyran, tetrahydro-2,2,6-trimethyl-6-vinyl- | | tetrahydro-2,2,6-trimethyl-6-vinyl-2H-pyran | (±)- | tetrahydro-2,6,6-trimethyl-2-vinyl-2H-pyran | | trimethoxy-2-vinyl tetrahydropyran | 2,6,6- | trimethoxy-2-vinyltetrahydropyran | 2,6,6- | trimethyl-2-vinyl tetrahydropyran | 2,6,6- | trimethyl-2-vinyltetrahydropyran | 2,2,6- | trimethyl-6-ethenyl tetrahydropyran | 2,2,6- | trimethyl-6-vinyl tetrahydro-2H-pyran | 2,2,6- | trimethyl-6-vinyl tetrahydropyran | 2,2,6- | trimethyl-6-vinyl-tetrahydropyran | 2,2,6- | trimethyl-6-vinyltetrahydropyran | 2,6,6- | trimethyl-6-vinyltetrahydropyran |
Articles:
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Blends well with wild notes.
Flavouring and fragrence ingredient. Present in roselle tea, muscat grapes, lime oil, alfalfa, Riesling wine, grapefruit, yellow passion fruit, apricot, blackberry, blueberry, nectarine, cherimoya, papaya and curuba fruits
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