cis-carveol
cis-2-methyl-5-(1-methylethenyl)-2-cyclohexen-1-ol
 
Notes:
None found
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CAS Number: 1197-06-4Picture of molecule3D/inchi
FDA UNII: OOZ105PLI9
Nikkaji Web: J9.138C
XlogP3-AA: 2.10 (est)
Molecular Weight: 152.23672000
Formula: C10 H16 O
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome or firefox)
Category: flavor and fragrance agents
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
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Physical Properties:
Appearance: colorless clear liquid (est)
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Boiling Point: 231.46 °C. @ 760.00 mm Hg (est)
Vapor Pressure: 0.012000 mmHg @ 25.00 °C. (est)
Flash Point: 196.00 °F. TCC ( 91.20 °C. ) (est)
logP (o/w): 2.819 (est)
Soluble in:
 alcohol
 water, 519.7 mg/L @ 25 °C (est)
Insoluble in:
 water
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Organoleptic Properties:
 
Odor Type: spicy
 
Odor Strength: medium
 
 caraway  spicy  
Odor Description:
at 100.00 %. 
caraway
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
None found
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Suppliers:
 None found
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Safety Information:
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: flavor and fragrance agents
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
Recommendation for cis-carveol usage levels up to:
  4.0000 % in the fragrance concentrate.
 
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Safety References:
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 330573
National Institute of Allergy and Infectious Diseases: Data
 (1R,5R)-2-methyl-5-prop-1-en-2-ylcyclohex-2-en-1-ol
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References:
Leffingwell: Chirality or Article
 (1R,5R)-2-methyl-5-prop-1-en-2-ylcyclohex-2-en-1-ol
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 330573
Pubchem (sid): 10505349
Flavornet: 1197-06-4
Pherobase: View
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Other Information:
(IUPAC): Atomic Weights of the Elements 2011 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
CHEBI: View
UM BBD: Search
KEGG (GenomeNet): C11395
HMDB (The Human Metabolome Database): Search
FooDB: FDB003843
Typical G.C.
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
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Potential Blenders and core components note
 
For Odor
citrus
 crithmum maritimum oilFR
green
3-hepten-2-oneFL/FR
herbal
 anethum graveolens herb oilFL/FR
 caraway oil terpenesFR
 caraway seed absoluteFL/FR
terpeneless caraway seed oilFL/FR
 caraway seed oil CO2 extractFL/FR
 carum carvi fruit extractFL/FR
 carum carvi fruit oilFL/FR
 carum carvi fruit tinctureFL/FR
 carum carvi seed extractFL/FR
 dill seed oil CO2 extract indianFL/FR
 dill seed oil indianFL/FR
 perilla leaf oilFL/FR
minty
laevo-carveolFL/FR
dextro-carvoneFL/FR
cis-carvone-5,6-oxideFL/FR
trans-para-menthan-2-oneFL/FR
spicy
isobutyl angelateFL/FR
 caraway seed oleoresinFL/FR
trans-carveolFL/FR
 cuminyl alcoholFL/FR
4-isopropyl-2-cyclohexenoneFL/FR
 
For Flavor
 
No flavor group found for these
trans-carveolFL/FR
laevo-carveolFL/FR
 perilla leaf oilFL/FR
4-isopropyl-2-cyclohexenoneFL/FR
creamy
3-hepten-2-oneFL/FR
green
isobutyl angelateFL/FR
(E)-2-hexenal diethyl acetalFL
herbal
 anethum graveolens herb oilFL/FR
 caraway oleoresinFL
 caraway seed absoluteFL/FR
terpeneless caraway seed oilFL/FR
 caraway seed oil CO2 extractFL/FR
 carum carvi fruitFL
 carum carvi fruit extractFL/FR
 carum carvi fruit oilFL/FR
 carum carvi fruit tinctureFL/FR
 carum carvi seed extractFL/FR
minty
dextro-carvoneFL/FR
cis-carvone-5,6-oxideFL/FR
trans-para-menthan-2-oneFL/FR
spicy
 caraway seed oleoresinFL/FR
 cuminyl alcoholFL/FR
 dill seed oil CO2 extract indianFL/FR
 dill seed oil indianFL/FR
 
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Potential Uses:
 acaciaFR
 allspiceFR
 allspiceFR
 angelicaFL/FR
 arnica flowerFR
 bay rumFR
 bayberryFR
 bayberryFR
 beeswax absolute replacerFR
 boldus oil replacer 
 calamus oil replacerFR
 caraway seedFL/FR
 cardamom oil replacerFR
 carnationFR
 carrot seedFL/FR
 cassiaFR
 cassia blossomFR
 chamomileFR
 cinnamonFR
 clary sage oil replacerFR
 cloveFR
 copaiba balsamFL/FR
 corianderFL/FR
 croton eluteria barkFL/FR
 cumin oil replacerFR
 currant bud absolute replacerFL/FR
 curry leafFL/FR
 cypress oil replacerFR
 dill weedFL/FR
 dogwoodFR
 elder flowerFR
 galangal rootFL/FR
 geraniumFR
 gingerFR
 ginger white gingerFR
 gingerbreadFR
 graham crackerFR
 guaiacwoodFL/FR
 habubaFR
 hinoki oil replacerFR
 hollyberryFR
 hopFR
 jonquilFR
 maceFR
 majaFR
 marjoramFL/FR
 mimosaFR
 mustardFL
 myrrhFR
 nutmegFR
 osmanthusFR
 parsley leafFL/FR
 pepperFR
 pepper black pepperFL/FR
 pepper chili pepper 
 pepper tabasco pepperFL
 pepper tree berryFL/FR
 pine needleFL/FR
 pizzaFR
 pumpkin pieFR
 resedaFR
 root beerFR
 rose dog roseFR
 rose moss roseFR
 saffronFR
 sarsaparillaFL
 sassafrasFR
 snake rootFL/FR
 spiceFR
 spicewoodFR
 spikenard oil replacerFR
 tansy oil replacerFL/FR
 tarragon oil replacerFL/FR
 tea black teaFL
 tolu balsamFR
 wasabiFL
 watercress nasturtium 
 worcestershire sauceFL
 wormwood oil replacerFR
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Occurrence (nature, food, other): note
 blood orange oil (citrus sinensis l. var. sanguinello) italy @ 0.010%
Data  GC  Search Trop  Picture
 blood orange oil (citrus sinensis l. var. tarocco) italy @ 0.005%
Data  GC  Search Trop  Picture
 blood orange oil italy @ 0.010%
Data  GC  Search Trop  Picture
 bombycilaena erecta oil greece @ 0.30%
Data  GC  Search Trop  Picture
 caraway flower oil
Search Trop  Picture
 caraway seed
Search Trop  Picture
 caraway seed oil @ 0.00-0.40%
Data  GC  Search Trop  Picture
 celery oil
Search Trop  Picture
 celery seed oil
Search Trop  Picture
 celery seed oil CO2 extract india @ 0.02%
Data  GC  Search Trop  Picture
 celery seed oil india @ 0.06%
Data  GC  Search Trop  Picture
 cistus oil @ 0.1%
Data  GC  Search Trop  Picture
 costmary oil @ 0.36%
Data  GC  Search Trop  Picture
 dill seed
Search Trop  Picture
 eucalyptus globulus bicostata oil @ 0.08%
Data  GC  Search Trop  Picture
 eucalyptus globulus maidenii f. muell oil @ 0.07%
Data  GC  Search Trop  Picture
 eucalyptus globulus pseudoglobulus oil @ 0.07%
Data  GC  Search Trop  Picture
 fleabane oil @ 0.30%
Data  GC  Search Trop  Picture
 gingergrass oil @ 0.68%
Data  GC  Search Trop  Picture
 grapefruit oil california @ trace%
Data  GC  Search Trop  Picture
 horsemint shoot
Search Trop  Picture
 labdanum oil @ 1.22%
Data  GC  Search Trop  Picture
 laurel leaf oil turkey @ 0.10%
Data  GC  Search Trop  Picture
 layana oil zimbabwe @ 0.1%
Data  GC  Search Trop  Picture
 lemon verbena oil turkey @ 0.12%
Data  GC  Search Trop  Picture
 lemongrass oil yunnan @ 0.27%
Data  GC  Search Trop  Picture
 mandarin fruit
Search Trop  Picture
 mandarin oil uruguay @ trace%
Data  GC  Search Trop  Picture
 mastic fruit oil @ 0.33%
Data  GC  Search Trop  Picture
 mikan peel oil @ trace%
Data  GC  Search Trop  Picture
 myrtle oil @ 0.06%
Data  GC  Search Trop  Picture
 orange peel oil sweet c.p. blond italy @ 0.005%
Data  GC  Search Trop  Picture
 orange peel oil sweet c.p. blond italy @ 0.006%
Data  GC  Search Trop  Picture
 orange peel oil sweet c.p. blond italy @ 0.006%
Data  GC  Search Trop  Picture
 orange peel oil sweet c.p. blond italy @ 0.006%
Data  GC  Search Trop  Picture
 orange peel oil sweet c.p. blond italy @ 0.007%
Data  GC  Search Trop  Picture
 pepper black pepper fruit
Search Trop  Picture
 pepper black pepper fruit oil
Search Trop  Picture
 petitgrain sweet oil @ 0.21%
Data  GC  Search  PMC Picture
 pteronia oil @ 0.20%
Data  GC  Search Trop  Picture
 sage oil reunion @ trace%
Data  GC  Search Trop  Picture
 spearmint leaf
Search Trop  Picture
 spearmint oil
Search Trop  Picture
 spearmint oil america @ 0.31-0.54%
Data  GC  Search Trop  Picture
 tagete oil CO2 extract @ 0.23%
Data  GC  Search Trop  Picture
 valerian root oil @ 0.1-0.2%
Data  GC  Search Trop  Picture
 wormseed oil america @ 0.25%
Data  GC  Search Trop  Picture
 wormseed oil spain @ 4.91%
Data  GC  Search Trop  Picture
 yarrow oil @ 0.10%
Data  GC  Search Trop  Picture
 yuzu peel oil c.p. @ trace%
Data  GC  Search Trop  Picture
 yuzu peel oil CO2 extract @ trace-0.01%
Data  GC  Search Trop  Picture
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Synonyms:
cis-p-mentha-1,8-dien-6-ol
cis-para-mentha-1,8-dien-6-ol
cis-2-methyl-5-(1-methyl ethenyl)-2-cyclohexen-1-ol
cis-2-methyl-5-(1-methylethenyl)-2-cyclohexen-1-ol
(1R,5R)-2-methyl-5-prop-1-en-2-ylcyclohex-2-en-1-ol
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Articles:
PubMed: GC-MS characterisation and antibacterial activity evaluation of Nigella sativa oil against diverse strains of Salmonella.
PubMed: Chemical composition, cytotoxicity and in vitro antitrypanosomal and antiplasmodial activity of the essential oils of four Cymbopogon species from Benin.
PubMed: Chemical composition and insecticidal activity of the essential oil of Illicium pachyphyllum fruits against two grain storage insects.
PubMed: Chemical composition and larvicidal activity of essential oil from Mentha spicata (Linn.) against three mosquito species.
PubMed: Insecticidal activity of essential oil of Carum Carvi fruits from China and its main components against two grain storage insects.
PubMed: Enhanced bioproduction of carvone in a two-liquid-phase partitioning bioreactor with a highly hydrophobic biocatalyst.
PubMed: Regio- and stereoselective fungal oxyfunctionalisation of limonenes.
PubMed: Analysis of volatile components from Ziziphora taurica subsp. taurica by steam distillation, superheated-water extraction, and direct thermal desorption with GCxGC-TOFMS.
PubMed: Repellency of essential oils of some Kenyan plants against Anopheles gambiae.
PubMed: Changes of the volatile profile and artifact formation in Daidai (Citrus aurantium) cold-pressed peel oil on storage.
PubMed: Hydroxylation of specifically deuterated limonene enantiomers by cytochrome p450 limonene-6-hydroxylase reveals the mechanism of multiple product formation.
PubMed: Hydroxylation of limonene enantiomers and analogs by recombinant (-)-limonene 3- and 6-hydroxylases from mint (Mentha) species: evidence for catalysis within sterically constrained active sites.
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