isopiperitenol
2-cyclohexen-1-ol, 3-methyl-6-(1-methylethenyl)-
 
Notes:
None found
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CAS Number: 491-05-4Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 207-726-9
Nikkaji Web: J76.400K
Beilstein Number: 2207765
XlogP3-AA: 2.10 (est)
Molecular Weight: 152.23672000
Formula: C10 H16 O
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Category: natural substances and extractives
 
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Physical Properties:
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Boiling Point: 206.00 to  207.00 °C. @ 760.00 mm Hg (est)
Vapor Pressure: 0.054000 mmHg @ 25.00 °C. (est)
Flash Point: 183.00 °F. TCC ( 84.10 °C. ) (est)
logP (o/w): 2.590 (est)
Soluble in:
 water, 372.6 mg/L @ 25 °C (est)
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Organoleptic Properties:
 
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: natural substances and extractives
Recommendation for isopiperitenol usage levels up to:
 not for fragrance use.
 
Recommendation for isopiperitenol flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
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EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 527822
National Institute of Allergy and Infectious Diseases: Data
 3-methyl-6-prop-1-en-2-ylcyclohex-2-en-1-ol
Chemidplus: 0000491054
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References:
 3-methyl-6-prop-1-en-2-ylcyclohex-2-en-1-ol
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 491-05-4
Pubchem (cid): 527822
Pubchem (sid): 135227193
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
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Typical G.C.
VCF-Online: VCF Volatile Compounds in Food
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Potential Blenders and core components note
 
None Found
 
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Potential Uses:
None Found
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Occurrence (nature, food, other): note
 gingergrass
Search Trop  Picture
 pimenta racemosa leaf oil lemon @ 0.15%
Data  GC  Search Trop  Picture
 shiranuhi mandarin
Search Trop  Picture
 ziziphora hispanica
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Synonyms:
2-cyclohexen-1-ol, 3-methyl-6-(1-methylethenyl)-
p-mentha-1,8-dien-3-ol
3-methyl-6-(1-methyl vinyl) cyclohex-2-en-1-ol
3-methyl-6-(1-methylethenyl)-2-cyclohexen-1-ol
3-methyl-6-(1-methylvinyl)cyclohex-2-en-1-ol
3-methyl-6-(prop-1-en-2-yl)cyclohex-2-en-1-ol
3-methyl-6-prop-1-en-2-ylcyclohex-2-en-1-ol
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Articles:
PubMed: Isolation and characterization of isopiperitenol dehydrogenase from piperitenone-type perilla.
PubMed: Monoterpene metabolism. Cloning, expression, and characterization of (-)-isopiperitenol/(-)-carveol dehydrogenase of peppermint and spearmint.
PubMed: Organization of monoterpene biosynthesis in Mentha. Immunocytochemical localizations of geranyl diphosphate synthase, limonene-6-hydroxylase, isopiperitenol dehydrogenase, and pulegone reductase.
PubMed: Metabolic engineering of monoterpene biosynthesis: two-step production of (+)-trans-isopiperitenol by tobacco.
PubMed: Biotransformation of limonene by bacteria, fungi, yeasts, and plants.
PubMed: Volatile chemicals identified in extracts from newly hybrid citrus, dekopon (Shiranuhi mandarin Suppl. J.).
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.
PubMed: Functional expression of regiospecific cytochrome P450 limonene hydroxylases from mint (Mentha spp.) in Escherichia coli and saccharomyces cerevisiae.
PubMed: Regiospecific cytochrome P450 limonene hydroxylases from mint (Mentha) species: cDNA isolation, characterization, and functional expression of (-)-4S-limonene-3-hydroxylase and (-)-4S-limonene-6-hydroxylase.
PubMed: Cytochrome P450 limonene hydroxylases of Mentha species.
PubMed: Biochemical characterization of a spearmint mutant that resembles peppermint in monoterpene content.
PubMed: Monoterpene biosynthesis: specificity of the hydroxylations of (-)-limonene by enzyme preparations from peppermint (Mentha piperita), spearmint (Mentha spicata), and perilla (Perilla frutescens) leaves.
PubMed: Metabolism of monoterpenes: oxidation of isopiperitenol to isopiperitenone, and subsequent isomerization to piperitenone by soluble enzyme preparations from peppermint (Mentha piperita) leaves.
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