(E)-linalool oxide
3,7-dimethyl-1,6-octadien-3-ol epoxy deriv., trans-
 
Notes:
None found
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CAS Number: 11063-78-8Picture of molecule3D/inchi
Nikkaji Web: J239.309C
XlogP3-AA: 1.40 (est)
Molecular Weight: 170.25186000
Formula: C10 H18 O2
NMR Predictor: Predict (works with chrome or firefox)
Category: flavor and fragrance agents
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
Google Books: Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Perfumer and Flavorist: Search
Google Patents: Search
US Patents: Search
EU Patents: Search
Pubchem Patents: Search
PubMed: Search
NCBI: Search
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Physical Properties:
Appearance: colorless to pale yellow clear liquid (est)
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Soluble in:
 water, 1669 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: flavor and fragrance agents
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
 
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Safety References:
EPI System: View
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 6432254
National Institute of Allergy and Infectious Diseases: Data
 2-[(2S,5S)-5-ethenyl-5-methyloxolan-2-yl]propan-2-ol
Chemidplus: 0011063788
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References:
 2-[(2S,5S)-5-ethenyl-5-methyloxolan-2-yl]propan-2-ol
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 6432254
Pubchem (sid): 135288125
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
CHEMBL: View
HMDB (The Human Metabolome Database): HMDB004072
FooDB: FDB006705
Export Tariff Code: 2932.19.0000
Typical G.C.
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Wikipedia: View
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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
 apricot fruit
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 basil oil var. glabratum turkey @ 0.60%
Data  GC  Search Trop  Picture
 bay leaf oil clove @ 0.1%
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 bergamot oil @ 0.000-trace%
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 champaca absolute (michelia alba) @ 0.23%
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 citrus unshiu peel oil @ trace%
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 coriander seed oil @ 0.30%
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 cymbopogon citratus dc. stapf. oil cuba @ <0.10%
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 geranium oil bourbon @ 0.13%
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 lavandin flower water @ 0.64%
Data  GC  Search Trop  Picture
 lavandula angustifolia flower water @ 0.61%
Data  GC  Search Trop  Picture
 lavender oil CO2 extract @ 0.91%
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 lavender oil spain @ 0.05%
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 lavender water @ 0.08%
Data  GC  Search Trop  Picture
 marjoram oil (thymus mastichina) spain @ 0.80%
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 neroli oil CO2 extract @ 0.16%
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 orangeflower water absolute @ 1.0-3.7%
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 salvia verbenaca seed oil tunisia @ 1.05%
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 witch hazel leaf oil @ 0.12%
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Synonyms:
(E)-3,7-dimethyl-1,6-octadien-3-ol epoxy deriv.
3,7-dimethyl-1,6-octadien-3-ol epoxy deriv., trans-
2-[(2S,5S)-5-ethenyl-5-methyloxolan-2-yl]propan-2-ol
trans-linalool oxide
 linalool oxide, trans-
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Articles:
Info: Volatile Flavor Components in Bogyojosaeng and Suhong Cultivars of Strawberry (Fragaria ananassa Duch.)
PubMed: trans-2-Tritylcyclohexanol as a chiral auxiliary in permanganate-mediated oxidative cyclization of 2-methylenehept-5-enoates: application to the synthesis of trans-(+)-linalool oxide.
PubMed: Enantiomer distribution of major chiral volatile organic compounds in selected types of herbal honeys.
PubMed: Analysis of aroma-active compounds in three sweet osmanthus (Osmanthus fragrans) cultivars by GC-olfactometry and GC-MS.
PubMed: Chemical composition of volatiles from Opuntia littoralis, Opuntia ficus-indica, and Opuntia prolifera growing on Catalina Island, California.
PubMed: Enantiomeric distribution of major chiral volatile organic compounds in juniper-flavored distillates.
PubMed: Bioorganic diversity of rare Coriandrum sativum L. honey: unusual chromatographic profiles containing derivatives of linalool/oxygenated methoxybenzene.
PubMed: Compositions of the volatile oils of Citrus macroptera and C. maxima.
PubMed: Composition of a monoterpenoid-rich essential oil from the rhizome of Zingiber officinale from north western Himalayas.
PubMed: Volatile fraction of lavender and bitter fennel infusion extracts.
PubMed: Essential oil composition and variability of Hypericum perforatum from wild populations of northern Turkey.
PubMed: Volatiles from a rare Acer spp. honey sample from Croatia.
PubMed: [Study on chemical constituents and antimicrobial activity of the essential oil from Acanthopanax brachypus].
PubMed: Screening of volatile composition from Portuguese multifloral honeys using headspace solid-phase microextraction-gas chromatography-quadrupole mass spectrometry.
PubMed: Quantitation of free and glycosidically bound volatiles in and effect of glycosidase addition on three tomato varieties (Solanum lycopersicum L.).
PubMed: [Studies on the chemical constituents of the volatiles of Clerodendron bungei].
PubMed: Application of HS-SPME and GC-MS to characterization of volatile compounds emitted from Osmanthus flowers.
PubMed: Rapid determination of volatile compounds emitted from Chimonanthus praecox flowers by HS-SPME-GC-MS.
PubMed: Volatile compounds emitted by sclerotia of Sclerotinia minor, Sclerotinia sclerotiorum, and Sclerotium rolfsii.
PubMed: Grapefruit gland oil composition is affected by wax application, storage temperature, and storage time.
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