(-)-lavandulyl acetate
4-hexen-1-ol, 5-methyl-2-(1-methylethenyl)-, acetate, (R)-
 
Notes:
None found
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      Product(s):
      20777-39-3 1,5-Dimethyl-1-vinyl-4-hexenylcetate 95%
       
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CAS Number: 20777-39-3 
Other(deleted CASRN): 22658-96-4
ECHA EC Number: 244-026-2
Nikkaji Web: J36.845H
XlogP3-AA: 3.60 (est)
Molecular Weight: 196.28980000
Formula: C12 H20 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
Boiling Point: 228.00 to  229.00 °C. @ 760.00 mm Hg (est)
Vapor Pressure: 0.072000 mmHg @ 25.00 °C. (est)
Flash Point: 159.00 °F. TCC ( 70.50 °C. ) (est)
logP (o/w): 3.518 (est)
Soluble in:
 alcohol
Insoluble in:
 water
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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:
BOC Sciences
For experimental / research use only.
1,5-Dimethyl-1-vinyl-4-hexenylcetate 95%
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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
RIFM Fragrance Material Safety Assessment: Search
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
 
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Safety References:
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 20777-39-3
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 30247
National Institute of Allergy and Infectious Diseases: Data
 (5-methyl-2-prop-1-en-2-ylhex-4-enyl) acetate
Chemidplus: 0020777393
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References:
 (5-methyl-2-prop-1-en-2-ylhex-4-enyl) acetate
Canada Domestic Sub. List: 20777-39-3
Pubchem (cid): 30247
Pubchem (sid): 134994553
Pherobase: View
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Other Information:
HMDB (The Human Metabolome Database): Search
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
 chamomile sweet false chamomile
Search Trop  Picture
 jacquinia macrocarpa
Search Trop  Picture
 primula farinosa
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Synonyms:
4-hexen-1-ol, 5-methyl-2-(1-methylethenyl)-, acetate, (2R)-
4-hexen-1-ol, 5-methyl-2-(1-methylethenyl)-, acetate, (R)-
(-)-(R)-lavandulyl acetate
(2R)-lavandulyl acetate
(R)-lavandulyl acetate
(2R)-5-methyl-2-(1-methyl ethenyl)-4-hexen-1-ol acetate
(R)-5-methyl-2-(1-methyl ethenyl)-4-hexen-1-ol acetate
(2R)-5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl acetate
(R)-2-isopropenyl-5-methyl hex-4-enyl acetate
(R)-2-isopropenyl-5-methylhex-4-enyl acetate
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Articles:
PubMed: The biosynthetic origin of irregular monoterpenes in Lavandula: isolation and biochemical characterization of a novel cis-prenyl diphosphate synthase gene, lavandulyl diphosphate synthase.
PubMed: Identification of the sex pheromone of the mealybug Dysmicoccus grassii Leonardi.
PubMed: Differential induction, purification and characterization of cold active lipase from Yarrowia lipolytica NCIM 3639.
PubMed: [Studies regarding chemical composition of lavender volatile oils].
PubMed: Hydrodistillation-headspace solvent microextraction, a new method for analysis of the essential oil components of Lavandula angustifolia Mill.
PubMed: Identification of a male-produced aggregation pheromone in the western flower thrips Frankliniella occidentalis.
PubMed: Enzymatic esterification of lavandulol--a partial kinetic resolution of (S)-lavandulol and preparation of optically enriched (R)-lavandulyl acetate.
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