longicyclene
1,2,4-methenoazulene, decahydro-1,5,5,8a-tetramethyl-
 
Notes:
None found
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CAS Number: 1137-12-8Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 214-504-5
Beilstein Number: 2039581
MDL: MFCD00042690
XlogP3-AA: 5.00 (est)
Molecular Weight: 204.35628000
Formula: C15 H24
NMR Predictor: Predict (works with chrome or firefox)
Category: natural substances and extractives
 
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
Google Patents: Search
US Patents: Search
EU Patents: Search
Pubchem Patents: Search
PubMed: Search
NCBI: Search
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Physical Properties:
Assay: 95.00 to 100.00 % sum of isomers
Food Chemicals Codex Listed: No
Boiling Point: 239.00 to  240.00 °C. @ 760.00 mm Hg
Vapor Pressure: 0.061000 mmHg @ 25.00 °C. (est)
Flash Point: 193.00 °F. TCC ( 89.44 °C. )
logP (o/w): 5.908 (est)
Soluble in:
 alcohol
 water, 0.1974 mg/L @ 25 °C (est)
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:
Santa Cruz Biotechnology
For experimental / research use only.
(+)-Longicyclene
Sigma-Aldrich: Aldrich
For experimental / research use only.
(+)-Longicyclene purum, ≥95.0% (sum of enantiomers, GC)
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Safety Information:
Preferred SDS: View
 
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 longicyclene usage levels up to:
 not for fragrance use.
 
Recommendation for longicyclene flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 564934
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 3
Chemidplus: 0001137128
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References:
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 564934
Pubchem (sid): 135051395
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
HMDB (The Human Metabolome Database): Search
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
 angelica root oil @ 0.07%
Data  GC  Search Trop  Picture
 croton cajucara benth. leaf oil brazil @ 0.90%
Data  GC  Search Trop  Picture
 croton flavens l. (welensali) leaf oil curacao @ 0.20%
Data  GC  Search Trop  Picture
 hinoki leaf oil @ 0.41%
Data  GC  Search Trop  Picture
 hinoki root oil @ 0.65%
Data  GC  Search Trop  Picture
 hinoki wood oil @ 0.05%
Data  GC  Search Trop  Picture
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Synonyms:
(1S- (1alpha,2alpha,3abeta, 4alpha,8abeta,9R*))-decahydro-1,5,5,8a-tetramethyl-1,2,4-methenoazulene
1,2,4-methenoazulene, decahydro-1,5,5,8a-tetramethyl-
1,5,5,8a-tetramethyldecahydro-1,2,4-(methanetriyl)azulene
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Articles:
PubMed: Suppression of SOS-inducing activity of chemical mutagens by metabolites from microbial transformation of (+)-longicyclene.
PubMed: Characterization of Szovitsia callicarpa volatile constituents obtained by micro- and hydrodistillation.
PubMed: Determination of the volatile composition in essential oil of Descurainia sophia (L.) Webb ex Prantl (Flixweed) by gas chromatography/mass spectrometry (GC/MS).
PubMed: Flavor characteristics of lapsang souchong and smoked lapsang souchong, a special Chinese black tea with pine smoking process.
PubMed: Male lures for mediterranean fruitfly (Ceratitis capitata wied.): Structural analogs of α-copaene.
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