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chrysanthemol
chrysanthemyl alcohol

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Name:[2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropyl]methanol
CAS Number: 5617-92-5Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg:227-045-0
FDA UNII: R52DEG7BXK
Nikkaji Web:J13.716B
MDL:MFCD00001305
XlogP3-AA:2.50 (est)
Molecular Weight:154.25266000
Formula:C10 H18 O
BioActivity Summary:listing
NMR Predictor:Predict (works with chrome, Edge 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
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Google Scholar: with word "odor"Search
Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
PubMed:Search
NCBI:Search
 
Physical Properties:
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Boiling Point: 264.39 °C. @ 760.00 mm Hg (est)
Vapor Pressure:0.001000 mmHg @ 25.00 °C. (est)
Flash Point: 185.00 °F. TCC ( 85.00 °C. ) (est)
logP (o/w): 2.837 (est)
Soluble in:
 alcohol
 water, 387.9 mg/L @ 25 °C (est)
Insoluble in:
 water
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
None found
 
Suppliers:
BOC Sciences
For experimental / research use only.
trans-CHRYSANTHEMYL ALCOHOL
ExtraSynthese
For experimental / research use only.
Chrysanthemyl alcohol
Santa Cruz Biotechnology
For experimental / research use only.
Chrysanthemyl alcohol, mixture of cis and trans
Sigma-Aldrich: Aldrich
For experimental / research use only.
Chrysanthemyl alcohol, mixture of cis and trans 98%
sds
 
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
 
Safety in Use Information:
Category:
natural substances and extractives
Recommendation for chrysanthemol usage levels up to:
 not for fragrance use.
 
Recommendation for chrysanthemol flavor usage levels up to:
 not for flavor use.
 
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 :110685
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:3
[2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropyl]methanol
Chemidplus:0005617925
 
References:
 [2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropyl]methanol
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):110685
Pubchem (sid):135068662
 
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
CHEMBL:View
KEGG (GenomeNet):C17611
HMDB (The Human Metabolome Database):Search
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 chrysanthemum indian chrysanthemum
Search Trop Picture
 
Synonyms:
 chrysanthemyl alcohol
 chrysanthemyl alcohol, mixture of cis and trans
 cyclopropanemethanol, 2,2-dimethyl-3-(2-methyl-1-propen-1-yl)-
 cyclopropanemethanol, 2,2-dimethyl-3-(2-methyl-1-propenyl)-
 cyclopropanemethanol, 2,2-dimethyl-3-(2-methyl-1-propenyl)-, (cis,trans-(±))-
2,2-dimethyl-3-(2-methyl propenyl) cyclopropane methanol
[2,2-dimethyl-3-(2-methyl-1-propenyl)cyclopropyl]methanol
[2,2-dimethyl-3-(2-methylprop-1-en-1-yl)cyclopropyl]methanol
[2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropyl]methan-1-ol
[2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropyl]methanol
2,2-dimethyl-3-(2-methylpropenyl)cyclopropanemethanol
 

Articles:

PubMed:A trichome-specific linoleate lipoxygenase expressed during pyrethrin biosynthesis in pyrethrum.
PubMed:Chirality and bioactivity of the sex pheromone of Madeira mealybug (Hemiptera: Pseudococcidae).
PubMed:Comparative characterization of Santolina insularis chemotypes by essential oil composition, 5S-rRNA-NTS sequencing and EcoRV RFLP-PCR.
PubMed:Eudesmane sesquiterpenes from the aquatic fungus Beltrania rhombica.
PubMed:Electron Transfer Photochemistry of Homochrysanthemol: Intramolecular Nucleophilic Attack on the Cyclopropane Ring.
PubMed:Stereoselective total synthesis of chrysanthemol.
PubMed:Chrysanthemyl diphosphate synthase: isolation of the gene and characterization of the recombinant non-head-to-tail monoterpene synthase from Chrysanthemum cinerariaefolium.
PubMed:Guaianolide-endoperoxide and monoterpene-hydroperoxides from Achillea nobilis.
PubMed:Chemical composition and antimicrobial activity of essential oils of Jasonia candicans and J. montana.
PubMed:Incorporation of [1-14C]-Isopentenyl Pyrophosphate into Monoterpenes by a Cell-Free Homogenate Prepared from Callus Cultures of Chrysanthemum cinerariaefolium.
PubMed:Microbiologically catalyzed enantio- and diastereoselective oxidation of chrysanthemol stereoisomers to chrysanthemic acids.
PubMed:Gas chromatographic determination of racemic cis- and trans-chrysanthemols and their potential aldehyde and carboxylic acid microbial metabolites.
PubMed:[Studies on the chemical constituents of Chrysanthemum indicum L].
 
Notes:
None found
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