chrysanthemol
chrysanthemyl alcohol
Identification
| Name | chrysanthemol |
| IUPAC | [2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropyl]methanol |
| CAS Number | 5617-92-5 |
| EINECS | 227-045-0 |
| FDA UNII | R52DEG7BXK |
| Molecular Formula | C10 H18 O |
| Molecular Weight | 154.25266000 |
| MDL Number | MFCD00001305 |
| Nikkaji Number | J13.716B |
Regulatory
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 |
| Insoluble in | water |
No sensory data available
Safety Information
| Preferred SDS | View |
| Oral/Parenteral Toxicity | Not determined |
| Dermal Toxicity | Not determined |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']
Safety in Use
| 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. |
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Potential Uses
Natural Occurrence
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
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].