3-methyl-1-penten-3-ol
1-penten-3-ol, 3-methyl-
Identification
| Name | 3-methyl-1-penten-3-ol |
| EINECS | 213-044-2 |
| FDA UNII | Search |
| Molecular Formula | C6 H12 O |
| Molecular Weight | 100.16084000 |
| MDL Number | MFCD00004481 |
| Nikkaji Number | J232.274I |
| Beilstein | 1361621 |
Regulatory
Physical Properties
| Appearance | colorless clear liquid (est) |
| Assay | 97.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Specific Gravity | 0.83800 @ 25.00 °C. |
| Refractive Index | 1.42800 @ 20.00 °C. |
| Boiling Point | 115.00 to 117.00 °C. @ 760.00 mm Hg |
| Vapor Pressure | 9.361000 mmHg @ 25.00 °C. (est) |
| Flash Point | 78.00 °F. TCC ( 25.56 °C. ) |
| logP (o/w) | 1.402 (est) |
| Soluble in | alcohol |
| Insoluble in | water |
No sensory data available
Safety Information
| Preferred SDS | View |
| European information | Most important hazard(s): |
| Oral/Parenteral Toxicity | oral-rat LD50 700 mg/kg |
| Dermal Toxicity | subcutaneous-mouse LD50 1160 mg/kg |
| 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 3-methyl-1-penten-3-ol usage levels up to | not for fragrance use. |
| Recommendation for 3-methyl-1-penten-3-ol flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
Synonyms
ethyl butenol
ethyl methyl vinyl carbinol
ethylbutenol
methyl ethyl vinyl carbinol
(±)-3-
methyl pent-1-en-3-ol
(±)-3-
methyl-1-penten-3-ol
methylethylvinyl carbinol
methylethylvinylcarbinol
3-
methylpent-1-en-3-ol
pent-1-en-3-ol, 3-methyl-
1-
penten-3-ol, 3-methyl-
PubMed:
Studies of the gas phase reactions of linalool, 6-methyl-5-hepten-2-ol and 3-methyl-1-penten-3-ol with O3 and OH radicals.
PubMed:
Bacterial degradation of tert-amyl alcohol proceeds via hemiterpene 2-methyl-3-buten-2-ol by employing the tertiary alcohol desaturase function of the Rieske nonheme mononuclear iron oxygenase MdpJ.
PubMed:
Sesquiterpenes from Laurencia similis.
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Sesquiterpene-like inhibitors of a 9-cis-epoxycarotenoid dioxygenase regulating abscisic acid biosynthesis in higher plants.
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Synthesis and reactivity studies of palladium(II) complexes containing the N-phosphorylated iminophosphorane-phosphine ligands Ph2PCH2P{=NP(=O)(OR)2}Ph2 (R=Et, Ph): application to the catalytic synthesis of 2,3-dimethylfuran.
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Selective hydrogenation by Pd nanoparticles embedded in polyelectrolyte multilayers.
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Four new bromotryptamine derivatives from the marine bryozoan Flustra foliacea.
PubMed:
A density-functional study of the mechanism for the diastereoselective epoxidation of chiral allylic alcohols by the titanium peroxy complexes.
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Anthracenone ABA analogue as a potential photoaffinity reagent for ABA-binding proteins.