dehydrovomifoliol
6-hydroxy-3-oxo-a-ionone
Identification
| Name | dehydrovomifoliol |
| IUPAC | 4-hydroxy-3,5,5-trimethyl-4-[(E)-3-oxobut-1-enyl]cyclohex-2-en-1-one |
| CAS Number | 7070-24-8 |
| FDA UNII | Search |
| Molecular Formula | C13 H18 O3 |
| Molecular Weight | 222.28406000 |
| Nikkaji Number | J1.228.338E |
| Beilstein | 2050826 |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Boiling Point | 367.42 °C. @ 760.00 mm Hg (est) |
| Flash Point | 374.00 °F. TCC ( 190.20 °C. ) (est) |
| logP (o/w) | 0.691 (est) |
| Soluble in | water, 1.428e+004 mg/L @ 25 °C (est) |
No sensory data available
Safety Information
| 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 dehydrovomifoliol usage levels up to | not for fragrance use. |
| Recommendation for dehydrovomifoliol flavor usage levels up to | not for flavor use. |
No supplier data available
Potential Uses
Natural Occurrence
Synonyms
2-
cyclohexen-1-one-4-ol, 3,5,5-trimethyl-4-(3-oxo-1-butenyl)
2-
cyclohexen-1-one, 4-hydroxy-3,5,5-trimethyl-4-(3-oxo-1-butenyl)-
(±)-6-
hydroxy-3-oxo-a-ionone
6-
hydroxy-3-oxo-a-ionone
4-
hydroxy-3,5,5-trimethyl-4-[(1E)-3-oxo-1-butenyl]-2-cyclohexen-1-one
4-
hydroxy-3,5,5-trimethyl-4-[(1E)-3-oxobut-1-en-1-yl]cyclohex-2-en-1-one
4-
hydroxy-3,5,5-trimethyl-4-[(E)-3-oxobut-1-enyl]cyclohex-2-en-1-one
4-
hydroxy-3,5,5-trimethyl-4-[3-oxo-1-butenyl]-2-cyclohexen-1-one
4-
hydroxy-4-(3-oxo-1-butenyl)-3,5,5-trimethylcyclohex-2-en-1-one
PubMed:
[Sesquiterpenoids from Solanum lyratum].
PubMed:
Tigliane diterpenes from Croton mauritianus as inhibitors of chikungunya virus replication.
PubMed:
Chemometrics as a tool of origin determination of Polish monofloral and multifloral honeys.
PubMed:
Bioactive compounds from Vitex leptobotrys.
PubMed:
[Chemical constituents of chloroform fraction from leaves of Chimonanthus salicifolius].
PubMed:
[Chemical consitituents from root of Isatis indigotica].
PubMed:
[Chemical constituents of Pilea cavaleriei subsp. cavaleriei].
PubMed:
Classification and characterization of manuka honeys based on phenolic compounds and methylglyoxal.
PubMed:
Evaluation of the antiproliferative activity of the leaves from Arctium lappa by a bioassay-guided fractionation.
PubMed:
[Isoprenoids and phenylpropanoids from Saussurea deltoidea].
PubMed:
Isolation of megastigmane sesquiterpenes from the silkworm (Bombyx mori L.) droppings and their promotion activity on HO-1 and SIRT1.
PubMed:
[Studies on the chemical constituents of rhizoma of Coniogramme japonica].
PubMed:
Anticholinesterase and antioxidant constituents from Gloiopeltis furcata.
PubMed:
The constituents of Urtica cannabina used in Uighur medicine.
PubMed:
Two new sesquiterpenoids from Solanum lyratum with cytotoxic activities.
PubMed:
5-Hydroxytryptamine2A receptor binding activity of compounds from Litsea sessilis.
PubMed:
New germacrane sesquiterpenes from Salvia chinensis.
PubMed:
[Studies on chemical constitutes of Acantophora spicifera].
PubMed:
Bioactive constituents from Rollinia emarginata (Annonaceae).
PubMed:
[Norisoprenoids from red alga Gymnogongrus flabelliformis].
PubMed:
[Chemical constituents from red alga Corallina pilulifera].
PubMed:
Lagaspholones A and B: two new jatropholane-type diterpenes from Euphorbia lagascae.
PubMed:
Two new megastigmanes from the leaves of Cucumis sativus.
PubMed:
A variety of volatile compounds as markers in unifloral honey from dalmatian sage (Salvia officinalis L.).
PubMed:
Chemical constituents of Glechoma longituba.
PubMed:
Norisoprenoids and hepatoprotective flavone glycosides from the aerial parts of Beta vulgaris var. cicla.
PubMed:
Diterpenes and other constituents from Croton draco (Euphorbiaceae).
PubMed:
Antimalarial compounds from Rhaphidophora decursiva.