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Grundinformationen
- CAS
1074-95-9- Standard-SMILES
CC(C)[C@@H]1CC[C@H](C)CC1=O- InChIKey
NFLGAXVYCFJBMK-IUCAKERBSA-N- Summenformel
- C10H18O
- Durchschnittliche Molmasse
- 154,253 g/mol
- Monoisotopische Masse
- 154,1357652
Namen und Bezeichner
- Bevorzugter Name
- (1S,4S)-Isomenthone
- IUPAC
- (2S,5S)-5-Methyl-2-(propan-2-yl)cyclohexan-1-one
- Lokaler Name
- (±)-Isomenthon
- Englischer Name
- Isomenthoneextra
- Summenformel
- C10H18O
- Molmasse
- 154.25
Namen und Synonyme
Datenbank-Bezeichner
- CAS
1074-95-9、18309-28-9、36977-92-1、491-07-6- PubChem CID
- 6432469
- DTXSID
DTXSID501315467- ChEBI
CHEBI:36496- UNII
- 11T7AFM2DS、9WZ3E2G6CL
- EC Number
- 207-727-4、214-049-2、242-194-1、253-295-5
- Nikkaji
- J100.108F
Eigenschaften
Physikochemische Eigenschaften
- FEMA
- 3460 · 3460 | D,L-ISOMENTHONE
- Farbe
- A colourless slightly oily liquid
- Geruch (Odor)
- The powerful, refreshing and clean-minty odour of moderate tenacity. Somewhat cooling mouthfeel and a refreshing, minty, but distinctly bitter taste.
- Wasserlöslichkeit
- Almost insoluble in water, soluble in alcohol, Propylene glycol, mineral oil and perfume and flavour materials. Very poorly soluble in Glycerin.
Sicherheit und Regulatorisches
Sicherheitsdaten
- Toxizität
- The acute dermal LD 5 0 in rabbits was reported as > 5 ml/kg (Levenstein, 1973).
Chemie und Industrie
Anwendungen
Occurrenced-Isomenthone has been reported to have been isolated from Micromeria abissinica Benth., Pelargonium tomentosum Jacquin and others. /-Isomenthone has been identified in Reunion geranium, Pelargonium capitatum and others (FenaroWs Handbook of Flavor Ingredients, 1971).
VerwendenIsomenthone has very interesting effects in Rose, Carnation, Muguet, Fougeres, Lavender-complexes, etc. The use concentration will normally be about 0.5 to 200, but it may be somewhat higher in Rose and Lavender. The spicy notes in certain types of Men’s fragrances can eliminate the unpleasant sweetness brought about by the conventional Spice and Fougere fixatives.
Darstellung
synthetischeBy hydrogénation of piperitone.
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