Thiomenthone®
Blackcurrant Body ; Blackcurrant Mercaptan® ; 5-methyl-2-(2-sulfanylpropan-2-yl)cyclohexan-1-one ; Buchu ketone ; Buchu mercaptan ; 2-(1-mercapto-1-methylethyl)-5-methyl-cyclohexanone ; Jallione ; Mangone ; Para-mentha-8-thiol-3-one ; P-menthane-8-thiol-3-one ; P-menthon-8-thiol ; 8-mercapto-3-p-menthanone ; Mercaptoisopropyl-5-methylcyclohexanone ; Thiomenthone ; Ribes mercaptan ; Pulegone mercaptan ; 5-methyl-2-(1-methyl-1-sulfanylethyl)cyclohexanone
Photo credits: ScenTree SAS
| Company | Ingredient Name | ID | Naturality | Purity | Latin name | Treated part | Geographical origin | Certifications | Comments | MOQ |
|---|---|---|---|---|---|---|---|---|---|---|
|
Corps Cassis - 30gr | - | - | - | - | - | - | more | - |
General Presentation
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CAS N° : : 38462-22-5
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EINECS number : 253-953-1
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FEMA number : 3177
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Density : 1
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Optical rotation : Lorem Ipsum
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Allergens : This ingredient does not contain any allergen.
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Refractive Index @20°C : Lorem Ipsum
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Volatility : Head
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Price Range : €€€
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Appearance : Colorless liquid
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FLAVIS number : 12.038
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JECFA number : 561
Information on synthetic ingredients
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Acid Value : Lorem Ipsum
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Boiling Point : 56°C (à 0,1 mmHg)
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Detection Threshold : Donnée indisponible.
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Molecular formula : C10H18OS
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Log P : 2,45
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Molecular Weight : 186,32 g/mol
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Fusion Point : Donnée indisponible.
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Flash Point : 108°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
Thiomenthone® is one of the most powerful molecule used in perfumery, as Grapefruit Mercaptan.
Stability :
Stable in perfumes and diverse functional bases
Uses in perfumery :
Thiomenthone® is used in grapefruit accords, exotic fruits, green, white flowers, red fruits and peach notes. Provides a powerful head note.
Year of discovery :
1968
Isomerism :
The asymmetric carbon of Thiomenthone® gives rise to two enantiomers (R) and (S). However, it is the racemic mixture of the two enantiomers that is used in perfumery.
Synthesis precursor :
Thiomenthone® is not a precursor to the synthesis of another compound of olfactory interest.
Natural availability :
Thiomenthone® is present in Buchu EO in its natural state, in very small quantities.
Synthesis route :
Thiomenthone® is synthesized by reaction between Pulegone and hydrogen sulfide in the presence of a base such as triethylamine.
Regulations & IFRA
This ingredient is not restricted
