Photo credits: ScenTree SAS

Sulfuric > Berries > Green

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	Comments	Naturality	Certifications	MOQ	Purity
	Corps Cassis - 30gr	-	Visit website	-		-	-
	P-MENTHA-8-THIOL-3-ONE	441M011000	Visit website	Synthetic Aroma Chemicals		-	-

Corps Cassis - 30gr

Certifications :

P-MENTHA-8-THIOL-3-ONE

ID : 441M011000

Certifications : Certifications : Kasher

General Presentation

CAS N° :
38462-22-5
EINECS number :
253-953-1
FEMA number :
3177
FLAVIS number :
12.038

JECFA number :
561
Volatility :
Head
Price Range :
€€€

Physico chemical properties

Appearance :
Colorless liquid
Density :
1
Refractive Index @20°C :
1,493 - 1,497
Optical rotation :
Data not available.
Vapor pressure :
Data not available.
Flash Point :
108°C

Molecular formula :
C₁₀H₁₈OS
Molecular Weight :
186,32 g/mol
Log P :
2,45
Fusion Point :
Donnée indisponible.
Boiling Point :
56°C (à 0,1 mmHg)
Detection Threshold :
Donnée indisponible.

Chemistry & Uses

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

Natural availability :

Thiomenthone® is present in Buchu EO in its natural state, in very small quantities.

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.

Synthesis route :

Thiomenthone® is synthesized by reaction between Pulegone and hydrogen sulfide in the presence of a base such as triethylamine.

Stability :

Stable in perfumes and diverse functional bases

Other comments :

Thiomenthone® is one of the most powerful molecule used in perfumery, as Grapefruit Mercaptan.

Thiomenthone®

I buy this ingredient

General Presentation

CAS N° :

EINECS number :

FEMA number :

FLAVIS number :

JECFA number :

Volatility :

Price Range :

Physico chemical properties

Appearance :

Density :

Refractive Index @20°C :

Optical rotation :

Vapor pressure :

Flash Point :

Molecular formula :

Molecular Weight :

Log P :

Fusion Point :

Boiling Point :

Detection Threshold :

Chemistry & Uses

Uses in perfumery :

Year of discovery :

Natural availability :

Isomerism :

Synthesis precursor :

Synthesis route :

Stability :

Other comments :

Regulations & IFRA

Allergens :

IFRA 51^th :

Thiomenthone®

I buy this ingredient

I buy this ingredient

General Presentation

CAS N° :

EINECS number :

FEMA number :

FLAVIS number :

JECFA number :

Volatility :

Price Range :

Physico chemical properties

Appearance :

Density :

Refractive Index @20°C :

Optical rotation :

Vapor pressure :

Flash Point :

Molecular formula :

Molecular Weight :

Log P :

Fusion Point :

Boiling Point :

Detection Threshold :

Chemistry & Uses

Uses in perfumery :

Year of discovery :

Natural availability :

Isomerism :

Synthesis precursor :

Synthesis route :

Stability :

Other comments :

Regulations & IFRA

Allergens :

IFRA 51th :

IFRA 51^th :