Photo credits: ScenTree SAS

Woody > Sandalwood > Milky > Fatty > Dry Woods

Javanol® Super

[(1R,2S)-1-methyl-2-[[(1R,3S,5S)-1,2,2-trimethyl-3-bicyclo[3.1.0]hexanyl]methyl]cyclopropyl]méthanol ; 1-methyl-2-[(1,2,2-trimethylbicyclo[3.1.0]hex-3-yl)methyl]-cyclopropanemethanol

Photo credits: ScenTree SAS

Company	Ingredient Name	ID	Comments	Naturality	Certifications	Purity	Latin name	Treated part	Geographical origin	MOQ
	Javanol® Super - 30gr	-	Visit website	-		-	-	-	-	-

Javanol® Super - 30gr

Certifications :

General Presentation

CAS N° :
198404-98-7
EINECS number :
427-900-1
FEMA number :
4776
FLAVIS number :
Donnée indisponible.

JECFA number :
2254
Volatility :
Base
Price Range :
€€€€

Physico chemical properties

Appearance :
Colorless viscous liquid
Density :
0,95
Refractive Index @20°C :
Data not available.
Optical rotation :
Data not available.
Vapor pressure :
Data not available.
Flash Point :
>93°C

Molecular formula :
C₁₅H₂₆O
Molecular Weight :
222,37 g/mol
Log P :
Donnée indisponible.
Fusion Point :
Donnée indisponible.
Boiling Point :
271°C
Detection Threshold :
Donnée indisponible.

Chemistry & Uses

Year of discovery :

Data not available.

Natural availability :

Javanol® is not available in its natural state.

Isomerism :

Javanol® has several asymmetric carbons that give rise to several possible isomers. Javanol® Super is a unique isomer. In addition, Javanol® is a constitutional isomer of Polysantol®. These two compounds have a similar structure, and are used for similar reasons in perfumes. Javanol® still has a less milky note than Polysantol®, but is more powerful.

Synthesis precursor :

Javanol® is not involved in the synthesis of another compound of olfactory interest.

Synthesis route :

Javanol® is synthesized by a Simmons-Smith double reaction, consisting of cyclopropanation from 2-methyl-4-(2,2,3-trimethyl-3-cyclopenten-1-yl)-2-buten-1-ol. This reaction involves a catalysis of Zinc and Copper, as well as diodomethane, to convert a double bond to a cyclopropane group. Javanol® Super corresponds to one isolated isomer of Javanol®.

Stability :

Unstable exclusively in acid cleaners and in bleach.

Other comments :

The detection limit of Javanol® is extremely low. This makes it one of the most used santal compounds, because it brings a milky and woody effect, even with a very small dosis.

Javanol® Super

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

Year of discovery :

Natural availability :

Isomerism :

Synthesis precursor :

Synthesis route :

Stability :

Other comments :

Regulations & IFRA

Allergens :

IFRA 51^th :

Javanol® Super

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

Year of discovery :

Natural availability :

Isomerism :

Synthesis precursor :

Synthesis route :

Stability :

Other comments :

Regulations & IFRA

Allergens :

IFRA 51th :

IFRA 51^th :