Photo credits: ScenTree SAS

Woody > Sandalwood > Milky > Grapefruit

Bacdanol®

Bangalol® ; Dartanol® ; Sandranol® ; Sanjinol® ; (E)-2-ethyl-4-(2,2,3-trimethyl-1-cyclopent-3-enyl)but-2-en-1-ol ; Bacdanix ; Bagdenol ; Dartanol ; Ethyl trimethyl cyclopentene butenol ; 2-ethyl-4-(2,2,2-trimethyl-1-cyclopent-3-enyl)but-2-en-1-ol ; Finalol ; Landacanol ; Levosandol ; Pracdonal ; Radjanol ; Sadacanol ; Sandal fleur ; Sandalrome ; Sandenol ; Sanderol ; Sandolene; Sandalmysore Core

Photo credits: ScenTree SAS

Company	Ingredient Name	ID	Comments	Naturality	Certifications	Purity	Latin name	Treated part	Geographical origin	MOQ
	Bacdanol - 30 Gr	-	Visit website	-		-	-	-	-	-

Bacdanol - 30 Gr

Certifications :

General Presentation

CAS N° :
28219-61-6
EINECS number :
248-908-8
FEMA number :
Donnée indisponible.
FLAVIS number :
Donnée indisponible.

JECFA number :
Donnée indisponible.
Volatility :
Base
Price Range :
€€

Physico chemical properties

Appearance :
Colorless viscous liquid
Density :
0,916
Refractive Index @20°C :
1,486 - 1,490
Optical rotation :
Data not available.
Vapor pressure :
0,0025 hPa @20°C 0,001065 mmHg @23°C
Flash Point :
93°C

Molecular formula :
C₁₄H₂₄O
Molecular Weight :
208,34 g/mol
Log P :
4,54
Fusion Point :
Donnée indisponible.
Boiling Point :
287,4°C à 760 mmHg
Detection Threshold :
Donnée indisponible.

Chemistry & Uses

Year of discovery :

Data not available.

Natural availability :

Bacdanol® is not available in its natural state.

Isomerism :

Bacdanol® has two diastereoisomers, as it has a double bond whose conformation can vary. Only the racemic mixture of the two isomers is used in perfumery.

Synthesis precursor :

Bacdanol® is not a precursor to the synthesis of another compound of olfactory interest.

Synthesis route :

Bacdanol® is synthesized in two stages by reacting campholenaldehyde with butanal. The intermediate aldehyde that is obtained is then partially hydrogenated to turn it into alcohol.

Stability :

Stable in perfumes and diverse functional bases

Other comments :

Among other sandalwood notes, Bacdanol® has a closer smell to Sandalore®, which also has a leather facet.

Bacdanol®

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 :

Bacdanol®

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 :