ScenTree, la nouvelle encyclopédie des ingrédients de parfum.

Exploring the branches of scent

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Crédits photo: ScenTree SAS

CAS number :

28219-61-6

EINECS number :

248-908-8

FEMA number :

Data not available.

JECFA number :

Data not available.

FLAVIS number :

Data not available.

Volatility :

Base

Appearance :

Colorless viscous liquid

Price Range :

€€

Stability :

Stable in perfumes and diverse functional bases

Density :

0.916

Molecular formula :

C₁₄H₂₄O

Molecular Weight :

208.34 g/mol

Flash Point :

199.4°F (93°C)

Log P :

4.54

Fusion Point :

Data not available.

Boiling Point :

287.4°C at 760 mmHg

Detection Threshold :

Data not available.

Crédits photo: ScenTree SAS

Year of discovery :

Data not available.

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.

Synthesis precursor :

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

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.

Natural availability :

Bacdanol® is not available in its natural state.

Allergens :

This ingredient does not contain any allergen.

For more information on allergens used in perfumery, please consult our article about allergens

IFRA :

This ingredient is not restricted

Maximum usage according to the product category :
Ingredients containing
Ingredient Name	CAS N°	Estimated Concentration
Geraniol	106-24-1	0,7

Cat.1	Cat.2	Cat.3	Cat.4	Cat.5	Cat.6	Cat.7	Cat.8	Cat.9	Cat.10	Cat.11
0,16 %	0,2 %	0,83 %	2,49 %	1,31 %	3,99 %	0,42 %	2 %	5 %	2,5 %	Not restricted

Skin contact products	Non skin contact products
Leave on products	Rinse off products

List of natural ingredients containing the material presented here
Ingredient Name	Botanical Name	CAS N°	Estimated Concentration

Maximum usage according to the product category :
Ingredients containing
Ingredient Name	CAS N°	Estimated Concentration
Geraniol	106-24-1	0,7
alpha-Cedrene	469-61-4	0,05
Farnesol	4602-84-0	11
alpha-Cedrene	469-61-4	0,2

Cat.1	Cat.2	Cat.3	Cat.4	Cat.5A	Cat.5B	Cat.5C	Cat.5D	Cat.6
0,00016 %	0,13 %	0,4 %	2,4 %	0,6 %	0,52 %	0,6 %	0,17 %	0,00016 %
Cat.7A	Cat.7B	Cat.8	Cat.9	Cat.10A	Cat.10B	Cat.11A	Cat.11B	Cat.12
0,87 %	0,87 %	0,17 %	2,2 %	2,2 %	4,4 %	0,17 %	0,17 %	Not restricted

List of natural ingredients containing the material presented here
Ingredient Name	Botanical Name	CAS N°	Estimated Concentration

To learn more about IFRA's standards : https://ifrafragrance.org/safe-use/library
To find out the specificities of each category and the ingredients prohibited by IFRA, click article about l'IFRA
ScenTree is solely responsible for the information provided here.

Uses in perfumery :

Bacdanol® is used in sandalwood reconstitutions, or in combination with rosy floral notes.

Other names :

Bangalol®, 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

Other comments :

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

Exploring the branches of scent

Year of discovery :

Data not available.

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.

Synthesis precursor :

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

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.

Natural availability :

Bacdanol® is not available in its natural state.

Allergens :

This ingredient does not contain any allergen.

Annexe I :

Restriction type :

RESTRICTION QRA

Cause of restriction :

DERMAL SENSITIZATION

Amendment :

48

Comments :

Quantitative usage limits :

Annexe I :

Annexe I :

Restriction type :

Cause of restriction :

DERMAL SENSITIZATION AND SYSTEMIC TOXICITY

Amendment :

49

Comments :

Quantitative limit on the use :

Annexe I :