Photo credits: ScenTree SAS
Bacdanol®
Woody > Sandalwood > Milky > Grapefruit
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 | Learn more | Naturality | Certifications | MOQ | Purity |
|---|---|---|---|---|---|---|
|
BAGDENOL
BAC-1
|
Discover | - | 10 grs | - | |
|
DARTANOL®
937490
|
Discover | Molecules |
|
- | - |
|
|
SANDEROL™
911520
|
Discover | Molecules |
|
- | - |
|
Bacdanol - 30 Gr | Discover | - | 30grs | - | |
|
Bacdanix/Bacdanol | Discover | Synthetic Aroma Chemicals | - | - |
BAC-1
937490
911520
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 :
Donnée indisponible. -
Vapor pressure :
0,00187 mmHg @20°C 0,001065 mmHg @23°C -
Flash Point :
93°C (199,4°F)
-
Molecular formula :
C14H24O -
Molecular Weight :
208,34 g/mol -
Log P :
4,54 -
Fusion Point :
Donnée indisponible. -
Boiling Point :
287°C (548,6°F) -
Detection Threshold :
Donnée indisponible.
Chemistry & Uses
Uses in perfumery :
Bacdanol® is used in sandalwood reconstitutions, or in combination with rosy floral notes.
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.
Labelling
Allergens :
This ingredient does not contain any allergen.
Signal word :
Warning
Hazard pictograms :
Precautionary statements :
| HAZARD | PRECAUTION |
|---|---|
| H315 Causes skin irritation.
H319 Causes serious eye irritation. H410 Very toxic to aquatic life with long lasting effects. |
P264 Wash ... thoroughly after handling. P273 Avoid release to the environment. P280 Wear protective gloves/protective clothing/eye protection/face protection. P337 + P313 If eye irritation persists: Get medical advice/attention. P391 Collect spillage. P501 Dispose of contents/container to… |
IFRA
IFRA 51th :
This ingredient is not restricted for the 51th amendment
