Bacdanol® (CAS N° 28219-61-6)​

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

Bacdanol® (CAS N° 28219-61-6)​

Photo credits: ScenTree SAS

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

Certifications :

Information Générales

General Presentation

  • CAS N° : 28219-61-6

  • EINECS number : 248-908-8

  • FEMA number : Donnée indisponible.

  • FLAVIS number : Donnée indisponible.

  • JECFA number : Donnée indisponible.

  • Appearance : Colorless viscous liquid

  • Density : 0,916

  • Volatility : Base

  • Price Range : €€

Physico-chemical properties

  • 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.

  • Optical rotation : Donnée indisponible

  • Vapor pressure : Donnée indisponible

  • Refractive Index @20°C : Donnée indisponible

  • Acid Value : Donnée indisponible.

  • Flash Point : 93°C

Utilisation

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.

Utilisation

Regulations & IFRA

Allergens :

This ingredient does not contain any allergen.

IFRA 51th :

This ingredient is not restricted for the 51th amendment

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