Woody > Ambery Woods > Ambergris > Dry Woods > Marine

Boisambrene Forte®

Boisambrene F® ; Amberwood F® ; Amberwood Forte® ; Ethoxymethoxycyclododecane ; Amber decane ; (ethoxymethoxy)-cyclododecane ; Formaldehyde cyclododecyl ethyl acetal ; Lanberwood forte

Boisambrene Forte® (CAS N° 58567-11-6)​

Photo credits: ScenTree SAS

Company Ingredient Name ID Naturality Purity Latin name Treated part Geographical origin Certifications Comments MOQ
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Boisambrene forte - 30 Gr - - - - - - more -
Information Générales

General Presentation

  • CAS N° : : 58567-11-6

  • EINECS number : 261-332-1

  • FEMA number : Donnée indisponible.

  • Density : 0,931

  • Optical rotation : Lorem Ipsum

  • Allergens : This ingredient does not contain any allergen.

  • Refractive Index @20°C : Lorem Ipsum

  • Volatility : Base

  • Price Range : €€€

  • Appearance : Colorless liquid

  • FLAVIS number : Donnée indisponible.

  • JECFA number : Donnée indisponible.

Information on synthetic ingredients

  • Acid Value : Lorem Ipsum

  • Boiling Point : 94°C (à 0,1 Pa)

  • Detection Threshold : Donnée indisponible.

  • Molecular formula : C15H30O2

  • Log P : Donnée indisponible.

  • Molecular Weight : 242,4 g/mol

  • Fusion Point : Donnée indisponible.

  • Flash Point : 150°C

  • Vapor pressure : Lorem Ipsum

Utilisation

Uses

Other comments :

The name Boisambrene Forte® exists as opposed to Boisambrene®, that has a very similar structure (one less carbon atom at the end of the chain) and a slightly different smell.

Stability :

Stable in perfumes and diverse functional bases.

Uses in perfumery :

Boisambrene Forte® is used in woody and ambery notes to bring strength and its characteristic note. This compound can also be used in alkaline bases such as soaps or detergents, thanks to its stability.

Year of discovery :

Discovered in 1974.

Isomerism :

Boisambrene Forte® does not have any isomer used in perfumery.

Synthesis precursor :

Boisambrene Forte® is not a precursor to the synthesis of antoher compound of olfactory interest.

Natural availability :

Boisambrene Forte® is not available in its natural state.

Synthesis route :

Boisambrene Forte® can be obtained by reaction between cyclododecanol and a gazeous complex of pure paraformaldehyde and hydrochloric acid. The intermediary product is called chloromethoxy cyclododecane. This byproduct can undergo an ethylation reaction with sodium ethanolate, prepared with pure sodium in ethanol.

Utilisation

Regulations & IFRA

  • IFRA 51th : This ingredient is restricted by IFRA

  • This ingredient is not restricted for the 49th amendment

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