Ambrettolide (CAS N° 28645-51-4)​

Photo credits: ScenTree SAS

Musky > Berries > White Flowers

Ambrettolide

17-oxacycloheptadec-6-en-1-one ; Isoambrettolide ; Ambrettozone ; Oxacycloheptadec-10-en-2-one ; Hexadec-9-en-1,16 lactone ; Lanbrettolide ; Moschus lactone ; Scentolide

Ambrettolide (CAS N° 28645-51-4)​

Photo credits: ScenTree SAS

Company Ingredient Name ID Comments Naturality Certifications Purity Latin name Treated part Geographical origin MOQ
Quosentis logo
Ambrettolide - 30 Gr - Visit website Je me procure cet ingrédient - - - - - -
MANE logo
AMBRETTOLIDE M_0040009 Visit website Je me procure cet ingrédient Synthétique - - - - -
Synarome logo
SCENTOLIDE 85705 Visit website Je me procure cet ingrédient Molecule - - - - -

Ambrettolide - 30 Gr

Certifications :

AMBRETTOLIDE

ID : M_0040009

Certifications :

SCENTOLIDE

ID : 85705

Certifications :

Information Générales

General Presentation

  • CAS N° :

    28645-51-4
  • EINECS number :

    249-120-7
  • FEMA number :

    4145
  • FLAVIS number :

    10.063
  • JECFA number :

    1991
  • Volatility :

    Base
  • Price Range :

    €€€
Physico-chemical properties

Physico chemical properties

  • Appearance :

    Colorless liquid
  • Density :

    0,956
  • Refractive Index @20°C :

    1,477 - 1,482
  • Optical rotation :

    Data not available.
  • Vapor pressure :

    0,000158 mmHg @23°C
  • Flash Point :

    99°C
  • Molecular formula :

    C16H28O2
  • Molecular Weight :

    252,4 g/mol
  • Log P :

    6,51
  • Fusion Point :

    Donnée indisponible.
  • Boiling Point :

    187°C (à 21 hPa)
  • Detection Threshold :

    0,3 ng/l air
Utilisation

Chemistry & Uses

Year of discovery :

Discovered in 1927.

Natural availability :

Ambrettolide is found naturally in angelica sap and in Ambrette Seeds Absolute, from which it is extracted in its natural state.

Isomerism :

Ambrettolide has a double bond, creating two possible diastereoisomers (Z) and (E). The Ambrettolide used in perfumery is a racemic mixture of these two isomers. Both diastereoisomers have a similar smell.

Synthesis precursor :

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

Synthesis route :

Ambrettolide is synthesized by reaction between aleuritic acid and trimethyl orthoformate. A second step consists in reacting the intermediate product that is obtained during the previous process with acetic anhydride, and potassium hydroxide afterwards, to cyclize the second intermediate product and obtain the final product.

Stability :

Musks are very stable, as in alcoholic and in functional fragrances, exept in acid cleaners, antiperspirants and bleaches.

Other comments :

Among other musks, Ambrettolide is comparable to Helvetolide® and Velvione® thanks to its white flowers facet.

Utilisation

Regulations & IFRA

Allergens :

This ingredient does not contain any allergen.

IFRA 51th :

This ingredient is not restricted for the 51th amendment

I am a chocolate hazelnut cookie. I come out of the oven. Impossible to refuse me.
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