Benzyl acetate (CAS N° 140-11-4)​

Photo credits: ScenTree SAS

Benzyl acetate

Floral > White Flowers > Solar > Benzyl

Phenylméthyl acetate ; Acetoxytoluene ; Benteine ; Benzyl Ethanoate ; Acetic acid benzyl ester ; Acetic phenyl methyl ester ; Benzene methanol acetate ; Benzene methanol ethanoate ; Benzyl alcohol acetate

Benzyl acetate (CAS N° 140-11-4)​

Photo credits: ScenTree SAS



Company Ingredient Name Learn more Naturality Certifications MOQ Purity
PCW logo BENZYL ACETATE
AB-1
Discover - 10 grs 99.5 - 100
Quosentis logo Acetate de Benzyle - 30 Gr Discover - 30grs -
Tilley Distribution logo Benzyl Acetate Discover Synthetic Aroma Chemicals - -
Tilley Distribution logo Benzyl Acetate natural Discover Natural Aroma Chemicals - -
PCW logo
BENZYL ACETATE

AB-1

Discover
Quosentis logo
Acetate de Benzyle - 30 Gr
Discover
Tilley Distribution logo
Benzyl Acetate
Discover
Tilley Distribution logo
Benzyl Acetate natural
Discover
General Presentation

General Presentation

  • CAS N° :

    140-11-4
  • EINECS number :

    205-399-7
  • FEMA number :

    2135
  • FLAVIS number :

    9,014
  • JECFA number :

    23
  • Volatility :

    Head
  • Price Range :

Physico-chemical properties

Physico-chemical properties

  • Appearance :

    Colorless liquid
  • Density :

    1,1
  • Refractive Index @20°C :

    1,501 - 1,504
  • Optical rotation :

    Donnée indisponible.
  • Vapor pressure :

    0,1643 mmHg @25°C
  • Flash Point :

    91°C (195,8°F)
  • Molecular formula :

    C9H10O2
  • Molecular Weight :

    150,18 g/mol
  • Log P :

    1,96
  • Fusion Point :

    -51°C (-59,8°F)
  • Boiling Point :

    206°C (402,8°F)
  • Detection Threshold :

    2 et 270 ppb (0,000027%)
Chemistry & Uses

Chemistry & Uses

Uses in perfumery :

Benzyl acetate is used in floral reconstructions, especially in jasmine, ylang-ylang and monoï notes.

Year of discovery :

Discovered in 1853. Benzyl acetate was first isolated from jasmine absolute during the 10's by german scientists Albert Hesse and Friedrich Müller, because this extract contains 20 to 35% of this molecule.

Natural availability :

Today, natural Benzyl acetate can be extracted from Grandiflorum Jasmine Absolute (and other origins), Ylang-Ylang Extra EO or Narcissus Absolute.

New
Ingredient % min % max
Champaca absolute 3 5
Jasmine Grandiflorum absolute 40 65
Jasmine Grandiflorum concrete 50 70
Jasmine Sambac absolute 15 20
Jasmine Sambac concrete
Ylang ylang oil extra (Comorres & Mayotte) 11 17.50
Ylang ylang oil extra (Madagascar) 5.50 14
Ylang ylang oil I (Comorres & Mayotte) 6 14
Ylang ylang oil I (Madagascar) 2.80 10
Ylang ylang oil III (Comorres & Mayotte) 4 8
Ylang ylang oil III (Madagascar) 0.10 2.20

Isomerism :

Para-Cresyl acetate is a constitutional isomer of Benzyl acetate. Both have the same formula, but para-Cresyl acetate is much more animalic and less floral-jasmine than Benzyl acetate.

Synthesis precursor :

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

Synthesis route :

Nowadays, Benzyl acetate is synthesized by an esterification reaction from acetic acid and Benzyl Alcohol, in the presence of an acid catalyst such as concentrated sulfuric acid.

Stability :

acetates may form acetic acid through time.
Most of the time, the occurrence of a benzenic cycle in a molecule causes a coloration of this molecule through time

Other comments :

Benzyl acetate has a different polarity than Benzylacetone. However, both molecules have a very similar smell. This is the case of several esters, correlated with their analogous ketone.

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