Floral > Rosy > Honeyed > Butyric

Phenylacetic acid

Phenyl Acetic Acid ; 2-phenylacetic Acid ; Benzene acetic acid ; Benzyl carboxylic acid ; Toluic acid

Phenylacetic acid (CAS N° 103-82-2)​

Photo credits: ScenTree SAS

Do you sell any of the raw materials? Would you like to let our users know?
Send an email to fournisseurs@scentree.coto learn about our advertising opportunities.

Information Générales

General Presentation

  • CAS N° : : 103-82-2

  • EINECS number : 203-148-6

  • FEMA number : 2878

  • Density : 1,08

  • Optical rotation : Lorem Ipsum

  • Allergens : This ingredient does not contain any allergen.

  • Refractive Index @20°C : Lorem Ipsum

  • Volatility : Heart

  • Price Range :

  • Appearance : White crystals

  • FLAVIS number : 08.038

  • JECFA number : 1007

Information on synthetic ingredients

  • Acid Value : Lorem Ipsum

  • Boiling Point : 265°C

  • Detection Threshold : 1 ppm (0,0001%)
    Ce qui fait de lui un composé moins facilement détectable que l'Alcool phényléthylique

  • Molecular formula : C8H8O2

  • Log P : 1,4

  • Molecular Weight : 136,14 g/mol

  • Fusion Point : 77°C

  • Flash Point : 132°C

  • Vapor pressure : Lorem Ipsum

Utilisation

Uses

Other comments :

In comparison with Phenyl Ethyl Alcohol, Phenylacetic Acid brings a more butyric and honeyed facet, but less pleasant and directly reminiscent of rose.

Stability :

Très stable en eau de toilette.
Most of the time, the occurrence of a benzenic cycle in a molecule causes a coloration of this molecule through time
Acids may lowen a perfume’s pH. An acid pH can help preserving a perfume, but can also be the source of other raw materials modification

Uses in perfumery :

Phenylacetic Acid gives a honeyed and sweet touch to a rose note.

Year of discovery :

1885

Isomerism :

Anisic Aldehyde and Methyl Benzoate are constitutional isomers of Phenylacetic Acid. However, their smell is not related.

Synthesis precursor :

Phenylacetic acid is the precursor for the synthesis of several esters called ''phenyl acetates '', by reacting it with an alcohol in the presence of a catalyst acid.

Natural availability :

Phenylacetic Acid is present in Tobacco Absolute, Cocoa Absolute and chicory from which it can be extracted in small quantities. Synthetic Phenylacetic Acid remains the most produced and used in perfumery.

Synthesis route :

Phenylacetic Acid is obtained according to a synthetic route in two steps, that involves benzyl chloride with sodium cyanide, followed by a hydrolysis to obtain the corresponding acid.

Utilisation

Regulations & IFRA

This ingredient is not restricted

I am a chocolate hazelnut cookie. I come out of the oven. Impossible to refuse me.
This website is using cookies
Our website uses cookies for statistics, performance, and security. These anonymous data allow us to give you an optimal navigation experience. You can always disable cookies in your browser settings.