Phenyl acetaldehyde (CAS N° 122-78-1)​

Photo credits: ScenTree SAS

Phenyl acetaldehyde

Floral > Rosy > Honeyed > Green

Phenyl Acetic Aldehyde ; 2-phenylacetaldehyde ; Benzacetaldehyde ; Phenylethanal ; Alpha-toluic aldehyde

Phenyl acetaldehyde (CAS N° 122-78-1)​

Photo credits: ScenTree SAS



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PCW logo PHENYLACETALDEHYDE EXTRA
PHAL-1
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Quosentis logo Aldéhyde Phénylacétique - 30 Gr Discover - 30grs -
Tilley Distribution logo Phenyl Acetaladehyde natural Discover Natural Aroma Chemicals - -
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PHENYLACETALDEHYDE EXTRA

PHAL-1

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Quosentis logo
Aldéhyde Phénylacétique - 30 Gr
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Tilley Distribution logo
Phenyl Acetaladehyde natural
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General Presentation

General Presentation

  • CAS N° :

    122-78-1
  • EINECS number :

    204-574-5
  • FEMA number :

    2874
  • FLAVIS number :

    5,03
  • JECFA number :

    1002
  • Volatility :

    Base
  • Price Range :

    €€€
Physico-chemical properties

Physico-chemical properties

  • Appearance :

    Colorless liquid
  • Density :

    1,03
  • Refractive Index @20°C :

    1,525 - 1,545
  • Optical rotation :

    Donnée indisponible.
  • Vapor pressure :

    0,3675 mmHg @25°C
  • Flash Point :

    68°C (154,4°F)
  • Molecular formula :

    C8H8O
  • Molecular Weight :

    120,15 g/mol
  • Log P :

    1,54
  • Fusion Point :

    -10°C (14°F)
  • Boiling Point :

    193°C (379,4°F)
  • Detection Threshold :

    4 ppb (0,0000004%)
Chemistry & Uses

Chemistry & Uses

Uses in perfumery :

Phenyl Acetaldehyde is used in rosy floral notes, citrus or leather notes.

Year of discovery :

1908

Natural availability :

Phenyl Acetaldehyde is present in many flowers such as chicory or flower of Lecythis usitata in Brazil, from which it can be extracted.

Isomerism :

Phenyl Acetaldehyde does not have any isomer used in perfumery.

Synthesis precursor :

Phenyl Acetaldehyde is a precursor to the synthesis of a Schiff base by reaction with Methyl Anthranilate. This molecule has a pinkish, green, honeydew and mandarin smell. Furthermore, a reaction with methanol in an acid medium synthesizes Viridine®.

Synthesis route :

Phenyl Acetaldehyde can be synthesized during the vapor phase isomerization of styrene oxide, in the presence of aluminum silicate, or from phenylethane-1,2-diol, always during the vapor phase and always in presence of aliminum silicate, used as catalysts.

Stability :

Aldehydes may form diethylacetals in alcoholic perfumes, with no real impact on their smell
Has a great capacity of polymerisation
Most of the time, the occurrence of a benzenic cycle in a molecule causes a coloration of this molecule through time

Other comments :

Phenyl Acetaldehyde is often marketed diluted in Phenyl Ethyl Alcohol. It has a more honeyed and less green facet than the latter.

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