Benzaldehyde (CAS N° 100-52-7)​

Photo credits: ScenTree SAS

Benzaldehyde

Balsamic Ambery > Almondy > Vanillic

Benzoic Aldehyde ; Almond artificial oil ; Benzanoaldehyde ; Benzarone ; Benzene carbaldehyde ; Benzene carbonal ; Benzene carboxaldehyde ; Benzene methylal ; Benzene carbinal ; Benzenecarbonal ; Benzenemehylal ; Benzoyl hydride ; Phenyl methanal ; Phenylformaldehyde ; Phenylketone ; Phenylmethanal

Benzaldehyde (CAS N° 100-52-7)​

Photo credits: ScenTree SAS



Company Ingredient Name Learn more Naturality Certifications MOQ Purity
PCW logo BENZALDEHYDE
ALDB-1
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Quosentis logo Benzaldéhyde - 30gr Discover - 30grs -
Tilley Distribution logo Benzaldehyde natural Discover Natural Aroma Chemicals - -
Tilley Distribution logo Benzaldehyde Synthetic Discover Synthetic Aroma Chemicals - -
PCW logo
BENZALDEHYDE

ALDB-1

Discover
Quosentis logo
Benzaldéhyde - 30gr
Discover
Tilley Distribution logo
Benzaldehyde natural
Discover
Tilley Distribution logo
Benzaldehyde Synthetic
Discover
General Presentation

General Presentation

  • CAS N° :

    100-52-7
  • EINECS number :

    202-860-4
  • FEMA number :

    2127
  • FLAVIS number :

    5,013
  • JECFA number :

    22
  • Volatility :

    Head
  • Price Range :

Physico-chemical properties

Physico-chemical properties

  • Appearance :

    Colorless viscous liquid
  • Density :

    1,045
  • Refractive Index @20°C :

    1,544 - 1,547
  • Optical rotation :

    Donnée indisponible.
  • Vapor pressure :

    1,2676 mmHg @25°C 3,7503 mmHg @45°C
  • Flash Point :

    64°C (147,2°F)
  • Molecular formula :

    C7H6O
  • Molecular Weight :

    106,12 g/mol
  • Log P :

    1,5
  • Fusion Point :

    -26°C (-14,8°F)
  • Boiling Point :

    179°C (354,2°F)
  • Detection Threshold :

    Varie selon les personnes entre 100 ppb et 4,6 ppm (0,00046%), lorsque son seuil de reconnaissance varie entre 330 ppb et 4,1 ppm
Chemistry & Uses

Chemistry & Uses

Uses in perfumery :

Benzaldehyde is used in almond, fruit stone and nutty notes. Gives nuances to vanilla notes.

Year of discovery :

Discovered in 1863.

Natural availability :

Benzaldehyde can be found in almond, several fruits, Vanilla Bourbon Absolute (and other origins), Grandiflorum Jasmine Absolute and fruit stones. In its natural state, it is extracted from Bitter Almond EO, of which it is the major compound.

Isomerism :

Benzaldehyde does not have any isomer used in perfumery.

Synthesis precursor :

Benzaldehyde is the precursor to the synthesis of many compounds used in perfumery. For example, its hydrogenation synthesizes benzoic alcohol. It condenses with other aldehydes to create many other compounds, replacing the aldehyde function with an alcene function. Finally, a Perkin reaction with several acids allows to obtain various compounds, such as Cinnamic Acid by reaction with acetic anhydride. Finally, benzaldehyde forms a Schiff base by reaction with Methyl Anthranilate or Indole for example.

Synthesis route :

Benzaldehyde is synthesized by hydrolysis of benzyl chloride, by an acidic route in the presence of iron chloride, or by an alkaline route in the presence of sodium carbonate. A toluene oxidation also allows to obtain both Benzoic Acid and Benzaldehyde.

Stability :

Tends to oxydize easily into perbenzoic acid, which can react with itself to onvert it into Benzoic Acid.
Tends to color through time.

Other comments :

As it can be compared to Furfural and Salicylaldehyde, Benzaldehyde is the reference almond note in perfumery.

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