2-Acetyl pyrazine (CAS N° 22047-25-2)​

Photo credits: ScenTree SAS

2-Acetyl pyrazine

Burnt Leather > Burnt

1-pyrazin-2-ylethanone ; Methyl-2-pyrazinyl ketone ; Popcorn pyrazine

2-Acetyl pyrazine (CAS N° 22047-25-2)​

Photo credits: ScenTree SAS



Company Ingredient Name Learn more Naturality Certifications MOQ Purity
PCW logo 2-ACETYL PYRAZINE
2AP-1
Discover - 10 grs 99 - 100
Quosentis logo 2-Acetyl Pyrazine - 30 Gr Discover - 30grs -
Tilley Distribution logo 2-Acetyl Pyrazine Discover Synthetic Aroma Chemicals - -
PCW logo
2-ACETYL PYRAZINE

2AP-1

Discover
Quosentis logo
2-Acetyl Pyrazine - 30 Gr
Discover
Tilley Distribution logo
2-Acetyl Pyrazine
Discover
General Presentation

General Presentation

  • CAS N° :

    22047-25-2
  • EINECS number :

    244-753-5
  • FEMA number :

    3126
  • FLAVIS number :

    14,032
  • JECFA number :

    784
  • Volatility :

    Heart
  • Price Range :

    €€€
Physico-chemical properties

Physico-chemical properties

  • Appearance :

    White solid
  • Density :

    1,107
  • Refractive Index @20°C :

    1,501 - 1,535
  • Optical rotation :

    Donnée indisponible.
  • Vapor pressure :

    Donnée indisponible.
  • Flash Point :

    Donnée indisponible.
  • Molecular formula :

    C6H6N2O
  • Molecular Weight :

    122,14 g/mol
  • Log P :

    0,2
  • Fusion Point :

    77°C (170,6°F)
  • Boiling Point :

    213°C (415,4°F)
  • Detection Threshold :

    62 ppb (0,0000062%)
Chemistry & Uses

Chemistry & Uses

Uses in perfumery :

2-acetyl Pyrazine is used in almond, praline, chocolate, coffee and rice notes.

Year of discovery :

Data not available.

Natural availability :

2-acetyl Pyrazine is not available in its natural state.

Isomerism :

2-acetyl Pyrazine has no known isomer in perfumery.

Synthesis precursor :

2-acetyl Pyrazine is not a precursor to the synthesis of another compound of olfactory interest.

Synthesis route :

2-acetyl Pyrazine is part of a family of molecules which scent is close to peanuts as well as cooked and roasted fruits. Pyrazines are often obtained with a Gutknecht or Gastaldi condensation reaction, in both cases to condense two amines on two ketones, under the effect of an acid and oxidation. Here, one of the reagents contains the acetyl group of the final molecule, while the other does not have any branches.

Stability :

Stable in perfumes and diverse functional bases

Other comments :

2-acetyl Pyrazine is less strong than 2-ethyl-3-methyl Pyrazine, with a closer aspect to roasted peanuts.

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