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Galbazine

Galbanum Pyrazine ; 2-methoxy-3-(2-methylpropyl)pyrazine ; Isobutyl methoxypyrazine ; 2-isobutyl-2-methoxypyrazine ; Galbanum pyrazine ; 2-methoxy-3-isobutyl pyrazine ; 2-methoxy-3-(2-methylpropyl)pyrazine ; 2-methoxy-3-isobutylpyrazine ; 2-2-methyl propyl-3-methoxypyrazine ; 2-isobutyl-3-methoxypyrazine ; 2-methoxy-3-isobutylpyrazine

Galbazine (CAS N° 24683-00-9)​

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Information Générales

General Presentation

  • CAS N° : : 24683-00-9

  • EINECS number : 246-402-1

  • FEMA number : 3132

  • Density : 0,99

  • Optical rotation : Lorem Ipsum

  • Allergens : This ingredient does not contain any allergen.

  • Refractive Index @20°C : Lorem Ipsum

  • Volatility : Head

  • Price Range : €€€€

  • Appearance : Colorless liquid

  • FLAVIS number : 14.043

  • JECFA number : 792

Information on synthetic ingredients

  • Acid Value : Lorem Ipsum

  • Boiling Point : 215°C

  • Detection Threshold : 2 ppt à 10 ppb (0,000001%)

  • Molecular formula : C9H14N2O

  • Log P : 2,62 (est,)

  • Molecular Weight : 166,22 g/mol

  • Fusion Point : Donnée indisponible.

  • Flash Point : 80°C

  • Vapor pressure : Lorem Ipsum

Utilisation

Uses

Other comments :

In comparision to 2-methoxy-3-isopropyl Pyrazine, Galbazine has a much more fruity note, linked to its raw vegetables note. For this facet, Galbazine is more used in perfumes.

Stability :

Stable in perfumes and diverse functional bases

Uses in perfumery :

Galbazine is used in green notes of tomato leaf or violet leaf, in orange blossom notes and woody-patchouli accords.

Year of discovery :

1969

Isomerism :

Galbazine does not have any isomer used in perfumery.

Synthesis precursor :

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

Natural availability :

Galbazine is found in traces in Galbanum EO for example, and can be extracted from it. In the majority of cases, synthetic Galbazine remains the most used.

Synthesis route :

Galbazine is a molecule of the Pyrazine family. Pyrazines are often obtained by a condensation reaction of Gutknecht or Gastaldi, aiming in both cases to condense two amines on two ketones, under the effect of an acid and oxidation. Here, one of the reagents contains an isobutyl group and a methoxy group of the final molecule, while the other does not have any branches.

Utilisation

Regulations & IFRA

This ingredient is not restricted

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