Green > Cut Grass > Green Fruits > Butyric

Cis-3-Hexenyl isobutyrate

Verdural B Extra ; [(Z)-hex-3-enyl] 2-methylpropanoate ; Propanoic acid ; 2-methyl-3-hexenyl ester

Cis-3-Hexenyl isobutyrate (CAS N° 41519-23-7)​

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Information Générales

General Presentation

  • CAS N° : : 41519-23-7

  • EINECS number : 255-424-0

  • FEMA number : 3929

  • Density : 0,88

  • 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 : 09.563

  • JECFA number : 1275

Information on synthetic ingredients

  • Acid Value : Lorem Ipsum

  • Boiling Point : 92°C

  • Detection Threshold : Donnée indisponible.

  • Molecular formula : C10H18O2

  • Log P : 3,52

  • Molecular Weight : 170,25 g/mol

  • Fusion Point : Donnée indisponible.

  • Flash Point : 67°C

  • Vapor pressure : Lorem Ipsum

Utilisation

Uses

Other comments :

Can be market with a trace of alpha tocopherol (0.1%) to prevent oxydation.

Stability :

Les esters ont tendance à former leur acide correspondant en stabilité. Cis-3-Hexenyl IsoButyrate is particularly unstable in a shower gel and shampoo base.

Uses in perfumery :

Brings naturalness to fruity notes. Thanks to its green (cut grass) and its yellow fruit facets, cis-3-hexenyl isobutyrate gives a ripe note to fruits. Interesting for the plum notes.
Suppliers recommend to use it below 1%.

Year of discovery :

Data not available.

Isomerism :

Cis-3-Hexenyl Isobutyrate is the positional isomer of cis-3-Hexenyl Butyrate and trans-2-Hexenyl Isobutyrate. The latter are less commonly used in perfumery, but have a similar odor. Trans-2-Hexenyl Isobutyrate has a more fruity and less green, apple-like smell. Trans-3-Hexenyl Isobutyrate, is not used in perfumery.

Synthesis precursor :

cis-3-Hexenyl IsoButyrate is not a precursor to the synthesis of another compound of olfactory interest.

Natural availability :

Reported found in guava, spearmint EO. Do not exist in its natural state but there is a nature identical quality for cis-3-Hexenyl IsoButyrate

Synthesis route :

Cis-3-Hexenyl Isobutyrate is synthesized by an esterification process between Isobutyric acid (or 2-methylpropanoic acid) and cis-3-Hexenol. This reaction involves acid catalysis using a small amount of a strong acid such as concentrated sulphuric acid.

Utilisation

Regulations & IFRA

This ingredient is not restricted

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