Photo credits: ScenTree SAS
Do you sell any of the raw materials? Would you like to let our users know?
Send an email to fournisseurs@scentree.coto learn about our advertising opportunities.
General Presentation
-
CAS N° : : 590-86-3
-
EINECS number : 209-691-5
-
FEMA number : 2692
-
Density : 0,803
-
Optical rotation : Lorem Ipsum
-
Allergens : This ingredient does not contain any allergen.
-
Refractive Index @20°C : Lorem Ipsum
-
Volatility : Head
-
Price Range : Data not available.
-
Appearance : Colorless liquid
-
FLAVIS number : 05.006
-
JECFA number : 258
Information on synthetic ingredients
-
Acid Value : Lorem Ipsum
-
Boiling Point : 90°C
-
Detection Threshold : Donnée indisponible.
-
Molecular formula : C5H10O
-
Log P : 1,5
-
Molecular Weight : 86,13 g/mol
-
Fusion Point : -51°C
-
Flash Point : 0,5°C
-
Vapor pressure : Lorem Ipsum
Uses
Other comments :
Isovaleraldehyde can be compared to Furfural, standing out thanks to its more pyrogenic and bitter almond gourmand note. Isovaleraldehyde is more etheric and fruity-cherry and pear.
Stability :
This molecule may form Schiff bases by reacting with Methyl Anthranilate or Indole for example, forming another colored and differently smelling compound.
Uses in perfumery :
Isovaleraldehyde is used in cherry and chocolate notes, to bring a liquorous head note.
Year of discovery :
Data not available.
Isomerism :
Isovaleraldehyde does not have any isomer used in perfumery.
Synthesis precursor :
Isovaleraldehyde can be used to synthesize Schiff bases, reacting with Methyl Anthranilate or Indole for example.
Natural availability :
Isovaleraldehyde is found in the odorous principle of many fruits and food we consume every day : apple, ginger, beef, lovage…
Synthesis route :
Isovaleraldehyde is synthesized by oxydation of Isoamyl Alcohol.
Regulations & IFRA
This ingredient is not restricted
