Helional

Helional (from heliotropin, from which is it commonly derived) is a chemical compound used as a perfume in soap and laundry detergent. Chemically it is an aldehyde with a hydrocinnamaldehyde motif; a structural element which is present in a number of other important commercial fragrances and odorants.[2]

Helional
Names
IUPAC name
3-(1,3-Benzodioxol-5-yl)-2-methylpropanal
Other names
2-Methyl-3-(3,4-methylenedioxyphenyl)propanal;
2-piperonylpropanal
Helional
Ocean propanal
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.013.528
UNII
Properties
C11H12O3
Molar mass 192.214 g·mol−1
Appearance clear colorless liquid
Odor floral, herbaceous
Density 1.162 g/ml
Boiling point 282°C
Hazards
Safety data sheet [1]
GHS pictograms
GHS Signal word Warning
GHS hazard statements
H315, H319, H335
P261, P305+351+338
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Synthesis

Several synthetic routes exist but the most common is a crossed-aldol condensation between piperonal (heliotropin) and propanal followed by selective hydrogenation of the intermediate alkene. This produces a racemic product.

gollark: A dodecahedron's the dual polyhedron of an icosahedron IIRC. But then you have to ask "why an icosahedron", so that doesn't really answer things.
gollark: Not unless you want to enter the farlands.
gollark: These are clearly different colors.
gollark: Ridiculous. The debug overview *clearly* says the biome. You can't fake that.
gollark: There's not an xkcd about there being an xkcd for everything, is there?

See also

References

  1. Sigma-Aldrich Co., 2-methyl-3-(3,4-methylenedioxyphenyl)propanal. Retrieved on 2016-03-02.
  2. Wetzel, Christian H.; Oles, Markus; Wellerdieck, Christiane; Kuczkowiak, Michael; Gisselmann, Gunter; Hatt, Hanns (1999). "Specificity and sensitivity of a human olfactory receptor functionally expressed in human embryonic kidney 293 cells and Xenopus laevis oocytes". Journal of Neuroscience. 19: 7426–7433. doi:10.1093/chemse/bji002. PMID 15647465.CS1 maint: uses authors parameter (link)


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