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Bourgeonal

From Wikipedia, the free encyclopedia
Bourgeonal
Names
Preferred IUPAC name
3-(4-tert-Butylphenyl)propanal
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.038.182 Edit this at Wikidata
EC Number
  • 242-016-2
UNII
  • InChI=1/C13H18O/c1-13(2,3)12-8-6-11(7-9-12)5-4-10-14/h6-10H,4-5H2,1-3H3
    Key: FZJUFJKVIYFBSY-UHFFFAOYAX
  • O=CCCc1ccc(cc1)C(C)(C)C
Properties
C13H18O
Molar mass 190.286 g·mol−1
Appearance Pale yellow liquid
Density 0.938 g/cm3
Boiling point 265.1 °C (509.2 °F; 538.2 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Bourgeonal is an aromatic aldehyde used in perfumery. It has a fragrance reminiscent of lily of the valley, otherwise described as floral, watery, green, and aldehydic. It is a pale yellow liquid at room temperature.

Synthesis

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Industrial synthesis of bourgeonal involved a mixed aldol reaction of 4-tert-butylbenzaldehyde and acetaldehyde, followed by hydrogenation. Alternatively it may be produced by the alkylation of tert-butylbenzene with propanal (often in it's acetal form).[1]

Biolobical effects

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In a 2003 study it was found that in vitro, bourgeonal acts as a chemo-attractant for human spermatozoa, activating an olfactory receptor called OR1D2 (formerly called hOR17-4)[2] which opens calcium ion channels in the sperm, leading them to swim twice as fast.[3] Bourgeonal is suspected to be involved in helping sperm locate the ovum.

As of 2010, bourgeonal is the only known odor substance to which males have a higher average sensitivity than females.[2] This is thought to be because the same olfactory receptor (OR1D2) is expressed in non-olfactory tissue in sperm cells as well as the olfactory tissue of the nose. The involvement with sperm chemotaxis causes an evolutionary pressure for males (sexual selection) that causes them to have more OR1D2 receptors on average, both in the nose as well as in sperm.

References

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  1. ^ Ramachanderan, Raghavendra; Schaefer, Bernd (June 2019). "Lily-of-the-valley fragrances". ChemTexts. 5 (2). doi:10.1007/s40828-019-0081-8.
  2. ^ a b Peter Olsson and Matthias Laska (2010). "Human Male Superiority in Olfactory Sensitivity to the Sperm Attractant Odorant Bourgeonal". Chemical Senses. 35 (5): 427–32. doi:10.1093/chemse/bjq030. PMID 20378596.
  3. ^ Spehr, M.; Gisselmann, G; Poplawski, A; Riffell, JA; Wetzel, CH; Zimmer, RK; Hatt, H (2003). "Identification of a Testicular Odorant Receptor Mediating Human Sperm Chemotaxis". Science. 299 (5615): 2054–58. Bibcode:2003Sci...299.2054S. doi:10.1126/science.1080376. PMID 12663925. S2CID 45306091.