PERILLALDEHYDE (2111-75-3)

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Suppliers

• Sigma-Aldrich - Search for PERILLALDEHYDE
• Fisher Scientific - Search for PERILLALDEHYDE
• TCI - PERILLALDEHYDE
  20.00 - 67.00 USD

Most-cited Publications

• Terpenoid biotransformation in mammals. V. Metabolism of (+)-citronellal, (+-)-7-hydroxycitronellal, citral, (-)-perillaldehyde, (-)-myrtenal, cuminaldehyde, thujone, and (+-)-carvone in rabbits. (Xenobiotica, 1989)
• Perillyl alcohol and perillaldehyde induced cell cycle arrest and cell death in BroTo and A549 cells cultured in vitro (Life Sciences, 2003)
• Enhanced antimicrobial action of lysozyme against Gram-negative and Gram-positive bacteria due to modification with perillaldehyde (Journal of Agricultural and Food Chemistry, 1994)
• Conformational flexibility in terpenes: vibrational circular dichroism (VCD), infrared and Raman study of S-(-)-perillaldehyde. (Journal of Physical Chemistry A, 2008)
• Antimicrobial Effect of trans-Cinnamaldehyde, ()-Perillaldehyde, ()-Citronellal, Citral, Eugenol and Carvacrol on Airborne Microbes Using an Airwasher (Biological & Pharmaceutical Bulletin, 2006)
• Antidepressant-like Effect of l-perillaldehyde in Stress-induced Depression-like Model Mice through Regulation of the Olfactory Nervous System (Evidence-based Complementary and Alternative Medicine, 2011)

Areas of Application

Safety

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Trends

Alternate Names

• perilla aldehyde
• 4-mentha-1,8-dien-7-al
• perillaldehyde, (+)-isomer
• p-mentha-1,8-dien-7-al
• SMILES
  CC(=C)C1CCC(=CC1)C=O
• InChIKey
  RUMOYJJNUMEFDD-UHFFFAOYSA-N

External Links

• Pubchem - PERILLALDEHYDE
• Wikipedia - perillaldehyde
  Perillaldehyde, or perilla aldehyde, is a natural organic compound found most abundantly in the annual herb perilla, but also in a wide variety of other plants and essential oils. It is a monoterpenoid containing an aldehyde functional group. Perillaldehyde, or volatile oils from perilla that are rich in perillaldehyde, are used as food additives for flavoring and in perfumery to add spiciness.

Synthesis

Perilla alcohol  +  dimethyl sulfide (Corey-Kim oxidation of secondary alcohols)

Synthesis of PERILLALDEHYDE ›

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PERILLALDEHYDE

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