Piperonal

Quality 0.50 · 2 views · Updated 2 months ago

title: "Piperonal" type: doc version: 1 created: 2026-02-28 author: "Wikipedia contributors" status: active scope: public tags: ["benzaldehydes", "benzodioxoles"] topic_path: "general/benzaldehydes" source: "https://en.wikipedia.org/wiki/Piperonal" license: "CC BY-SA 4.0" wikipedia_page_id: 0 wikipedia_revision_id: 0

| Verifiedfields = changed | Watchedfields = changed | verifiedrevid = 394986228 | Name = Piperonal | ImageFile = Piperonal structure.png | ImageClass = skin-invert | ImageName = | PIN = 2H-1,3-Benzodioxole-5-carbaldehyde | OtherNames= Heliotropin; Heliotropine; Piperonyl aldehyde; Protocatechuic aldehyde methylene ether; 3,4-methylenedioxybenzaldehyde; |Section1={{Chembox Identifiers | UNII_Ref = | UNII = KE109YAK00 | ChEBI_Ref = | ChEBI = 8240 | ChEMBL_Ref = | ChEMBL = 271663 | StdInChI_Ref = | StdInChI = 1S/C8H6O3/c9-4-6-1-2-7-8(3-6)11-5-10-7/h1-4H,5H2 | StdInChIKey_Ref = | StdInChIKey = SATCULPHIDQDRE-UHFFFAOYSA-N | SMILES1 = c1cc2c(cc1C=O)OCO2 | CASNo_Ref = | CASNo = 120-57-0 | Beilstein = 131691 | ChemSpiderID_Ref = | ChemSpiderID = 13859497 | EC_number = 204-409-7 | Gmelin = 4186 | KEGG = C10812 | PubChem = 8438 | SMILES = O=Cc1ccc2OCOc2c1 |Section2={{Chembox Properties | C=8 | H=6 | O=3 | Appearance = Colorless crystals | Density = 1.337 g/cm3 | MeltingPtC = 37 | MeltingPt_ref = | BoilingPtC = 263 | BoilingPt_ref = | Solubility = Soluble in 500 parts |Section3={{Chembox Hazards | GHSPictograms = | GHSSignalWord = Warning | HPhrases = | PPhrases = | MainHazards = | FlashPt = | AutoignitionPt = | LD50 = 2700 mg/kg (orally in rats) }} |Section4={{Chembox Legal status | legal_AU = | legal_BR = D1 | legal_BR_comment = | legal_EU = category 1 precursor | legal_EU_comment = | legal_US = List I | legal_US_comment = | legal_UK = | legal_UN =

Piperonal, also known as heliotropin, is an organic compound which is commonly found in fragrances and flavors. The molecule is structurally related to other aromatic aldehydes such as benzaldehyde and vanillin. The methylenedioxyphenyl group is found in other fragrances.

Natural occurrence

Piperonal naturally occurs in various plants. Examples include dill, violet flowers, and black pepper.

Preparation

Piperonal can be prepared by the oxidative cleavage of isosafrole or by using a multistep sequence from catechol or 1,2-methylenedioxybenzene. Synthesis from the latter chemical is accomplished through a condensation reaction with glyoxylic acid followed by cleaving the resulting α-hydroxy acid with an oxidizing agent. Synthesis from catechol requires an additional step, Williamson ether synthesis using dichloromethane.

Reactions

Piperonal, like all aldehydes, can be reduced to its alcohol (piperonyl alcohol) or oxidized to give its acid (piperonylic acid).

Piperonal can be used in the synthesis of some pharmaceutical drugs including tadalafil, L-DOPA, and atrasentan.

Fragrance

Piperonal has a floral odor which is commonly described as being similar to that of vanillin or cherry. For this reason it is commonly used in fragrances and artificial flavors. Perfumers began to use the fragrance for the first time by the early 1880s. It is commonly used to add vanilla or almond nuances, generally imparting balsamic, powdery, and floral aspects to a scent's character.

Piperonyl acetate is a synthetic cherry flavoring.

Use in MDMA manufacture

Due to their role in the manufacture of MDMA, safrole, isosafrole, and piperonal are Category I precursors under regulation no. 273/2004 of the European Community.

References

References

  1. {{Merck12th
  2. Anvisa. (2023-03-31). "RDC Nº 784 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial". [[Diário Oficial da União]].
  3. {{CELEX. 32004R0273
  4. (19 September 2025). "List I and II Regulated Chemicals - Alphabetical Order". DEA Diversion - US DOJ.
  5. (2016). "Ullmann's Encyclopedia of Industrial Chemistry".
  6. (1974). "An Improved Procedure for Synthesis of DL-4-Hydroxy-3-methoxymandelic Acid (DL-"Vanillyl"-mandelic Acid, VMA)". Journal of Research of the National Bureau of Standards Section A.
  7. (1982). "Oxidative cleavage of α-diols, α-diones, α-hydroxy-ketones and α-hydroxy- and α-keto acids with calcium hypochlorite [Ca(OCl)2]". Tetrahedron Letters.
  8. (1969). "The methylenation of catechols". Journal of the Chemical Society.
  9. (2013). "Synthesis and characterization of related substances and metabolite of tadalafil, a PDE-5 inhibitor". Organic Communications.
  10. (1962). "Studies on Optically Active Amino Acids. I. Preparation of 3-(3, 4-Methylenedioxyphenyl)-D-, and -L-alanine". Chemical & Pharmaceutical Bulletin.
  11. (1996). "2,4-Diarylpyrrolidine-3-carboxylic AcidsPotent ETASelective Endothelin Receptor Antagonists. 1. Discovery of A-127722". Journal of Medicinal Chemistry.
  12. 9781409404927
  13. The Good Scents Company database entry for [http://www.thegoodscentscompany.com/data/rw1005891.html Heliotropin] {{Webarchive. link. (2020-08-01)
  14. Fenaroli's Handbook of Flavor Ingredients.

::callout[type=info title="Wikipedia Source"] This article was imported from Wikipedia and is available under the Creative Commons Attribution-ShareAlike 4.0 License. Content has been adapted to SurfDoc format. Original contributors can be found on the article history page. ::

benzaldehydesbenzodioxoles