CHEBI:32687 - piperonyl butoxide

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name piperonyl butoxide
ChEBI ID CHEBI:32687
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information ChemicalBook:CB6851738
Download Molfile XML SDF
Wikipedia License
Ozone () (or trioxygen) is an inorganic molecule with the chemical formula O3. It is a pale blue gas with a distinctively pungent smell. It is an allotrope of oxygen that is much less stable than the diatomic allotrope O2, breaking down in the lower atmosphere to O2 (dioxygen). Ozone is formed from dioxygen by the action of ultraviolet (UV) light and electrical discharges within the Earth's atmosphere. It is present in very low concentrations throughout the atmosphere, with its highest concentration high in the ozone layer of the stratosphere, which absorbs most of the Sun's ultraviolet (UV) radiation. Ozone's odor is reminiscent of chlorine, and detectable by many people at concentrations of as little as 0.1 ppm in air. Ozone's O3 structure was determined in 1865. The molecule was later proven to have a bent structure and to be weakly diamagnetic. At standard temperature and pressure, ozone is a pale blue gas that condenses at cryogenic temperatures to a dark blue liquid and finally a violet-black solid. Ozone's instability with regard to more common dioxygen is such that both concentrated gas and liquid ozone may decompose explosively at elevated temperatures, physical shock, or fast warming to the boiling point. It is therefore used commercially only in low concentrations. Ozone is a powerful oxidizing agent (far more so than dioxygen) and has many industrial and consumer applications related to oxidation. This same high oxidizing potential, however, causes ozone to damage mucous and respiratory tissues in animals, and also tissues in plants, above concentrations of about 0.1 ppm. While this makes ozone a potent respiratory hazard and pollutant near ground level, a higher concentration in the ozone layer (from two to eight ppm) is beneficial, preventing damaging UV light from reaching the Earth's surface.
Read full article at Wikipedia
Formula C19H30O5
Net Charge 0
Average Mass 338.43850
Monoisotopic Mass 338.20932
InChI InChI=1S/C19H30O5/c1-3-5-7-20-8-9-21-10-11-22-14-17-13-19-18(23-15-24-19)12-16(17)6-4-2/h12-13H,3-11,14-15H2,1-2H3
InChIKey FIPWRIJSWJWJAI-UHFFFAOYSA-N
SMILES CCCCOCCOCCOCc1cc2OCOc2cc1CCC
Roles Classification
Application(s): pesticide synergist
A substance that increases the efficacy of a pesticide.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing piperonyl butoxide (CHEBI:32687) has role pesticide synergist (CHEBI:25943)
piperonyl butoxide (CHEBI:32687) is a benzodioxoles (CHEBI:38298)
IUPAC Name
5-{[2-(2-butoxyethoxy)ethoxy]methyl}-6-propyl-1,3-benzodioxole
Synonyms Sources
(3,4-methylenedioxy-6-propylbenzyl) (butyl) diethylene glycol ether NIST Chemistry WebBook
(butylcarbityl)(6-propylpiperonyl)ether ChemIDplus
2-(2-butoxyethoxy)ethyl 6-propylpiperonyl ether ChemIDplus
5-propyl-4-(2,5,8-trioxa-dodecyl)-1,3-benzodioxole NIST Chemistry WebBook
6-propylpiperonyl butyl diethylene glycol ether NIST Chemistry WebBook
α-(2-(2-n-butoxyethoxy)-ethoxy)-4,5-methylenedioxy-2-propyltoluene NIST Chemistry WebBook
α-[2-(2-butoxyethoxy)ethoxy]-4,5-(methylenedioxy)-2-propyltoluene NIST Chemistry WebBook
butyl carbitol 6-propylpiperonyl ether ChemIDplus
Manual Xrefs Databases
4276 DrugCentral
529 VSDB
529 PPDB
C18880 KEGG COMPOUND
D08383 KEGG DRUG
Piperonyl_Butoxide Wikipedia
View more database links
Registry Numbers Types Sources
288063 Beilstein Registry Number Beilstein
51-03-6 CAS Registry Number NIST Chemistry WebBook
51-03-6 CAS Registry Number ChemIDplus
Last Modified
22 February 2017