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Details

Stereochemistry ACHIRAL
Molecular Formula C8H6O3
Molecular Weight 150.1314
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PIPERONAL

SMILES

O=CC1=CC2=C(OCO2)C=C1

InChI

InChIKey=SATCULPHIDQDRE-UHFFFAOYSA-N
InChI=1S/C8H6O3/c9-4-6-1-2-7-8(3-6)11-5-10-7/h1-4H,5H2

HIDE SMILES / InChI
Molecular Formula C8H6O3
Molecular Weight 150.1314
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

2010
435
PubMed

PubMed

TitleDatePubMed
[Morphological features of the thymus in heliotrin hepatitis upon administration of immunostimulators].
2001
Antioxidant properties of 8.0.4'-neolignans.
2001 Nov
A short synthesis of (+/-)-epiasarinin.
2002 Apr 4
[Comparative evaluation of antioxidant properties of neoselen and berberin in chronic heliotrinal hepatitis].
2002 Apr-Jun
Concentrations of nine alkenylbenzenes, coumarin, piperonal and pulegone in Indian bidi cigarette tobacco.
2003 Feb
[Succivil efficacy in endogenous intoxication].
2003 Jul-Aug
Bhc-diol as a photolabile protecting group for aldehydes and ketones.
2003 Jun 12
Chemical profiling of 3,4-methylenedioxymethamphetamine (MDMA) tablets seized in Hong Kong.
2003 Nov
Microbiologic oxidation of isosafrole into piperonal.
2003 Spring
First total synthesis of justicidone, a p-quinone-lignan derivative from Justicia hyssopifolia.
2005 Aug
A study of impurities in intermediates and 3,4-methylenedioxymethamphetamine (MDMA) samples produced via reductive amination routes.
2005 Dec 20
Determination of synthesis method of ecstasy based on the basic impurities.
2005 Sep 10
Synthesis of 7-deoxypancratistatin from carbohydrates by the use of olefin metathesis.
2006 Apr 12
The fumigant and repellent activity of aliphatic lactones against Pediculus humanus capitis (Anoplura: Pediculidae).
2006 Feb
Alpha-phenyl-N-tert-butyl nitrone (PBN) derivatives: synthesis and protective action against microvascular damages induced by ischemia/reperfusion.
2007 May 15
Influence of chalcone analogues on serum glucose levels in hyperglycemic rats.
2008 Feb 15
Synthesis and use of 4-peptidylhydrazido-N-hexyl-1,8-naphthalimides as fluorogenic histochemical substrates for dipeptidyl peptidase IV and tripeptidyl peptidase I.
2009 Jan
Enhancement in sample collection for the detection of MDMA using a novel planar SPME (PSPME) device coupled to ion mobility spectrometry (IMS).
2009 Jul
3',6'-Bis(ethyl-amino)-2',7'-dimethyl-2-{[2-[(E)-3,4-methyl-enedioxy-benzyl-idene-amino]eth-yl}spiro-[isoindoline-1,9'-xanthen]-3-one.
2009 Jul 15
4-Methyl-1,3-bis-(3,4-methyl-enedioxy-benz-yl)-2-(3,4-methyl-enedioxy-phen-yl)imidazolidine.
2009 Nov 11
Total synthesis of (+)-virgatusin via AlCl3-catalyzed [3+2] cycloaddition.
2009 Sep 14
(E)-N'-(1,3-Benzodioxol-5-ylmethyl-ene)nicotinohydrazide monohydrate.
2009 Sep 5
1-(2-Bromobenzoyl)-6,7-(methylene-dioxy)isoquinoline.
2010 Dec 11
Detection of piperonal emitted from polymer controlled odor mimic permeation systems utilizing Canis familiaris and solid phase microextraction-ion mobility spectrometry.
2010 Feb 25
Toxicological methods for tracing drug abuse: chromatographic, spectroscopic and biological characterisation of ecstasy derivatives.
2010 Mar
Preparation and In vitro / In vivo characterization of spray dried microsphere formulation encapsulating 4-chlorocurcumin.
2010 May
N-[(E)-1,3-Benzodioxol-5-yl-methyl-idene]-4-methyl-aniline.
2010 Nov 24
14-(1,3-Benzodioxol-5-yl)-7,14-dihydro-dibenzo[a,j]acridine.
2010 Nov 6
(2E)-3-(1,3-Benzodioxol-5-yl)-1-(3-bromo-2-thien-yl)prop-2-en-1-one.
2010 Sep 4
Patents

Patents

04014885
1
04024274
1
04073798
8
04125541
3
04125714
3
04182729
3
04227015
1
04344954
3
05182404
5
05233057
5
05517350
1
05574056
1
05594006
2
05661168
3
05716984
3
05719183
1
05731321
1
06133456
1
06162927
2
06218427
1
06252080
1
06306870
4
06310076
4
06310211
1
06329387
1
06448260
2
06498172
5
JP2001288179A
1
JP2004124078A
1
JP2004203839A
3
JP2004250334A
2
JP2004269376A
1
JP2006095182A
1
JP2006325902A
2
JP2006340785A
1
JP2007502860A
3
JP2011207797A
1
JPH03215835A
1
JPH0383904A
1
JPH0390004A
1
JPH04124123A
1
JPH04178388A
1
JPH04342511A
2
JPH07330755A
2
JPH0827144A
1
JPH09227568A
1
JPH10259121A
1
JPH11228368A
3
JPS5522615A
1
JPS55314A
1
JPS5535003A
1
Substance Class Chemical
Created
by admin
on Fri Dec 16 19:21:45 UTC 2022
Edited
by admin
on Fri Dec 16 19:21:45 UTC 2022
Record UNII
KE109YAK00
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PIPERONAL
FCC   FHFI   HSDB   MART.   MI   WHO-DD  
Common Name English
PIPERONAL (CONSTITUENT OF BLACK PEPPER) [DSC]
Common Name English
HELIOTROPINE [INCI]
Common Name English
PIPERONAL [HSDB]
Common Name English
DIOXYMETHYLENEPROTOCATECHUIC ALDEHYDE
Common Name English
3,4-(METHYLENEDIOXY)BENZALDEHYDE
Systematic Name English
2H-BENZO(3,4-D)-1,3-DIOXOLAN-5-YLFORMALDEHYDE
Systematic Name English
NSC-26826
Code English
PIPERONAL [FHFI]
Common Name English
1,3-BENZODIOXOLE-6-CARBOXALDEHYDE
Systematic Name English
PIPERONAL [FCC]
Common Name English
FEMA NO. 2911
Code English
GELIOTROPIN
Common Name English
Piperonal [WHO-DD]
Common Name English
HELIOTROPINE
INCI  
INCI  
Official Name English
PIPERONAL [MI]
Common Name English
PIPERONAL [MART.]
Common Name English
PIPERONYLALDEHYDE
Systematic Name English
Classification Tree Code System Code
JECFA EVALUATION PIPERONAL
Created by admin on Fri Dec 16 19:21:45 UTC 2022 , Edited by admin on Fri Dec 16 19:21:45 UTC 2022
Code System Code Type Description
EVMPD
SUB37596
Created by admin on Fri Dec 16 19:21:45 UTC 2022 , Edited by admin on Fri Dec 16 19:21:45 UTC 2022
PRIMARY
WIKIPEDIA
PIPERONAL
Created by admin on Fri Dec 16 19:21:45 UTC 2022 , Edited by admin on Fri Dec 16 19:21:45 UTC 2022
PRIMARY
HSDB
581
Created by admin on Fri Dec 16 19:21:45 UTC 2022 , Edited by admin on Fri Dec 16 19:21:45 UTC 2022
PRIMARY
EPA CompTox
DTXSID7025924
Created by admin on Fri Dec 16 19:21:45 UTC 2022 , Edited by admin on Fri Dec 16 19:21:45 UTC 2022
PRIMARY
RXCUI
33753
Created by admin on Fri Dec 16 19:21:45 UTC 2022 , Edited by admin on Fri Dec 16 19:21:45 UTC 2022
PRIMARY RxNorm
CHEBI
8240
Created by admin on Fri Dec 16 19:21:45 UTC 2022 , Edited by admin on Fri Dec 16 19:21:45 UTC 2022
PRIMARY
NSC
26826
Created by admin on Fri Dec 16 19:21:45 UTC 2022 , Edited by admin on Fri Dec 16 19:21:45 UTC 2022
PRIMARY
FDA UNII
KE109YAK00
Created by admin on Fri Dec 16 19:21:45 UTC 2022 , Edited by admin on Fri Dec 16 19:21:45 UTC 2022
PRIMARY
DAILYMED
KE109YAK00
Created by admin on Fri Dec 16 19:21:45 UTC 2022 , Edited by admin on Fri Dec 16 19:21:45 UTC 2022
PRIMARY
MESH
C005454
Created by admin on Fri Dec 16 19:21:45 UTC 2022 , Edited by admin on Fri Dec 16 19:21:45 UTC 2022
PRIMARY
PUBCHEM
8438
Created by admin on Fri Dec 16 19:21:45 UTC 2022 , Edited by admin on Fri Dec 16 19:21:45 UTC 2022
PRIMARY
MERCK INDEX
M8858
Created by admin on Fri Dec 16 19:21:45 UTC 2022 , Edited by admin on Fri Dec 16 19:21:45 UTC 2022
PRIMARY Merck Index
CAS
120-57-0
Created by admin on Fri Dec 16 19:21:45 UTC 2022 , Edited by admin on Fri Dec 16 19:21:45 UTC 2022
PRIMARY
ECHA (EC/EINECS)
204-409-7
Created by admin on Fri Dec 16 19:21:45 UTC 2022 , Edited by admin on Fri Dec 16 19:21:45 UTC 2022
PRIMARY
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