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Details

Stereochemistry ACHIRAL
Molecular Formula C14H14O4
Molecular Weight 246.2586
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIALLYL PHTHALATE

SMILES

C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C

InChI

InChIKey=QUDWYFHPNIMBFC-UHFFFAOYSA-N
InChI=1S/C14H14O4/c1-3-9-17-13(15)11-7-5-6-8-12(11)14(16)18-10-4-2/h3-8H,1-2,9-10H2

HIDE SMILES / InChI
Molecular Formula C14H14O4
Molecular Weight 246.2586
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
149124
PubMed

PubMed

TitleDatePubMed
Structure-dependent activity of phthalate esters and phthalate monoesters binding to human constitutive androstane receptor.
2015-06-15
Evaluation of aggregating brain cell cultures for the detection of acute organ-specific toxicity.
2013-06
FT Raman--a valuable tool for surveying kinetics in RCM of functionalized dienes.
2010-09-15
A proteomics based approach to assessing the toxicity of bisphenol A and diallyl phthalate to the abalone (Haliotis diversicolor supertexta).
2010-04
Chemical analysis and risk assessment of diethyl phthalate in alcoholic beverages with special regard to unrecorded alcohol.
2009-12-02
Screening method for phthalate esters in water using liquid-phase microextraction based on the solidification of a floating organic microdrop combined with gas chromatography-mass spectrometry.
2008-08-15
Multixenobiotic resistance, acetyl-choline esterase activity and total oxyradical scavenging capacity of the Arctic spider crab, Hyasaraneus, following exposure to bisphenol A, tetra bromo diphenyl ether and diallyl phthalate.
2008-08
Release kinetics of procaine hydrochloride (PrHy) from pH-responsive nanogels: theory and experiments.
2008-06-05
Evaluation of the developmental toxicity of diallyl phthalate administered orally to rats.
2008-06
Effect of ultrasonic separation on the structure and properties of diallyl phthalate prepolymer.
2008-04
Comparative drug release studies of two cationic drugs from pH-responsive nanogels.
2007-12
Development of dispersive liquid-liquid microextraction combined with gas chromatography-mass spectrometry as a simple, rapid and highly sensitive method for the determination of phthalate esters in water samples.
2007-11-23
Identification of proteomic signatures of exposure to marine pollutants in mussels (Mytilus edulis).
2006-07
An overview of the BEEP Stavanger workshop.
2006-06-01
An ecotoxicoproteomic approach (SELDI-TOF mass spectrometry) to biomarker discovery in crab exposed to pollutants under laboratory conditions.
2006-06-01
Induction of micronuclei and other nuclear abnormalities in mussels exposed to bisphenol A, diallyl phthalate and tetrabromodiphenyl ether-47.
2006-06-01
Protein responses in blue mussels (Mytilus edulis) exposed to organic pollutants: a combined CYP-antibody/proteomic approach.
2006-06-01
Specificity of the peroxisome proliferation response in mussels exposed to environmental pollutants.
2006-06-01
Expression of cytoskeletal proteins, cross-reacting with anti-CYP1A, in Mytilus sp. exposed to organic contaminants.
2006-06-01
Effects of seawater pollutants on protein tyrosine phosphorylation in mussel tissues.
2006-06-01
Preliminary study of responses in mussel (Mytilus edilus) exposed to bisphenol A, diallyl phthalate and tetrabromodiphenyl ether.
2006-06-01
Alteration of steroid hormone balance in juvenile turbot (Psetta maxima) exposed to nonylphenol, bisphenol A, tetrabromodiphenyl ether 47, diallylphthalate, oil, and oil spiked with alkylphenols.
2006-05
Biomarkers of exposure and reproduction-related effects in mussels exposed to endocrine disruptors.
2006-04
Adsorption of phthalic acid and its esters onto high-area activated carbon-cloth studied by in situ UV-spectroscopy.
2005-06-30
Differential effects of phthalate esters on transcriptional activities via human estrogen receptors alpha and beta, and androgen receptor.
2005-06-01
Microstructure and rheology of stimuli-responsive microgel systems--effect of cross-linked density.
2005-05-30
Osmotic compressibility of soft colloidal systems.
2005-05-10
Microstructure and rheology of stimuli-responsive nanocolloidal systems-effect of ionic strength.
2004-12-21
A simple and reproducible testing method for dialkyl phthalate migration from polyvinyl chloride products into saliva simulant.
2003-02
Patents

Patents

JP2000147212A
1
JP2000284237A
1
JP2001040179A
1
JP2002061716A
1
JP2002241566A
1
JP2003040948A
1
JP2003192858A
1
JP2003246872A
1
JP2003515642A
2
JP2004043563A
1
JP2004526030A
6
JP2007324142A
1
JP2008255338A
1
JP2009074065A
1
JP2011168791A
1
JP2011506746A
2
JPH02123139A
1
JPH02129265A
1
JPH0291146A
1
JPH03217409A
1
JPH03247613A
1
JPH03281512A
1
JPH0411648A
1
JPH04136857A
1
JPH04159324A
1
JPH05148392A
1
JPH06136075A
1
JPH06157690A
1
JPH06279557A
1
JPH07126425A
1
JPH0952971A
1
JPH11106445A
1
JPH11116750A
1
JPH11140777A
1
JPH11240923A
1
JPH11255864A
1
JPS05569610A
1
JPS06123641A
1
JPS06126660A
1
JPS06164733A
1
JPS06222811A
1
JPS5291033A
1
JPS5410346A
1
JPS5422336A
1
JPS5473900A
1
JPS55149940A
1
JPS56122820A
1
JPS56155211A
1
JPS5636526A
1
JPS5643335A
1
JPS5681381A
1
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:54:26 GMT 2025
Edited
by admin
on Mon Mar 31 21:54:26 GMT 2025
Record UNII
F79L0UL6ST
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DAPON 35
Preferred Name English
DIALLYL PHTHALATE
HSDB  
Systematic Name English
ALLYL PHTHALATE
Systematic Name English
DI-2-PROPENYL 1,2-BENZENEDICARBOXYLATE
Systematic Name English
DIALLYL PHTHALATE [HSDB]
Common Name English
1,2-BENZENEDICARBOXYLIC ACID, 1,2-DI-2-PROPEN-1-YL ESTER
Systematic Name English
1,2-BENZENEDICARBOXYLIC ACID, DI-2-PROPENYL ESTER
Common Name English
PHTHALIC ACID, DIALLYL ESTER
Systematic Name English
O-PHTHALIC ACID, DIALLYL ESTER
Systematic Name English
NSC-7667
Code English
Code System Code Type Description
CAS
131-17-9
Created by admin on Mon Mar 31 21:54:26 GMT 2025 , Edited by admin on Mon Mar 31 21:54:26 GMT 2025
PRIMARY
EPA CompTox
DTXSID7020392
Created by admin on Mon Mar 31 21:54:26 GMT 2025 , Edited by admin on Mon Mar 31 21:54:26 GMT 2025
PRIMARY
ECHA (EC/EINECS)
205-016-3
Created by admin on Mon Mar 31 21:54:26 GMT 2025 , Edited by admin on Mon Mar 31 21:54:26 GMT 2025
PRIMARY
NSC
7667
Created by admin on Mon Mar 31 21:54:26 GMT 2025 , Edited by admin on Mon Mar 31 21:54:26 GMT 2025
PRIMARY
FDA UNII
F79L0UL6ST
Created by admin on Mon Mar 31 21:54:26 GMT 2025 , Edited by admin on Mon Mar 31 21:54:26 GMT 2025
PRIMARY
SMS_ID
300000053316
Created by admin on Mon Mar 31 21:54:26 GMT 2025 , Edited by admin on Mon Mar 31 21:54:26 GMT 2025
PRIMARY
HSDB
4169
Created by admin on Mon Mar 31 21:54:26 GMT 2025 , Edited by admin on Mon Mar 31 21:54:26 GMT 2025
PRIMARY
PUBCHEM
8560
Created by admin on Mon Mar 31 21:54:26 GMT 2025 , Edited by admin on Mon Mar 31 21:54:26 GMT 2025
PRIMARY
NIH
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