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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

PubMed

PubMed

TitleDatePubMed
A simple and reproducible testing method for dialkyl phthalate migration from polyvinyl chloride products into saliva simulant.
2003 Feb
Microstructure and rheology of stimuli-responsive nanocolloidal systems-effect of ionic strength.
2004 Dec 21
Differential effects of phthalate esters on transcriptional activities via human estrogen receptors alpha and beta, and androgen receptor.
2005 Jun 1
Osmotic compressibility of soft colloidal systems.
2005 May 10
Biomarkers of exposure and reproduction-related effects in mussels exposed to endocrine disruptors.
2006 Apr
An overview of the BEEP Stavanger workshop.
2006 Jun 1
An ecotoxicoproteomic approach (SELDI-TOF mass spectrometry) to biomarker discovery in crab exposed to pollutants under laboratory conditions.
2006 Jun 1
Induction of micronuclei and other nuclear abnormalities in mussels exposed to bisphenol A, diallyl phthalate and tetrabromodiphenyl ether-47.
2006 Jun 1
Protein responses in blue mussels (Mytilus edulis) exposed to organic pollutants: a combined CYP-antibody/proteomic approach.
2006 Jun 1
Specificity of the peroxisome proliferation response in mussels exposed to environmental pollutants.
2006 Jun 1
Expression of cytoskeletal proteins, cross-reacting with anti-CYP1A, in Mytilus sp. exposed to organic contaminants.
2006 Jun 1
Effects of seawater pollutants on protein tyrosine phosphorylation in mussel tissues.
2006 Jun 1
Preliminary study of responses in mussel (Mytilus edilus) exposed to bisphenol A, diallyl phthalate and tetrabromodiphenyl ether.
2006 Jun 1
Comparative drug release studies of two cationic drugs from pH-responsive nanogels.
2007 Dec
Effect of ultrasonic separation on the structure and properties of diallyl phthalate prepolymer.
2008 Apr
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 Aug
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 Aug 15
Chemical analysis and risk assessment of diethyl phthalate in alcoholic beverages with special regard to unrecorded alcohol.
2009 Dec 2
Evaluation of aggregating brain cell cultures for the detection of acute organ-specific toxicity.
2013 Jun
Structure-dependent activity of phthalate esters and phthalate monoesters binding to human constitutive androstane receptor.
2015 Jun 15
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 08:08:56 GMT 2023
Edited
by admin
on Sat Dec 16 08:08:56 GMT 2023
Record UNII
F79L0UL6ST
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
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
DAPON 35
Brand 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 Sat Dec 16 08:08:56 GMT 2023 , Edited by admin on Sat Dec 16 08:08:56 GMT 2023
PRIMARY
EPA CompTox
DTXSID7020392
Created by admin on Sat Dec 16 08:08:56 GMT 2023 , Edited by admin on Sat Dec 16 08:08:56 GMT 2023
PRIMARY
ECHA (EC/EINECS)
205-016-3
Created by admin on Sat Dec 16 08:08:56 GMT 2023 , Edited by admin on Sat Dec 16 08:08:56 GMT 2023
PRIMARY
NSC
7667
Created by admin on Sat Dec 16 08:08:56 GMT 2023 , Edited by admin on Sat Dec 16 08:08:56 GMT 2023
PRIMARY
FDA UNII
F79L0UL6ST
Created by admin on Sat Dec 16 08:08:56 GMT 2023 , Edited by admin on Sat Dec 16 08:08:56 GMT 2023
PRIMARY
HSDB
4169
Created by admin on Sat Dec 16 08:08:56 GMT 2023 , Edited by admin on Sat Dec 16 08:08:56 GMT 2023
PRIMARY
PUBCHEM
8560
Created by admin on Sat Dec 16 08:08:56 GMT 2023 , Edited by admin on Sat Dec 16 08:08:56 GMT 2023
PRIMARY