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Merck
CN

36925

Diallyl phthalate

analytical standard

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About This Item

Linear Formula:
C6H4-1,2-(CO2CH2CH=CH2)2
CAS Number:
131-17-9
Molecular Weight:
246.26
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329755540
EC Number:
205-016-3
Beilstein/REAXYS Number:
1880877
MDL number:
MFCD00008646

Key Documents

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InChI key

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

SMILES string

C=CCOC(=O)c1ccccc1C(=O)OCC=C

grade

analytical standard

vapor density

8.3 (vs air)

vapor pressure

2.3 mmHg ( 150 °C)

autoignition temp.

725 °F

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

Quality Level

100

bp

165-167 °C/5 mmHg (lit.)

density

1.121 g/mL at 25 °C (lit.)

application(s)

cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

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General description

This substance is listed on the positive list of the EU regulation 10/2011 for plastics intended to come into contact with food. Find all available reference materials for compounds listed in 10/2011 here

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Other Notes

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1B

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

330.8 °F - closed cup

flash_point_c

166 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
BCCP2638
BCCN1846
BCCG6132
BCCF2972
BCBT9657

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A M Saillenfait et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 46(6), 2150-2156 (2008-04-01)
The objective of this study was to evaluate the developmental toxic potential of diallyl phthalate (DAP) in rats. Pregnant Sprague-Dawley rats were given DAP at doses of 0 (olive oil), 100, 150, 200, and 250mg/kg/day, by gavage (5ml/kg), on Gestational
Christophe Minier et al.
Marine pollution bulletin, 56(8), 1410-1415 (2008-07-05)
The Arctic has become a sink for persistent organic pollutants (POPs) originating from lower latitudes, and relatively high levels have been found in different biota. Recent studies have identified detrimental effects on wildlife including endocrine disruption, impairment of enzyme activity
Jin Zhou et al.
Chemosphere, 79(5), 595-604 (2010-03-02)
The contamination of marine ecosystems by endocrine disrupting compounds (EDCs) is of great concern. Protein expression profile maybe a good method to help us understand the molecular mechanisms of EDCs-toxicity to aquatic organisms. In this study, the abalone (Haliotis diversicolor
Beng H Tan et al.
Advances in colloid and interface science, 113(2-3), 111-120 (2005-06-07)
The effect of cross-linked density on the rheological behavior of model pH-responsive microgel systems consisting of methacrylic acid-ethyl acrylate (MAA-EA) cross-linked with di-allyl phthalate (DAP) was examined. Neutralization of acid groups increases the osmotic pressure exerted by counter-ions trapped in
Janina Barsiene et al.
Aquatic toxicology (Amsterdam, Netherlands), 78 Suppl 1, S105-S108 (2006-04-18)
Analysis of micronuclei, nuclear buds, bi-polynucleated and fragmented-apoptotic cells was performed in gills of blue mussels exposed for 3 weeks to sublethal concentrations of bisphenol A, diallyl phthalate (for the both nominal concentration 50 ppb) and to tetrabromodiphenyl ether-47 (nominal
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