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Supelco

Diallyl phthalate

analytical standard

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About This Item

Linear Formula:
C6H4-1,2-(CO2CH2CH=CH2)2
CAS Number:
Molecular Weight:
246.26
Beilstein:
1880877
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

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

refractive index

n20/D 1.519 (lit.)

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

SMILES string

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

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

InChI key

QUDWYFHPNIMBFC-UHFFFAOYSA-N

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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.

Recommended products

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

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

330.8 °F - closed cup

Flash Point(C)

166 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number

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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
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
N Aarab et al.
Aquatic toxicology (Amsterdam, Netherlands), 78 Suppl 1, S86-S92 (2006-04-04)
Environmental pollutants with hormonal activity including bisphenol, diallyl phtalate and tetrabromodiphenyl ether, have the potential to alter gonadal development and reproduction in aquatic wildlife. Little is known about the biological impact of environmentally relevant concentrations in mussels. To investigate some
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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