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About This Item
Empirical Formula (Hill Notation):
C14H18O6
CAS Number:
Molecular Weight:
282.29
Beilstein:
2056929
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
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grade
technical
Assay
≥90% (GC)
form
liquid
refractive index
n20/D 1.503
bp
230 °C/10 mmHg (lit.)
density
1.173 g/mL at 20 °C (lit.)
SMILES string
COCCOC(=O)c1ccccc1C(=O)OCCOC
InChI
1S/C14H18O6/c1-17-7-9-19-13(15)11-5-3-4-6-12(11)14(16)20-10-8-18-2/h3-6H,7-10H2,1-2H3
InChI key
HSUIVCLOAAJSRE-UHFFFAOYSA-N
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Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Repr. 1B
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 1
Flash Point(F)
249.8 °F - closed cup
Flash Point(C)
121 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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E J Ritter et al.
Teratology, 32(1), 25-31 (1985-08-01)
It is hypothesized that the known teratogen di(2-methoxyethyl) phthalate (DMEP) acts by in vivo hydrolysis to 2-methoxyethanol (2-ME), also a known teratogen, which in turn is metabolized to methoxyacetic acid (MAA), the proximate teratogen. Teratological studies were conducted with Wistar
Yuki Ito et al.
Journal of occupational health, 49(3), 172-182 (2007-06-19)
Di(2-ethylhexyl)phthalate (DEHP), a commonly used industrial plasticizer, causes liver tumorigenesis presumably via activation of peroxisome proliferator-activated receptor alpha (PPARalpha). The mechanism of DEHP tumorigenesis has not been fully elucidated, and to clarify whether DEHP tumorigenesis is induced via PPARalpha, we
S L Cassidy et al.
Archives of toxicology, 53(1), 71-78 (1983-05-01)
Single dosages of DMEP (1,000-2,000 mg/kg), GMCH (50 mg/kg), ECH (25 and 50 mg/kg), FA (100 and 200 mg/kg), and MMS (100-400 mg/kg) were administered orally to 10 week old male Wistar rats. The rats were necropsied on the 11th
R Gollamudi et al.
Journal of applied toxicology : JAT, 5(6), 368-371 (1985-12-01)
Di(2-ethylhexyl)phthalate (DEHP) inhibited UDP-glucuronyltransferase activity of rat liver in vitro and in vivo. Diethyl phthalate and dimethoxyethyl phthalate also inhibited this enzyme in vitro. On the other hand, DEHP did not inhibit the activity of the cytosolic enzyme N-acetyltransferase; it
J Campbell et al.
Journal of applied toxicology : JAT, 4(1), 35-41 (1984-02-01)
The rat foetus, in contrast with the maternal liver and placenta, has little or no ability to hydrolyse di-(2-methoxyethyl)-phthalate (DMEP) to mono-2-methoxyethyl)-phthalate (MMEP). At short times after the administration of DMEP to the dam on the 14th day of gestation
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