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524972

Sigma-Aldrich

Diethyl phthalate

99.5%

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Synonym(s):
1,2-Benzodioic acid diethyl ester, 1,2-Diethyl benzene-1,2-dicarboxylate, Diethyl 1,2-benzenedicarboxylate, Ethyl phthalate, Neantine, o-Benzenedicarboxylic acid diethyl ester
Linear Formula:
C6H4-1,2-(CO2C2H5)2
CAS Number:
Molecular Weight:
222.24
Beilstein/REAXYS Number:
1912500
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor density

7.66 (vs air)

Quality Level

vapor pressure

1 mmHg ( 100 °C)

assay

99.5%

form

liquid

autoignition temp.

854 °F

expl. lim.

0.75 %, 187 °F

impurities

≤0.18% water

color

APHA: ≤15

refractive index

n20/D 1.502 (lit.)

bp

298-299 °C (lit.)

mp

−3 °C (lit.)

density

1.12 g/mL at 25 °C (lit.)

SMILES string

CCOC(=O)c1ccccc1C(=O)OCC

InChI

1S/C12H14O4/c1-3-15-11(13)9-7-5-6-8-10(9)12(14)16-4-2/h5-8H,3-4H2,1-2H3

InChI key

FLKPEMZONWLCSK-UHFFFAOYSA-N

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General description

Diethyl phthalate (DEP) is a phthalic anhydride ester (PAE) that is commonly used as a solvent in cosmetics and also as a plasticizer.

Application

Diethyl phthalate can be used as a solvent for the antimony reduction of aluminum chloride-phosphorus trichloride-alkyl chloride complexes to form the corresponding alkylphosphonous dichlorides. It can undergo condensation with o-phenylenediamine in the presence of sodium hydride to form dibenzo (b,f)(1,4)diazocine-6,11(5H, 12H)-dione.

Other Notes

Plasticizer.

wgk_germany

WGK 2

ppe

Eyeshields, Gloves


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Dimethyl phthalate PESTANAL®, analytical standard

Supelco

41320

Dimethyl phthalate

Diisononyl phthalate ester content ≥99 % (mixture of C9 isomers), technical grade

Sigma-Aldrich

376663

Diisononyl phthalate

Dioctyl phthalate ≥99.5%

Sigma-Aldrich

D201154

Dioctyl phthalate

Dibutyl phthalate PESTANAL®, analytical standard

Supelco

36736

Dibutyl phthalate

Diazocine chemistry. V. Synthesis and rearrangement of dibenzo [b, f][1, 4] diazocine-6, 11 (5H, 12H)-dione.
Paudler W W and Zeiler A G
The Journal of Organic Chemistry, 34(7), 2138-2140 (1969)
The synthesis of alkylphosphonous dichlorides from aluminum chloride?phosphorus trichloride?alkyl chloride complexes.
Perry B J, et al.
Canadian Journal of Chemistry, 41(9), 2299-2302 (1963)
Maik Hadorn et al.
Proceedings of the National Academy of Sciences of the United States of America, 109(50), 20320-20325 (2012-11-24)
Higher-order structures that originate from the specific and reversible DNA-directed self-assembly of microscopic building blocks hold great promise for future technologies. Here, we functionalized biotinylated soft colloid oil-in-water emulsion droplets with biotinylated single-stranded DNA oligonucleotides using streptavidin as an intermediary
Lee-Ju Cheng et al.
Aquatic toxicology (Amsterdam, Netherlands), 109, 166-175 (2011-10-28)
The toxicity and effects of diethyl phthalate (DEP), a potent allelochemical, on the growth of greater duckweed were studied. Biochemical analyses and physiological methods were combined to investigate oxidative stress, adverse effects and their mechanisms in greater duckweeds grown in
Antonia M Calafat et al.
Environmental health perspectives, 114(11), 1783-1789 (2006-11-17)
The probability of nonoccupational exposure to phthalates is high given their use in a vast range of consumables, including personal care products (e.g., perfumes, lotions, cosmetics), paints, industrial plastics, and certain medical devices and pharmaceuticals. Phthalates are of high interest

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