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W512206

Sigma-Aldrich

Diethyl phthalate

≥99%

Synonym(s):

Anozol, Diethyl benzene-1,2-dicarboxylate

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About This Item

Linear Formula:
C6H4-1,2-(CO2C2H5)2
CAS Number:
Molecular Weight:
222.24
Beilstein:
1912500
EC Number:
MDL number:
UNSPSC Code:
12164502
PubChem Substance ID:
NACRES:
NA.21

biological source

synthetic

vapor density

7.66 (vs air)

vapor pressure

1 mmHg ( 100 °C)

Assay

≥99%

form

liquid

autoignition temp.

854 °F

expl. lim.

0.75 %, 187 °F

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.)

application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

food allergen

no known allergens

Organoleptic

odorless

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 is commonly used as a vehicle for fragrances and cosmetic ingredients. It is one of the volatile compounds found in rice cultivars and starfruit.

Disclaimer

For R&D or non-EU Food use. Not for retail sale.

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

338.0 °F - closed cup

Flash Point(C)

170 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Volatile profiles of aromatic and non-aromatic rice cultivars using SPME/GC-MS
Bryant RJ and McClung AM.
Food Chemistry, 124(2), 501-513 (2011)
Volatile components of starfruit
MacLeod G and Ames JM
Phytochemistry, 29(1), 165-172 (1990)
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
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
Raphael J Witorsch et al.
Critical reviews in toxicology, 40 Suppl 3, 1-30 (2010-10-12)
This article reviews laboratory and epidemiological research into the endocrine disruptive effects of components of personal care products, namely, phthalate esters, parabens, ultraviolet (UV) filters, polycyclic musks, and antimicrobials. High doses of phthalates in utero can produce “phthalate syndrome,” demasculinizing

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