524972
Diethyl phthalate
99.5%
Sinónimos:
DEP
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Fórmula lineal:
C6H4-1,2-(CO2C2H5)2
Número CAS:
Peso molecular:
222.24
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-550-6
Beilstein/REAXYS Number:
1912500
MDL number:
Assay:
99.5%
Bp:
298-299 °C (lit.)
Vapor pressure:
1 mmHg ( 100 °C)
Servicio técnico
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Permítanos ayudarlevapor density
7.66 (vs air)
Quality Level
vapor pressure
1 mmHg ( 100 °C)
assay
99.5%
autoignition temp.
854 °F
expl. lim.
0.75 %, 187 °F
impurities
≤0.18% water
color
APHA: ≤25
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.)
functional group
ester
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
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.
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Clase de almacenamiento
10 - Combustible liquids
wgk
WGK 2
flash_point_f
338.0 °F - closed cup
flash_point_c
170 °C - closed cup
ppe
Eyeshields, Gloves
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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)
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