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Merck

86440

Dimethyl terephthalate

purum, ≥99.0% (GC)

Synonym(s):

DMT, Dimethyl 1,4-benzenedicarboxylate, Dimethyl p-benzenedicarboxylate, Dimethyl p-phthalate, Methyl 4-(carbomethoxy)benzoate

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About This Item

Linear Formula:
C6H4-1,4-(CO2CH3)2
CAS Number:
Molecular Weight:
194.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-411-8
Beilstein/REAXYS Number:
1107185
MDL number:
Assay:
≥99.0% (GC)
Form:
powder, crystals or chunks
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InChI key

WOZVHXUHUFLZGK-UHFFFAOYSA-N

InChI

1S/C10H10O4/c1-13-9(11)7-3-5-8(6-4-7)10(12)14-2/h3-6H,1-2H3

SMILES string

COC(=O)c1ccc(cc1)C(=O)OC

vapor density

1.04 (vs air)

vapor pressure

1.15 mmHg ( 93 °C)

grade

purum

assay

≥99.0% (GC)

form

powder, crystals or chunks

autoignition temp.

1058 °F

mp

139-141 °C (lit.), 140-142 °C

functional group

ester

Quality Level

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Storage Class

11 - Combustible Solids

wgk

WGK 1

flash_point_f

309.2 °F - (External MSDS)

flash_point_c

154 °C - (External MSDS)

ppe

Eyeshields, Gloves, type N95 (US)


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S Monarca et al.
Mutation research, 262(2), 85-92 (1991-02-01)
Dimethyl terephthalate (DMTP), the para configuration of dimethyl phthalate, is one of the basic monomers used in the synthesis of polyethylene terephthalate (PET) plastics. Human exposure to DMTP may primarily occur during the manufacture of PET fibers and films. The
S H Ganji et al.
Biodegradation, 6(1), 61-66 (1995-01-01)
Aspergillus niger (AG-1) metabolized dimethylterephthalate through monomethylterephthalate, terephthalate and protocatechuate. Degradation of dimethylterephthalate was followed by extraction of residual dimethylterephthalate from the spent medium. The quantitative UV analysis showed that 58% of the dimethylterephthalate supplement was taken up in 144
Minoru Genta et al.
Waste management (New York, N.Y.), 27(9), 1167-1177 (2006-08-18)
To apply PET depolymerization in supercritical methanol to commercial recycling, the benefits of supercritical methanol usage in PET depolymerization was investigated from the viewpoint of the reaction rate and energy demands. PET was depolymerized in a batch reactor at 573
[Use of statistical values in plotting dose-effect relationships and determining the action thresholds of factors].
M G Shandala et al.
Gigiena i sanitariia, (7)(7), 26-28 (1986-07-01)
Zhiqiang Guo et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 68(2), 337-340 (2007-02-28)
Two 10-hydroxybenzo[h]quinoline metal complexes, bis(10-hydroxybenzo[h]quinolinato) beryllium (Bebq2) and bis(10-hydroxybenzo[h]quinolinato)zincum (Znbq2), have been synthesized. The structure are characterized by 1HNMR, IR and so on. The photophysical processes of Bebq2 and Znbq2 have been carefully investigated by fluorescence spectra. The results show

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