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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:
Product Name
Dimethyl terephthalate, purum, ≥99.0% (GC)
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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R I Goncharova et al.
Mutation research, 204(4), 703-709 (1988-04-01)
The mutagenic activity of dimethyl terephthalate (DMtP) was evaluated in the micronucleus test in mice. A clear clastogenic effect was obtained at all concentrations studied (0.2-1.0 mmole/kg body weight). The maximum number of micronuclei occurred 24 h after a single
Yu Ping Wang et al.
Ecotoxicology (London, England), 15(6), 549-557 (2006-09-07)
Two strains of bacteria were isolated from deep-ocean sediments of the South China Sea using enrichment culturing technique and they were identified as Sphingomonas yanoikuyae DOS01 (AY878409) and Variovorax paradoxus T4 (AY878410) based on 16S rRNA gene sequences. S. yanoikuyae
Liheng Feng et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 61(11-12), 2505-2509 (2005-07-27)
A novel luminescent compound, 9,9-bis[4'-(beta-naphthyl-methacrylate)phenyl]fluorene (F-NMAP) is synthesized by Heck reaction of beta-naphthyl methacrylic ester (NMAE) and 9,9-bis(4'-iodophenyl)-fluorene (BIPF). The structure is characterized by MS, 1H NMR, IR, and UV-vis spectroscopy. The photophysical processes of F-NMAP have been carefully investigated
[The basophil degranulation reaction as a method for detecting allergy and autoallergy to common chemical compounds].
G I Vinogradov et al.
Laboratornoe delo, (6)(6), 339-341 (1984-01-01)
Jiaxi Li et al.
Ecotoxicology (London, England), 15(4), 391-397 (2006-05-06)
Pasteurella multocida Sa, a bacterial strain isolated from mangrove sediment by enrichment technique, was capable of transforming dimethyl terephthalate (DMT). Biodegradation of DMT was shown to take place as a series of sequential steps involving the hydrolysis of two ester
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