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About This Item
Linear Formula:
C6H4-1,3-(CO2CH3)2
CAS Number:
Molecular Weight:
194.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
215-951-9
Beilstein/REAXYS Number:
1912251
MDL number:
Assay:
99%
Product Name
Dimethyl isophthalate, ReagentPlus®, 99%
InChI key
VNGOYPQMJFJDLV-UHFFFAOYSA-N
InChI
1S/C10H10O4/c1-13-9(11)7-4-3-5-8(6-7)10(12)14-2/h3-6H,1-2H3
SMILES string
COC(=O)c1cccc(c1)C(=O)OC
vapor density
6.8 (vs air)
vapor pressure
93.7 mmHg ( 208 °C)
product line
ReagentPlus®
assay
99%
mp
64-68 °C (lit.)
functional group
ester
Quality Level
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Application
Dimethyl isophthalate was used in the synthesis of:
- polybutylene isophthalate end-capped with N-ethyl-pentadecafluorooctanamide
- poly(ethylene terephthalate-co-isophthalate-co-5-tert-butylisophthalate) terpolyesters
General description
Dimethyl isophthalate is dimethyl phthalate ester based plasticizer.
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
343.4 °F - closed cup
flash_point_c
173 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Poly(ethylene terephthalate) terpolyesters containing isophthalic and 5-tert-butylisophthalic units
Kint DPR, et al.
Journal of Polymer Science: Part A, General Papers, 41(1), 124-134 (2003)
Zhonggang Wang et al.
The journal of physical chemistry. B, 113(46), 15204-15211 (2009-10-22)
Polybutylene isophthalates (PBI) end-capped with N-ethyl-pentadecafluorooctanamide were synthesized from dimethyl isophthalate, 1,4-butanediol, and N-(2-hydroxyethyl)-perfluorooctanamide with fluorine monomer content from 0 to 5 mol %. The results demonstrated that there was an obvious gradient drop of fluorine concentration from the film
Zhu-Hua Luo et al.
Environmental science and pollution research international, 18(9), 1653-1660 (2011-06-01)
Dimethyl phthalate esters (DMPEs) are a group of plasticizers commonly detected in the environment with potential adverse human health impact. The degradation of DMPEs by fungal systems has been studied to a limited extent, particularly by yeasts. In this study
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