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| MeSHName = Dimethyl+4-phthalate | | MeSHName = Dimethyl+4-phthalate | ||
| RTECS = WZ1225000 | | RTECS = WZ1225000 | ||
| StdInChI = 1S/C10H10O4/c1-13-9(11)7-3-5-8(6-4-7)10(12)14-2/h3-6H,1-2H3 | |||
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| StdInChIKey = WOZVHXUHUFLZGK-UHFFFAOYSA-N | |||
⚫ | | SMILES = COC(=O)C1=CC=C(C=C1)C(=O)OC | ||
| SMILES1 = O=C(OC)c1ccc(cc1)C(=O)OC | | SMILES1 = O=C(OC)c1ccc(cc1)C(=O)OC | ||
| InChI = 1S/C10H10O4/c1-13-9(11)7-3-5-8(6-4-7)10(12)14-2/h3-6H,1-2H3 | | InChI = 1S/C10H10O4/c1-13-9(11)7-3-5-8(6-4-7)10(12)14-2/h3-6H,1-2H3 |
Revision as of 15:08, 8 August 2011
Names | |
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Preferred IUPAC name Dimethyl terephthalate | |
Systematic IUPAC name 1,4-Dimethyl benzene-1,4-dicarboxylate | |
Other names
1,4-Benzenedicarboxylic acid dimethyl ester Dimethyl 4-phthalate | |
Identifiers | |
CAS Number | |
3D model (JSmol) | |
Abbreviations | DMT |
Beilstein Reference | 1107185 |
ChemSpider | |
ECHA InfoCard | 100.004.011 |
EC Number |
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MeSH | Dimethyl+4-phthalate |
PubChem CID | |
RTECS number |
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CompTox Dashboard (EPA) | |
InChI
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SMILES
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Properties | |
Chemical formula | C10H10O4 |
Molar mass | 194.186 g·mol |
Appearance | white solid |
Density | 1.2 g/cm³, ? |
Melting point | 142 °C (288 °F; 415 K) |
Boiling point | 288 °C (550 °F; 561 K) |
Acidity (pKa) | -7.21 |
Basicity (pKb) | -6.60 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Y verify (what is ?) Infobox references |
Dimethyl terephthalate (DMT) is an organic compound with the formula C6H4(CO2CH3)2. It is the diester formed from terephthalic acid and methanol. It is a white solid that melts to give a distillable colourless liquid.
Production
DMT has been produced in a number of ways. Conventionally and still of commercial value is the direct esterification of terephthalic acid. Alternatively, it can be prepared by alternating oxidation and methyl-esterification steps from p-xylene via methylp-toluate.
Use
DMT is used in the production of polyesters, including polyethylene terephthalate (PET) and polytrimethylene terephthalate. It consists of benzene substituted with carboxymethyl groups (CO2CH3) at the 1 and 4 positions. Because DMT is volatile, it is an intermediate is some schemes for the recyclic of PET, e.g. from plastic bottles.
Hydrogenation of DMT affords the diol cyclohexanedimethanol, which is a useful monomer.
References
- ^ Richard J. Sheehan "Terephthalic Acid, Dimethyl Terephthalate, and Isophthalic Acid" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2005.doi:10.1002/14356007.a26_193
External links
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