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185124

Sigma-Aldrich

Dimethyl terephthalate

ReagentPlus®, ≥99%

Sinonimo/i:

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

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About This Item

Formula condensata:
C6H4-1,4-(CO2CH3)2
Numero CAS:
120-61-6
Peso molecolare:
194.18
Beilstein:
1107185
Numero CE:
204-411-8
Numero MDL:
MFCD00008440
Codice UNSPSC:
12352100
eCl@ss:
39024601
ID PubChem:
24850669
NACRES:
NA.22

Densità del vapore

1.04 (vs air)

Livello qualitativo

200

Tensione di vapore

1.15 mmHg ( 93 °C)

Nome Commerciale

ReagentPlus®

Saggio

≥99%

Forma fisica

(Powder or Crystals or Chunk(s))

Temp. autoaccensione

1058 °F

Punto di fusione

139-141 °C (lit.)

Solubilità

water: slightly soluble 0.0493 g/L at 20 °C

Stringa SMILE

COC(=O)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
WOZVHXUHUFLZGK-UHFFFAOYSA-N

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Descrizione generale

Dimethyl terephthalate undergoes enzymatic polycondensation with 1,8-diaminooctane to yield oligo(octamethylene terephthalamide).

Applicazioni

Dimethyl terephthalate was used to synthesize silicone aromatic polyesters by the transesterification reaction with α,ω-bis(hydroxyalkyl)-terminated poly(dimethylsiloxane) in toluene. It was used in the synthesis of multiblock copolymers consisting of polyiso-butylene, dimethyl terephthalate and 1,4-butanediol.

Note legali

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

309.2 °F - (External MSDS)

Punto d’infiammabilità (°C)

154 °C - (External MSDS)

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

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Certificati d'analisi (COA)

Lot/Batch Number
BCCH3676
BCCF6710
BCCD5713
BCBX9603
BCBW3254

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Yadagiri Poojari et al.
Chemical communications (Cambridge, England), (44)(44), 6834-6835 (2009-11-04)
Immobilized Candida antarctica lipase B (CALB) was successfully employed as a catalyst to synthesize silicone aromatic polyesters by the transesterification of dimethyl terephthalate with alpha,omega-bis(hydroxyalkyl)-terminated poly(dimethylsiloxane) in toluene under mild reaction conditions.
Tristan A Geervliet et al.
Chemistry, an Asian journal, 14(6), 877-883 (2018-12-15)
This study reports for the first time the use of bio-based alternatives for PMMA as host matrix for luminescent solar concentrators (LSCs). Notably, two types of renewable polyesters were synthesized in varying molar ratios via a two-step melt-polycondensation reaction with
E Stavila et al.
Biomacromolecules, 14(5), 1600-1606 (2013-04-03)
Enzymatically catalyzed polycondensation of p-xylylenediamine and diethyl sebacate resulted in oligo(p-xylylene sebacamide) with high melting temperatures (223-230 °C) and the enzymatic polycondensation of dimethyl terephthalate and 1,8-diaminooctane leads to oligo(octamethylene terephthalamide) with two melting temperatures at 186 and 218 °C.
Copolyesters containing polyisobutylene soft segments and polybutylene terephthalate as the crystalline segments.
Deak G and Kennedy JP.
Journal of Macromolecular Science, Part A: Pure and Applied Chemistry, 33(S7-8), 439-449 (1996)
R I Goncharova et al.
Genetika, 24(7), 1226-1233 (1988-07-01)
Mutagenic activity of dimethyl terephthalate (DMtP) was evaluated using the bone marrow micronucleus test in mice. Clear clastogenic effect with the highest response in 24 h after a single i.p. injection was obtained at all concentrations used (0.2-1.0 mM/kg). The
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