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Merck
CN

31298

Dimethyl terephthalate

analytical standard

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About This Item

Linear Formula:
C6H4-1,4-(CO2CH3)2
CAS Number:
120-61-6
Molecular Weight:
194.18
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329753745
EC Number:
204-411-8
Beilstein/REAXYS Number:
1107185
MDL number:
MFCD00008440

Key Documents

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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

grade

analytical standard

vapor density

1.04 (vs air)

vapor pressure

1.15 mmHg ( 93 °C)

assay

≥98% (HPLC)

form

powder, crystals or chunks ((pellets))

autoignition temp.

1058 °F

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

Quality Level

100

application(s)

environmental

format

neat

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General description

This substance is listed on the positive list of the EU regulation 10/2011 for plastics intended to come into contact with food.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Other Notes

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Legal Information

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

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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Certificates of Analysis (COA)

Lot/Batch Number
BCBW5357

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D S Patel et al.
Indian journal of experimental biology, 36(3), 321-324 (1998-10-01)
Comamonas acidovorans D-4, capable of utilizing dimethylterephthalate (DMT) as the sole carbon source, was isolated from the activated sludge of petrochemical wastewater treatment plant. Almost complete utilization of as high as 0.5% (w/v) DMT was observed in 72 hr. Growth
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
L Tserovska et al.
Acta microbiologica Bulgarica, 30, 61-66 (1993-01-01)
The microbial association 189 was isolated from soil treated with dimethylterephthalate (DMT) for a long time. The dynamics of its growth, respectively the degradation of the terephthalate ester known as an environmental pollutant has been studied.
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
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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