07038

Supelco

Dimethyl terephthalate

Standard for quantitative NMR, TraceCERT®

Linear Formula:
C6H4-1,4-(CO2CH3)2
CAS Number:
Molecular Weight:
194.18
Beilstein/REAXYS Number:
1107185
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.24
Pricing and availability is not currently available.

Quality Level

grade

Standard for quantitative NMR
certified reference material
TraceCERT®

vapor density

1.04 (vs air)

vapor pressure

1.15 mmHg ( 93 °C)

description

qNMR Standard for DMSO-d6 (9.2 ppm)

CofA

certificate is enclosed in each package

autoignition temp.

1058 °F

shelf life

limited shelf life, expiry date on the label

application(s)

gas chromatography (GC): suitable
qNMR: suitable

mp

139-141 °C (lit.)

Featured Industry

Cleaning Products
Cosmetics
Environmental
Flavors and Fragrances
Food and Beverages
Personal Care

format

neat

SMILES string

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

InChI key

WOZVHXUHUFLZGK-UHFFFAOYSA-N

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General description

This certified reference material (CRM) is produced and certified in accordance with ISO/IEC 17025 and ISO 17034. This CRM is traceable to primary material from an NMI, e.g. NIST or NMIJ.
Certified content by quantitative NMR incl. uncertainty and expiry date are given on the certificate.
Download your certificate at: http://www.sigma-aldrich.com.

Caution

Store under Argon.

Other Notes

Chemcial Shift: 8.1 and 3.9 ppm (chemical shifts may slightly vary depending on the experimental conditions)
Suitable NMR solvents: Acetonitrile, Chloroform, MeOD, DMSO-d6

Legal Information

TraceCERT is a registered trademark of Sigma-Aldrich Co. LLC

RIDADR

NONH for all modes of transport

WGK Germany

WGK 1

Flash Point(F)

303.8 °F - closed cup

Flash Point(C)

151 °C - closed cup

Certificate of Analysis
Certificate of Origin
[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)
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...
Z Chen et al.
Guang pu xue yu guang pu fen xi = Guang pu, 21(3), 362-365 (2003-09-02)
The fluorescence quenching of perylene and pyrene by dimethyl terephthalate (DMTP) and N,N-dimethylaniline (DMA) have been investigated. The results show that pyrene can form exciplex with DMTP or DMA at room temperature and perylene can only form exciplex with DMA....
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...
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...
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