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409758

Sigma-Aldrich

N,N-Dimethyl-1,4-phenylenediamine oxalate

98%

Synonym(s):

N,N-Dimethyl-p-phenylenediamine hemioxalate salt

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About This Item

Linear Formula:
[(CH3)2NC6H4NH2]2·H2C2O4
CAS Number:
62778-12-5
Molecular Weight:
362.42
EC Number:
263-723-2
MDL number:
MFCD00036387
UNSPSC Code:
12352100
PubChem Substance ID:
24865671
NACRES:
NA.22

Assay

98%

form

powder

mp

205 °C (dec.) (lit.)

SMILES string

OC(=O)C(O)=O.CN(C)c1ccc(N)cc1.CN(C)c2ccc(N)cc2

InChI

1S/2C8H12N2.C2H2O4/c2*1-10(2)8-5-3-7(9)4-6-8;3-1(4)2(5)6/h2*3-6H,9H2,1-2H3;(H,3,4)(H,5,6)

InChI key

MNUINXKPLPIOEF-UHFFFAOYSA-N

Application

N,N-Dimethyl-1,4-phenylenediamine oxalate (N,N-dimethyl-p-phenylenediamine hemioxalate salt, DPD) was used as reagent in a study to evaluate the catalytic effects of elemental sulfur nanoparticles on CrVI reduction. It was also used to study the transformation of trichloroethene (TCE), caused by heating contaminated soil and groundwater samples.

Pictograms

Skull and crossbones
GHS06

Signal Word

Danger

Hazard Classifications

Acute Tox. 2 Oral - Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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On-line electrochemical-mass spectrometry study of the mechanism of oxidation of N, N-dimethyl-p-phenylenediamine in aqueous electrolytes.
Modestov AD, et al.
Journal of Electroanalytical Chemistry, 565(1), 7-19 (2004)
Jed Costanza et al.
Environmental science & technology, 43(3), 909-914 (2009-02-28)
This study explores the transformation of trichloroethene (TCE) caused by heating contaminated soil and groundwater samples obtained from the East Gate Disposal Yard (EGDY) located in Fort Lewis, WA. After field samples transferring into glass ampules and introducing 1.5 micromol
Yeqing Lan et al.
Environmental science & technology, 39(7), 2087-2094 (2005-05-06)
Chromate (CrVI) reduction by sulfide was conducted in anaerobic batch experimental systems. The molar ratio of the reduced CrVI to the oxidized S(-II) was 1:1.5 during the reaction, suggesting that the product of sulfide oxidation was elemental sulfur. Under the
S Marroquí et al.
Journal of bacteriology, 183(3), 854-864 (2001-02-24)
We isolated a Tn5-induced Rhizobium tropici mutant that has enhanced capacity to oxidize N,N-dimethyl-p-phenylendiamine (DMPD) and therefore has enhanced respiration via cytochrome oxidase. The mutant had increased levels of the cytochromes c(1) and CycM and a small increase in the
Xiang-yuan Huang et al.
Guang pu xue yu guang pu fen xi = Guang pu, 22(4), 627-630 (2003-08-27)
A new catalytic spectrophotometic method for the determination of trace chromium (VI) is reported in this paper. The method is based on the catalytic action of chromium (VI) on the oxidative coupling of p-Amino-N,N-dimethylaniline dihydrochloride and 1-Amino-8-naphthol-3,6-disulfonic acid to form
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