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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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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
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)
Claudineia R Silva et al.
Talanta, 85(3), 1703-1705 (2011-08-03)
A spectrophotometric flow injection procedure involving N,N-dimethyl-p-phenylenediamine (DMPD) is applied to the sulfide monitoring of a sugar fermentation by Saccharomyces cerevisiae under laboratory conditions. The gaseous chemical species evolving from the fermentative process, mainly CO(2), are trapped allowing a cleaned
C Li et al.
The Biochemical journal, 300 ( Pt 1), 31-36 (1994-05-15)
C-terminal alpha-amidation is a structural feature essential to the biological activity of many peptide hormones. Peptidylglycine alpha-amidating mono-oxygenase (PAM; EC 1.14.17.3) catalyses conversion of glycine-extended peptide hormone precursors into their corresponding alpha-hydroxyglycine derivatives. This reaction is the first step in
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