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186384

Sigma-Aldrich

N,N-Dimethyl-p-phenylenediamine sulfate salt

98%

Sinónimos:

4-(Dimethylamino)aniline sulfate salt, 4-Amino-N,N-dimethylaniline sulfate salt, DMPPDA

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About This Item

Fórmula lineal:
(CH3)2NC6H4NH2·H2SO4
Número de CAS:
536-47-0
Peso molecular:
234.27
Beilstein/REAXYS Number:
4612278
EC Number:
208-636-2
MDL number:
MFCD00012992
UNSPSC Code:
12352100
PubChem Substance ID:
24851217
NACRES:
NA.22

Quality Level

200

assay

98%

form

solid

bp

495 °C (lit.)

mp

200-205 °C (dec.) (lit.)

solubility

water: soluble 50 mg/mL, clear to hazy, colorless to faintly yellow or pink

functional group

amine

SMILES string

OS(O)(=O)=O.CN(C)c1ccc(N)cc1

InChI

1S/C8H12N2.H2O4S/c1-10(2)8-5-3-7(9)4-6-8;1-5(2,3)4/h3-6H,9H2,1-2H3;(H2,1,2,3,4)

InChI key

GLUKPDKNLKRLHX-UHFFFAOYSA-N

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Application

N,N-Dimethyl-p-phenylenediamine sulfate salt was used:
  • to investigate the role of H2S in cardioprotection induced by ischemic preconditioning in rat heart
  • in spectrophotometric determination of gold(III) in gold-pharmaceuticals such as sodium aurothimaleate and auranofin
  • to investigate colonic tissue H2S production using the acetate trapping assay system

pictograms

Skull and crossbones
GHS06

signalword

Danger

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

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

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

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Certificados de análisis (COA)

Lot/Batch Number
BCCG1432
BCCF8733
BCCF8732
BCCF8731
BCCF7895

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New and sensitive spectrophotometric determination of gold (III) with N, N-dimethyl-p-phenylenediamine and potassium persulfate.
Mori I, et al.
Analytical Letters, 30(5), 953-961 (1997)
Jin-Song Bian et al.
The Journal of pharmacology and experimental therapeutics, 316(2), 670-678 (2005-10-06)
Endogenous H(2)S is synthesized mainly by cystathionine gamma-lyase in the heart. The present study investigated the role of H(2)S in cardioprotection induced by ischemic preconditioning. We have examined the effect of endogenous H(2)S and exogenous application of NaHS (H(2)S donor)
Kyle L Flannigan et al.
American journal of physiology. Gastrointestinal and liver physiology, 301(1), G188-G193 (2011-04-09)
Hydrogen sulfide (H(2)S) is an important modulator of many aspects of digestive function, both in health and disease. Colonic tissue H(2)S synthesis increases markedly during injury and inflammation and appears to contribute to resolution. Some of the bacteria residing in
Kraiwan Punyain et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 83(1), 368-378 (2011-09-20)
Organic radical cations form dicationic dimers in solution, observed experimentally as diamagnetic species in temperature-dependent EPR and low temperature UV/Vis spectroscopy. Dimerization of paraphenylenediamine, N,N-dimethyl-paraphenylenediamine and 2,3,5,6-tetramethyl-paraphenylenediamine radical cation in ethanol/diethylether mixture was investigated theoretically according to geometry, energetics and
F Tessier et al.
International journal for vitamin and nutrition research. Internationale Zeitschrift fur Vitamin- und Ernahrungsforschung. Journal international de vitaminologie et de nutrition, 66(2), 166-170 (1996-01-01)
An HPLC micro-method with fluorescence detection has been developed to determine total vitamin C (vit C) and dehydroascorbic acid (DHA) concentrations in human plasma samples. This method is based on the rapid, specific reaction of DHA with dimethyl-o-phenylenediamine (DMPD) to
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