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292265

Sigma-Aldrich

N,N′-Diphenyl-p-phenylenediamine

98%

Synonym(s):

N,N′-Diphenyl-1,4-phenylenediamine

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About This Item

Linear Formula:
C6H5NHC6H4NHC6H5
CAS Number:
74-31-7
Molecular Weight:
260.33
Beilstein:
2215944
EC Number:
200-806-4
MDL number:
MFCD00003015
UNSPSC Code:
12162002
PubChem Substance ID:
24857574
NACRES:
NA.23

Assay

98%

bp

220-225 °C/0.5 mmHg (lit.)

mp

143-145 °C (lit.)

SMILES string

N(c1ccccc1)c2ccc(Nc3ccccc3)cc2

InChI

1S/C18H16N2/c1-3-7-15(8-4-1)19-17-11-13-18(14-12-17)20-16-9-5-2-6-10-16/h1-14,19-20H

InChI key

UTGQNNCQYDRXCH-UHFFFAOYSA-N

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Application

  • TPA-induced inhibition of gap junctional intercellular communication is not mediated through free radicals.: This research explores the role of N,N′-Diphenyl-p-phenylenediamine (DPPD) in cellular communication, providing insights into its applications in high-performance rubber stabilizers and life science manufacturing chemicals. (Hasler et al., 1990).

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H317,H412

Hazard Classifications

Aquatic Chronic 3 - Skin Sens. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

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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Yoshiko Kawai et al.
Journal of pharmacological sciences, 111(4), 433-439 (2009-12-08)
Cisplatin causes chronic interstitial disease with fibrosis, but the development mechanism of interstitial fibrosis is not yet understood. We examined the effect of an antioxidant, N,N'-diphenyl-1,4-phenylenediamine (DPPD), on development of interstitial fibrosis induced by cisplatin. Cisplatin increased blood urea nitrogen
Sung Min Park et al.
Pharmacology & toxicology, 92(1), 43-50 (2003-04-25)
This study was undertaken in order to examine the roles of lipid peroxidation and poly (ADP-ribose) polymerase (PARP) activation in oxidant-induced renal cell death. Opossum kidney cell cultures were used as the renal epithelial cell model, and an inorganic hydroperoxide
Xiaobo Ji et al.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 23(11), 1317-1320 (2007-11-14)
The oxidation of N,N'-diphenyl-1,4-phenylenediamine (DPPD) has been studied by cyclic voltammetry at glassy carbon electrodes in propylene carbonate. Next, the reaction between ammonia and DPPD was similarly investigated. It has been shown that ammonia reversibly removes protons from oxidized DPPD
I Rath et al.
Zeitschrift fur Naturforschung. C, Journal of biosciences, 55(11-12), 957-964 (2001-02-24)
The primary reactions leading to Al toxicity in plant cells have not yet been elucidated. We used soybean (Glycine max [L.] Merr.) cell suspension cultures to address the question whether lipid peroxidation plays an important role in Al toxicity. Upon
A Campos-Neto et al.
Tuberculosis (Edinburgh, Scotland), 81(5-6), 353-358 (2002-01-22)
Although the tuberculin test has aided in the diagnosis of tuberculosis for more than 85 years, its interpretation is difficult particularly because sensitization with non-tuberculous mycobacteria leads to false positive tests. Using the guinea pig model of tuberculosis, we have
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