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292265

Sigma-Aldrich

N,N′-Diphenyl-p-phenylendiamin

98%

Synonym(e):

N,N′-Diphenyl-1,4-phenylendiamin

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About This Item

Lineare Formel:
C6H5NHC6H4NHC6H5
CAS-Nummer:
74-31-7
Molekulargewicht:
260.33
Beilstein:
2215944
EG-Nummer:
200-806-4
MDL-Nummer:
MFCD00003015
UNSPSC-Code:
12162002
PubChem Substanz-ID:
24857574
NACRES:
NA.23

Qualitätsniveau

100

Assay

98%

bp

220-225 °C/0.5 mmHg (lit.)

mp (Schmelzpunkt)

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

InChIKey

UTGQNNCQYDRXCH-UHFFFAOYSA-N

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Verwandte Kategorien

Anwendung

  • 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).

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

H-Sätze

H317 - H412

Gefahreneinstufungen

Aquatic Chronic 3 - Skin Sens. 1

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 1

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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N,N,N′,N′-Tetramethyl-p-phenylendiamin 99%, powder

Sigma-Aldrich

T7394

N,N,N′,N′-Tetramethyl-p-phenylendiamin

N,N′-Dimethyl-1,3-propandiamin 97%

Sigma-Aldrich

308110

N,N′-Dimethyl-1,3-propandiamin

Phthalamsäure 97%

Sigma-Aldrich

556998

Phthalamsäure

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
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
Florian Seyfarth et al.
Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG, 7(9), 770-772 (2009-04-24)
A ten-year-old boy presented with recurrent eczema on the dorsal of both feet and the thighs. His symptoms became worse when he used racing swim fins. Patch testing included the standard, ointments, preservatives, leather, textile dyes, rubber component, and corticosteroid
Stefania Miccadei et al.
Nutrition and cancer, 60(2), 276-283 (2008-04-30)
Cultured rat hepatocytes and human hepatoma HepG2 cells were used to evaluate the hepatoprotective properties of polyphenolic extracts from the edible part of artichoke (AE). The hepatocytes were exposed to H2O2generated in situ by glucose oxidase and were treated with
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