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크기 선택
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
C6H4[N(CH3)2]2
CAS 번호:
Molecular Weight:
164.25
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-831-6
Beilstein/REAXYS Number:
1564025
MDL number:
제품 이름
N,N,N′,N′-Tetramethyl-p-phenylenediamine, 99%, powder
InChI key
CJAOGUFAAWZWNI-UHFFFAOYSA-N
InChI
1S/C10H16N2/c1-11(2)9-5-7-10(8-6-9)12(3)4/h5-8H,1-4H3
SMILES string
CN(C)c1ccc(cc1)N(C)C
assay
99%
form
flakes
powder
color
off-white to brown
bp
260 °C (lit.)
mp
49-51 °C (lit.)
Quality Level
유사한 제품을 찾으십니까? 방문 제품 비교 안내
Application
N,N,N′,N′-Tetramethyl-p-phenylenediamine (TMPDA) can be used:
- In the flow injection analysis of benzoyl peroxide.
- To study photoinduced electron transfer to halogenated solvents.
Disclaimer
May darken in storage.
General description
N,N,N′,N′-Tetramethyl-p-phenylenediamine (TMPDA) is a redox reagent with low ionization potential widely used as an electron donor for photosystem I. It also acts as an electron acceptor in photosystem II.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral
저장 등급
11 - Combustible Solids
wgk
WGK 1
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
Interaction of N, N, N′ ,N′ -tetramethyl-p-phenylenediamine with photosystem II as revealed by thermoluminescence: reduction of the higher oxidation states of the Mn cluster and displacement of plastoquinone from the QB niche
Gauthier A, et al.
Biochimica et Biophysica Acta, 1757(11), 1547-1556 (2006)
Flow injection analysis of benzoyl peroxide using N, N, N, N-tetramethyl-p-phenylenediamine (TMPDA) and surfactants
Pharr DY & Tomsyck JA
Analytical Letters, 42(5), 821-832 (2009)
Ultrafast photoinduced electron transfer from N, N, N′ , N′ -tetramethyl-p-phenylenediamine and N, N, N′ , N′ -tetramethylbenzidine to dichloromethane
Boilet L, et al.
Journal of Photochemistry and Photobiology A: Chemistry, 163(3), 529-536 (2004)
P P Bawol et al.
Physical chemistry chemical physics : PCCP, 20(33), 21447-21456 (2018-08-09)
The reversibility of current Li-O2 batteries suffers from high charging overpotentials. To address this problem, the use of redox mediators has been proposed, which are supposed to improve the sluggish reaction kinetics of the oxygen evolution reaction via a solution
Toshiaki Miura
Chemico-biological interactions, 236, 67-73 (2015-04-30)
To investigate the mechanisms of cardiotoxicity induced by adriamycin (ADM), the enzymatic activities of ADM-Fe(3+), including the peroxidase and lipoxygenase (LOX) activity, and participation of active oxygen species in the damage to biological components were examined. ADM-Fe(3+), but not ADM
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