168343
N,N-Diethyl-p-phenylenediamine sulfate salt
97%
Synonym(s):
4-Amino-N,N-diethylaniline sulfate salt
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About This Item
Linear Formula:
(C2H5)2NC6H4NH2 · H2SO4
CAS Number:
Molecular Weight:
262.33
EC Number:
228-500-6
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
4219768
MDL number:
InChI key
AYLDJQABCMPYEN-UHFFFAOYSA-N
InChI
1S/C10H16N2.H2O4S/c1-3-12(4-2)10-7-5-9(11)6-8-10;1-5(2,3)4/h5-8H,3-4,11H2,1-2H3;(H2,1,2,3,4)
SMILES string
OS(O)(=O)=O.CCN(CC)c1ccc(N)cc1
assay
97%
mp
184-186 °C (lit.)
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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Joanne Paquin et al.
Arzneimittel-Forschung, 55(7), 359-369 (2005-08-06)
Oxidative stress may involve overproduction of hydrogen peroxide which can generate highly cytotoxic hydroxyl radicals in the presence of ferrous ions. This work demonstrates that TCAT (Tricomponent Antioxidant Therapy), an association of pyruvate, vitamin E and fatty acids, provides neuronal
Masoumeh Hasani et al.
Journal of hazardous materials, 157(1), 161-169 (2008-02-15)
A multicomponent analysis method based on principal component analysis-artificial neural network models (PC-ANN) is proposed for the determination of phenolic compounds. The method relies on the oxidative coupling of phenols (phenol, 2 chlorophenol, 3-chlorophenol and 4-chlorophenol) to N,N-diethyl-p-phenylenediamine in the
Allergic contact dermatitis in a photographer.
A Aguirre et al.
Contact dermatitis, 27(5), 340-341 (1992-11-01)
Jessica A Kershaw et al.
Analytical and bioanalytical chemistry, 379(4), 707-713 (2004-06-04)
The effect of Cu(II) on the determination of homocysteine via its electrochemically initiated reaction with N, N-diethyl-p-phenylenediamine is examined. The presence of copper inhibited the detection process for homocysteine owing to a complexation reaction occurring. This provided an indirect route
Z B Ogel et al.
Applied microbiology and biotechnology, 71(6), 853-862 (2006-01-04)
Scytalidium thermophilum produces an extracellular phenol oxidase on glucose-containing medium. Certain phenolic acids, specifically gallic acid and tannic acid, induce the expression of the enzyme. Production at 45 degrees C in batch cultures is growth-associated and is enhanced in the
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