07672
N,N-Diethyl-p-phenylenediamine sulfate salt
≥98.0% (T)
Synonym(s):
4-Amino-N,N-diethylaniline sulfate salt
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About This Item
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Quality Level
Assay
≥98.0% (T)
form
solid
mp
184-186 °C (lit.)
184-187 °C
SMILES string
OS(O)(=O)=O.CCN(CC)c1ccc(N)cc1
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)
InChI key
AYLDJQABCMPYEN-UHFFFAOYSA-N
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Application
N,N-Diethyl-p-phenylenediamine sulfate salt has been used to prepare N,N-diethyl-p-phenylenediamine (DPD) solution, which is commonly used as a chromogenic indicator for the determination of free and total chlorine by titrimetric, colorimetric and spectroscopic methods.{50
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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An improved N, N?-diethyl-p-phenylenediamine (DPD) method for the determination of free chlorine based on multiple wavelength detection.
Analytica Chimica Acta, 407(1-2), 127-133 (2000)
Improvements in the N, N-diethyl-p-phenylenediamine method for the determination of free and combined residual chlorine through the use of FIA.
Talanta, 38(2), 145-149 (1991)
Allergic contact dermatitis in a photographer.
Contact dermatitis, 27(5), 340-341 (1992-11-01)
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
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
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