Chemodex

N,N-Diethyl-p-phenylenediamine sulfate salt

CHF 45.00
In stock
CDX-D0932-G05050 gCHF 45.00
CDX-D0932-G250250 gCHF 90.00
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Product Details
Synonyms DPD sulfate; 4-Amino-N,N-diethylaniline sulfate salt; N,N-Diethyl-1,4-phenylenediammonium sulfate; Color Developing Agent 1
Product Type Chemical
Properties
Formula C10H18N2O4S
MW 262.33
CAS 6283-63-2
RTECS SS9625000
Source/Host Chemicals Synthetic
Purity Chemicals ≥99%
Appearance White crystalline powder.
Solubility Soluble in water (100mg/ml).
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

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Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key AYLDJQABCMPYEN-UHFFFAOYSA-N
Smiles CCN(CC)C1=CC=C(C=C1)N.OS(=O)(=O)O
Shipping and Handling
Shipping AMBIENT
Short Term Storage +20°C
Long Term Storage +20°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at RT.
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Product Specification Sheet
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Description

N,N-Diethyl-p-phenylenediamine sulfate (DPD) is used as a chromogenic indicator or reagent in analytical chemistry and in water quality testing. It is commonly used in a test called the DPD method, primarily for the measurement of free and total chlorine by titrimetric, colorimetric and spectroscopic methods in water. DPD reacts with free chlorine (hypochlorous acid and hypochlorite ions) to form a pink or magenta-colored compound. The intensity of the color is directly proportional to the concentration of chlorine, making it a convenient method for chlorine quantification. In general, it is used for spectrophotometric determination KIO4 levels, drugs (containing phenolic groups or aromatic amino groups) and as a peroxidase substrate. DPD has been developed as a color developing agent in photgraphy.

Product References

(1) G. Gordon, et al.; Talanta 38, 145 (1991) | (2) L. Moberg & B. Karlberg; Anal. Chim. Acta 407, 127 (2000) | (3) F.H. Metwally, et al.; Farmaco 56, 601 (2001) | (4) M. Hasani, et al.; J. Hazard. Mat. 157, 161 (2008) | (5) P. Nagaraja, et al.; Acta Pharm. 60, 217 (2010) | (6) F. Yang, et al.; Mikrochim. Acta 186, 417 (2019) | (7) M. Zhou, et al.; Anal. Chem. 93, 769 (2021)

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