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| Names | |
|---|---|
| Preferred IUPAC name
 N1,N1-Diethylbenzene-1,4-diamine  | |
| Other names
 N,N-diethyl-p-phenylenediamine DPD  | |
| Identifiers | |
3D model (JSmol)  | 
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| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.002.014 | 
| EC Number | 
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PubChem CID  | 
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| UNII | |
| UN number | 1673 | 
CompTox Dashboard (EPA)  | 
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| Properties | |
| C10H16N2 | |
| Molar mass | 164.252 g·mol−1 | 
| Hazards | |
| GHS labelling: | |
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| Danger | |
| H301, H314 | |
| P260, P264, P270, P280, P301+P310, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P330, P363, P405, P501 | |
| Related compounds | |
Related compounds  | 
Color Developing Agent 2; Color Developing Agent 3; Color Developing Agent 4; | 
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). 
Infobox references  | |
Color Developing Agent 1 (CD-1) is the first in the series of color developing agents used in developing color films. It is the organic compound N,N-diethyl-1,4-benzenediamine (DPD), which is usually in the form of the monohydrochloride salt.[1] In color development, after reducing a silver atom in a silver halide crystal, the oxidized developing agent combines with a color coupler to form a color dye molecule.
Arthur Thomas Palin, a Fellow of the Royal Society of Chemistry, developed a widely used color based method of water testing using DPD to indicate the chlorine content of treated water.
See also
References
- ↑ "1,4-Benzenediamine, N,N-diethyl-, monohydrochloride". U.S. National Center for Biotechnology Information. Retrieved 21 January 2020.
 
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