DPPH

DPPH
Skeletal formula of DPPH
sample
Names
Preferred IUPAC name
2,2-Diphenyl-1-(2,4,6-trinitrophenyl)hydrazin-1-yl
Other names
2,2-Diphenyl-1-picrylhydrazyl
1,1-Diphenyl-2-picrylhydrazyl radical
2,2-Diphenyl-1-(2,4,6-trinitrophenyl)hydrazyl
Diphenylpicrylhydrazyl
Identifiers
3D model (JSmol)
Abbreviations DPPH
ChemSpider
ECHA InfoCard 100.015.993 Edit this at Wikidata
UNII
  • InChI=1S/C18H12N5O6/c24-21(25)15-11-16(22(26)27)18(17(12-15)23(28)29)19-20(13-7-3-1-4-8-13)14-9-5-2-6-10-14/h1-12H checkY
    Key: HHEAADYXPMHMCT-UHFFFAOYSA-N checkY
  • InChI=1/C18H13N5O6/c24-21(25)15-11-16(22(26)27)18(17(12-15)23(28)29)19-20(13-7-3-1-4-8-13)14-9-5-2-6-10-14/h1-12,19H
    Key: WCBPJVKVIMMEQC-UHFFFAOYAG
  • InChI=1/C18H12N5O6/c24-21(25)15-11-16(22(26)27)18(17(12-15)23(28)29)19-20(13-7-3-1-4-8-13)14-9-5-2-6-10-14/h1-12H
    Key: HHEAADYXPMHMCT-UHFFFAOYAG
  • c1ccc(cc1)N(c2ccccc2)[N]c3c(cc(cc3[N+](=O)[O-])[N+](=O)[O-])[N+](=O)[O-]
Properties
C18H12N5O6
Molar mass 394.32 g/mol
Appearance Black to green powder, purple in solution
Density 1.4 g/cm3
Melting point 135 °C (275 °F; 408 K) (decomposes)
insoluble
Solubility in methanol 10 mg/mL
Hazards
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 0: Exposure under fire conditions would offer no hazard beyond that of ordinary combustible material. E.g. sodium chlorideFlammability 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oilInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
0
1
0
Safety data sheet (SDS) MSDS
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)

DPPH is a common abbreviation for the organic chemical compound 2,2-diphenyl-1-picrylhydrazyl. It is a dark-colored crystalline powder composed of stable free radical molecules. DPPH has two major applications, both in laboratory research: one is a monitor of chemical reactions involving radicals, most notably it is a common antioxidant assay,[1] and another is a standard of the position and intensity of electron paramagnetic resonance signals.

  1. ^ Sharma, Om P.; Bhat, Tej K. (15 April 2009). "DPPH antioxidant assay revisited". Journal of Food Chemistry. 113 (4): 1202–1205. doi:10.1016/j.foodchem.2008.08.008.

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