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2,6-Dichlorophenol is a compound with formula C 6 H 3 Cl 2 OH. It is one of the six isomers of dichlorophenol. It is a colorless solid. Its pK a is 6.78, which is about 100x more acidic than 2-chlorophenol (8.52) and 1000x more acidic than phenol itself (9.95). [3]
3,5-Dichlorophenol Dichlorophenols are used as intermediates in the manufacture of more complex chemical compounds, including the common herbicide 2,4-dichlorophenoxyacetic acid (2,4-D). [ 1 ]
2,6-Dichlorophenolindophenol (DCPIP, DCIP or DPIP) is a chemical compound used as a redox dye. When oxidized , DCPIP is blue with a maximal absorption at 600 nm; when reduced , DCPIP is colorless. DCPIP can be used to measure the rate of photosynthesis .
Chemical structure of 2-chlorophenol. A chlorophenol is any organochloride of phenol that contains one or more covalently bonded chlorine atoms. There are five basic types of chlorophenols (mono- to pentachlorophenol) and 19 different chlorophenols in total when positional isomerism is taken into account.
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Oxidized form Color of Reduced form Sodium 2,6-Dibromophenol-indophenol or Sodium 2,6-Dichlorophenol-indophenol +0.64 +0.22 blue colorless Sodium o-Cresol indophenol +0.62 +0.19 blue colorless Thionine (syn. Lauth's violet) +0.56 +0.06 violet colorless Methylene blue +0.53 +0.01 [2] blue colorless Indigotetrasulfonic acid +0.37 -0.05 blue colorless
Download as PDF; Printable version; In other projects Wikidata item; Appearance. move to sidebar hide ... 2,6-Dichlorophenol; 3,4-Dichlorophenol; 3,5-Dichlorophenol
2,4,6-Trichlorophenol, for example, has two chlorine atoms in the ortho positions and one chlorine atom in the para position. There are six different isomers: 2,3,4-Trichlorophenol