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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]
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. It is part of the Hill reagents family. When exposed to light in a photosynthetic system, the ...
(However, PE only dissolves at temperatures well above 100 °C.) Poly(styrene) has a solubility parameter of 9.1 cal 1/2 cm −3/2, and thus ethyl acetate is likely to be a good solvent. Nylon 6,6 has a solubility parameter of 13.7 cal 1/2 cm −3/2, and ethanol is likely to be the best solvent of those tabulated. However, the latter is polar ...
2,6-Di-tert-butylphenol is an organic compound with the structural formula 2,6-((CH 3) 3 C) 2 C 6 H 3 OH. This colorless solid alkylated phenol and its derivatives are used industrially as UV stabilizers and antioxidants for hydrocarbon -based products ranging from petrochemicals to plastics. [ 1 ]
The density of quartz is around 2.65 g/cm 3 but the (dry) bulk density of a mineral soil is normally about half that density, between 1.0 and 1.6 g/cm 3. In contrast, soils rich in soil organic carbon and some friable clays tend to have lower bulk densities ( <1.0 g/cm 3 ) due to a combination of the low-density of the organic materials ...
2,6-DMP is produced by the methylation of phenol. With production >100,000 tons/y, it is the most important xylenol. The methylation is carried out by contacting gaseous phenol and methanol at elevated temperatures in the presence of a solid acid catalyst: [2] [3] C 6 H 5 OH + 2 CH 3 OH → (CH 3) 2 C 6 H 3 OH + 2 H 2 O
o-Xylene (ortho-xylene) is an aromatic hydrocarbon with the formula C 6 H 4 (CH 3) 2, with two methyl substituents bonded to adjacent carbon atoms of a benzene ring (the ortho configuration). It is a constitutional isomer of m-xylene and p-xylene, the mixture being called xylene or xylenes. o-Xylene is a colourless slightly oily flammable ...
C 6 H 5 CH 3 + C 6 H 6 → C 6 H 5 −C 6 H 5 + CH 4. The other principal route is by the oxidative dehydrogenation of benzene: 2 C 6 H 6 + ½ O 2 → C 6 H 5 −C 6 H 5 + H 2 O. Annually 40,000,000 kg are produced by these routes. [13] In the laboratory, biphenyl can also be synthesized by treating phenylmagnesium bromide with copper(II) salts.