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Mass concentration, g/(100 ml) at 15.56 °C Density relative to 4 °C water Density at 20 °C relative to 20 °C water Density at 25 °C relative to 25 °C water Freezing temperature, °C 10 °C 20 °C 25 °C 30 °C
Cyclohexanone is produced by the oxidation of cyclohexane in air, typically using cobalt catalysts: [11]. C 6 H 12 + O 2 → (CH 2) 5 CO + H 2 O. This process forms cyclohexanol as a by-product, and this mixture, called "KA Oil" for ketone-alcohol oil, is the main feedstock for the production of adipic acid.
2 c 6 h 12 + o 2 → 2 c 6 h 11 oh This process coforms cyclohexanone , and this mixture ("KA oil" for ketone-alcohol oil) is the main feedstock for the production of adipic acid . The oxidation involves radicals and the intermediacy of the hydroperoxide C 6 H 11 O 2 H. Alternatively, cyclohexanol can be produced by the hydrogenation of phenol :
The ideal gas equation can be rearranged to give an expression for the molar volume of an ideal gas: = = Hence, for a given temperature and pressure, the molar volume is the same for all ideal gases and is based on the gas constant: R = 8.314 462 618 153 24 m 3 ⋅Pa⋅K −1 ⋅mol −1, or about 8.205 736 608 095 96 × 10 −5 m 3 ⋅atm⋅K ...
The reaction conducted in two steps beginning with the conversion of DMT to the diester dimethyl 1,4-cyclohexanedicarboxylate (DMCD): C 6 H 4 (CO 2 CH 3) 2 + 3 H 2 → C 6 H 10 (CO 2 CH 3) 2. In the second step DMCD is further hydrogenated to CHDM: C 6 H 10 (CO 2 CH 3) 2 + 4 H 2 → C 6 H 10 (CH 2 OH) 2 + 2 CH 3 OH. A copper chromite catalyst ...
1-Ethynylcyclohexanol (ECX) is an alkynyl alcohol derivative which is both a synthetic precursor to, and an active metabolite of the tranquilizer ethinamate, and has similar sedative, anticonvulsant and muscle relaxant effects. It has been sold as a designer drug, first being identified in the UK in March 2012. [1] [2] [3] [4]
Ethenone is produced by thermal dehydration of acetic acid at 700–750 °C in the presence of triethyl phosphate as a catalyst: [7] [8] CH 3 CO 2 H → CH 2 =C=O + H 2 O. It has also been produced on a laboratory scale by the thermolysis of acetone at 600–700 °C. [9] [10] CH 3 COCH 3 →CH 2 =C=O + CH 4. This reaction is called the ...
Cyclohexylmethanol is an organic compound with the formula C 6 H 11 −CH 2 −OH. It is a cyclohexane ring functionalized with an alcohol , specifically a hydroxymethyl group. The compound is a colorless liquid, although commercial samples can appear yellow.