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1-Hexanol (IUPAC name hexan-1-ol) is an organic alcohol with a six-carbon chain and a condensed structural formula of CH 3 (CH 2) 5 OH. This colorless liquid is slightly soluble in water, but miscible with diethyl ether and ethanol .
3,5,5-Trimethyl-1-hexanol is a nine carbon primary alcohol, and it makes up the mixture isononanol along with isononyl alcohol. It is used for fragrance in many toiletries and household cleaning products. Between one and ten metric tonnes are produced every year for use as a fragrance. [1]
The molar mass of atoms of an element is given by the relative atomic mass of the element multiplied by the molar mass constant, M u ≈ 1.000 000 × 10 −3 kg/mol ≈ 1 g/mol. For normal samples from Earth with typical isotope composition, the atomic weight can be approximated by the standard atomic weight [ 2 ] or the conventional atomic weight.
Hexanol may refer to any of the following isomeric organic compounds with the formula C 6 H 13 OH: Structure Type IUPAC name Boiling point (°C) Primary Hexan-1-ol: 158
Cyclohexanol is produced by the oxidation of cyclohexane in air, typically using cobalt catalysts: [5]. 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.
Cyclohexane-1,2,3,4,5,6-hexol is a family of chemical compounds with formula C 6 H 12 O 6, whose molecule consists of a ring of six carbon atoms, each bound to one hydrogen atom and one hydroxyl group (–OH).
Molar mass: 98.145 g·mol −1 Density: 0.851 g/cm 3: Boiling point: 126 °C (259 °F; 399 K) Related compounds ... 1-Hexanol, another volatile organic compound, ...
178.0 K (–95.1 °C), 1.23 Pa Critical point: 507.6 K (234.5 °C), 3020 kPa Std enthalpy change of fusion, Δ fus H o: 13 kJ/mol Std entropy change of fusion, Δ fus S o: 70 J/(mol·K) Std enthalpy change of vaporization, Δ vap H o: 28.85 kJ/mol at 68.8 °C Std entropy change of vaporization, Δ vap S o? J/(mol·K) Solid properties Std ...