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0.8243 g/cm 3 at 20 °C Boiling point: 126.5 °C (259.7 °F; 399.6 K) ... 2-Methyl-3-pentanol (IUPAC name: 2-methylpentan-3-ol) is an organic chemical compound.
This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.
2-Methylbutan-1-ol: 128.7 3-methyl-1-butanol or isoamyl alcohol or isopentyl alcohol primary 3-Methylbutan-1-ol: 131.2 2,2-dimethyl-1-propanol or neopentyl alcohol primary 2,2-Dimethylpropan-1-ol: 113.1 2-pentanol or sec-amyl alcohol or methyl (n) propyl carbinol secondary Pentan-2-ol: 118.8 3-methyl-2-butanol or sec-isoamyl alcohol or methyl ...
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2-Methyl-3-pentanol; 3-Methyl-3-pentanol; 2,2-Dimethyl-1-butanol; 2,3-Dimethyl-1-butanol ... Text is available under the Creative Commons Attribution-ShareAlike 4.0 ...
3-Methyl-2-pentanol (IUPAC name: 3-methylpentan-2-ol) is an organic chemical compound. It has been identified as a component of hops . [ 2 ] Its presence in urine can be used to test for exposure to 3-methylpentane .
2-Methyl-2-pentanol (IUPAC name: 2-methylpentan-2-ol) is an organic chemical compound. It can be added to a gas chromatograph to help distinguish between branched compounds, especially alcohols. [2] Its presence in urine can be used to test for exposure to 2-methylpentane. [3]
The synthesis of methyl benzoate by Fischer–Speier esterification. Fischer esterification or Fischer–Speier esterification is a special type of esterification by refluxing a carboxylic acid and an alcohol in the presence of an acid catalyst. The reaction was first described by Emil Fischer and Arthur Speier in 1895. [1]