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The branching in 2-ethyl-1-butanol makes it harder to crystallize due to packing disruption, which results in a very low freezing point. Esters of 2-ethyl-1-butanol are similarly effected and it therefore finds application as a feedstock in the production of plasticizers and lubricants, where its presence helps reduce viscosity and lower freezing points.
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.
Boiling point (°C) K b (°C⋅kg/mol) Freezing point (°C) ... [2] Ethyl Acetate: 77.1 [5] Acetic Anhydride: ... n-Butanol: 117.7 [12] Hydrochloric Acid: 84.8
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 ...
C 8 H 10 N 4 O 2: Molar mass: 194.194 g·mol −1 Appearance Odorless, white needles or powder Density: 1.23 g/cm 3, solid [1] Melting point: 227 to 228 °C (441 to 442 °F; 500 to 501 K) (anhydrous) 234 to 235 °C (453 to 455 °F; 507 to 508 K) (monohydrate) Boiling point: 178 °C (352 °F; 451 K) (sublimation)
Butanol (also called butyl alcohol) is a four-carbon alcohol with a formula of C 4 H 9 O H, which occurs in five isomeric structures (four structural isomers), from a straight-chain primary alcohol to a branched-chain tertiary alcohol; [1] all are a butyl or isobutyl group linked to a hydroxyl group (sometimes represented as BuOH, sec-BuOH, i-BuOH, and t-BuOH).
The molecular formula C 6 H 14 O may refer to: tert-Amyl methyl ether; Diisopropyl ether; Dimethylbutanols. 2,2-Dimethyl-1-butanol; 3,3-Dimethyl-1-butanol; Dipropyl ether; 2-Ethyl-1-butanol; Ethyl tert-butyl ether; Hexanols. 1-Hexanol; 2-Hexanol; 3-Hexanol; Methylpentanols. 2-Methyl-1-pentanol; 3-Methyl-1-pentanol; 4-Methyl-1-pentanol; 2-Methyl ...
Theoretically 2-methylhexane also burns with a less sooty flame, emitting higher-frequency radiation; however, as heptane and 2-methylhexane differ by only one carbon atom, in terms of branching, both burn with a bright yellow flame when ignited. Compared to n-heptane, 2-methylhexane also has lower melting and boiling points. A lower density of ...