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Make-up artists use acetone to remove skin adhesive from the netting of wigs and mustaches by immersing the item in an acetone bath, then removing the softened glue residue with a stiff brush. [70] Acetone is a main ingredient in many nail polish removers because it breaks down nail polish. [71]
This Wikipedia page provides a comprehensive list of boiling and freezing points for various solvents.
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.
A well-known example of a positive azeotrope is an ethanol–water mixture (obtained by fermentation of sugars) consisting of 95.63% ethanol and 4.37% water (by mass), which boils at 78.2 °C. [10] Ethanol boils at 78.4 °C, water boils at 100 °C, but the azeotrope boils at 78.2 °C, which is lower than either of its constituents. [11]
This is crucial to remember when partitioning compounds between solvents and water in a separatory funnel during chemical syntheses. Often, specific gravity is cited in place of density. Specific gravity is defined as the density of the solvent divided by the density of water at the same temperature. As such, specific gravity is a unitless value.
The simplest ketone is acetone (where R and R' is methyl), with the formula (CH 3) 2 CO. Many ketones are of great importance in biology and industry. Examples include many sugars , many steroids (e.g., testosterone), and the solvent acetone. [1]
ethyl acetate < acetone < ethanol < methanol < acetone:water (7:3) < ethanol:water (8:2) < methanol:water (8:2) < water. Solid-liquid extractions at laboratory scales can use Soxhlet extractors. A solid sample containing the desired compound along with impurities is placed in the thimble.
In 90% acetone-water, the peak absorption wavelengths of chlorophyll a are 430 nm and 664 nm; peaks for chlorophyll b are 460 nm and 647 nm; peaks for chlorophyll c 1 are 442 nm and 630 nm; peaks for chlorophyll c 2 are 444 nm and 630 nm; peaks for chlorophyll d are 401 nm, 455 nm and 696 nm. [27]