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Diethyl ether is a popular non-polar solvent in liquid-liquid extraction. As an extractant, it is immiscible with and less dense than water. Although immiscible, it has significant solubility in water (6.05 g/(100 ml) at 25 °C [ 2 ] ) and dissolves 1.5 g/(100 g) (1.0 g/(100 ml)) water at 25 °C.
The handling of this chemical may incur notable safety precautions. It is highly recommended that you seek the Material Safety Datasheet for this chemical from a reliable source such as SIRI, and follow its directions.
For example, ethyl methyl ether (CH 3 OC 2 H 5), diphenylether (C 6 H 5 OC 6 H 5). As for other organic compounds, very common ethers acquired names before rules for nomenclature were formalized. Diethyl ether is simply called ether, but was once called sweet oil of vitriol. Methyl phenyl ether is anisole, because it was originally found in ...
Ethers like diethyl ether and tetrahydrofuran (THF) can form highly explosive organic peroxides upon exposure to oxygen and light. THF is normally more likely to form such peroxides than diethyl ether. One of the most susceptible solvents is diisopropyl ether, but all ethers are considered to be potential peroxide sources.
Diethyl ether has a long history as a medical anesthetic; when starting fluid was mostly ether, a similar effect could be obtained using it. Use at the present time directly as an inhalant includes the effect of the petroleum solvents, which are more toxic as inhalants than diethyl ether.
Fluoroboric acid is corrosive and attacks the skin. It is available commercially as a solution in water and other solvents such as diethyl ether. It is a strong acid with a weakly coordinating, non-oxidizing conjugate base. [2] It is structurally similar to perchloric acid, but lacks the hazards associated with oxidants.
Tetrafluoroborate salts are commonly employed as non-coordinating anions. The adduct with diethyl ether, boron trifluoride diethyl etherate, or just boron trifluoride etherate, (BF 3 ·O(CH 2 CH 3) 2) is a conveniently handled liquid and consequently is widely encountered as a laboratory source of BF 3. [16]
1,4-Dioxane (/ d aɪ ˈ ɒ k s eɪ n /) is a heterocyclic organic compound, classified as an ether. It is a colorless liquid with a faint sweet odor similar to that of diethyl ether. The compound is often called simply dioxane because the other dioxane isomers (1,2-and 1,3-) are rarely encountered.