Search results
Results from the WOW.Com Content Network
Dimethyl ether (DME; also known as methoxymethane) is the organic compound with the formula CH 3 OCH 3, (sometimes ambiguously simplified to C 2 H 6 O as it is an isomer of ethanol). The simplest ether , it is a colorless gas that is a useful precursor to other organic compounds and an aerosol propellant that is currently being demonstrated for ...
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.
This Wikipedia page provides a comprehensive list of boiling and freezing points for various solvents.
Diglyme, or bis(2-methoxyethyl) ether, is an organic compound with the chemical formula (CH 3 OCH 2 CH 2) 2 O. It is a colorless liquid with a slight ether-like odor. It is a solvent with a high boiling point. It is the dimethyl ether of diethylene glycol. The name diglyme is a portmanteau of diglycol methyl ether. It is miscible with water as ...
Dimethoxyethane, also known as glyme, monoglyme, dimethyl glycol, ethylene glycol dimethyl ether, dimethyl cellosolve, and DME, is a colorless, aprotic, and liquid ether that is used as a solvent, especially in batteries. [2] Dimethoxyethane is miscible with water.
Dimethyl ether: A colourless gas that is used as an aerosol spray propellant. A potential renewable alternative fuel for diesel engines with a cetane rating as high as 56–57. Diethyl ether: A colourless liquid with sweet odour. A common low boiling solvent (b.p. 34.6 °C) and an early anaesthetic. Used as starting fluid for diesel engines.
Methoxyethane, also known as ethyl methyl ether, is a colorless gaseous ether with the formula CH 3 OCH 2 CH 3. Unlike the related dimethyl ether and diethyl ether , which are widely used and studied, this mixed alkyl ether has no current applications.
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.