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Diethyl ether hydroperoxide forms polymers known as diethyl ether peroxide, or ethylidene peroxide: The peroxide is a colorless oil that is an extremely brisant and friction sensitive explosive material , however the polymeric materials are solid making them more dangerous as evaporation of the volatile diethyl ether can leave thin films of ...
Methyl ethyl ketone peroxide, benzoyl peroxide and to a smaller degree acetone peroxide are used as initiators for radical polymerization of some thermosets, e.g. unsaturated polyester and vinyl ester resins, often encountered when making fiberglass or carbon fiber composites (CFRP), with examples including boats, RV units, bath tubs, pools ...
A cyclic ether, one of the most polar simple ethers that is used as a solvent. Anisole (methoxybenzene) An aryl ether and a major constituent of the essential oil of anise seed. Crown ethers: Cyclic polyethers that are used as phase transfer catalysts. Polyethylene glycol (PEG) A linear polyether, e.g. used in cosmetics and pharmaceuticals.
This hydrogen peroxide then releases hydrogen peroxide: [(HO) 3 B(OOH)] − + H 2 O ⇌ B(OH) − 4 + H 2 O 2. Several metal hydroperoxide complexes have been characterized by X-ray crystallography. Some form by the reaction of metal hydrides with oxygen gas: [17] L n M−H + O 2 → L n M−O−O−H (L n refers to other ligands bound to the ...
Hydrogen peroxide is a chemical compound with the formula H 2 O 2.In its pure form, it is a very pale blue [5] liquid that is slightly more viscous than water.It is used as an oxidizer, bleaching agent, and antiseptic, usually as a dilute solution (3%–6% by weight) in water for consumer use and in higher concentrations for industrial use.
A tincture is typically an extract of plant or animal material dissolved in ethanol (ethyl alcohol). Solvent concentrations of 25–60% are common, but may run as high as 90%. [ 1 ] In chemistry , a tincture is a solution that has ethanol as its solvent.
A generic epoxide. In organic chemistry, an epoxide is a cyclic ether, where the ether forms a three-atom ring: two atoms of carbon and one atom of oxygen.This triangular structure has substantial ring strain, making epoxides highly reactive, more so than other ethers.
The use of hydrogen peroxide as an oxidant would be advantageous, making the reaction more environmentally friendly as the sole byproduct is water. [7] Benzeneseleninic acid derivatives as catalysts have been reported to give high selectivity with hydrogen peroxide as the oxidant. [ 25 ]