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A closely related mixture, sometimes called "base piranha", is a 5:1:1 mixture of water, ammonia solution (NH 4 OH, or NH 3 (aq)), and 30% hydrogen peroxide. [2] [3] As hydrogen peroxide is less stable at high pH than under acidic conditions, NH 4 OH (pH c. 11.6) also accelerates its decomposition.
Common cerumenolytics such as hydrogen peroxide and hydrogen peroxide - urea (also called carbamide peroxide) are topical preparations used to facilitate the removal of ear wax. Their side effects tend to be mild, including ear discomfort , transient loss of hearing, dizziness , and local irritation.
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.
Docusate is the common chemical and pharmaceutical name of the anion bis(2-ethylhexyl) sulfosuccinate, also commonly called dioctyl sulfosuccinate (DOSS). [ 2 ] [ 3 ] [ 4 ] Salts of this anion, especially docusate sodium , are widely used in medicine as an emollient laxative and as stool softeners , by mouth or rectally. [ 1 ]
hydrogen sulfide: Claus process: vanadium pentoxide (heterogeneous) sulfur: remediation of byproduct of oil refinery: methane, ammonia: Andrussow process: platinum (heterogeneous) hydrogen cyanide: basic chemicals, gold mining extractant ethylene: epoxidation: mixed Ag oxides (heterogeneous) ethylene oxide: basic chemicals, surfactants ...
Catalase is also used in the textile industry, removing hydrogen peroxide from fabrics to make sure the material is peroxide-free. [ 45 ] A minor use is in contact lens hygiene – a few lens-cleaning products disinfect the lens using a hydrogen peroxide solution; a solution containing catalase is then used to decompose the hydrogen peroxide ...
The Dakin oxidation. The Dakin oxidation (or Dakin reaction) is an organic redox reaction in which an ortho- or para-hydroxylated phenyl aldehyde (2-hydroxybenzaldehyde or 4-hydroxybenzaldehyde) or ketone reacts with hydrogen peroxide (H 2 O 2) in base to form a benzenediol and a carboxylate.
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 ...
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