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Permanganates sodium permanganate

Permanganate. Sodium permanganate, permanganate of soda, [CAS 10101-50-5], NaMn0 3H20. purple solid, soluble, formed by oxidation of acidified sodium manganate solution with chlorine, and then evaporating. Used (1) as disinfectant and bactericide, (2) in medicine. [Pg.1492]

Hydrogen chloride Acetic anhydride, aluminum, 2-aminoethanol, ammonia, chlorosulfonic acid, ethylenediamine, fluorine, metal acetylides and carbides, oleum, perchloric acid, potassium permanganate, sodium, sulfuric acid... [Pg.1208]

Sofid sodium permanganate monohydrate has been shown to be a selective synthetic reagent (156). It is typically used in hexane for the heterogeneous oxidation of aldehydes, alcohols, and sulfides. Synthetic methodology based on crystal surfaces exhibited greater selectivity, higher yield, and easier work-up as compared to aqueous permanganate reactions. [Pg.522]

Chemical Treatment. Some organic compounds are attacked by chemical reagents such as potassium permanganate, sodium hydroxide, calcium hypochlorite, and o2one (29,30). [Pg.226]

Bromophenol blue Potassium permanganate Sodium carbonate decahydrate Ethanol... [Pg.228]

The effect of inorganic additives upon ignition delay in anilinium nitrate-red finning nitric acid systems was examined. The insoluble compounds copper(I) chloride, potassium permanganate, sodium pentacyanonitrosylferrate and vanadium(V) oxide were moderately effective promoters, while the soluble ammonium or sodium metavanadates were very effective, producing vigorous ignition. [Pg.1573]

As an example, bulk modification by the organic reaction of unsaturated PHA with sodium permanganate resulted in the incorporation of dihydroxyl or carboxyl functional groups [106]. Due to the steric hindrance of the isotactic pendant chains, complete conversion could not be obtained. However, the solubility of the modified polymers was altered in such a way that they were now completely soluble in acetone/water and water/bicarbonate mixtures, respectively [106]. Solubility can play an important role in certain applications, for instance in hydrogels. Considering the biosynthetic pathways, the dihydroxyl or carboxyl functional groups are very difficult to incorporate by microbial synthesis and therefore organic chemistry actually has an added value to biochemistry. [Pg.271]

Sodium perborate monohydrate Sodium perborate tetrahydrate Sodium percarbonate Sodium perchlorate Sodium perchlorate monohydrate Sodium permanganate Sodium peroxide Sodium persulfate Strontium chlorate Strontium perchlorate Strontium peroxide Tetranitromethane Thallium chlorate Trichloro-s-triazinetrione (trichloroisocyanuric) (acid all forms)... [Pg.64]

The acid, referred to as tetra acid , is prepared as follows In a Friedel-Crafts reaction, acenaphthene 72 is reacted with malonic dinitrile and aluminum chloride. The resulting condensation product 75 is oxidized with sodium chlorate/hy-drochloric acid to form the dichloroacenaphthindandione 76. Oxidation with sodium hypochlorite solution/sodium permanganate affords naphthalene tetracar-boxylic acid 68, mostly existing as the monoanhydride 68a. The dianhydride, on the other hand, evolves only after drying at approx. 150°C. [Pg.483]

Bis(benzene)chromium dichromate, 3851 Calcium chromate, 3926 Copper chromate oxide, 4223 Dibismuth dichromium nonaoxide, 0232 Lead chromate, 4243 Lithium chromate, 4236 Magnesium permanganate, 4691 Potassium dichromate, 4248 Potassium permanganate, 4647 Sodium dichromate, 4250 Sodium molybdate, 4713 Sodium permanganate, 4703 Zinc permanganate, 4710... [Pg.249]

Sodium perchlorate, 4040 Sodium permanganate, 4703 Sodium peroxide, 4803 Sodium peroxodisulfate, 4809 f Sulfur, 4897 Sulfuric acid, 4479 Sulfur trioxide, 4849... [Pg.310]

Sodium permanganate (NaMnO ) is a purple crystal that is soluble in water and is used as an oxidizing agent, disinfectant, and bactericide and as an antidote for morphine poisoning. [Pg.53]

Piroxicam Piroxicam, 1,1 -dioxid-4-hydroxy-2-methyl-iV-2-pyradyl-2//-1,2-benzothiazine-3-carboxamide (3.2.78), is synthesized from saccharin (3.2.70). Two methods for saccharin synthesis are described. It usually comes from toluene, which is sulfonated by chlorosulfonic acid, forming isomeric 4- and 2-toluenesulfonyl chlorides. The isomeric products are separated by freezing (chilling). The liquid part, 2-toluenesulfonyl chloride (3.2.68) is separated from the crystallized 4-toluenesulfochloride and reacted with ammonia, giving 2-toluenesul-fonylamide (3.2.69). Oxidation of the product with sodium permanganate or chromium (VI) oxide in sulfuric acid gives saccharin—o-sulfobenzoic acid imide (3.2.70) [123-126]. [Pg.51]

The position and geometry of the side chain double bonds can be determined by ozonolysis and a potassium permanganate-sodium periodate oxidation, as well as by the IR spectrum. Results have shown that the side chain double bonds are always Z 16,122,126). [Pg.238]

Many classical oxidations are frequently performed in aqueous media, using oxidants such as potassium permanganate, sodium periodate, or sodium or calcium hypochlorite (Hudlicky, 1990). Cyclohexene can now be oxidized directly to colorless crystalline adipic acid with aqueous 30 percent hydrogen peroxide under organic solvent-and halide-free conditions, as discussed earlier (Sato et al., 1998) (see fig. 6.1). [Pg.164]

Addition of potassium permanganate removes colored impurities that otherwise persist through subsequent distillations of the acid. The maximum concentration of potassium permanganate in water at room temperature is about 5%. It may be more convenient to use a concentrated solution of sodium permanganate, which is very soluble in water. However, the end point is difficult to observe with sodium permanganate. [Pg.78]

Decomposition was initiated by the addition of a concentrated aqueous solution of calcium and sodium permanganate to the hydrogen peroxide. The use of potassium permanganate proved ineffective since KMn04 is insufficiently soluble in water and the solution contains inadequate MnO -ions for rapid initiation of the reaction. [Pg.302]

Aluminum sulfate Calcium hydroxide Calcium sulfate Copper sulfate Ferric chloride Potassium permanganate Sodium chloride Anhydrous TSP Hydrated TSP Sodium hydroxide... [Pg.418]


See other pages where Permanganates sodium permanganate is mentioned: [Pg.365]    [Pg.9]    [Pg.908]    [Pg.516]    [Pg.96]    [Pg.95]    [Pg.657]    [Pg.338]    [Pg.984]    [Pg.984]    [Pg.1026]    [Pg.1768]    [Pg.1477]    [Pg.860]    [Pg.348]    [Pg.1123]    [Pg.29]    [Pg.368]    [Pg.469]    [Pg.471]    [Pg.395]    [Pg.96]    [Pg.908]    [Pg.1492]    [Pg.185]   
See also in sourсe #XX -- [ Pg.8 , Pg.180 ]




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Alcohols, primary with sodium permanganate

Alcohols, secondary, oxidation with sodium permanganate

Oxidation sodium permanganate monohydrate

Oxidation with Sodium Periodate and Potassium Permanganate

Potassium permanganate and sodium

Potassium permanganate and sodium periodate

Potassium permanganate-sodium periodate

Sodium permanganate

Sodium permanganate carboxylic acids

Sodium permanganate monohydrate

Sodium permanganate monohydrate oxidant

Sodium permanganate oxidation

Sodium permanganate primary amines

Sodium permanganate, decomposition

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