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Amines amine salts

Substances determined amines, amine salts, amino acids, salts of acids... [Pg.590]

CF3S03H phosphonitrilic chlorides such as (Cl3PN(PCl2N) PCl3)+PCl-6 strong bases such as KOH, NaOH, and (CH3)4NOH as well as amines, amine salts of carboxylic acids, ion exchange resin, and clays activated with mineral acids. One of the most efficient and extensively used in industry is the catalytic system based on phosphonitrilic chlorides (70—72). [Pg.45]

There is no difference in water solubilities for amines and amine salts containing up to four carbons. Both are miscible with water in all proportions. However, there is a large difference for amines and amine salts of five or more carbons. Amines of five or more carbons are much less soluble than amines of less than five carbons. The polar portion of the molecule is water-compatible while the nonpolar portion is not. Water solubility occurs unless the nonpolar portion is too large. Too large is five or more carbons for all families except for salts such as the amine salts. Amine salts are ionic and much more water-compatible than the polar amines. Amine salts show water solubility even when there are more than five carbons. [Pg.322]

Biocides can be subdivided according to their chemical structure into seven main types inorganic compounds hydrocarbons, halogenated hydrocarbons and nitrocompounds alcohols, phenols and their derivatives aldehydes, ketones, organic acids and their derivatives amines, amine salts and quaternary ammonium compositions metal-organic compositions heterocyclic compounds. The characteristics of the most useful biocides are shown in Table 4. [Pg.125]

Inhibitors may be classified as shown in Fig. 6.1. There are two major classes inorganic and organic. The anodic type of inorganic inhibitors includes chromates, nitrites, molybdates and phosphates, and the cathodic type includes zinc and polyphosphate inhibitors. The film forming class is the major class of organic inhibitor as it includes amines, amine salts and imidazolines - sodium benzoate mercaptans, esters, amines and ammonia derivatives. [Pg.354]


See other pages where Amines amine salts is mentioned: [Pg.45]    [Pg.789]    [Pg.45]    [Pg.2628]    [Pg.203]    [Pg.901]    [Pg.901]    [Pg.903]    [Pg.905]    [Pg.907]    [Pg.1204]    [Pg.396]    [Pg.7583]    [Pg.566]    [Pg.114]    [Pg.915]    [Pg.915]    [Pg.917]    [Pg.919]    [Pg.921]    [Pg.923]    [Pg.127]    [Pg.363]   
See also in sourсe #XX -- [ Pg.901 , Pg.908 ]

See also in sourсe #XX -- [ Pg.915 , Pg.916 , Pg.917 , Pg.918 , Pg.919 , Pg.920 , Pg.921 , Pg.922 , Pg.923 , Pg.924 , Pg.925 , Pg.926 , Pg.927 , Pg.928 , Pg.929 , Pg.930 , Pg.931 , Pg.932 ]




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1, 2, 4, Thiadiazole diazonium salts with amines

1.2- Dithiolylium salts reaction with amines

1.3- Propanediamine, monopotassium salt deprotonation of amines

Acid salts, of amines

Alkylation with amines and ammonium salts

Amides, tertiary Amine salts

Amidinium salts aminal ester synthesis

Amine Salts as Phase-Transfer Catalysts

Amine alkylammonium salt

Amine oxides salt formation

Amine picrate salts

Amine salt cross-linking

Amine salt, preparation

Amine salts, coordination compound

Amine salts, coordination compound synthesis with

Amine salts, group frequencies

Amine salts, infrared spectra

Amine salts, unsaturated

Amine-salt process

Amines Diazonium salts

Amines acridinium salts

Amines amidinium salt synthesis

Amines aminium salts

Amines ammonium salts

Amines ammonium salts, quaternar

Amines arenediazonium salts

Amines base metal salts

Amines compounds, diazonium salts

Amines conversion into diazonium salts

Amines copper salt-catalyzed

Amines coupling with diazonium salts

Amines cyclimmonium salts

Amines from ammonium salts

Amines iminium salts

Amines mercury salts

Amines quaternary ammonium salts

Amines salt formation

Amines salts

Amines salts

Amines salts formed between carboxylic acids

Amines via diazonium salts

Amines, acetylation salts

Ammonium salts, alkyl amines

Aromatic Amines and Diazonium Salts

Azomethinium salts aminals

Basicity of Amines Amine Salts

Benzopyrylium salts, amination

Binaphthyl-derived Cyclic Amines and Their Salts as Asymmetric Organocatalysts

Copper salts amine complexes

Cyclimmonium salts amines, tert

Cyclimmonium salts amines, tert., cyclic

Diazonium salts amine deamination

Diazonium salts formation from primary amines

Diazonium salts from amines

Diazonium salts from aryl amines

Diazonium salts, amine reactions

Diazonium salts, amine reactions coupling

Diazonium salts, amine reactions preparation

Diazonium salts, amine reactions reduction

Dithiocarbamic acid salts, from amines

Formamidinium salts amines

Fremy’s salt primary amines

Fremy’s salt secondary amines

Hydrazinium salts amines, tert

Hydrochloride salts, of amines

Imine salts from amines

Iminium salts, addition amines with aldehydes

Iminium salts, from amines

Ketene aminals amidinium salt synthesis

Ketene aminals amidinium salts

Magnesium, tris salts amines

Metal amine salts

Metal reaction with amine salts

Methyl iodide quaternary amine salt

Nitrogen as a nucleophile ammonium salts, amines

Onium salts, from amines

Oxazolium salts amines

Pharmacologically active amine salts

Picric acid amine salts

Picric acid salts with amines

Primary amines with carboxylic acid salts

Primary amines, derivatives diazonium salt reaction

Pyridinium salt amine

Pyridinium salt amine 2518 Transformation

Pyrylium salts reactions with primary amines

Quaternary amine salts

Reaction of Amines with Strong Acids Amine Salts

Reaction with amine acid salts

Reactions with amine salts

Salt synthesis neutralized amines

Salts of amines

Solvent extraction amine salts

Subject amine salts

Sulphonate salts amination

Tertiary Amines and Quaternary Ammonium Salts

Tertiary amines quaternary salt formation

Thiopyrylium salts, reaction with amines

Triflate salts, amine neutralization

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