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Basic sulfonates

For chemical processes, some examples are the elimination of aromatics by sulfonation, the elimination of olefins by bromine addition on the double bond (bromine number), the elimination of conjugated diolefins as in the case of the maleic anhydride value (MAV), and the extraction of bases or acids by contact with aqueous acidic or basic solutions. [Pg.26]

Imino-4-thiazolines are far more basic than their isomeric 2-aminothiazoles (see Table VI-1). They react with most electrophDic centers through the exocyclic nitrogen and are easily acylated (37, 477, 706) and sulfonated (652). The reaction of 2-imino-3-methyi-4-thiazoline (378) with a-chloracetic anhydride yields 379 (Scheme 217) (707). This exclusive reactivity of the exocyclic nitrogen precludes the direct synthesis of endocyclic quaternary salts of 2-imino-4-thiazolines. although this class of compounds was prepared recently according to Scheme 218 (493). [Pg.124]

Oxidation, already described in neutral and acidic media, may also be performed in basic medium. An alkaline solution of H2O2 reacts with 4-thiazoline 2-thione to yield thiazole-2-sulfonic acid (201-203), whereas alkaline oxidation performed with (NH )2S20g yields the disulfides (148). [Pg.397]

Most xanthene dyes are classified as basic dyes by their method of appHcation acid dyes can be produced by introduction of sulfonic acid groups. The fluoresceins, which contain carboxy and hydroxy substituents, are also acid dyes for coloration of silk. Some of the fluoresceins in which the carboxy group has been esterified, are soluble in alcohol or other organic solvents and can be classified as solvent dyes. Mordant dyes can be produced by introducing o-dihydroxy or sahcyhc acid groups (2), which when metallised can have very good lightfastness. [Pg.399]

The basic flow sheet for the flotation-concentration of nonsulfide minerals is essentially the same as that for treating sulfides but the family of reagents used is different. The reagents utilized for nonsulfide mineral concentrations by flotation are usually fatty acids or their salts (RCOOH, RCOOM), sulfonates (RSO M), sulfates (RSO M), where M is usually Na or K, and R represents a linear, branched, or cycHc hydrocarbon chain and amines [R2N(R)3]A where R and R are hydrocarbon chains and A is an anion such as Cl or Br . Collectors for most nonsulfides can be selected on the basis of their isoelectric points. Thus at pH > pH p cationic surfactants are suitable collectors whereas at lower pH values anion-type collectors are selected as illustrated in Figure 10 (28). Figure 13 shows an iron ore flotation flow sheet as a representative of high volume oxide flotation practice. [Pg.50]

The history of the discovery of amino acids is closely related to advances ia analytical methods. Initially, quantitative and qualitative analysis depended exclusively upon crystallization from proteia hydrolysates. The quantitative precipitation of several basic amino acids including phosphotungstates, the separation of amino acid esters by vacuum distillation, and precipitation by sulfonic acid derivatives were developed successively duriag the last century. [Pg.271]

Dyes, Dye Intermediates, and Naphthalene. Several thousand different synthetic dyes are known, having a total worldwide consumption of 298 million kg/yr (see Dyes AND dye intermediates). Many dyes contain some form of sulfonate as —SO H, —SO Na, or —SO2NH2. Acid dyes, solvent dyes, basic dyes, disperse dyes, fiber-reactive dyes, and vat dyes can have one or more sulfonic acid groups incorporated into their molecular stmcture. The raw materials used for the manufacture of dyes are mainly aromatic hydrocarbons (67—74) and include ben2ene, toluene, naphthalene, anthracene, pyrene, phenol (qv), pyridine, and carba2ole. Anthraquinone sulfonic acid is an important dye intermediate and is prepared by sulfonation of anthraquinone using sulfur trioxide and sulfuric acid. [Pg.79]

Historically, these sulfonates have been difficult to produce in good quaUty and to formulate into laundry powders because of thermal and hydrolytic stabihty problems. Used basically as an anionic, oleochemically sourced replacement for LAS, FAE sulfonate benefits include good detergency at low concentration, low environmental load, and good supply of high quaUty material (71). To avoid possible thermal stabihty problems, these sulfonates have found apphcation in Hquid products. They are used in at least one U.S. dishwashing Hquid, and the cocoyl derivative, Alpha-Step MC48, is marketed by Stepan Chemical Company. [Pg.242]

Dyes in these classes are generally basic dyes ie, the chiomophoie is cationic. Some stmctures have been sulfonated to acid dyes, eg, the Nigrosine, (Cl Solvent Black 5 Cl 50415), (8) to Cl Acid Black 2 [8005-03-6] (Cl 50420) (9). [Pg.420]

Diazophenols, ie, o-hydroxyaryldiazonium salts, couple to 1-naphthol in weaMy basic solution primarily in the para position, but as the hydroxyl ion concentration is increased, formation of the ortho isomer is favored and is frequentiy the sole product. Pyridine and pyridine derivatives, urea, and acetate, etc, used as buffers can also catalyze azo coupling reactions (28). l-amino-2-naphthol-4-sulfonic acid [116-63-2] (1,2,4-acid) and 1-naphthol yield the important Eriochrome Black A [3564-14-5] (18a, R = H) (Cl Mordant Black 3 Cl 14640) which is reportedly (20) a mixture of ortho and para isomers. [Pg.428]


See other pages where Basic sulfonates is mentioned: [Pg.360]    [Pg.583]    [Pg.589]    [Pg.140]    [Pg.909]    [Pg.1065]    [Pg.308]    [Pg.68]    [Pg.909]    [Pg.1065]    [Pg.201]    [Pg.208]    [Pg.125]    [Pg.360]    [Pg.583]    [Pg.589]    [Pg.140]    [Pg.909]    [Pg.1065]    [Pg.308]    [Pg.68]    [Pg.909]    [Pg.1065]    [Pg.201]    [Pg.208]    [Pg.125]    [Pg.323]    [Pg.303]    [Pg.591]    [Pg.134]    [Pg.278]    [Pg.118]    [Pg.316]    [Pg.278]    [Pg.339]    [Pg.439]    [Pg.257]    [Pg.258]    [Pg.331]    [Pg.460]    [Pg.461]    [Pg.184]    [Pg.158]    [Pg.74]    [Pg.82]    [Pg.86]    [Pg.109]    [Pg.199]    [Pg.259]    [Pg.267]    [Pg.425]    [Pg.426]   
See also in sourсe #XX -- [ Pg.308 ]




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