Tetrabutyl ammonium hydrogen sulfate

The sodium and potassium salts of glutaconaldehyde are soluble only in polar solvents such as water, dimethyl sulfoxide, N,N-dimethylformamide, pyridine, and methanol. However, the stable tetrabutylammonium salt is soluble in relatively nonpolar solvents such as chloroform and ethyl acetate. It may be prepared from the potassium salt in the following manner. In a 1-1. Erlenmeyer flask equipped with a magnetic stirring bar are placed a solution of 13.6g. (0.1 mole) of crude glutaconaldehyde potassium salt in 200 ml. of water and a solution of 33.9 g. (0.1 mole) of tetrabutyl-ammonium hydrogen sulfate in 200 ml. of ice-cold water, the pH of wliich was adjusted to 10 by adding aqueous 2M sodium hydroxide. 

Amine extraction of penicillins has been examined in a pilot scale extractor and its performance has been analyzed through suitable mathematical models 117-19]. Extraction efficiency as high as 90% was achieved under suitable conditions. The procedure for selection of volume ratios of the aqueous to organic phase and concentration ratio of carrier (Amberlite LA-2) to penicillin-G at a desired degree of extraction and enrichment has recently been described [20]. Ion-pair extraction of penicillin-V and phenoxy acetic acid with Amberlite LA-2 hydrochloride and tetrabutyl ammonium hydrogen sulfate can be effective in... 

Facilitated transport of penicilHn-G in a SLM system using tetrabutyl ammonium hydrogen sulfate and various amines as carriers and dichloromethane, butyl acetate, etc., as the solvents has been reported [57,58]. Tertiary and secondary amines were found to be more efficient carriers in view of their easy accessibility for back extraction, the extraction being faciUtated by co-transport of a proton. The effects of flow rates, carrier concentrations, initial penicilHn-G concentration, and pH of feed and stripping phases on transport rate of penicillin-G was investigated. Under optimized pH conditions, i. e., extraction at pH 6.0-6.5 and re-extraction at pH 7.0, no decomposition of peniciUin-G occurred. The same SLM system has been applied for selective separation of penicilHn-G from a mixture containing phenyl acetic acid with a maximum separation factor of 1.8 under a liquid membrane diffusion controlled mechanism [59]. Tsikas et al. [60] studied the combined extraction of peniciUin-G and enzymatic hydrolysis of 6-aminopenicillanic acid (6-APA) in a hollow fiber carrier (Amberlite LA-2) mediated SLM system. 

Ten benzimidazoles Milk NaOH addn, EtOAc extn, liq-liq partn 5 Nucleosil 120 Ci8, 5 m O.OIM H3PO4/ ACN (80 20) contg 5 mM tetrabutyl-ammonium hydrogen sulfate, at 50 C UV 292 nm 2-40 ppb/ 59-100% 343... 

Procedure (See Chromatography, Appendix IIA.) Use a high-performance liquid chromatograph capable of separating acesulfame potassium and 4-hydroxybenzoic acid ethyl ester with a resolution of 2. Use a chromatograph equipped with a UV or diode array (227 nm) detector and a 25-cm x 4.6-mm (id) stainless steel column, or equivalent, packed with 3 to 5 p,m of reversed phase C18 silica gel, or equivalent. The elution is isocratic. Use a 40 60 (v/v) solution of acetoni-trile 0.01 MlL tetrabutyl ammonium hydrogen sulfate (TBAHS) in water as the mobile phase, with a flow rate of about 1 mL/min. 

This reaction was carried out in a water-chlorobenzene mixtin-e in the presence of NaOH and tetrabutyl ammonium hydrogen sulfate (484). 

While a number of different phase transfer catalysts such as tetrabutyl ammonium halides (Ref. 10, 11), tetrabutyl ammonium hydroxide (Ref. 16-18), tetrabutyl ammonium hydrogen sulfate (Ref. 21-22), Adogen-464 (Ref. 16, 18), tetrabutyl phosphonium bromide (Ref. 19, 20), 18-crown-6 (Ref. 12, 13, 19, 20), cryptand [222] (Ref. 21, 22), etc., have been used in the chemical modification of polymers, few systematic studies of the influence of the catalyst on the reactions have been done. It is presumed that the same considerations which govern the choice of a phase transfer catalyst for classical organic synthesis also apply in the case of reactions with polymers. 

Tetrabutyl ammonium phosphate, and tetramethyl ammonium hydrogen sulfate. 

See Tetra-n-butyl ammonium hydroxide 1-Butanaminium, N,N,N-tributyl-, iodide. See Tetrabutyl ammonium iodide 1-Butanaminium, N,N,N-tributyl-, sulfate (1 1). See Tetra-n-butyl ammonium hydrogen sulfate Butanaminium, N,N,N-trimethyl-4-(2-acetamidoethoxy), chloride. See Acetamidoethoxybutyl trimonium chloride... 

TBAEMA. See t-Butylaminoethyl methacrylate TBAF. See Tetrabutyl ammonium fluoride TBAHS. See Tetra-n-butyl ammonium hydrogen sulfate... 

Benzyl trimethyl ammonium hydroxide Cetrimonium bromide Dimethyl diallyl ammonium chloride Laurtrimonium bromide Laurtrimonium chloride Methyl tributyl ammonium chloride Tetrabutyl ammonium bromide Tetrabutyl ammonium chloride Tetrabutyl ammonium fluoride Tetra-n-butyl ammonium hydrogen sulfate Tetra-n-butyl ammonium hydroxide Tetrabutyl ammonium iodide Tetrabutylphosphonium acetate, monoacetic acid Tetrabutylphosphonium bromide Tetrabutylphosphonium chloride Tetraethylammonium bromide Tetraethylammonium hydroxide Tetrakis (hydroxymethyl) phosphonium chloride Tetramethylammonium bromide Tetramethylammonium chloride Tetramethylammonium hydroxide Tetramethyl ammonium iodide Tetraphenyl phosphonium bromide Tetrapropyl ammonium bromide Tetrapropyl ammonium iodide Tributylamine Tributyl phosphine Tributyl (tetradecyl) phosphonium chloride Trioctyl (octadecyl) phosphonium iodide catalyst, phase-transfer Tetraethylammonium chloride Tetraoctylphosphonium bromide Tri-n-butyl methyl ammonium chloride Tri methyl phenyl ammonium hydroxide catalyst, phenolics Triethylamine... 

Ion-pair chromatography has also been used for the separation of aspartame from other sweeteners. The ion-pair reagents commonly used are triethylammonium phosphate (32), tetra-ethylammonium hydroxyde (47), tetrapropylammonium hydroxide (40), pentanesulfonate (52), tetrabutylammonium phosphate (34), tetrabutylammonium hydrogen sulfate (66), and tetrabutyl-ammonium p-toluenesulfonate (24). 

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