Benactyzine

Benactyzine hydrochloride Benoxinate hydrochloride Caramiphen edisylate Chloroprocaine HCI Dicyclomine HCI Valethamate bromide 4-( -Diethylaminoethoxy) benzophenone Clomiphene dihydrogen citrate 2-(2-Diethylaminoethyl) acetic acid ethyl ester Chromonar HCI 2-Diethylaminoethyiamine Ambenonium chloride Chlorisondamine chloride Diethylaminoethyl chloride Captodiamine Dlltiazem HCI Flurazepam Penthienate bromide Tiropramide Tripara nol... 

CftH 5NO 100-37-8) see Adiphenine Benactyzine Bielamiverine Dicycloverine Otilonium bromide Oxybuprocaine Oxyphenonium bromide Parethoxycaine Procaine Valethamate bromide 2-(diethylamino)ethanol hydrochloride (C HijCINO 14426-20-1) see Chloroprocaine... 

C,ftHij03 52182-15-7) see Benactyzine Benzilonium bromide Bevonium metilsulfate Propiverine Tropenziline bromide... 

Various drugs used in the treatment of Parkinson s disease (e.g., Benactyzine) can be hallucinogenic at higher doses. However, since they seem to produce a trip like that of the glycolate esters (Ditran, etc.), which they structurally resemble, these compounds should be avoided. 

Many organic chemicals are analyzed by RPC. These include various arylhydroxylamines as the N-hydroxyurea derivative with methyl isocyanate (614) alkyl- and alkoxy-disubstituted azoxybenzenes (6t5), n-alkyl-4-nitrophenylcarbonate esters ranging in length from methyl to octyl (616), 4-nitrophenol in the presence of 4-nitrophenyl phosphate (617), ben-zilic acid, and benactyzine-HCI using ion-pair chromatography (618), as well as aniline and its various metabolites (619), stereoisomers of 4,4 -dihydroxyhydrobenzoin (620), and aldehydes and ketones as the 2,4-dinitrophenylhydrazones (621). The technique has also been used to analyze propellants and hydrazine and 1,1-dimethylhydrazine were quantitita-vely determined (622, 623). 

When stored at 10-20 °C, solutions of III had their greatest stabilities at an initial pH of 6. 33 When the temperature of storage was 30°C or more, the initial pH that provided the greatest stability of the oxime in an aqueous solution was 5. With that initial pH, the estimated half-life of III in solutions stored at 40°C was 9.6 yr. The half-life of I in solutions at the pH of greatest stability, initially 4, for storage at 40°C was estimated to be 9 yr. In a solution containing also atropine and benactyzine at a pH of 2.8, 1.42 of the protective potency due to III was lost after 1 yr at 25°C.134... 

Berger and Wilson also reported the separation of 10 antidepressants (amitriptyline, imipramine, nortriptyline, desipramine, protripyline, bucliz-ine, benactyzine, hydroxyzine, perphenazine, and thioridazine) using a packed-column SFC with a tertiary mobile phase [37], A Lichrosphere cyanopropyl column with a mobile phase consisting of supercritical fluid carbon dioxide with 10% modifier (methanol with 0.5% isopropylamine) was used for the separation. It was noted that solutes did not elute without the addition of isopropylamine. Detection limits obtained were as low as 88 ppb for a 5-jul injection. 

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