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Amezinium Methyl Sulfate

Chemical Name 4-Amlno-6-methoxy-1ishenylpyridazinium methyl sulfate Common Name — [Pg.57]

Reicheneder, F. and Kropp, R. U.S. Patent 3,631 P38 December 28,1971 assigned to Badische Anilin und Soda-Fabrik A.G. [Pg.57]

Chemical Name (S)-0-3-amino-3-deoxy-oi-D-glucopyranosyl-(1- 6)-0-[6-amino-6-deoxy-oi-D-glucopyranosyl-(1- 4)] -N -(4-amino-2-hydroxy-1-oxobutyl)-2-deoxy-D-streptamine [Pg.57]

Trade Name Manufacturer Country Year Introduced [Pg.58]

L-(-)-7-Amino-a-hydroxybutyric Acid N-hydroxysuccinimide 6 -Monobenzyloxy-carbonyl-kanamycin A Sulfuric Acid [Pg.58]

7 parts of 1 i3henyl-4.aminopyridazone-(6) and 19 parts of dimethyl sulfate in 400 parts of xylene are kept at 120°C for one hour while mixing well. The reaction mixture Is suction filtered, 28 parts (895% of the theory) of 1-phenyl-4.amino-6-methoxypyridazinium metho-sulfate is obtained having a melting point of 173° to 174°C after recrystallization from acetonitrile. The perchlorate has a melting point of 179° to 182°C. [Pg.57]

Amezinium methyl sulfate Bromopride Cefoxitin sodium Cimetide... [Pg.1630]

See other pages where Amezinium Methyl Sulfate is mentioned: [Pg.56]    [Pg.1735]    [Pg.243]    [Pg.64]    [Pg.56]    [Pg.1735]    [Pg.56]    [Pg.1735]    [Pg.12]    [Pg.56]    [Pg.1735]    [Pg.243]    [Pg.64]    [Pg.56]    [Pg.1735]    [Pg.56]    [Pg.1735]    [Pg.12]    [Pg.404]    [Pg.435]    [Pg.404]    [Pg.435]   


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