Title: Phenocoll
CAS Registry Number: 103-97-9
CAS Name: 2-Amino-N-(4-ethoxyphenyl)acetamide
Additional Names: 2-amino-p-acetophenetidide; a-amino-p-acetophenetide; aminoacetophenetidine; 4-glycylaminophenol ethyl ether; glycine p-phenetidide; 4-glycylaminophenetol; glycocoll-p-phenetidide; phenokoll
Trademarks: Phenamine
Molecular Formula: C10H14N2O2
Molecular Weight: 194.23
Percent Composition: C 61.84%, H 7.27%, N 14.42%, O 16.47%
Literature References: Prepn: Majert, DE 59121; DE 59874 (1891 to Schering), Frdl. 3, 915, 918; DE 346809 (1921 to Schering), Frdl. 13, 1066; Karrer, Haebler, Helv. Chim. Acta 7, 534 (1924).
Properties: Crystals, mp 100.5°.
Melting point: mp 100.5°
Derivative Type: Monohydrate
Properties: Crystals, mp 95°.
Melting point: mp 95°
Derivative Type: Hydrochloride
CAS Registry Number: 539-10-6
Molecular Formula: C10H14N2O2.HCl
Molecular Weight: 230.69
Percent Composition: C 52.06%, H 6.55%, N 12.14%, O 13.87%, Cl 15.37%
Properties: Cryst powder. Sol in 20 parts water, in alcohol. More sol in hot water; slightly sol in benzene, chloroform, ether. Aq soln is neutral. Incompat. Alkali hydroxides or carbonates.
Derivative Type: Salicylate
CAS Registry Number: 140-47-6
Trademarks: Salocoll
Molecular Formula: C10H14N2O2.C7H6O3
Molecular Weight: 332.35
Percent Composition: C 61.44%, H 6.07%, N 8.43%, O 24.07%
Properties: Fine needles. Sweetish taste. Sol in 200 parts cold, 20 parts hot water. Incompat. As for the hydrochloride; with substances incompat with salicylates.
Therap-Cat: Antipyretic, analgesic.
Keywords: Analgesic (Non-Narcotic); Antipyretic.

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