Identification | Back Directory | [Name]
PHENETHICILLIN POTASSIUM SALT | [CAS]
132-93-4 | [Synonyms]
cvk alpen darcil broxil pen200 penova pensig brl152 brocsil penemve maxipen optipen semopen synapen peniplus priospen oralopen chemipen alticina bendralan ro-cillin syncillin synerpenin alfacillin alfocillin chemipen-c astracillin dramcillin-s synthecillin penicillinmv synthecilline synthepentabl feneticilline penicillin-152 alpha-oralopen alpha-oracillin kphenethicillin pheno-m-penicillin penicillin B potassium penicillin-152potassium potassiumphenethicillin pheneticillin potassium PHENETHICILLIN POTASSIUM PHENETHICILLIN POTASSIUM SALT phenoxyaethylpenicillink-salz potassium(1-phenoxyethyl)penicillin alpha-phenoxyethylpenicillinpotassium -heptane-2-carboxylicacidpotassiumsalt potassiummethylphenoxymethylpenicillin PHENETHICILLIN POTASSIUM SALT USP/EP/BP potassium(alpha-phenoxyethyl)penicillin alpha-phenoxyethylpenicillinpotassiumsalt (2s-(2alpha,5alpha,6beta))-nopotassiumsal PHENETICILLIN POTASSIUM WHO(CRM STANDARD) α-Phenoxyethylpenicillinic acid, potassium a-phenoxyethylpenicillinicacidpotassiumsalt ALPHA-PHENOXYETHYLPENICILLINIC ACID POTASSIUM SALT potassium6-(alpha-phenoxypropionamido)penicillanate 6-(a-phenoxypropionamido)penicillanicacidpotassiumsalt 6-[α-Phenoxypropionamido] penicillanic acid potassium salt 3,3-dimethyl-7-oxo-6--4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylicacimo 4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylicacid,3,3-dimethyl-7-oxo-6-(2-p 3,3-dimethyl-7-oxo-6-[(1-oxo-2-phenoxypropyl)amino]-4-thia-1-azabicyclo[3.2.0] | [EINECS(EC#)]
205-084-4 | [Molecular Formula]
C17H19KN2O5S | [MDL Number]
MFCD00082379 | [MOL File]
132-93-4.mol | [Molecular Weight]
402.51 |
Hazard Information | Back Directory | [Originator]
Syncillin, Bristol, US ,1959 | [Definition]
ChEBI: Phenethicillin potassium is an organic potassium salt. It contains a phenethicillin(1-). | [Manufacturing Process]
Triethylamine (1.5 ml) was added to a cold solution (10°C) of αphenoxypropionic acid (1.66 g, 0.01 mol) in 15 ml of pure dioxane, with stirring and cooling to 5°C to 10°C while isobutyl chloroformate (1.36 g, 0.01 mol) in 5 ml of dioxane was added dropwise. Then the mixture was stirred for ten minutes at 5°C to 8°C. A solution of 6-amino-penicillanic acid (2.16 g, 0.01 mol) in 15 ml of water and 2 ml of triethylamine was then added dropwise while the temperature was maintained below 10°C. The resulting mixture was stirred in the cold for 15 minutes then at room temperature for 30 minutes, diluted with 30 ml of cold water and extracted with ether which was discarded. The cold aqueous solution was then covered with 75 ml of ether and acidified to pH 2 with 5 N H2SO4. After shaking, the ether layer containing the product 6-(α-phenoxypropionamido)penicillanic acid, was dried for ten minutes over anhydrous sodium sulfate and filtered. Addition of 6 ml of dry n-butanol containing 0.373 g/ml of potassium 2-ethylhexanoate precipitated the potassium salt of the product as a colorless oil which crystallized on stirring and scratching and was collected, dried in vacuo and found to weigh 2.75 g, to melt at 217°C to 219°C. | [Brand name]
Chemipen
(Bristol-Myers Squibb); Syncillin (Bristol-Myers
Squibb) [Name previously used: Phenethicillin.]. | [Therapeutic Function]
Antibacterial | [Safety Profile]
Poison by intravenous route. Moderately toxic by intraperitoneal route. When heated to decomposition it emits toxic fumes of K2O, SOx, and NOx. |
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