Detail of > 2016-36-6
- CAS Number:
- 2016-36-6
- Name:
Choline salicylate
- Formula:
- C7H5O3.C5H14NO
- Molecular Structure:

- Synonyms:
- (2-Hydroxyethyl)trimethylammonium salicylate
- Molecular Weight:
- 241.32
- EINECS:
- 217-948-8
- Density:
- g/cm3
- Boiling Point:
- 336.3 °C at 760 mmHg
- Flash Point:
- 144.5 °C
- Appearance:
- Clear, colourless liquid
- Safety:
- Moderately toxic by ingestion, intraperitoneal, and subcutaneous routes. An analgesic and antipyretic. When heated to decomposition it emits toxic fumes of NOx and NH3. See also CHOLINE.Details
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Reference
- Stabilized solid choline salicylate mixtures
- Stabilized solid choline salicylate mixtures. Sasmor, Ernest J. (Mundipharma A.-G., Switz.). Ger. Offen. DE 2701553 28 Jul 1977, 27 pp. (German). (Germany). CODEN: GWXXBX. CLASS: IC: C08B015-00. PRIORITY: US 76-651110 21 Jan 1976. DOCUMENT TYPE: Patent CA Section: 63 (Pharmaceuticals) Complexes of choline salicylate (I) [2016-36-6], carboxymethyl cellulose [9000-11-7], and divalent metal ions are prepd. In contrast to I, the complexes are not hygroscopic, are stable for £4 years, and can be made into tablets. For example, an aq. soln. of 90% I was mixed with an equimolar amt. of anhyd. aluminum hydroxy salicylate, and 2.5-25% (of the total wt.) I was added. The compn. was hardened and ground to give a stable, dry, free-flowing powder. The powder ws compressed with additives into tablets each contg. 435 mg I.
- Evaluation of drug bioavailability under clinical conditions
- Evaluation of drug bioavailability under clinical conditions. Cepelak, V.; Mayer, O.; Cepelakova, H.; Vitous, J.; Petrlik, M. (Dep. Clin. Pharmacol., Fac. Hosp., Plzen, Czech.). Zentralbl. Pharm., Pharmakother. Laboratoriumsdiagn., 116(4), 345-53 (German) 1977. CODEN: ZPPLBF. DOCUMENT TYPE: Journal CA Section: 1 (Pharmacodynamics) Serum levels of trimethazone [13221-27-7] (500 mg orally, i.m. or i.v.), ketazone [853-34-9] (500 mg in aq. and nonaq. solns., i.m.), xanthinol nicotinate [437-74-1] (1500 mg as xanidil or complamin, i.v.), salicylate (as arthropan [2016-36-6], acylpyrin [50-78-2], Syrap [2016-36-6], or choline salicylate [2016-36-6]) and several tribenoside [10310-32-4] prepns. or jaritin [37750-83-7] were compared in rats or man. Bioavailability was affected by drug form and administration route.
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