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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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CAS No. 

2016-36-6 Choline salicylate

China (Mainland)   2360
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CAS No. 

2016-36-6 Choline salicylate

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CAS No. 

2016-36-6 Choline salicylate

India   6
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CAS No. 

2016-36-6 Choline Salicylate

Chemistry: TOXICITY: SAFETY: Production: Others: Name: Choline salicylate Synonyms:(2-Hydroxyethyl)trimethylammonium salicylate Molecular Formula C7H5O3.C5H14NO Molecular Weight 241.28 CAS Registry Number 2016-36-6 EINECS 217-948-8
China (Mainland)   6
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CAS No. 

2016-36-6 Choline salicylate

Choline Salicylate Solution B.P 5 MT
India  
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CAS No. 

2016-36-6 CHOLINE SALICYLATE

As per BP
India   20
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CAS No. 

2016-36-6 Choline salicylate

It is an OTC product and used as a gel for the treatment of oral ulcers
India  
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CAS No. 

2016-36-6 CHOLINE SALICYLATE

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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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