Ranitidine hydrochloride

Cat. No. 1967

Ranitidine hydrochloride C13H22N4O3S.HCl [66357-59-3]

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Chemical Name: N-[2-[[[5-[(Dimethylamino)methyl]-2-furanyl]methyl]thio]ethyl]-N'-methyl-2-nitro-1,1-ethanediamine hydrochloride

Biological Activity

Potent, selective and competitive histamine H2 receptor antagonist (pA2 = 6.95 - 7.2). Inhibits gastric acid secretion induced by histamine, pentagastrin, bethanecol and food in vivo. Also inhibits aspirin-induced gastric lesions.

Technical Data

M.Wt:
350.86
Formula:
C13H22N4O3S.HCl
Solubility:
Soluble to 50 mM in water
Purity:
>99 %
Storage:
Desiccate at +4°C
CAS No:
66357-59-3

The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
All Tocris products are intended for laboratory research use only.

Certificate of Analysis / Safety Data Sheet

Certificate of Analysis: View current batch
Safety Data Sheet: View Safety Data Sheet

Brittain and Daly (1981) A review of the animal pharmacology of ranitidine - a new, selective histamine H2-antagonist. Scand.J.Gastroenterol.Suppl. 69 1.

Daly et al (1981) Some in vitro and in vivo actions of the new histamine H2-receptor antagonist, ranitidine. Br.J.Pharmacol. 72 49. PMID: 6112034.

Daly et al (1981) Antagonism of vasodepressor and gastric secretory responses to histamine by the H2-receptor antagonists, ranitidine and cimetidine, in the anaesthetized dog. Br.J.Pharmacol. 72 55. PMID: 6112035.

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Citations are publications that use Tocris products. Selected citations for Ranitidine hydrochloride include:

Kwiatkowski et al (2013) Coordination of distinct but interacting rhythmic motor programs by a modulatory projection neuron using different co-transmitters in different ganglia. J Exp Biol 216 1827. PMID: 23393282.

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Keywords: Ranitidine hydrochloride, supplier, Selective, H2, antagonists, receptors, histamine, histaminergic, h2, antagonist, Tocris Bioscience, Histamine H2 Receptor Antagonist products

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