Product overview

Name Ranitidine hydrochloride
Purity >99%
Description Potent, selective, competitive H2 receptor antagonist
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Biological Data

Biological description Potent, selective and competitive H2 receptor antagonist (Ki = 0.14 µM). Decreases the secretion of gastric acid and pepsin. Shows antioxidant, antinociceptive and hepatoprotective actions.

Solubility & Handling

Storage instructions +4°C (desiccate)
Solubility overview Soluble in water (50 mM)
Important This product is for RESEARCH USE ONLY and is not intended for therapeutic or diagnostic use. Not for human or veterinary use.

Calculators

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Dilution

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Chemical Data

Purity >99%
Chemical name N-[2-[[[5-[(Dimethylamino)methyl]-2 -furanyl]methyl]thio]ethyl]-N'-methyl-2-nitro-1,1-e thanediamine hydrochloride
Molecular Weight 350.86
Chemical structure Ranitidine hydrochloride [66357-59-3] Chemical Structure
Molecular Formula C13H22N4O3S.HCl
CAS Number 66357-59-3
PubChem identifier 3033332
SMILES CN/C(=C\[N+](=O)[O-])/NCCSCC1=CC=C(O1)CN(C)C.Cl
InChi InChI=1S/C13H22N4O3S.ClH/c1-14-13(9-17(18)19)15-6-7-21-10-12-5-4-11(20-12)8-16(2)3;/h4-5,9,14-15H,6-8,10H2,1-3H3;1H/b13-9+;
InChiKey GGWBHVILAJZWKJ-KJEVSKRMSA-N
MDL number MFCD00069339