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Ranitidine hydrochloride
Cat. No.:
OB0225LY-0100
Appearance:
Solid
Purity:
≥99%
Identity:
Confirmed by NMR and LC-MS.
Size:
Product Overview
Description:
Ranitidine hydrochloride is an H2 receptor antagonist used to reduce gastric acid secretion. Its salt form, hydrochloride, is its usual dosage form.
Synonym:
AH19065; 66357-59-3; 1,1-Ethenediamine, N-(2-(((5-((Dimethylamino)methyl)-2-furanyl)methyl)thio)ethyl)-N'-methyl-2-nitro-; 1,1-Ethenediamine, N-[2-[[[5-[(dimethylamino)methyl]-2-furanyl]methyl]thio]ethyl]-N'-methyl-2-nitro-; (E)-1-N'-[2-[[5-[(dimethylamino)methyl]furan-2-yl]methylsulfanyl]ethyl]-1-N-methyl-2-nitroethene-1,1-diamine; N-[2-[[[5-[(Dimethylamino)methyl]-2-furanyl]methyl]thio]ethyl]-n'-methyl-2-nitro-1,1-ethenediamine
CAS No.:
66357-59-3
Compound CID:
3001055
Formula:
C13H23ClN4O3S
Formula Weight:
350.86
Specification
Relative Density:
1.044 g/cm3
Stability:
3 years in powder form.
Storage:
Storage at -20°C.
Applications:
Ranitidine hydrochloride is Mainly used to study the treatment of gastroesophageal reflux disease (GERD), peptic ulcer, and prevention of recurrence of gastric acid-related diseases.
Library Information
Targets:
Antibacterial; P450; Histamine receptor
Receptors:
H2 receptor
Pathways:
GPCR/G protein; Immunology/Inflammation; Neuronal signaling; Microbiology/Virology; Metabolism
Plate Number:
AOCL-2
Plate Location:
c3
Empty Location:
a1-h1; a12-h12
Container:
96-well plate
Formulation:
10 mM DMSO
DMSO Max Solubility:
60 mg/mL; 171.01 mM
Water Max Solubility:
142.51 mM





