CAS No. 76824-35-6

Batch: Purity:99.48
Famotidine  Chemical Structure
Chemical Structure
Check the Famotidine product page for in-depth specifications, including solubility, stock solutions, MOA, and working concentrations.

Chemical Information

IUPAC Name 3-[[2-(diaminomethylideneamino)-1,3-thiazol-4-yl]methylsulfanyl]-N'-sulfamoylpropanimidamide
CAS Number 76824-35-6
Molecular Formula

C8H15N7O2S3

Molecular Weight (MW) 337.45
SMILES C1=C(N=C(S1)N=C(N)N)CSCCC(=NS(=O)(=O)N)N
InChIKey XUFQPHANEAPEMJ-UHFFFAOYSA-N

Ordering Information

Biological Activity

Famotidine is a potent histamine H2 receptor antagonist that selectively blocks H2 receptor activity. By inhibiting histamine binding to parietal cells, famotidine suppresses histamine-stimulated gastric acid secretion and lowers basal acid levels. This competitive antagonism attenuates intracellular cAMP accumulation, resulting in significant gastric mucosal protection and inhibition of ulcer formation in cellular and animal lesion models. [1]

How to Prepare Stock Solution?

Concentration Volume Mass
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Solubility

Batch:
All in vitro solubility values are batch-tested experimental data (non-literature values).
Solvent Solubility & Note
DMSO 67 mg/mL (198.54 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO. The recommended stock concentration is 10 mM in DMSO.)
Water Insoluble
Ethanol Insoluble
FAQ
Q: Why does a DMSO stock precipitate in media/saline?
A: It is caused by unheated aqueous media (supersaturation), local solvent shock, or incorrect mixing sequence.
How to fix it?
  • Preheat media/saline to 37°C.
  • Mix rapidly (pipette/vortex) upon addition.
  • For complex mixes, always add the aqueous phase last.
  • Re-dissolve minor precipitates with a 37°C water bath and sonication (≤30 min).

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Note: Technical data last updated: Sep 1, 2026.