Sodium (R)-6-methoxy-2-(((4-methoxy-3,5-dimethylpyridin-2-yl)methyl)sulfinyl)benzo[d]imidazol-1-ide

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Reagent Code: #232775
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CAS Number 161796-77-6

science Other reagents with same CAS 161796-77-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 367.4 g/mol
Formula C₁₇H₁₈N₃NaO₃S
badge Registry Numbers
MDL Number MFCD23160332
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Widely used in the pharmaceutical industry as a key component in proton pump inhibitors (PPIs), this (R)-enantiomer is effective in reducing gastric acid production. It is primarily employed in the treatment of gastroesophageal reflux disease (GERD), peptic ulcers, and Zollinger-Ellison syndrome. Due to its enantiomeric purity, it provides a defined pharmacokinetic profile distinct from racemic mixtures. It is often formulated in enteric-coated tablets to protect the compound from degradation in the acidic environment of the stomach, ensuring targeted release in the small intestine for optimal absorption.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿4,680.00

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Sodium (R)-6-methoxy-2-(((4-methoxy-3,5-dimethylpyridin-2-yl)methyl)sulfinyl)benzo[d]imidazol-1-ide
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Widely used in the pharmaceutical industry as a key component in proton pump inhibitors (PPIs), this (R)-enantiomer is effective in reducing gastric acid production. It is primarily employed in the treatment of gastroesophageal reflux disease (GERD), peptic ulcers, and Zollinger-Ellison syndrome. Due to its enantiomeric purity, it provides a defined pharmacokinetic profile distinct from racemic mixtures. It is often formulated in enteric-coated tablets to protect the compound from degradation in the acid

Widely used in the pharmaceutical industry as a key component in proton pump inhibitors (PPIs), this (R)-enantiomer is effective in reducing gastric acid production. It is primarily employed in the treatment of gastroesophageal reflux disease (GERD), peptic ulcers, and Zollinger-Ellison syndrome. Due to its enantiomeric purity, it provides a defined pharmacokinetic profile distinct from racemic mixtures. It is often formulated in enteric-coated tablets to protect the compound from degradation in the acidic environment of the stomach, ensuring targeted release in the small intestine for optimal absorption.

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