High-Purity Rabeprazole Sulfide: CAS 117977-21-6 for Pharmaceutical Research
Discover a critical pharmaceutical intermediate essential for R&D and quality control in the pharmaceutical industry.
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![1H-Benzimidazole,2-[[[4-(3-methoxypropoxy)-3-methyl-2-pyridinyl]methyl]thio]-](https://www.nbinno.com/2025/webimg/gemini_688ce9a233711_1754065314.png)
1H-Benzimidazole,2-[[[4-(3-methoxypropoxy)-3-methyl-2-pyridinyl]methyl]thio]-
This high-purity chemical compound, identified by CAS 117977-21-6, serves as a vital pharmaceutical intermediate and reference standard. Its primary utility lies in supporting analytical method development and validation for critical drug substances, ensuring the quality and safety of pharmaceutical products.
- High Purity for Reliable Analysis: With a purity of u226599%, this compound ensures accurate results in Rabeprazole Sulfide CAS 117977-21-6 purity assays and other critical analytical procedures.
- Essential for Pharmaceutical R&D: As a key pharmaceutical reference standard for Rabeprazole, it is indispensable for researchers developing new drug formulations and analytical techniques.
- Key Role in Quality Control: This Rabeprazole EP Impurity B chemical intermediate is crucial for quality control departments to ensure that drug products meet stringent regulatory requirements.
- Facilitates Synthesis and Evaluation: The availability of this compound supports the precise CAS 117977-21-6 intermediate synthesis, enabling thorough evaluation of Rabeprazole-related compounds.
Key Advantages Offered
Uncompromising Purity
Benefit from u226599% purity, ensuring the reliability of your research findings and analytical outcomes when utilizing this Rabeprazole Sulfide CAS 117977-21-6 purity compound.
Dedicated Research Support
This product is an ideal choice for buy Rabeprazole Sulfide for R&D, providing researchers with a trusted source for critical developmental work.
Regulatory Compliance Assurance
Utilizing this compound as a pharmaceutical reference standard for Rabeprazole aids in meeting regulatory guidelines and demonstrating product quality.
Key Applications
API Intermediate
Serve as a crucial building block in the synthesis of Active Pharmaceutical Ingredients (APIs), contributing to the development of new therapeutic agents.
Reference Standard
Function as a precisely characterized reference standard for analytical testing, essential for method validation and quality assurance in the pharmaceutical sector.
Analytical Method Development
Aid in the development and optimization of analytical methods for identifying and quantifying related substances, ensuring the purity and efficacy of pharmaceutical products.
Impurity Profiling
Assist in the detailed impurity profiling of pharmaceutical compounds, a critical step in meeting stringent drug regulatory requirements.