Darunavir Impurity A (CAS 169280-56-2): Your Key Pharmaceutical Intermediate
High-purity intermediate essential for Darunavir synthesis, meeting global pharmaceutical standards.
Get a Quote & SampleProduct Core Value
![4-AMINO-N-[(2R,3S)-3-AMINO-2-HYDROXY-4-PHENYLBUTYL]-N-ISOBUTYLBENZENE-1-SULFONAMIDE](https://www.nbinno.com/2025/webimg/gemini_688c8b9ded440_1754041245.png)
4-AMINO-N-[(2R,3S)-3-AMINO-2-HYDROXY-4-PHENYLBUTYL]-N-ISOBUTYLBENZENE-1-SULFONAMIDE
As a critical building block for Darunavir, this high-purity intermediate ensures the efficacy and safety of the final antiviral drug. Its stringent quality control and adherence to pharmacopeial standards make it indispensable for pharmaceutical research and manufacturing.
- Discover the essential role of Darunavir Impurity A in robust drug development workflows, ensuring compliance and quality.
- Learn about sourcing high-purity pharmaceutical intermediates like this Darunavir synthesis intermediate for your research needs.
- Understand the importance of a reliable 4-AMINO-N-[(2R,3S)-3-AMINO-2-HYDROXY-4-PHENYLBUTYL]-N-ISOBUTYLBENZENE-1-SULFONAMIDE supplier for consistent product quality.
- Explore the advantages of using this intermediate in your drug development process, from early research to batch release testing.
Advantages You Gain
Uncompromised Purity
Achieve reliable results with an intermediate that boasts a minimum assay of 98%, meeting USP, BP, EP, and FCC standards for pharmaceutical applications, crucial for pharmaceutical impurity reference standard consistency.
Streamlined Synthesis
Accelerate your Darunavir production with a precisely manufactured intermediate, ensuring a smooth and efficient Darunavir synthesis intermediate process.
Global Compliance
Trust in a product that adheres to international pharmacopeial standards, facilitating easier regulatory submissions and broader market access for your pharmaceutical products.
Key Applications
Pharmaceutical Synthesis
Essential as a Darunavir intermediate for the synthesis of the active pharmaceutical ingredient, supporting the development of antiviral therapies.
Drug Development
Serves as a critical 4-AMINO-N-[(2R,3S)-3-AMINO-2-HYDROXY-4-PHENYLBUTYL]-N-ISOBUTYLBENZENE-1-SULFONAMIDE supplier's product for early-stage research, formulation, and validation.
Quality Control
Utilized as a reference standard in quality control processes to ensure the purity and consistency of Darunavir products.
Research & Development
A key component for R&D labs focusing on antiviral drug discovery and the development of new therapeutic agents.