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Surzebiclimab CAS NO 2342597-90-2
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CAS No.:2342597-90-2
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Surzebiclimab CAS NO 2342597-90-2 is a high-purity pharmaceutical intermediate and active ingredient of significant interest in modern therapeutic development. This compound is critical for research and manufacturing processes requiring precise molecular structures for biological activity. It is primarily utilized by pharmaceutical companies, biotechnology research institutions, and advanced chemical synthesis laboratories engaged in the development of novel therapeutic agents.
Application
- Pharmaceutical Intermediate: Serves as a key building block in the synthesis of active pharmaceutical ingredients (APIs) for investigational drugs.
- Biopharmaceutical Research: Used in preclinical and clinical research for studying biological pathways and therapeutic mechanisms of action.
- Process Chemistry & Development: Employed in route scouting, optimization, and scale-up activities within process R&D departments.
- Contract Manufacturing (CMO): Supplied to contract manufacturing organizations for the production of clinical trial materials and commercial drug substances.
- Reference Standard: Functions as an analytical reference standard for quality control, method development, and regulatory submissions.
- Life Science Reagent: Utilized in biochemical assays and as a tool compound for target validation in academic and industrial settings.
Basic Information
| Product Name | Surzebiclimab |
| CAS No. | 2342597-90-2 |
| Molecular Formula | Contact for details |
| Molecular Weight | Contact for details |
| Synonyms | Surzebiclimab; UNII-5V2W6S145Q; 5V2W6S145Q; (S)-2-((S)-2-(3-(4-(2-((2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindolin-4-yl)amino)ethoxy)phenyl)propanamido)-3-phenylpropanamido)pentanedioic acid; BMS-986405; CC-95775 |
| EINECS | Contact for details |
Quality Control
Our Surzebiclimab is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including identification, purity assay, and impurity profiling, to ensure it meets the stringent requirements for pharmaceutical development. Certificates of Analysis (COA) detailing all test results are provided and can be tailored to support regulatory filings (e.g., FDA, EMA).
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (typically 15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed in a dry environment to prevent degradation. For long-term storage, consider conditions under an inert atmosphere.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white solid |
| Identification (IR) | Conforms to structure |
| Identification (HPLC) | Retention time matches reference standard |
| Purity (HPLC) | ≥ 98.0% |
| Water Content (KF) | ≤ 1.0% |
| Residue on Ignition | ≤ 0.1% |
| Heavy Metals | ≤ 20 ppm |
| Single Unknown Impurity (HPLC) | ≤ 0.5% |
| Total Impurities (HPLC) | ≤ 2.0% |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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Trusted Manufacturer
With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.
Rigorous Quality Assurance
Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.
Advanced R&D Expertise
Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.






