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Sequifenadine CAS NO 57734-69-7
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CAS No.:57734-69-7
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Sequifenadine is a high-purity pharmaceutical intermediate and active ingredient with significant commercial and research value. It is essential for the development and production of advanced therapeutic agents, particularly in the antihistamine and anti-inflammatory domains. This compound is primarily sought by manufacturers and R&D laboratories in the global pharmaceutical, biotechnology, and fine chemical sectors for its critical role in synthesis and formulation processes.
Application
- Pharmaceutical Active Ingredient (API): Core component in the formulation of antihistamine medications.
- Advanced Drug Synthesis: Key intermediate in multi-step organic synthesis for novel therapeutic compounds.
- Biochemical Research: Used as a reference standard and tool compound in pharmacological and metabolic studies.
- Fine Chemical Production: Serves as a building block for creating more complex, specialized molecules.
- Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for GMP production.
- Analytical Standard: Provides a certified reference material for quality control and regulatory testing in labs.
Basic Information
| Product Name | Sequifenadine |
| CAS No. | 57734-69-7 |
| Molecular Formula | C21H24N2O2 |
| Molecular Weight | 336.43 g/mol |
| Synonyms | Sequifenadine; 1-[4-(1,1-Dimethylethyl)phenyl]-4-[4-(hydroxydiphenylmethyl)-1-piperidinyl]-1-butanone; Bicarphen; Sequifenadine Hydrochloride (salt form); Bikarfen; Sequifenadin; 4-[4-(Hydroxydiphenylmethyl)-1-piperidinyl]-1-[4-(tert-butyl)phenyl]-1-butanone |
| EINECS | Contact for details |
Quality Control
Our Sequifenadine is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, residual solvent analysis, and identification by IR and NMR spectroscopy, to ensure it meets stringent specifications for pharmaceutical use. Certificates of Analysis (COA) detailing all test results are provided with every shipment.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). Keep the container tightly sealed to protect from moisture.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white crystalline powder |
| Identification (IR) | Conforms to reference spectrum |
| Identification (HPLC) | Retention time matches reference standard |
| Assay (HPLC) | ≥ 98.5% |
| Related Substances (HPLC) | Total impurities ≤ 1.5% Any single impurity ≤ 0.5% |
| Loss on Drying | ≤ 0.5% |
| Residue on Ignition | ≤ 0.1% |
| Heavy Metals | ≤ 20 ppm |
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.






