Description

Budipine is a high-purity pharmaceutical intermediate and active pharmaceutical ingredient (API) with significant importance in neurological research and development. This compound is valued for its specific pharmacological profile, making it a critical component in the synthesis of advanced therapeutic agents. It is primarily utilized by pharmaceutical manufacturers and research institutions focused on developing treatments for central nervous system disorders.

Application

• Pharmaceutical API Synthesis: Serves as a key intermediate in the production of prescription neurological medications.
• Neurological Research: Used as a reference standard and active compound in preclinical and clinical studies targeting Parkinson's disease and related movement disorders.
• Chemical Intermediate: Acts as a building block for the synthesis of more complex, patented pharmaceutical molecules.
• Analytical Standard: Employed in quality control laboratories for method development, validation, and assay calibration.
• Academic & Institutional Research: Utilized in university and government labs for pharmacological and toxicological investigations.

Basic Information

Product Name	Budipine
CAS No.	57982-78-2
Molecular Formula	C19H31N
Molecular Weight	273.46 g/mol
Synonyms	1-tert-Butyl-4,4-diphenylpiperidine; 1-(1,1-Dimethylethyl)-4,4-diphenylpiperidine; BY 701; Budipin; Parkinsan
EINECS	Contact for details

Quality Control

Our Budipine is manufactured under strict quality management systems to ensure batch-to-batch consistency and reliability. The product undergoes rigorous analytical testing, including HPLC for purity and identity confirmation via IR and NMR spectroscopy, to meet the stringent requirements of pharmaceutical applications. A comprehensive Certificate of Analysis (COA) detailing all test results is provided with each shipment to support your regulatory and quality assurance needs.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed in a dry environment to prevent moisture absorption. Keep away from incompatible materials.

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 ≤ 1.0% Any single impurity ≤ 0.5%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.