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Butriptyline CAS NO 15686-37-0
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CAS No.:15686-37-0
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Butriptyline is a tricyclic antidepressant (TCA) compound with the CAS registry number 15686-37-0. It is valued in pharmaceutical research and development for its specific neurochemical activity profile, which serves as a reference point for studying antidepressant mechanisms. This compound is primarily utilized by pharmaceutical manufacturers, research institutions, and analytical laboratories engaged in the development and quality control of psychotropic medications.
Application
- Pharmaceutical Reference Standard: Used as a certified standard for the identification, purity assay, and impurity profiling of active pharmaceutical ingredients (APIs) in quality control laboratories.
- Biochemical Research: Employed in preclinical studies to investigate the pharmacology, metabolism, and structure-activity relationships (SAR) of tricyclic antidepressant agents.
- Analytical Method Development: Serves as a key analyte for developing and validating analytical methods, such as High-Performance Liquid Chromatography (HPLC) and Mass Spectrometry (MS), for antidepressant compounds.
- Metabolite Synthesis: Acts as a precursor or intermediate in the synthesis of specific metabolites for pharmacokinetic and toxicological studies.
Basic Information
| Product Name | Butriptyline |
| CAS No. | 15686-37-0 |
| Molecular Formula | C21H27N |
| Molecular Weight | 293.45 g/mol |
| Synonyms | 10,11-Dihydro-N,N,β-trimethyl-5H-dibenzo[a,d]cycloheptene-5-propylamine; Butriptyline Hydrochloride (salt form); Evadyne; Centroton; 5-(3-Methylaminopropylidene)-10,11-dihydro-5H-dibenzo[a,d]cycloheptene; Wy-2245; NSC-112682 |
| EINECS | Contact for details |
Quality Control
Our Butriptyline is manufactured under strict quality management systems to ensure high purity and batch-to-batch consistency. Each lot is accompanied by a comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles. We support compliance with cGMP (current Good Manufacturing Practice) and ICH (International Council for Harmonisation) guidelines for pharmaceutical ingredients, ensuring the material is suitable for research and development applications.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Keep the container tightly sealed in a dry environment to maintain stability.
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) | ≥98.0% |
| Related Substances (HPLC) | Total impurities ≤2.0% |
| 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.
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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.






