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Mazapertine CAS NO 134208-17-6
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CAS No.:134208-17-6
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Mazapertine CAS NO 134208-17-6 is a high-purity pharmaceutical intermediate and research chemical of significant interest in medicinal chemistry. Its primary value lies in its role as a key building block for the synthesis of novel therapeutic agents targeting the central nervous system. This compound is essential for pharmaceutical R&D laboratories, contract manufacturing organizations (CMOs), and academic institutions engaged in neuropharmacology and drug discovery programs.
Application
- Pharmaceutical Intermediate: A critical precursor in the synthesis of advanced active pharmaceutical ingredients (APIs) for neurological research.
- Neurological Research: Used in preclinical studies to investigate mechanisms related to specific receptor activity within the central nervous system.
- Medicinal Chemistry: Serves as a versatile scaffold for the design and development of new chemical entities with potential psychotropic or neuroprotective properties.
- Reference Standard: Employed as an analytical standard in quality control laboratories for method development and impurity profiling.
- Academic & Institutional Research: Utilized in university and government research programs focused on neuropsychiatric disorders.
- Contract Research & Manufacturing: Supplied to CROs and CMOs for custom synthesis projects and scale-up development.
Basic Information
| Product Name | Mazapertine |
| CAS No. | 134208-17-6 |
| Molecular Formula | C23H28N2O2 |
| Molecular Weight | 364.48 g/mol |
| Synonyms | Mazapertine; Mazapertine Succinate; 134208-17-6; 4-(4-Fluorophenyl)-1-[3-(4-fluorophenoxy)propyl]-4-piperidinol; 4-(4-Fluorophenyl)-1-[3-(4-fluorophenoxy)propyl]-4-piperidinyl alcohol; 4-Piperidinol, 4-(4-fluorophenyl)-1-[3-(4-fluorophenoxy)propyl]-; BIIP-1; BIIP 1 |
| EINECS | Contact for details |
Quality Control
Our Mazapertine is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. We adhere to ICH Q7 guidelines for active pharmaceutical ingredients (APIs) and provide comprehensive analytical documentation. A detailed Certificate of Analysis (COA) is supplied with each batch, confirming identity, purity, and impurity profiles as determined by validated methods such as HPLC, NMR, and MS.
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 in a dry environment to protect the product from moisture.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white 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% |
| Any single unknown impurity | ≤0.5% |
| Residual Solvents (GC) | Complies with ICH Q3C guidelines |
| Loss on Drying | ≤0.5% |
| 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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Why choose US
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.





