share

Mazapertine CAS NO 134208-17-6


Unit Price:

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.

Complete Your RFQ

0/ 2000

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.