Description

Pentapiperide is a synthetic organic compound with specific pharmacological activity, primarily utilized as a key intermediate in advanced pharmaceutical synthesis. Its precise chemical structure makes it valuable for developing active pharmaceutical ingredients (APIs) targeting specific receptor pathways. This compound is essential for research and development chemists, process chemists, and manufacturers in the pharmaceutical and fine chemical industries seeking high-purity building blocks for complex molecule construction.

Application

• Pharmaceutical Intermediate: Serves as a critical building block in the synthesis of novel therapeutic agents and active pharmaceutical ingredients (APIs).
• Medicinal Chemistry Research: Used in research laboratories for the discovery and development of new drug candidates, particularly in neurological and metabolic disorder studies.
• Process Chemistry & Scale-up: Employed in the optimization and pilot-scale production of pharmaceutical compounds requiring its specific molecular framework.
• Reference Standard: Can be supplied as a high-purity standard for analytical method development, validation, and quality control in pharmaceutical manufacturing.
• Fine Chemical Synthesis: Acts as a specialized reagent or precursor in the multi-step synthesis of complex organic molecules for various applications.

Basic Information

Product Name	Pentapiperide
CAS No.	7009-54-3
Molecular Formula	C21H28N2O2
Molecular Weight	340.46 g/mol
Synonyms	Pentapiperide; 1-Methyl-4-piperidyl α,α-diphenyl-2-piperidineacetate; 1-Methyl-4-piperidyl α-phenyl-α-(2-piperidyl)acetate; α,α-Diphenyl-2-piperidineacetic acid 1-methyl-4-piperidyl ester; 1-Methyl-4-piperidyl α-phenyl-α-(2-piperidyl)acetate; 1-Methyl-4-piperidyl diphenyl(2-piperidyl)acetate; 1-Methyl-4-piperidyl α,α-diphenyl-2-piperidineacetate
EINECS	Contact for details

Quality Control

Our Pentapiperide is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, identity confirmation by IR and NMR spectroscopy, and residual solvent analysis to ensure it meets stringent specifications for pharmaceutical intermediate use. A detailed Certificate of Analysis (COA) is provided with every shipment, confirming compliance with agreed-upon specifications.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated place at a controlled room temperature (typically 15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after opening to prevent degradation from atmospheric moisture. 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)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0% 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.