Description

n-Butyl-n-Methyl-4-Piperidinecarboxamidehydrochloride is a high-purity, synthetically derived piperidine derivative, primarily used as a critical pharmaceutical intermediate. This compound is essential for the research and development of novel active pharmaceutical ingredients (APIs), particularly in the central nervous system (CNS) and therapeutic agent categories. It is a key building block for medicinal chemists and manufacturers requiring a reliable, high-quality intermediate for complex synthesis pathways.

Application

• Pharmaceutical Intermediate: A crucial precursor in the synthesis of novel drug candidates and active pharmaceutical ingredients (APIs).
• Medicinal Chemistry Research: Used in lead optimization and structure-activity relationship (SAR) studies for new therapeutic agents.
• Chemical Synthesis: Serves as a versatile building block for constructing complex heterocyclic and piperidine-based molecular frameworks.
• Reference Standard: Utilized as an analytical standard for quality control and method development in pharmaceutical analysis.
• Biochemical Research: Employed in the study of biological pathways and receptor interactions where piperidine motifs are relevant.

Basic Information

Product Name	n-Butyl-n-Methyl-4-Piperidinecarboxamidehydrochloride
CAS No.	1193389-21-7
Molecular Formula	C12H25ClN2O
Molecular Weight	248.79 g/mol
Synonyms	N-Butyl-N-methylpiperidine-4-carboxamide hydrochloride; 1-Butyl-1-methyl-4-piperidinecarboxamide hydrochloride; 4-(N-Butyl-N-methylcarbamoyl)piperidine hydrochloride; N-Methyl-N-butylisonipecotamide hydrochloride; 1-Methyl-1-butyl-4-carbamoylpiperidinium chloride; Piperidine-4-carboxamide, N-butyl-N-methyl-, hydrochloride
EINECS	Contact for details

Quality Control

Our n-Butyl-n-Methyl-4-Piperidinecarboxamidehydrochloride is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC, NMR, and IR spectroscopy, to ensure identity, purity, and consistency. Certificates of Analysis (COA) are provided with every shipment, detailing all relevant specifications. We adhere to cGMP principles for pharmaceutical intermediates to support our clients' regulatory requirements.

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). This product is hygroscopic (moisture-sensitive) and must be kept under dry, inert conditions to maintain stability and purity.

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%
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Total impurities ≤ 2.0%

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