Description

2,2-Diphenyl-n-((1-Methyl-3-Piperidyl)Methyl)Acetanilide Hydriodide is a specialized organic salt compound of significant interest in advanced chemical synthesis. This compound serves as a crucial intermediate or reference standard in the development of novel pharmacologically active molecules. It is primarily utilized by research institutions and pharmaceutical companies engaged in medicinal chemistry and drug discovery programs. The high-purity grade of this material ensures reliable and reproducible results in sensitive applications.

Application

• Pharmaceutical Intermediate: Key building block in the research and synthesis of new chemical entities (NCEs) targeting neurological and receptor-based pathways.
• Medicinal Chemistry Research: Used as a precursor or analog in structure-activity relationship (SAR) studies to optimize drug candidate profiles.
• Reference Standard: Serves as an analytical standard for quality control and method development in pharmaceutical analysis.
• Biochemical Research: Employed in vitro studies to investigate interactions with biological targets and enzymes.
• Fine Chemical Synthesis: Intermediate for the preparation of more complex, functionalized organic molecules in custom synthesis projects.

Basic Information

Product Name	2,2-Diphenyl-n-((1-Methyl-3-Piperidyl)Methyl)Acetanilide Hydriodide
CAS No.	101651-72-3
Molecular Formula	C27H31IN2O
Molecular Weight	526.46 g/mol
Synonyms	N-[(1-Methylpiperidin-3-yl)methyl]-2,2-diphenylacetamide hydroiodide; 2,2-Diphenyl-N-[(1-methyl-3-piperidinyl)methyl]acetamide hydroiodide; Acetanilide, 2,2-diphenyl-N-[(1-methyl-3-piperidinyl)methyl]-, hydroiodide; 1-Methyl-3-[(2,2-diphenylacetamido)methyl]piperidinium iodide
EINECS	Contact for details

Quality Control

Our 2,2-Diphenyl-n-((1-Methyl-3-Piperidyl)Methyl)Acetanilide Hydriodide is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity suitable for research applications. Each lot is accompanied by a comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles. We adhere to relevant Good Manufacturing Practice (GMP) principles for pharmaceutical intermediates, and specifications can be aligned with client requirements for specific research or development projects.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (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 structure
Assay (HPLC)	≥ 98.0%
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Individual impurity ≤ 0.5%; Total impurities ≤ 2.0%

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