Description

1,2,3,6-Tetrahydro-1-Methyl-4-Pyridinemethanol α-Hydroxy-α,α-Diphenylacetate is a specialized organic compound with a complex molecular structure, serving as a key intermediate in advanced pharmaceutical synthesis. This compound is valued for its precise chemical functionality, enabling the development of targeted active pharmaceutical ingredients (APIs). It is primarily required by research institutions and manufacturers in the pharmaceutical and fine chemical industries for the development of new therapeutic agents.

Application

• Pharmaceutical Intermediate: A critical building block in the synthesis of novel central nervous system (CNS) active drugs and other therapeutic compounds.
• Research & Development (R&D): Used in medicinal chemistry for structure-activity relationship (SAR) studies and the development of new chemical entities.
• Active Pharmaceutical Ingredient (API) Synthesis: Serves as a precursor in multi-step synthetic routes for complex API manufacturing.
• Fine Chemical Production: Employed in the production of high-value, low-volume specialty chemicals requiring specific chiral or structural motifs.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for custom synthesis projects.

Basic Information

Product Name	1,2,3,6-Tetrahydro-1-Methyl-4-Pyridinemethanol α-Hydroxy-α,α-Diphenylacetate
CAS No.	93101-29-2
Molecular Formula	C22H25NO3
Molecular Weight	351.44 g/mol
Synonyms	1-Methyl-1,2,3,6-tetrahydropyridin-4-ylmethyl mandelate; 4-((Hydroxy(diphenyl)acetyl)oxy)methyl)-1-methyl-1,2,3,6-tetrahydropyridine; 1-Methyl-4-piperidylmandelate; Tropanyl mandelate derivative; 93101-29-2; α-Hydroxy-α,α-diphenylacetate ester of 1-methyl-4-piperidinemethanol
EINECS	Contact for details

Quality Control

Our products undergo rigorous quality testing to ensure compliance with industry standards for pharmaceutical intermediates. We employ advanced analytical techniques including HPLC, GC, and NMR to verify identity, purity, and consistency. Certificates of Analysis (COA) are available upon request, detailing batch-specific results. Our quality management system supports development under cGMP guidelines as required.

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 away from incompatible materials such as strong oxidizing agents.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Loss on Drying	≤ 0.5%

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