Description

2-Piperidinoethyl o-(Ethoxymethyl)Carbanilate Oxalate (1:1) is a specialized organic salt compound of significant interest in advanced chemical synthesis. This compound serves as a crucial intermediate or active pharmaceutical ingredient (API) in the research and development of novel therapeutic agents. It is primarily sought by pharmaceutical R&D laboratories, fine chemical manufacturers, and academic institutions engaged in medicinal chemistry and process development.

Application

• Pharmaceutical Intermediate: Key building block in the synthesis of potential drug candidates, particularly in central nervous system (CNS) or cardiovascular research.
• Medicinal Chemistry Research: Used as a reference standard or a precursor in structure-activity relationship (SAR) studies for new chemical entities.
• Fine Chemical Synthesis: Serves as a specialized reagent in multi-step organic syntheses requiring a protected or modified carbamate functionality.
• Biochemical Research: Potential application in the study of enzyme inhibition or receptor binding assays due to its structural features.
• Process Development: Used by manufacturers to scale up and optimize production routes for target molecules in a GMP environment.

Basic Information

Product Name	2-Piperidinoethyl o-(Ethoxymethyl)Carbanilate Oxalate (1:1)
CAS No.	80171-70-6
Molecular Formula	C18H28N2O5 • C2H2O4
Molecular Weight	424.46 g/mol
Synonyms	2-(1-Piperidinyl)ethyl [o-(ethoxymethyl)phenyl]carbamate oxalate; o-(Ethoxymethyl)carbanilic acid 2-piperidinoethyl ester oxalate; Carbamic acid, N-[2-(ethoxymethyl)phenyl]-, 2-(1-piperidinyl)ethyl ester, oxalate (1:1); PECO; 2-Piperidinoethyl o-ethoxymethylcarbanilate oxalate
EINECS	Contact for details

Quality Control

Our 2-Piperidinoethyl o-(Ethoxymethyl)Carbanilate Oxalate (1:1) is produced under strict quality management systems. Each batch undergoes comprehensive analytical testing including HPLC for purity, identity confirmation by IR and NMR, and residual solvent analysis to ensure it meets the stringent requirements for pharmaceutical intermediates. A Certificate of Analysis (COA) documenting all test results is provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed after each use to prevent moisture absorption, which may affect stability and handling properties.

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 ≤ 1.0%
Loss on Drying	≤ 1.0%
Residue on Ignition	≤ 0.1%

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