Description

Anileridine Phosphate is a synthetic opioid analgesic compound. It is primarily utilized in pharmaceutical research and development for its potent analgesic properties. This chemical is of significant interest to researchers and manufacturers in the pharmaceutical and life sciences sectors for developing and studying pain management solutions.

Application

• Pharmaceutical Intermediate: Serves as a key building block in the synthesis of specialized analgesic formulations.
• Analgesic Research: Used in preclinical and clinical research to study opioid receptor activity and mechanisms of pain relief.
• Reference Standard: Employed as a certified reference material (CRM) in analytical laboratories for quality control and method validation.
• Biochemical Studies: Applied in pharmacological studies to investigate the structure-activity relationships (SAR) of opioid compounds.
• Controlled Substance Analog Research: Used in legitimate forensic and regulatory science to develop detection and analysis methods.

Basic Information

Product Name	Anileridine Phosphate
CAS No.	4268-37-5
Molecular Formula	C22H30N2O5S
Molecular Weight	434.55 g/mol
Synonyms	Anileridine Dihydrogen Phosphate; Ethyl 1-(4-Aminophenethyl)-4-phenylisonipecotate Phosphate; WIN 14,098-2; Leritine Phosphate; Apodol; Nipecotan; NSC 17774; 1-(2-(p-Aminophenyl)ethyl)-4-phenyl-4-piperidinecarboxylic Acid Ethyl Ester Phosphate
EINECS	Contact for details

Quality Control

Our Anileridine Phosphate is produced under strict quality management systems. Each batch undergoes comprehensive analytical testing, including identification, purity assay, and impurity profiling, to ensure it meets the stringent requirements for research and development use. A detailed Certificate of Analysis (COA) is provided with every shipment to guarantee traceability and batch-to-batch consistency.

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 nature, the container must be kept tightly sealed to prevent moisture absorption.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	≥ 98.0%
Water Content (KF)	≤ 2.0%
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.