Description

Ifenprodil Glucuronide is a key glucuronide metabolite of the pharmaceutical agent Ifenprodil. This compound is of significant importance for pharmaceutical research and development, particularly in the fields of metabolism and pharmacokinetic studies. It serves as a critical reference standard for analytical method development and validation in bioanalytical laboratories. Researchers and quality control specialists in the pharmaceutical and contract research organization (CRO) sectors require this high-purity metabolite to ensure accurate drug metabolism and safety profiling.

Application

• Pharmaceutical Reference Standard: Primary use as a certified reference material (CRM) for quantitative and qualitative analysis in drug development.
• Metabolite Identification & Profiling: Essential for studying the metabolic pathways and biotransformation of Ifenprodil in preclinical and clinical research.
• Bioanalytical Method Development: Used to develop and validate sensitive LC-MS/MS, HPLC, or UPLC methods for the detection of Ifenprodil and its metabolites in biological matrices.
• Pharmacokinetic (PK) Studies: Critical for understanding the absorption, distribution, metabolism, and excretion (ADME) properties of the parent drug.
• Doping Control & Forensic Analysis: Potential application as a marker in specialized toxicological screenings.
• Quality Control & Assurance: Serves as an impurity standard to monitor and control the quality of Ifenprodil active pharmaceutical ingredient (API) and related formulations.

Basic Information

Product Name	Ifenprodil Glucuronide
CAS No.	66516-92-5
Molecular Formula	C27H38N2O8
Molecular Weight	518.60 g/mol
Synonyms	Ifenprodil β-D-Glucuronide; 4-[2-(4-Benzylpiperidin-1-yl)-1-hydroxypropyl]phenol β-D-Glucopyranosiduronic Acid; Ifenprodil O-β-D-Glucuronide; 1-[4-(β-D-Glucopyranuronosyloxy)phenyl]-2-[(4-phenylmethyl-1-piperidinyl)methyl]propyl Alcohol; Ifenprodil Glucuronide Metabolite
EINECS	Contact for details

Quality Control

Our Ifenprodil Glucuronide is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including identification by spectroscopic methods (NMR, IR, MS), purity assessment by HPLC, and control of specific impurities. We provide a comprehensive Certificate of Analysis (COA) with each shipment, detailing batch-specific results. Our quality commitment ensures the material is suitable for use as a high-purity reference standard in regulated research environments.

Storage

Preserve in a tightly closed container, protected from light. Store at controlled room temperature (15-25°C) or as indicated on the label or COA. This product is hygroscopic (moisture-sensitive) and should be handled in a dry environment to maintain stability and purity. For long-term storage, consider desiccants.

Specification

Item	Specification
Appearance	White to off-white solid
Identification (HPLC)	Conforms to reference standard
Identification (MS)	Conforms to structure
Purity (HPLC)	≥ 98.0%
Water Content (KF)	≤ 2.0%
Residue on Ignition	≤ 0.1%
Single Unknown Impurity (HPLC)	≤ 0.5%
Total Impurities (HPLC)	≤ 2.0%

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