Description

Propofol Related Compound C (50 Mg) (2,6-Diisopropylphenyl Isopropylether) is a high-purity analytical reference standard used for pharmaceutical quality control and research. This compound is critical for the accurate identification and quantification of process-related impurities in the synthesis of the anesthetic agent Propofol. It is essential for analytical chemists, quality assurance laboratories, and research institutions involved in pharmaceutical development and manufacturing to ensure product safety and regulatory compliance.

Application

• Pharmaceutical Impurity Profiling: Primary use as a certified reference standard for HPLC, GC, and LC-MS analysis to monitor and control the synthesis of Propofol.
• Method Development and Validation: Critical for developing and validating analytical methods in compliance with ICH Q2(R1) and other regulatory guidelines.
• Quality Control (QC) Testing: Used in in-process testing and release testing of active pharmaceutical ingredients (APIs) to ensure impurity levels are within specified limits.
• Stability Studies: Employed as a marker compound in forced degradation and shelf-life studies of Propofol formulations.
• Regulatory Submissions: Provides essential data for drug master files (DMFs), investigational new drug (IND) applications, and new drug applications (NDAs).
• Academic and Contract Research: Serves as a key reagent in university and CRO laboratories for pharmacological and metabolic pathway research related to anesthetic agents.

Basic Information

Product Name	Propofol Related Compound C (50 Mg) (2,6-Diisopropylphenyl Isopropylether)
CAS No.	141214-18-8
Molecular Formula	C15H24O
Molecular Weight	220.35 g/mol
Synonyms	2,6-Diisopropylphenyl Isopropyl Ether; 1-Isopropoxy-2,6-diisopropylbenzene; Propofol Isopropyl Ether; Propofol Impurity C; Propofol Related Substance C; 2,6-Bis(1-methylethyl)phenyl 1-methylethyl ether; Diisopropylphenoxypropane
EINECS	Contact for details

Quality Control

Every batch of Propofol Related Compound C is manufactured and analyzed under strict quality management systems. The product undergoes rigorous identity confirmation, purity analysis, and impurity profiling using advanced chromatographic techniques. A comprehensive Certificate of Analysis (COA) is provided with each unit, detailing batch-specific results for assay, related substances, and residual solvents. Our quality standards align with ICH guidelines to support regulatory requirements for pharmaceutical reference materials.

Storage

Preserve in a tightly closed container, protected from light. Store at controlled room temperature, 15-25°C (59-77°F). The product is supplied in a sealed vial to ensure stability and prevent contamination. For long-term storage, keep the container in a cool, dry, and well-ventilated area.

Specification

Item	Specification
Appearance	Colorless to pale yellow liquid
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single unknown impurity ≤ 0.5%
Water Content (KF)	≤ 0.5%
Residual Solvents (GC)	Complies with ICH Q3C

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