1A01050

6-Methyl-4-Phenylchromanol

Pharmaceutical Analytical Impurity (PAI)

• Sinónimos: (6-Methyl-4-phenylchroman-2-ol)
• Fórmula empírica (notación de Hill): C₁₆H₁₆O₂
• Número CAS: 209747-04-6
• Peso molecular: 240.30
• MDL number: MFCD00236118
• NACRES: NA.24
• UNSPSC Code: 41116107

Propiedades

• grade: pharmaceutical analytical impurity (PAI)
• agency: USP
• manufacturer/tradename: USP
• application(s): pharmaceutical
• format: neat
• storage temp.: 2-8°C

Descripción

General description

[6-Methyl-4-phenylchromanol (25 mg) (6-Methyl-4-phenylchroman-2-ol)] - CAS [209747-04-6] (usp.org)6-Methyl-4-Phenylchromanol is a USP Pharmaceutical Analytical Impurity (PAI).

USP PAI are a product line of impurities suitable for research and analytical purposes, which help to ensure the quality and safety of medicines.

Associated Drug Substance: Tolterodine tartrate.

Therapeutic Area: Renal.

For more information about this PAI, visit here.

Application

6-Methyl-4-Phenylchromanol (USP PAI) is intendedfor use in analytical testing to detect, identify, and measure pharmaceuticalimpurities.

Features and Benefits

USP PAI advance your early analytical R&D and process development. PAI can be used in the following applications:
1. Conduct analytical tests during early formulation feasibility studies.
2. Determine degradation impurities produced during stress studies.
3. Develop, validate, and transfer analytical methods.
4. Perform spiking studies during process R&D to demonstrate depletion upon recrystallization.
5. Record retention times and/or spectra
6. Determine relative response factors.
7. Identify unknown impurities that formed during ICH stability conditions.
8. Identify impurities that are present in the Reference Listed Drug
9. Test for and profile impurities not listed in drug substance and drug product monographs.

Información de seguridad

• Clase de almacenamiento: 11 - Combustible Solids
• wgk: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable