1A01040

11-Ketofluticasone Propionate

Pharmaceutical Analytical Impurity (PAI)

Manufacturer: Sigma Aldrich

CAS Number: 1219174-94-3

Synonym(S): 6alpha, 9-difluoro-17- [[(fluoromethyl)sulfanyl] carbonyl]-16alpha-methyl-3,11-dioxoandrosta-1-4dien-17alpha-yl-propanoate, (6S,8S,9R,10S,13S,14S,16R,17R)-6,9-Difluoro-17-(((fluoromethyl)thio) carbonyl)-10,13,16-trimethyl-3,11-dioxo-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-17-yl propionate, (6S,8S,9R,10S,13S,14S,16R,17R)-6,9-Difluoro-17-(((fluoromethyl)thio)carbonyl)-10,13,16-trimethyl-3,11-dioxo6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-17-yl propionate

Select a Size

Pack Size SKU Availability Price
25 MG 1A01040-25-MG In Stock ₹ 1,37,964.63

1A01040 - 25 MG

₹ 1,37,964.63

In Stock

Quantity

1

Base Price: ₹ 1,37,964.63

GST (18%): ₹ 24,833.633

Total Price: ₹ 1,62,798.263

grade

pharmaceutical analytical impurity (PAI)

Agency

USP

manufacturer/tradename

USP

application(s)

pharmaceutical

format

neat

storage temp.

2-8°C

Description

  • General description: Fluticasone Related Compound F 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: Fluticasone PropionateTherapeutic Area: SteroidsFor more information about this PAI, visit here.
  • Application: Fluticasone Related Compound F (USP PAI) is intended for use in analytical testing to detect, identify, and measure pharmaceutical impurities.
  • 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 spectra6. Determine relative response factors.7. Identify unknown impurities that formed during ICH stability conditions.8. Identify impurities that are present in the Reference Listed Drug9. Test for and profile impurities not listed in drug substance and drug product monographs.
  • Analysis Note: These products are for test and assay use only. They are not meant for administration to humans or animals and cannot be used to diagnose, treat, or cure diseases of any kind.
  • Other Notes: Sales restrictions may apply.

SAFETY INFORMATION

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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