898562-94-2 R9Y8EY0G42 PF-2545920 Mardepodect [USAN] UNII-R9Y8EY0G42 MP-10 PF 2545920 Quinoline, 2-((4-(1-methyl-4-(4-pyridinyl)-1H-pyrazol-3-yl)phenoxy)methyl)- 2-(4-(1-Methyl-4-pyridin-4-yl-1H-pyrazol-3-yl)-phenoxymethyl)quinoline PF-0254920 Mardepodect PF-02545920 CAS 898562-94-2

Purity 97%+In StockPharmaceutical Standards
CAS No.898562-94-2
Molecular FormulaC25H20N4O
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

898562-94-2 R9Y8EY0G42 PF-2545920 Mardepodect [USAN] UNII-R9Y8EY0G42 MP-10 PF 2545920 Quinoline, 2-((4-(1-methyl-4-(4-pyridinyl)-1H-pyrazol-3-yl)phenoxy)methyl)- 2-(4-(1-Methyl-4-pyridin-4-yl-1H-pyrazol-3-yl)-phenoxymethyl)quinoline PF-0254920 Mardepodect PF-02545920 CAS 898562-94-2 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 898562-94-2 R9Y8EY0G42 PF-2545920 Mardepodect [USAN] UNII-R9Y8EY0G42 MP-10 PF 2545920 Quinoline, 2-((4-(1-methyl-4-(4-pyridinyl)-1H-pyrazol-3-yl)phenoxy)methyl)- 2-(4-(1-Methyl-4-pyridin-4-yl-1H-pyrazol-3-yl)-phenoxymethyl)quinoline PF-0254920 Mardepodect PF-02545920.

CATO supplies 898562-94-2 R9Y8EY0G42 PF-2545920 Mardepodect [USAN] UNII-R9Y8EY0G42 MP-10 PF 2545920 Quinoline, 2-((4-(1-methyl-4-(4-pyridinyl)-1H-pyrazol-3-yl)phenoxy)methyl)- 2-(4-(1-Methyl-4-pyridin-4-yl-1H-pyrazol-3-yl)-phenoxymethyl)quinoline PF-0254920 Mardepodect PF-02545920 (CAS 898562-94-2), a certified reference material (molecular formula C25H20N4OHCl, MW 428.92 g/mol) for analytical method development and quality control.

The molecular framework of 898562-94-2 R9Y8EY0G42 PF-2545920 Mardepodect [USAN] UNII-R9Y8EY0G42 MP-10 PF 2545920 Quinoline, 2-((4-(1-methyl-4-(4-pyridinyl)-1H-pyrazol-3-yl)phenoxy)methyl)- 2-(4-(1-Methyl-4-pyridin-4-yl-1H-pyrazol-3-yl)-phenoxymethyl)quinoline PF-0254920 Mardepodect PF-02545920 (C25H20N4OHCl) is characterized by a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

As a certified reference material (CRM), 898562-94-2 R9Y8EY0G42 PF-2545920 Mardepodect [USAN] UNII-R9Y8EY0G42 MP-10 PF 2545920 Quinoline, 2-((4-(1-methyl-4-(4-pyridinyl)-1H-pyrazol-3-yl)phenoxy)methyl)- 2-(4-(1-Methyl-4-pyridin-4-yl-1H-pyrazol-3-yl)-phenoxymethyl)quinoline PF-0254920 Mardepodect PF-02545920 meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC25H20N4O HCl
Molecular Weight428.92 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at room temperature, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)17.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentCl-containing
Nitrogen Atoms4

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