N-(2-chloro-6-iodo-4-(trimethylsilyl)pyridin-3-yl)pivalamide CAS 1305325-24-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1305325-24-9
Molecular FormulaC13H20ClIN2OSi
Molecular Weight410.75 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(2-chloro-6-iodo-4-(trimethylsilyl)pyridin-3-yl)pivalamide CAS 1305325-24-9 chemical structure

Description

CATO supplies N-(2-chloro-6-iodo-4-(trimethylsilyl)pyridin-3-yl)pivalamide (CAS 1305325-24-9), a certified reference material (molecular formula C13H20ClIN2OSi, MW 410.75 g/mol) for analytical method development and quality control.

The molecular framework of N-(2-chloro-6-iodo-4-(trimethylsilyl)pyridin-3-yl)pivalamide (C13H20ClIN2OSi) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine/iodine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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

CATO manufactures N-(2-chloro-6-iodo-4-(trimethylsilyl)pyridin-3-yl)pivalamide under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC13H20ClIN2OSi
Molecular Weight410.75 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, low volatility)
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)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentCl/I-containing
Nitrogen Atoms2

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