(S)-2-[(5-Fluoro-2,4-dinitrophenyl)amino]-3-methylbutanamide CAS 132679-61-9

Purity 97%+In StockPharmaceutical Standards
CAS No.132679-61-9
Molecular FormulaC11H13FN4O5
Molecular Weight300.24 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(S)-2-[(5-Fluoro-2,4-dinitrophenyl)amino]-3-methylbutanamide CAS 132679-61-9 chemical structure

Description

Based on its molecular formula C11H13FN4O5, (S)-2-[(5-Fluoro-2,4-dinitrophenyl)amino]-3-methylbutanamide contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 300.24 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

(S)-2-[(5-Fluoro-2,4-dinitrophenyl)amino]-3-methylbutanamide (CAS 132679-61-9) is a high-purity analytical reference standard with the molecular formula C11H13FN4O5 and a molecular weight of 300.24 g/mol.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

CATO manufactures (S)-2-[(5-Fluoro-2,4-dinitrophenyl)amino]-3-methylbutanamide 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 FormulaC11H13FN4O5
Molecular Weight300.24 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1994
Halogen ContentF-containing
Nitrogen Atoms4

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