1-Phenyl-1H-indole-2,3-dione 3-[N-(4-nitrophenyl)hydrazone] CAS 303984-77-2

Purity 97%+In StockPharmaceutical Standards
CAS No.303984-77-2
Molecular FormulaC20H14N4O3
Molecular Weight358.35 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-Phenyl-1H-indole-2,3-dione 3-[N-(4-nitrophenyl)hydrazone] CAS 303984-77-2 chemical structure

Description

CATO manufactures 1-Phenyl-1H-indole-2,3-dione 3-[N-(4-nitrophenyl)hydrazone] 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.

1-Phenyl-1H-indole-2,3-dione 3-[N-(4-nitrophenyl)hydrazone] (CAS 303984-77-2) is a high-purity analytical reference standard with the molecular formula C20H14N4O3 and a molecular weight of 358.35 g/mol.

Owing to a steroid core, an amide group, a hydroxyl group, an ether linkage, 1-Phenyl-1H-indole-2,3-dione 3-[N-(4-nitrophenyl)hydrazone] is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 358.35 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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.

Physical & Chemical Properties

Molecular FormulaC20H14N4O3
Molecular Weight358.35 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)16.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Nitrogen Atoms4

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