6-Chloro-2-methoxy-N-(4-nitrophenyl)acridin-9-amine CAS 5442-55-7

Purity 97%+In StockPharmaceutical Standards
CAS No.5442-55-7
Molecular FormulaC20H14ClN3O3
Molecular Weight379.80 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-Chloro-2-methoxy-N-(4-nitrophenyl)acridin-9-amine CAS 5442-55-7 chemical structure

Description

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

6-Chloro-2-methoxy-N-(4-nitrophenyl)acridin-9-amine (CAS 5442-55-7), molecular formula C20H14ClN3O3 and molecular weight 379.80 g/mol, is a CATO reference standard with documented purity and traceability.

Based on its molecular formula C20H14ClN3O3, 6-Chloro-2-methoxy-N-(4-nitrophenyl)acridin-9-amine contains a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 379.80 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO manufactures 6-Chloro-2-methoxy-N-(4-nitrophenyl)acridin-9-amine 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 FormulaC20H14ClN3O3
Molecular Weight379.80 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)15.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1958
Halogen ContentCl-containing
Nitrogen Atoms3

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