1,4-Diamino-6-chloro-2-(3-methoxyphenoxy)anthracene-9,10-dione CAS 88605-23-6

Purity 97%+In StockPharmaceutical Standards
CAS No.88605-23-6
Molecular FormulaC21H15ClN2O4
Molecular Weight394.81 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1,4-Diamino-6-chloro-2-(3-methoxyphenoxy)anthracene-9,10-dione CAS 88605-23-6 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.

CATO supplies 1,4-Diamino-6-chloro-2-(3-methoxyphenoxy)anthracene-9,10-dione (CAS 88605-23-6), a certified reference material (molecular formula C21H15ClN2O4, MW 394.81 g/mol) for analytical method development and quality control.

Structurally, 1,4-Diamino-6-chloro-2-(3-methoxyphenoxy)anthracene-9,10-dione (C21H15ClN2O4) contains a flavonoid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 15.0, corresponding to approximately 15 ring(s) or double-bond equivalent(s). With a molecular weight of 394.81 g/mol, it falls into the moderately-high-molecular-weight range. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

CATO manufactures 1,4-Diamino-6-chloro-2-(3-methoxyphenoxy)anthracene-9,10-dione 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 FormulaC21H15ClN2O4
Molecular Weight394.81 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.)1982
Halogen ContentCl-containing
Nitrogen Atoms2

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