5-[2-[4-Chloro-2-(Trifluoromethyl)Phenyl]Hydrazinyl]-6-Imino-4-Oxonaphthalene-2-Sulfonic Acid CAS 3836-78-0

Purity 97%+In StockPharmaceutical Standards
CAS No.3836-78-0
Molecular FormulaC17H11ClF3N3O4S
Molecular Weight445.80 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-[2-[4-Chloro-2-(Trifluoromethyl)Phenyl]Hydrazinyl]-6-Imino-4-Oxonaphthalene-2-Sulfonic Acid CAS 3836-78-0 chemical structure

Description

5-[2-[4-Chloro-2-(Trifluoromethyl)Phenyl]Hydrazinyl]-6-Imino-4-Oxonaphthalene-2-Sulfonic Acid (C17H11ClF3N3O4S) contains a flavonoid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine/chlorine substitution. It is notably hygroscopic, halogen substitution raises its density and boiling point, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

5-[2-[4-Chloro-2-(Trifluoromethyl)Phenyl]Hydrazinyl]-6-Imino-4-Oxonaphthalene-2-Sulfonic Acid (CAS 3836-78-0) is a high-purity analytical reference standard with the molecular formula C17H11ClF3N3O4S and a molecular weight of 445.80 g/mol.

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 5-[2-[4-Chloro-2-(Trifluoromethyl)Phenyl]Hydrazinyl]-6-Imino-4-Oxonaphthalene-2-Sulfonic Acid 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 FormulaC17H11ClF3N3O4S
Molecular Weight445.80 g/mol
Purity97%+
StorageStore in a cool place (≤25°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)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1958
Halogen ContentF/Cl-containing
Nitrogen Atoms3
Sulfur Atoms1

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