3-Chloro-6-(2,2,2-trifluoroethoxy)pyridazine CAS 99366-83-3

Purity 97%+In StockPharmaceutical Standards
CAS No.99366-83-3
Molecular FormulaC6H4ClF3N2O
Molecular Weight212.56 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-Chloro-6-(2,2,2-trifluoroethoxy)pyridazine CAS 99366-83-3 chemical structure

Description

CATO supplies 3-Chloro-6-(2,2,2-trifluoroethoxy)pyridazine (CAS 99366-83-3), a certified reference material (molecular formula C6H4ClF3N2O, MW 212.56 g/mol) for analytical method development and quality control.

Owing to an amide group, a hydroxyl group, an ether linkage, fluorine/chlorine substitution, an aromatic ring system, 3-Chloro-6-(2,2,2-trifluoroethoxy)pyridazine is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 212.56 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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).

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 3-Chloro-6-(2,2,2-trifluoroethoxy)pyridazine 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 FormulaC6H4ClF3N2O
Molecular Weight212.56 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1985
Halogen ContentF/Cl-containing
Nitrogen Atoms2

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