3-(4-Chlorobenzyl)tetrahydro-2H-pyran-4-amine hydrochloride CAS 1956376-60-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1956376-60-5
Molecular FormulaC12H16ClNO
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(4-Chlorobenzyl)tetrahydro-2H-pyran-4-amine hydrochloride CAS 1956376-60-5 chemical structure

Description

CATO manufactures 3-(4-Chlorobenzyl)tetrahydro-2H-pyran-4-amine hydrochloride 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.

3-(4-Chlorobenzyl)tetrahydro-2H-pyran-4-amine hydrochloride (CAS 1956376-60-5) is a high-purity analytical reference standard with the molecular formula C12H16ClNOHCl and a molecular weight of 262.17 g/mol.

3-(4-Chlorobenzyl)tetrahydro-2H-pyran-4-amine hydrochloride (C12H16ClNOHCl) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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 FormulaC12H16ClNO HCl
Molecular Weight262.17 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
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.)1996
Halogen ContentCl-containing
Nitrogen Atoms1

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