{1-[4-(Trifluoromethyl)benzyl]cyclobutyl}methanamine hydrochloride CAS 1439903-10-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1439903-10-2
Molecular FormulaC13H16F3N
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

{1-[4-(Trifluoromethyl)benzyl]cyclobutyl}methanamine hydrochloride CAS 1439903-10-2 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.

{1-[4-(Trifluoromethyl)benzyl]cyclobutyl}methanamine hydrochloride (CAS 1439903-10-2) is a high-purity analytical reference standard with the molecular formula C13H16F3NHCl and a molecular weight of 279.73 g/mol.

{1-[4-(Trifluoromethyl)benzyl]cyclobutyl}methanamine hydrochloride (C13H16F3NHCl) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, fluorine/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.

CATO manufactures {1-[4-(Trifluoromethyl)benzyl]cyclobutyl}methanamine 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.

Physical & Chemical Properties

Molecular FormulaC13H16F3N HCl
Molecular Weight279.73 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
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.)1991
Halogen ContentF/Cl-containing
Nitrogen Atoms1

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