trans-3-(p-Tolyloxy)cyclobutanamine Hydrochloride CAS 1630906-70-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1630906-70-5
Molecular FormulaC11H15NO
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

trans-3-(p-Tolyloxy)cyclobutanamine Hydrochloride CAS 1630906-70-5 chemical structure

Description

CATO supplies trans-3-(p-Tolyloxy)cyclobutanamine Hydrochloride (CAS 1630906-70-5), a certified reference material (molecular formula C11H15NOHCl, MW 213.70 g/mol) for analytical method development and quality control.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution, trans-3-(p-Tolyloxy)cyclobutanamine Hydrochloride is typically off-white to pale yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 213.70 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

As a certified reference material (CRM), trans-3-(p-Tolyloxy)cyclobutanamine Hydrochloride meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC11H15NO HCl
Molecular Weight213.70 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.)1993
Halogen ContentCl-containing
Nitrogen Atoms1

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