3,4-Dihydro-2H-spiro[naphthalene-1,3'-pyrrolidine] hydrochloride CAS 73593-94-9

Purity 97%+In StockPharmaceutical Standards
CAS No.73593-94-9
Molecular FormulaC13H17N
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3,4-Dihydro-2H-spiro[naphthalene-1,3'-pyrrolidine] hydrochloride CAS 73593-94-9 chemical structure

Description

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.

3,4-Dihydro-2H-spiro[naphthalene-1,3'-pyrrolidine] hydrochloride (CAS 73593-94-9), molecular formula C13H17NHCl and molecular weight 223.74 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of 3,4-Dihydro-2H-spiro[naphthalene-1,3'-pyrrolidine] hydrochloride (C13H17NHCl) is characterized by a nitrogen-containing heterocyclic scaffold, a nitrile group, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

As a certified reference material (CRM), 3,4-Dihydro-2H-spiro[naphthalene-1,3'-pyrrolidine] 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 FormulaC13H17N HCl
Molecular Weight223.74 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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1978
Halogen ContentCl-containing
Nitrogen Atoms1

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