4,5,6,7-tetrahydro-1H-1,3-benzodiazol-5-ol hydrochloride CAS 1909336-27-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1909336-27-1
Molecular FormulaC7H10N2O
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4,5,6,7-tetrahydro-1H-1,3-benzodiazol-5-ol hydrochloride CAS 1909336-27-1 chemical structure

Description

The molecular framework of 4,5,6,7-tetrahydro-1H-1,3-benzodiazol-5-ol hydrochloride (C7H10N2OHCl) is characterized by an amide group, a hydroxyl group, an ether linkage, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, 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.

4,5,6,7-tetrahydro-1H-1,3-benzodiazol-5-ol hydrochloride (CAS 1909336-27-1) is a high-purity analytical reference standard with the molecular formula C7H10N2OHCl and a molecular weight of 174.63 g/mol.

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), 4,5,6,7-tetrahydro-1H-1,3-benzodiazol-5-ol 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 FormulaC7H10N2O HCl
Molecular Weight174.63 g/mol
AppearanceWhite to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor)
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)3.0
UV AbsorptionUV-absorbing
CAS Registry Year (est.)1995
Halogen ContentCl-containing
Nitrogen Atoms2

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