1-(p-Tolyl)-4,5,6,7-tetrahydro-1H-indazol-4-amine CAS 1255099-48-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1255099-48-9
Molecular FormulaC14H17N3
Molecular Weight227.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(p-Tolyl)-4,5,6,7-tetrahydro-1H-indazol-4-amine CAS 1255099-48-9 chemical structure

Description

The occurrence of 1-(p-Tolyl)-4,5,6,7-tetrahydro-1H-indazol-4-amine is closely related to a nitrogen-containing heterocyclic scaffold, a nitrile group in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies 1-(p-Tolyl)-4,5,6,7-tetrahydro-1H-indazol-4-amine (CAS 1255099-48-9), a certified reference material (molecular formula C14H17N3, MW 227.30 g/mol) for analytical method development and quality control.

1-(p-Tolyl)-4,5,6,7-tetrahydro-1H-indazol-4-amine (C14H17N3) contains a nitrogen-containing heterocyclic scaffold, a nitrile group. 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.

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), 1-(p-Tolyl)-4,5,6,7-tetrahydro-1H-indazol-4-amine 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 FormulaC14H17N3
Molecular Weight227.30 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Nitrogen Atoms3

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