1-(4-(Tert-butyl)phenyl)-4,5,6,7-tetrahydro-1H-indazol-4-amine CAS 1203661-49-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1203661-49-7
Molecular FormulaC17H23N3
Molecular Weight269.38 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(4-(Tert-butyl)phenyl)-4,5,6,7-tetrahydro-1H-indazol-4-amine CAS 1203661-49-7 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 1-(4-(Tert-butyl)phenyl)-4,5,6,7-tetrahydro-1H-indazol-4-amine.

CATO supplies 1-(4-(Tert-butyl)phenyl)-4,5,6,7-tetrahydro-1H-indazol-4-amine (CAS 1203661-49-7), a certified reference material (molecular formula C17H23N3, MW 269.38 g/mol) for analytical method development and quality control.

1-(4-(Tert-butyl)phenyl)-4,5,6,7-tetrahydro-1H-indazol-4-amine (C17H23N3) 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.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

As a certified reference material (CRM), 1-(4-(Tert-butyl)phenyl)-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 FormulaC17H23N3
Molecular Weight269.38 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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