1-(Furan-2-ylmethyl)-1H-pyrazol-5-amine CAS 3528-56-1

Purity 97%+In StockPharmaceutical Standards
CAS No.3528-56-1
Molecular FormulaC8H9N3O
Molecular Weight163.18 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(Furan-2-ylmethyl)-1H-pyrazol-5-amine CAS 3528-56-1 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-(Furan-2-ylmethyl)-1H-pyrazol-5-amine.

CATO supplies 1-(Furan-2-ylmethyl)-1H-pyrazol-5-amine (CAS 3528-56-1), a certified reference material (molecular formula C8H9N3O, MW 163.18 g/mol) for analytical method development and quality control.

1-(Furan-2-ylmethyl)-1H-pyrazol-5-amine (C8H9N3O) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. Its physicochemical properties are representative of its class; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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-(Furan-2-ylmethyl)-1H-pyrazol-5-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 FormulaC8H9N3O
Molecular Weight163.18 g/mol
AppearanceOff-white to pale yellow crystalline powder. (faint amine-like odor)
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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1958
Nitrogen Atoms3

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