1-(3-Methoxyphenyl)-1H-pyrazol-5-amine CAS 14679-00-6

Purity 97%+In StockPharmaceutical Standards
CAS No.14679-00-6
Molecular FormulaC10H11N3O
Molecular Weight189.21 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(3-Methoxyphenyl)-1H-pyrazol-5-amine CAS 14679-00-6 chemical structure

Description

The occurrence of 1-(3-Methoxyphenyl)-1H-pyrazol-5-amine is closely related to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

1-(3-Methoxyphenyl)-1H-pyrazol-5-amine (CAS 14679-00-6) is a high-purity analytical reference standard with the molecular formula C10H11N3O and a molecular weight of 189.21 g/mol.

1-(3-Methoxyphenyl)-1H-pyrazol-5-amine (C10H11N3O) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. 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-(3-Methoxyphenyl)-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 FormulaC10H11N3O
Molecular Weight189.21 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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1961
Nitrogen Atoms3

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