1-((4-Chloro-3,5-dimethylphenoxy)methyl)-3,5-dimethyl-1h-pyrazol-4-amine CAS 1004192-81-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1004192-81-7
Molecular FormulaC14H18ClN3O
Molecular Weight279.77 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-((4-Chloro-3,5-dimethylphenoxy)methyl)-3,5-dimethyl-1h-pyrazol-4-amine CAS 1004192-81-7 chemical structure

Description

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution, 1-((4-Chloro-3,5-dimethylphenoxy)methyl)-3,5-dimethyl-1h-pyrazol-4-amine is typically off-white to pale yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 279.77 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

1-((4-Chloro-3,5-dimethylphenoxy)methyl)-3,5-dimethyl-1h-pyrazol-4-amine (CAS 1004192-81-7) is a high-purity analytical reference standard with the molecular formula C14H18ClN3O and a molecular weight of 279.77 g/mol.

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

CATO manufactures 1-((4-Chloro-3,5-dimethylphenoxy)methyl)-3,5-dimethyl-1h-pyrazol-4-amine under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC14H18ClN3O
Molecular Weight279.77 g/mol
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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Halogen ContentCl-containing
Nitrogen Atoms3

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