1-(3,5-Dimethyl-1H-pyrazol-4-yl)-N-methylethan-1-amine oxalate CAS 1263987-41-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1263987-41-2
Molecular FormulaC8H15N3
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(3,5-Dimethyl-1H-pyrazol-4-yl)-N-methylethan-1-amine oxalate CAS 1263987-41-2 chemical structure

Description

Structurally, 1-(3,5-Dimethyl-1H-pyrazol-4-yl)-N-methylethan-1-amine oxalate (C8H15N3C2H2O4) contains an amino-acid-derived structure, an amide group, a hydroxyl group, an ether linkage. The molecule exhibits a degree of unsaturation (DBE) of 4.0, corresponding to approximately 4 ring(s) or double-bond equivalent(s). With a molecular weight of 243.26 g/mol, it falls into the medium-molecular-weight range. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO supplies 1-(3,5-Dimethyl-1H-pyrazol-4-yl)-N-methylethan-1-amine oxalate (CAS 1263987-41-2), a certified reference material (molecular formula C8H15N3C2H2O4, MW 243.26 g/mol) for analytical method development and quality control.

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-(3,5-Dimethyl-1H-pyrazol-4-yl)-N-methylethan-1-amine oxalate 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 FormulaC8H15N3 C2H2O4
Molecular Weight243.26 g/mol
AppearanceOff-white to pale yellow crystalline powder. (faint amine-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Nitrogen Atoms3

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