(Z)-3-(tert-butyl)-N'-hydroxy-1-methyl-1H-pyrazole-5-carboximidamide CAS 1355338-28-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1355338-28-1
Molecular FormulaC9H16N4O
Molecular Weight196.25 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(Z)-3-(tert-butyl)-N'-hydroxy-1-methyl-1H-pyrazole-5-carboximidamide CAS 1355338-28-1 chemical structure

Description

As a certified reference material (CRM), (Z)-3-(tert-butyl)-N'-hydroxy-1-methyl-1H-pyrazole-5-carboximidamide 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.

CATO supplies (Z)-3-(tert-butyl)-N'-hydroxy-1-methyl-1H-pyrazole-5-carboximidamide (CAS 1355338-28-1), a certified reference material (molecular formula C9H16N4O, MW 196.25 g/mol) for analytical method development and quality control.

Structurally, (Z)-3-(tert-butyl)-N'-hydroxy-1-methyl-1H-pyrazole-5-carboximidamide (C9H16N4O) contains a nitrogen-containing heterocyclic scaffold, 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 196.25 g/mol, it falls into the medium-molecular-weight range. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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.

Physical & Chemical Properties

Molecular FormulaC9H16N4O
Molecular Weight196.25 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)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Nitrogen Atoms4

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