N-(5-Ethyl-4-(heptan-4-yl)-1H-pyrazol-3-yl)acetimidamide CAS 647854-08-8

Purity 97%+In StockPharmaceutical Standards
CAS No.647854-08-8
Molecular FormulaC14H26N4
Molecular Weight250.38 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(5-Ethyl-4-(heptan-4-yl)-1H-pyrazol-3-yl)acetimidamide CAS 647854-08-8 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 N-(5-Ethyl-4-(heptan-4-yl)-1H-pyrazol-3-yl)acetimidamide.

CATO supplies N-(5-Ethyl-4-(heptan-4-yl)-1H-pyrazol-3-yl)acetimidamide (CAS 647854-08-8), a certified reference material (molecular formula C14H26N4, MW 250.38 g/mol) for analytical method development and quality control.

N-(5-Ethyl-4-(heptan-4-yl)-1H-pyrazol-3-yl)acetimidamide (C14H26N4) contains a nitrogen-containing heterocyclic scaffold, a nitrile group. 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.

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), N-(5-Ethyl-4-(heptan-4-yl)-1H-pyrazol-3-yl)acetimidamide 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 FormulaC14H26N4
Molecular Weight250.38 g/mol
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.)1985
Nitrogen Atoms4

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