N-(3-(Trifluoromethoxy)phenyl)hydrazinecarbothioamide CAS 1152549-22-8

Purity 97%+In StockPharmaceutical Standards
CAS No.1152549-22-8
Molecular FormulaC8H8F3N3OS
Molecular Weight251.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(3-(Trifluoromethoxy)phenyl)hydrazinecarbothioamide CAS 1152549-22-8 chemical structure

Description

Based on its molecular formula C8H8F3N3OS, N-(3-(Trifluoromethoxy)phenyl)hydrazinecarbothioamide contains a nitrogen-containing heterocyclic scaffold, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, fluorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 251.23 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

N-(3-(Trifluoromethoxy)phenyl)hydrazinecarbothioamide (CAS 1152549-22-8) is a high-purity analytical reference standard with the molecular formula C8H8F3N3OS and a molecular weight of 251.23 g/mol.

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-(3-(Trifluoromethoxy)phenyl)hydrazinecarbothioamide 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 FormulaC8H8F3N3OS
Molecular Weight251.23 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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Halogen ContentF-containing
Nitrogen Atoms3
Sulfur Atoms1

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