4-(3-(Methylthio)phenyl)-1H-pyrrole-3-carbonitrile CAS 87388-26-9

Purity 97%+In StockPharmaceutical Standards
CAS No.87388-26-9
Molecular FormulaC12H10N2S
Molecular Weight214.29 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(3-(Methylthio)phenyl)-1H-pyrrole-3-carbonitrile CAS 87388-26-9 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 214.29 g/mol gives 4-(3-(Methylthio)phenyl)-1H-pyrrole-3-carbonitrile distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

4-(3-(Methylthio)phenyl)-1H-pyrrole-3-carbonitrile (CAS 87388-26-9), molecular formula C12H10N2S and molecular weight 214.29 g/mol, is a CATO reference standard with documented purity and traceability.

4-(3-(Methylthio)phenyl)-1H-pyrrole-3-carbonitrile (C12H10N2S) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, sulfur-containing functionality. 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), 4-(3-(Methylthio)phenyl)-1H-pyrrole-3-carbonitrile 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 FormulaC12H10N2S
Molecular Weight214.29 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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1981
Nitrogen Atoms2
Sulfur Atoms1

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