1-(3-Iodophenyl)-N-methylmethanamine CAS 90389-93-8

Purity 97%+In StockPharmaceutical Standards
CAS No.90389-93-8
Molecular FormulaC8H10IN
Molecular Weight247.08 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(3-Iodophenyl)-N-methylmethanamine CAS 90389-93-8 chemical structure

Description

As a certified reference material (CRM), 1-(3-Iodophenyl)-N-methylmethanamine 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 1-(3-Iodophenyl)-N-methylmethanamine (CAS 90389-93-8), a certified reference material (molecular formula C8H10IN, MW 247.08 g/mol) for analytical method development and quality control.

The molecular framework of 1-(3-Iodophenyl)-N-methylmethanamine (C8H10IN) is characterized by a nitrogen-containing heterocyclic scaffold, a nitrile group, iodine substitution. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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 FormulaC8H10IN
Molecular Weight247.08 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, acetonitrile, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1982
Halogen ContentI-containing
Nitrogen Atoms1

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