Tolperisone 4-Carboxylic Acid-d10 Hydrochloride Hydrate CAS 1346603-66-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1346603-66-4
Molecular Formula-
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Tolperisone 4-Carboxylic Acid-d10 Hydrochloride Hydrate CAS 1346603-66-4 chemical structure

Description

CATO manufactures Tolperisone 4-Carboxylic Acid-d10 Hydrochloride Hydrate under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

CATO supplies Tolperisone 4-Carboxylic Acid-d10 Hydrochloride Hydrate (CAS 1346603-66-4), a certified reference material (molecular formula C16H11D10NO3HCl, MW 321.87 g/mol) for analytical method development and quality control.

The molecular framework of Tolperisone 4-Carboxylic Acid-d10 Hydrochloride Hydrate (C16H11D10NO3HCl) is characterized by deuterium isotope labeling, a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), 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 FormulaC16H11D10NO3 HCl
Molecular Weight321.87 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentCl-containing
Nitrogen Atoms1

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