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Chemical Structure
Chemical Structure
Chemical Structure

Azomethine-H monosodium salt hydrate [206752-32-1]

Research Use Only
CDX-A0149
Chemodex
CAS Number206752-32-1
Product group Chemicals
Estimated Purity>95%
Molecular Weight445.40 (anhydrous basis)
Price on request
Packing Size
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Overview

  • Supplier
    Chemodex
  • Product Name
    Azomethine-H monosodium salt hydrate [206752-32-1]
  • Delivery Days Customer
    10
  • CAS Number
    206752-32-1
  • Certification
    Research Use Only
  • Estimated Purity
    >95%
  • Hazard Information
    Warning
  • Molecular Formula
    C17H12NNaO8S2 . xH2O
  • Molecular Weight
    445.40 (anhydrous basis)
  • Scientific Description
    Chemical. CAS: 206752-32-1. Formula: C17H12NNaO8S2 . xH2O. MW: 445.40 (anhydrous basis). Synthetic Probe for the colorimetric determination of boron in samples such us soils, plants, composts, manure, water, nutirent solution, glass or steel (microgram levels of boron). It forms an orange complex with boron in aqueous solution (absorption maxima at ~415nm). The detection range of boron in sample solutions is 1.0-6ppm. To detect boron in plant samples EDTA is used to mask copper, iron and aluminium ions. It is also used in electrocyclization reactions in the synthesis of martinellic acid, spirotryprostatin A and benzodiazepinones. Was shown to produce free radicals and might have anti-malarial and anti-cancer properties. - Probe for the colorimetric determination of boron in samples such us soils, plants, composts, manure, water, nutirent solution, glass or steel (microgram levels of boron). It forms an orange complex with boron in aqueous solution (absorption maxima at ~415nm). The detection range of boron in sample solutions is 1.0-6ppm. To detect boron in plant samples EDTA is used to mask copper, iron and aluminium ions. It is also used in electrocyclization reactions in the synthesis of martinellic acid, spirotryprostatin A and benzodiazepinones. Was shown to produce free radicals and might have anti-malarial and anti-cancer properties.
  • SMILES
    O.[Na+].OC1=C(\C=N\C2=CC(=CC3=CC(=CC(O)=C23)S([O-])(=O)=O)S(O)(=O)=O)C=CC=C1
  • Storage Instruction
    RT
  • UNSPSC
    41116134