Atomfair Quinizarin C14H8O4

Description Quinizarin (CAS 105640-07-1) is a high-purity anthraquinone derivative with the molecular formula C14H8O4and IUPAC name 1,4-dihydroxyanthracene-9,10-dione . This orange-red crystalline compound is widely utilized in organic synthesis, dye manufacturing, and analytical chemistry due to its excellent chelating and chromogenic properties. Our Quinizarin is rigorously tested for purity (??98% by HPLC) and is supplied with comprehensive analytical documentation, including1H NMR, FT-IR, and mass spectrometry data. Available in research quantities (1g to 1kg) with customizable packaging options under inert atmosphere for optimal stability. Suitable for use as a precursor in photodynamic therapy agents, metal ion indicators, and as a key intermediate…

Description

Description

Quinizarin (CAS 105640-07-1) is a high-purity anthraquinone derivative with the molecular formula C14H8O4 and IUPAC name 1,4-dihydroxyanthracene-9,10-dione. This orange-red crystalline compound is widely utilized in organic synthesis, dye manufacturing, and analytical chemistry due to its excellent chelating and chromogenic properties. Our Quinizarin is rigorously tested for purity (??98% by HPLC) and is supplied with comprehensive analytical documentation, including 1H NMR, FT-IR, and mass spectrometry data. Available in research quantities (1g to 1kg) with customizable packaging options under inert atmosphere for optimal stability. Suitable for use as a precursor in photodynamic therapy agents, metal ion indicators, and as a key intermediate for advanced materials synthesis.

  • CAS No: 105640-07-1
  • Molecular Formula: C14H8O4
  • Molecular Weight: 240.21
  • Exact Mass: 240.04225873
  • Monoisotopic Mass: 240.04225873
  • IUPAC Name: 1,4-dihydroxyanthracene-9,10-dione
  • SMILES: C1=CC=C2C(=C1)C(=O)C3=C(C=CC(=C3C2=O)O)O
  • Synonyms: Quinizarin, 1,4-Dihydroxyanthraquinone, 1,4-Dihydroxyanthra-9,10-quinone, CHEBI:37487, NSC-15367

Application

Quinizarin serves as a versatile intermediate in the synthesis of anthraquinone dyes and pigments for textile applications. In analytical chemistry, it functions as a sensitive chromogenic reagent for spectrophotometric determination of metal ions, particularly aluminum and beryllium. The compound’s redox-active quinoid structure makes it valuable for developing organic semiconductors and electrochromic materials in advanced material science research.

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