Quinalizarin
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| General | ||||||||||||||||||||||
| Surname | Quinalizarin | |||||||||||||||||||||
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| Molecular formula | C 14 H 8 O 6 | |||||||||||||||||||||
| Brief description |
dark red needles with a green metallic sheen |
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| properties | ||||||||||||||||||||||
| Molar mass | 272.20 g mol −1 | |||||||||||||||||||||
| Physical state |
firmly |
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| Melting point |
> 275 ° C |
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| solubility |
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| As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . | ||||||||||||||||||||||
Quinalizarin is an organic chemical compound that belongs to the group of alizarin dyes and thus the anthraquinones . It is used for the detection and colorimetric determination of beryllium , magnesium , boron , aluminum , gallium , indium and fluorides and was previously used for dyeing cotton. Quinalizarin is made from alizarin by heating with fuming sulfuric acid and boric acid .
Individual evidence
- ↑ a b c Entry on quinalizarin. In: Römpp Online . Georg Thieme Verlag, accessed on March 5, 2014.
- ↑ a b Omikron Online: Chinalizarin data sheet ( Memento from May 7, 2012 in the Internet Archive )
- ↑ a b Data sheet quinalizarin, ≥95% (HPLC) from Sigma-Aldrich , accessed on June 2, 2016 ( PDF ).