Rosindulin
Structural formula | |||||||||||||||||||
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General | |||||||||||||||||||
Surname | Rosindulin | ||||||||||||||||||
other names |
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Molecular formula | C 28 H 18 N 3 NaO 6 S 2 | ||||||||||||||||||
Brief description |
dark red solid |
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properties | |||||||||||||||||||
Molar mass | 579.59 g mol −1 | ||||||||||||||||||
Physical state |
firmly |
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solubility |
very little in water (1 mg l −1 ) |
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safety instructions | |||||||||||||||||||
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As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
Rosindulin or Azocarmine G is a red dye that is mainly used in microscopy. It has no relation to carmine .
properties
Rosindulin is a dark red solid that is only sparingly soluble in water.
use
In microscopy , biological specimens are colored with Azocarmine G. Histologically , azocarmine G ( Az for short ) and aniline blue ( An ) are used as azan stains to differentiate between cells and the surrounding matrix.
Related links
In addition to Azocarmin G, there is also Azocarmin B ( CI 50090, Acid Red 103), which has improved water solubility.
The term rosinduline also stands for the substance group of the monoamino derivatives of phenylnaphthophenazonium. Varying the position of the amino group results in a large number of chemical compounds that were thoroughly investigated by Friedrich Kehrmann .
Web links
- Entry Azocarmine at Stainsfile
Individual evidence
- ↑ a b c d e data sheet Azocarmine G at AlfaAesar, accessed on February 10, 2018 ( PDF )(JavaScript required) .
- ↑ Datasheet Azocarmin G from Sigma-Aldrich , accessed on October 22, 2016 ( PDF ).
- ↑ External identifiers of or database links to Azocarmin B : CAS number: 25360-72-9, EC number: 246-897-4, ECHA InfoCard: 100.042.620 , PubChem : 6099365 , ChemSpider : 3578780 , Wikidata : Q27159446 .
- ↑ Entry Azocarmine at Stainsfile, accessed on February 10, 2018.
- ^ F. Kehrmann: On the constitution of the fluorine indines and rosindulines. Two preliminary communications. In: Reports of the German Chemical Society. 27, 1894, pp. 3348-3350, doi : 10.1002 / cber.189402703140 .
- ↑ F. Kehrmann, Ferd. Rademacher, O. Feder: About Nitro- and Amino-Rosinduline. In: Reports of the German Chemical Society. 31, 1898, pp. 3076-3087, doi : 10.1002 / cber.18980310387 .
- ^ Paul Karrer: Textbook of Organic Chemistry , 10th Edition, Georg Thieme Verlag, Stuttgart 1948, p. 653.