Proflavine
Structural formula | ||||||||||||||||||||||
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General | ||||||||||||||||||||||
Surname | Proflavine | |||||||||||||||||||||
other names |
3,6-diaminoacridine |
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Molecular formula | C 13 H 11 N 3 | |||||||||||||||||||||
Brief description |
yellow solid |
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properties | ||||||||||||||||||||||
Molar mass | 210.25 g mol −1 | |||||||||||||||||||||
Physical state |
firmly |
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Melting point |
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pK s value |
9.7 |
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solubility |
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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 . |
Proflavine is an aromatic heterocyclic compound. At room temperature it is a brown-green powder. The structure of proflavine is based on an acridine backbone. Proflavin is sold as chloride or hemisulfate and is used as an antiseptic and disinfectant .
properties
The melting point of proflavine is 285 ° C. It is readily soluble in water because the heterocyclic nitrogen atom is protonated in aqueous solution. This means that the proflavine is ionic. It shows yellow fluorescence in aqueous solution . The absorption maximum of proflavine is in aqueous solution and at a pH of 7 at 450 nm.
When introduced into the organism, proflavine acts as an intercalator in the DNA and is therefore potentially mutagenic.
swell
- Silke Korn, Michael W. Tausch: Laboratory Simulation for Coupled Cycles of Photosynthesis and Respiration. In: Journal of Chemical Education. Vol. 78 no. September 9 , 2001; doi : 10.1021 / ed078p1238 .
Individual evidence
- ↑ a b c d e Entry on Proflavine in the Hazardous Substances Data Bank , accessed on July 29, 2012.
- ↑ Data sheet 3,6-Diaminoacridine hydrochloride, Dye content 95% from Sigma-Aldrich , accessed on July 12, 2012 ( PDF ).
- ↑ a b Data sheet Proflavine hemisulfate salt hydrate, powder at Sigma-Aldrich , accessed on July 12, 2012 ( PDF ).
- ↑ ( page no longer available , search in web archives )