Ornithuric acid
Structural formula | |||||||||||||
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General | |||||||||||||
Surname | Ornithuric acid | ||||||||||||
other names |
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Molecular formula | C 19 H 20 N 2 O 4 | ||||||||||||
Brief description |
colorless needles |
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properties | |||||||||||||
Molar mass | 340.37 g mol −1 | ||||||||||||
Physical state |
firmly |
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Melting point |
189 ° C |
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solubility |
poorly soluble in water |
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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 . |
Ornithuric acid , also known as dibenzoylornithine, is an excretion product in birds that is used to detoxify benzoic acid . It is synthesized from the amino acid L - ornithine and two molecules of benzoic acid.
history
The compound was discovered by Charles Upham Shepard in the mid-19th century , but mistaken for a different acid. In 1877 it was examined more closely by Max Jaffé .
Individual evidence
- ↑ a b c d August Kekulé, Richard Anschütz, Gustav Schultz, Wilhelm LaCoste: Textbook of organic chemistry . 1867, p. 447 ( limited preview in Google Book search).
- ↑ Entry on l-ornithine. In: Römpp Online . Georg Thieme Verlag, accessed on June 20, 2014.
- ↑ This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.
- ^ Heinz Penzlin: Textbook of Animal Physiology. 5th edition. Gustav Fischer Verlag, Jena 1991, ISBN 3-334-60363-6 .
- ↑ Zeitschrift für rational Medicin, Volume 3, 1868, limited preview in the Google book search.