Collidinic acid
Appearance
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Names | |
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Preferred IUPAC name
Pyridine-2,4,6-tricarboxylic acid | |
Other names
2,4,6-Pyridinetricarboxylic acid
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Identifiers | |
3D model (JSmol)
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ChEMBL | |
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PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C8H5NO6 | |
Molar mass | 211.129 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Collidinic acid[1][2] (pyridine-2,4,6-tricarboxylic acid) is an organic compound that belongs to the heterocycles (more precisely the heteroaromatics). It belongs to the group of pyridinetricarboxylic acids and consists of a pyridine ring which carries three carboxy groups in the 2-, 4- and 6-positions. The name is derived from 2,4,6-collidine (2,4,6-trimethylpyridine).
Preparation
[edit]The compound can be obtained from the oxidation of 2,4,6-collidine by potassium permanganate.[3]
Uses
[edit]Collidinic acid can be used in the spectrophotometric determination of iron.[4]
References
[edit]- ^ B. Chatterjee: Donor properties of pyridine carboxylic acids: chromium(III) complexes, in: Journal of Inorganic and Nuclear Chemistry, Band 43, Nr. 10, 1981, S. 2553–2555; doi:10.1016/0022-1902(81)80300-4.
- ^ Raymond L. Richards: Vanadium: Inorganic & Coordination Chemistry, in: Encyclopedia of Inorganic and Bioinorganic Chemistry, 2011; doi:10.1002/9781119951438.eibc0236.
- ^ Zhu, Hong-Lin; Xu, Wei; Wang, Jian-Fei; Zheng, Yue-Qing (2012). "Synthesis, crystal structures and properties of two supramolecular polymers constructed by lanthanide with pyridine-2,4,6-tricarboxylic acid". Synthetic Metals. 162 (13–14): 1327–1334. doi:10.1016/j.synthmet.2012.05.016.
- ^ Pyridine and its derivatives. Supplement. Part Three. R. A. Abramovitch. New York: John Wiley & Sons. 1974. p. 298. ISBN 978-0-470-18822-4. OCLC 506484960.
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