Collidinic acid

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Collidinic acid
Trimesitinsaure Strukturformel V1.svg
Names
Preferred IUPAC name
Pyridine-2,4,6-tricarboxylic acid
Other names
2,4,6-Pyridinetricarboxylic acid
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
PubChem CID
UNII
  • InChI=1S/C8H5NO6/c10-6(11)3-1-4(7(12)13)9-5(2-3)8(14)15/h1-2H,(H,10,11)(H,12,13)(H,14,15)
    Key: CHGYKYXGIWNSCD-UHFFFAOYSA-N
  • C1=C(C=C(N=C1C(=O)O)C(=O)O)C(=O)O
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).

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).

Contents

Preparation

The compound can be obtained from the oxidation of 2,4,6-collidine by potassium permanganate. [3]

Uses

Collidinic acid can be used in the spectrophotometric determination of iron. [4]

Related Research Articles

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Pyridine is a basic heterocyclic organic compound with the chemical formula C5H5N. It is structurally related to benzene, with one methine group (=CH−) replaced by a nitrogen atom (=N−). It is a highly flammable, weakly alkaline, water-miscible liquid with a distinctive, unpleasant fish-like smell. Pyridine is colorless, but older or impure samples can appear yellow, due to the formation of extended, unsaturated polymeric chains, which show significant electrical conductivity. The pyridine ring occurs in many important compounds, including agrochemicals, pharmaceuticals, and vitamins. Historically, pyridine was produced from coal tar. As of 2016, it is synthesized on the scale of about 20,000 tons per year worldwide.

Sulfur trioxide (alternative spelling sulphur trioxide) is the chemical compound with the formula SO3. It has been described as "unquestionably the most [economically] important sulfur oxide". It is prepared on an industrial scale as a precursor to sulfuric acid.

<span class="mw-page-title-main">Phosphorine</span> Chemical compound

Phosphorine is a heavier element analog of pyridine, containing a phosphorus atom instead of an aza- moiety. It is also called phosphabenzene and belongs to the phosphaalkene class. It is a colorless liquid that is mainly of interest in research.

<span class="mw-page-title-main">Chromium(III) chloride</span> Chemical compound

Chromium(III) chloride (also called chromic chloride) is an inorganic chemical compound with the chemical formula CrCl3. It forms several hydrates with the formula CrCl3·nH2O, among which are hydrates where n can be 5 (chromium(III) chloride pentahydrate CrCl3·5H2O) or 6 (chromium(III) chloride hexahydrate CrCl3·6H2O). The anhydrous compound with the formula CrCl3 are violet crystals, while the most common form of the chromium(III) chloride are the dark green crystals of hexahydrate, CrCl3·6H2O. Chromium chlorides find use as catalysts and as precursors to dyes for wool.

<span class="mw-page-title-main">Triazine</span> Aromatic, heterocyclic compound

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<span class="mw-page-title-main">Collidine</span> Index of chemical compounds with the same name

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Vanadium(III) chloride describes the inorganic compound with the formula VCl3 and its hydrates. It forms a purple anhydrous form and a green hexahydrate [VCl2(H2O)4]Cl·2H2O. These hygroscopic salts are common precursors to other vanadium(III) complexes and is used as a mild reducing agent.

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2
[Os
4
(CO)
13
]
and Na
2
[Os(CO)
4
]
are used in the synthesis of osmium cluster compounds.

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<span class="mw-page-title-main">Methanesulfonic anhydride</span> Chemical compound

Methanesulfonic anhydride (Ms2O) is the acid anhydride of methanesulfonic acid. Like methanesulfonyl chloride (MsCl), it may be used to generate mesylates (methanesulfonyl esters).

<span class="mw-page-title-main">Arsabenzene</span> Chemical compound

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<span class="mw-page-title-main">2,4,6-Trimethylpyridine</span> Chemical compound

2,4,6-Trimethylpyridine (2,4,6-collidine) is an organic compound which belongs to the heterocycles. It consists of a pyridine ring substituted with three methyl groups. It belongs to the substance group of the collidines, a group of six constitutional isomers. 2,4,6-trimethylpyridine is the most well-known isomer of this group.

<span class="mw-page-title-main">Berberonic acid</span> Chemical compound

Berberonic acid is an organic compound that belongs to the heterocycles. It belongs to the group of pyridinetricarboxylic acids and consists of a pyridine ring which carries three carboxy groups in the 2-, 4- and 5-positions. The name is derived from berberine.

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References

  1. 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.
  2. Raymond L. Richards: Vanadium: Inorganic & Coordination Chemistry, in: Encyclopedia of Inorganic and Bioinorganic Chemistry , 2011; doi:10.1002/9781119951438.eibc0236.
  3. 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.
  4. 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.{{cite book}}: CS1 maint: others (link)