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3,5-Dinitrobenzoic acid

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This is an old revision of this page, as edited by Emeldir (talk | contribs) at 22:42, 18 September 2016 (preferred IUPAC name (PIN) according to ''Nomenclature of Organic Chemistry – IUPAC Recommendations and Preferred Names 2013 (Blue Book)''). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

3,5-Dinitrobenzoic acid
Skeletal formula
Ball-and-stick model
Names
Preferred IUPAC name
3,5-Dinitrobenzoic acid
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.002.501 Edit this at Wikidata
  • InChI=1S/C7H4N2O6/c10-7(11)4-1-5(8(12)13)3-6(2-4)9(14)15/h1-3H,(H,10,11) checkY
    Key: VYWYYJYRVSBHJQ-UHFFFAOYSA-N checkY
  • InChI=1/C7H4N2O6/c10-7(11)4-1-5(8(12)13)3-6(2-4)9(14)15/h1-3H,(H,10,11)
    Key: VYWYYJYRVSBHJQ-UHFFFAOYAQ
  • O=[N+]([O-])c1cc(cc([N+]([O-])=O)c1)C(=O)O
Properties
C7H4O6N2
Molar mass 212.118 g/mol
Appearance Yellow or colourless crystals
Melting point 205 to 207 °C (401 to 405 °F; 478 to 480 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

3,5-Dinitrobenzoic acid is an organic chemical that is an important corrosion inhibitor and is also used in photography. This aromatic compound is used by chemists to identify alcohol components in esters and in the fluorometric analysis of creatinine.

Identification of isopropanol as a derivate of 3,5-dinitrobenzoic acid:
3,5-dinitrobenzoic acid-2-propylester (mp.: 123 °C[1]).

References

  1. ^ CRC Handbook of Tables for Organic Compound Identification, Third Edition, 1984, ISBN 0-8493-0303-6.

Literature

  • "3,5-dinitrobenzoic acid". Combined Chemical Dictionary. Chapman and Hall/CRC Press. 2007.
  • B. C. Saunders, G. J. Stacey, I. G. E. Wilding: "The Preparation of 3:5-Dinitrobenzoic Acid and 3:5-Dinitrobenzoyl Chloride – Observations on the Acylation of Amino-acids by means of 3:5-Dinitrobenzoyl Chloride and certain other Acid Chlorides", Biochem. J., 1942, 36 (3–4), p. 368–375; Text; PDF.
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