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Wikipedia

3-Hydroxybenzoic acid

3-Hydroxybenzoic acid is a monohydroxybenzoic acid.

3-Hydroxybenzoic acid
Names
Preferred IUPAC name
3-Hydroxybenzoic acid
Other names
m-Hydroxybenzoic acid
meta-Hydroxybenzoic acid
3-Carboxyphenol
m-Salicylic acid
Identifiers
  • 99-06-9 Y
3D model (JSmol)
  • Interactive image
  • Interactive image
ChEBI
  • CHEBI:30764 Y
ChEMBL
  • ChEMBL65369 Y
ChemSpider
  • 7142 Y
ECHA InfoCard 100.002.478
  • 7420
UNII
  • 2ZFW40OJ7U Y
  • DTXSID6021610
  • InChI=1S/C7H6O3/c8-6-3-1-2-5(4-6)7(9)10/h1-4,8H,(H,9,10) Y
    Key: IJFXRHURBJZNAO-UHFFFAOYSA-N Y
  • C1=CC(=CC(=C1)O)C(=O)O
  • O=C(O)c1cc(O)ccc1
Properties
C7H6O3
Molar mass 138.12 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is YN ?)

Preparation edit

3-Hydroxybenzoic acid can be obtained by the alkali fusion of 3-sulfobenzoic acid between 210 – 220°C.[1]

Natural occurrence edit

3-Hydroxybenzoic acid is a component of castoreum, the exudate from the castor sacs of the mature North American beaver (Castor canadensis) and the European beaver (Castor fiber), used in perfumery.

It can also be formed by a Pseudomonas species from 3-Chlorobenzoic acid.[2]

3-Hydroxybenzoic Acid can be found in the pineapple fruit as well.

References edit

  1. ^ Clarke, M. F.; Owen, L. N. (1950). "434. Alicyclic glycols. Part V. 3-Hydroxymethylcyclohexanol". Journal of the Chemical Society (Resumed): 2108–2115. doi:10.1039/JR9500002108.
  2. ^ H.W. Johnston, G.G. Briggs and M. Alexander (1972). "Metabolism of 3-chlorobenzoic acid by a pseudomonad". Soil Biology and Biochemistry. 4 (2): 187–190. doi:10.1016/0038-0717(72)90010-7.

hydroxybenzoic, acid, monohydroxybenzoic, acid, namespreferred, iupac, name, other, names, hydroxybenzoic, acidmeta, hydroxybenzoic, acid3, carboxyphenolm, salicylic, acididentifierscas, number, model, jsmol, interactive, imageinteractive, imagechebi, chebi, 3. 3 Hydroxybenzoic acid is a monohydroxybenzoic acid 3 Hydroxybenzoic acid NamesPreferred IUPAC name 3 Hydroxybenzoic acidOther names m Hydroxybenzoic acidmeta Hydroxybenzoic acid3 Carboxyphenolm Salicylic acidIdentifiersCAS Number 99 06 9 Y3D model JSmol Interactive imageInteractive imageChEBI CHEBI 30764 YChEMBL ChEMBL65369 YChemSpider 7142 YECHA InfoCard 100 002 478PubChem CID 7420UNII 2ZFW40OJ7U YCompTox Dashboard EPA DTXSID6021610InChI InChI 1S C7H6O3 c8 6 3 1 2 5 4 6 7 9 10 h1 4 8H H 9 10 YKey IJFXRHURBJZNAO UHFFFAOYSA N YSMILES C1 CC CC C1 O C O OO C O c1cc O ccc1PropertiesChemical formula C7H6O3Molar mass 138 12 g molExcept where otherwise noted data are given for materials in their standard state at 25 C 77 F 100 kPa Y verify what is Y N Infobox referencesPreparation edit3 Hydroxybenzoic acid can be obtained by the alkali fusion of 3 sulfobenzoic acid between 210 220 C 1 Natural occurrence edit3 Hydroxybenzoic acid is a component of castoreum the exudate from the castor sacs of the mature North American beaver Castor canadensis and the European beaver Castor fiber used in perfumery It can also be formed by a Pseudomonas species from 3 Chlorobenzoic acid 2 3 Hydroxybenzoic Acid can be found in the pineapple fruit as well References edit Clarke M F Owen L N 1950 434 Alicyclic glycols Part V 3 Hydroxymethylcyclohexanol Journal of the Chemical Society Resumed 2108 2115 doi 10 1039 JR9500002108 H W Johnston G G Briggs and M Alexander 1972 Metabolism of 3 chlorobenzoic acid by a pseudomonad Soil Biology and Biochemistry 4 2 187 190 doi 10 1016 0038 0717 72 90010 7 nbsp This article about an aromatic compound is a stub You can help Wikipedia by expanding it vte Retrieved from https en wikipedia org w index php title 3 Hydroxybenzoic acid amp oldid 1018541614, wikipedia, wiki, book, books, library,

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