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Indoxyl

In organic chemistry, indoxyl is a nitrogenous substance with the chemical formula: C8H7NO.[1][2] Indoxyl is isomeric with oxindol and is obtained as an oily liquid.

Indoxyl
Names
Preferred IUPAC name
1H-Indol-3-ol
Identifiers
  • 480-93-3 Y
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:17840 Y
ChemSpider
  • 45861 Y
ECHA InfoCard 100.216.308
EC Number
  • 689-424-0
KEGG
  • C05658 Y
  • 50591
UNII
  • BZ24HY3WPJ Y
  • InChI=1S/C8H7NO/c10-8-5-9-7-4-2-1-3-6(7)8/h1-5,9-10H Y
    Key: PCKPVGOLPKLUHR-UHFFFAOYSA-N Y
  • InChI=1/C8H7NO/c10-8-5-9-7-4-2-1-3-6(7)8/h1-5,9-10H
    Key: PCKPVGOLPKLUHR-UHFFFAOYAR
  • Oc2c1ccccc1[nH]c2
Properties
C8H7NO
Molar mass 133.14728
Hazards
GHS labelling:
Danger
H302, H311, H319, H400
P264, P270, P273, P280, P301+P312, P302+P352, P305+P351+P338, P312, P322, P330, P337+P313, P361, P363, P391, P405, P501
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 ?)

Indoxyl is obtained from indican, which is a glycoside. The hydrolysis of indican yields β-D-glucose and indoxyl.

Indigo dye is a product of the reaction of indoxyl with a mild oxidizing agent such as atmospheric oxygen.

Indoxyl can be found in urine and is titrated with Obermayer's reagent, which is a dilute solution of ferric chloride (FeCl3) in hydrochloric acid (HCl).[3]

References edit

  1. ^ Katritzky, A. R.; Pozharskii, A. F. (2000). Handbook of Heterocyclic Chemistry (2nd ed.). Academic Press. ISBN 0080429882.
  2. ^ Clayden, J.; Greeves, N.; Warren, S.; Wothers, P. (2001). Organic Chemistry. Oxford, Oxfordshire: Oxford University Press. ISBN 0-19-850346-6.
  3. ^ Lide, David (1998). CRC - Handbook of Chemistry and Physics. CRC press LLC. pp. Section 8 page 3. ISBN 0-8493-0479-2.

indoxyl, organic, chemistry, indoxyl, nitrogenous, substance, with, chemical, formula, c8h7no, isomeric, with, oxindol, obtained, oily, liquid, namespreferred, iupac, name, indol, olidentifierscas, number, model, jsmol, interactive, imagechebi, chebi, 17840, y. In organic chemistry indoxyl is a nitrogenous substance with the chemical formula C8H7NO 1 2 Indoxyl is isomeric with oxindol and is obtained as an oily liquid Indoxyl NamesPreferred IUPAC name 1H Indol 3 olIdentifiersCAS Number 480 93 3 Y3D model JSmol Interactive imageChEBI CHEBI 17840 YChemSpider 45861 YECHA InfoCard 100 216 308EC Number 689 424 0KEGG C05658 YPubChem CID 50591UNII BZ24HY3WPJ YInChI InChI 1S C8H7NO c10 8 5 9 7 4 2 1 3 6 7 8 h1 5 9 10H YKey PCKPVGOLPKLUHR UHFFFAOYSA N YInChI 1 C8H7NO c10 8 5 9 7 4 2 1 3 6 7 8 h1 5 9 10HKey PCKPVGOLPKLUHR UHFFFAOYARSMILES Oc2c1ccccc1 nH c2PropertiesChemical formula C8H7NOMolar mass 133 14728HazardsGHS labelling PictogramsSignal word DangerHazard statements H302 H311 H319 H400Precautionary statements P264 P270 P273 P280 P301 P312 P302 P352 P305 P351 P338 P312 P322 P330 P337 P313 P361 P363 P391 P405 P501Except 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 references Indoxyl is obtained from indican which is a glycoside The hydrolysis of indican yields b D glucose and indoxyl Indigo dye is a product of the reaction of indoxyl with a mild oxidizing agent such as atmospheric oxygen Indoxyl can be found in urine and is titrated with Obermayer s reagent which is a dilute solution of ferric chloride FeCl3 in hydrochloric acid HCl 3 References edit Katritzky A R Pozharskii A F 2000 Handbook of Heterocyclic Chemistry 2nd ed Academic Press ISBN 0080429882 Clayden J Greeves N Warren S Wothers P 2001 Organic Chemistry Oxford Oxfordshire Oxford University Press ISBN 0 19 850346 6 Lide David 1998 CRC Handbook of Chemistry and Physics CRC press LLC pp Section 8 page 3 ISBN 0 8493 0479 2 nbsp This article about a heterocyclic compound is a stub You can help Wikipedia by expanding it vte Retrieved from https en wikipedia org w index php title Indoxyl amp oldid 1176031846, wikipedia, wiki, book, books, library,

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