Xanthydrol

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Structural formula
Structural formula of Xanthydrol
General
Surname Xanthydrol
other names
  • 9-hydroxyxanthene
  • 9-xanthenol
  • 9 H -xanthene-9-ol
Molecular formula C 13 H 10 O 2
Brief description

colorless to beige solid

External identifiers / databases
CAS number 90-46-0
EC number 201-996-1
ECHA InfoCard 100.001.815
PubChem 72861
ChemSpider 65693
Wikidata Q4021716
properties
Molar mass 198.22 g mol −1
Physical state

firmly

Melting point

127-128 ° C

solubility
  • soluble in methanol (50 g l −1 )
  • soluble in chloroform
  • practically insoluble in water
safety instructions
GHS labeling of hazardous substances
no GHS pictograms
H and P phrases H: no H-phrases
P: no P-phrases
Toxicological data

500 mg kg −1 ( LD Loratoral )

As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions .

Xanthydrol is a heterocyclic chemical compound .

Extraction and presentation

Xanthydrol can be obtained by reducing xanthone with sodium amalgam in an alcoholic solution.

properties

Xanthydrol is a colorless to beige solid that is soluble in methanol . It can easily be oxidized to xanthone and forms salts with mineral acids.

use

Xanthydrol is used as a derivatizing reagent for the determination of acrylamide in surface and drinking water according to the GC-MS method and of urea (for example in blood) by HPLC with fluorescence detection. It is also used for the determination of phenol and as a reagent in the thin-layer chromatographic determination of indole and indole derivatives.

The xanthydrol reaction is the reaction of xanthydrol, acetic acid and hydrochloric acid with 2-deoxy sugar and 2,6-dideoxy sugar with the formation of color products.

Individual evidence

  1. a b c d e f g h i data sheet Xanthydrol, 98% from Sigma-Aldrich , accessed on September 25, 2017 ( PDF ).
  2. a b c d e f Lexikon der Chemie: Xanthydrol - Lexikon der Chemie , accessed on September 25, 2017.
  3. RST BOWDEN: The Estimation of Blood Urea by the Xanthydrol Reaction. In: Journal of Small Animal Practice. 3, 1962, p. 217, doi : 10.1111 / j.1748-5827.1962.tb04191.x .
  4. ^ Gerhard Franz, Hildegard Koehler: Drugs and natural substances, basics and practice of chemical analysis . Springer-Verlag, 2013, ISBN 978-3-642-77376-1 , p. 105 ( limited preview in Google Book search).