Xanthydrol

Last updated
Xanthydrol
Xanthydrol.svg
Xanthydrol-3D-balls.png
Names
Preferred IUPAC name
9H-Xanthen-9-ol
Other names
Xanthanol, 9-Hydroxyxanthene, 9-Xanthydrol, Xanthen-9-ol, 9-Xanthenol, Xanthydrol solution
Identifiers
3D model (JSmol)
10395
ChemSpider
ECHA InfoCard 100.001.815 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 201-996-1
PubChem CID
UNII
  • InChI=1S/C13H10O2/c14-13-9-5-1-3-7-11(9)15-12-8-4-2-6-10(12)13/h1-8,13-14H Yes check.svgY
    Key: JFRMYMMIJXLMBB-UHFFFAOYSA-N Yes check.svgY
  • O2C1=C(C=CC=C1)C(C3=C2C=CC=C3)O
Properties
C13H10O2
Molar mass 198.221 g·mol−1
Melting point 124 to 126 °C (255 to 259 °F; 397 to 399 K) [1]
Hazards [2]
GHS labelling:
GHS-pictogram-exclam.svg GHS-pictogram-pollu.svg
Warning
H302, H315, H319, H335, H411
P261, P264, P270, P271, P273, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P391, P403+P233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Yes check.svgY  verify  (what is  Yes check.svgYX mark.svgN ?)

Xanthydrol is an organic chemical compound. Its formula is C 13 H 10 O 2. Its total molecular weight is 198.221 g/mol. Xanthydrol is used to test the levels of urea in the bloodstream. [3] Xanthidrol/acetonitrile solution is used for the simultaneous extraction and derivatisation of ethyl carbamate. [4]

Contents

Synthesis

Xanthydrol can be produced by the reduction of xanthone.

See also

References

  1. Goldberg; Wragg (1957). "972. Spasmolytics derived from xanthen". Journal of the Chemical Society: 4823–4829. doi:10.1039/JR9570004823.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  2. "9H-Xanthen-9-ol". pubchem.ncbi.nlm.nih.gov.
  3. Bowden, R. S. T. (1962). "The Estimation of Blood Urea by the Xanthydrol Reaction". Journal of Small Animal Practice. 3 (4): 217–218. doi:10.1111/j.1748-5827.1962.tb04191.x.
  4. "Determination of ethyl carbamate in spirits using salting-out assisted liquid–liquid extraction and high performance liquid chromatography with fluorimetric detection". Analytical Methods. 6: 9136–9141. 2014. doi:10.1039/C4AY02075H.