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Xanthydrol

From Wikipedia, the free encyclopedia
Xanthydrol
Skeletal formula
Ball-and-stick model
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 Edit this at Wikidata
EC Number
  • 201-996-1
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 checkY
    Key: JFRMYMMIJXLMBB-UHFFFAOYSA-N checkY
  • 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:
GHS07: Exclamation markGHS09: Environmental hazard
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).
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Xanthydrol is an organic chemical compound. Its formula is C13H10O2. Its total molecular weight is 198.221 g/mol. Xanthydrol is used to test the levels of urea in the bloodstream.[3]

Synthesis

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Xanthydrol can be produced by the reduction of xanthone.

See also

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References

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  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.