Xanthydrol
Appearance
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Names | |
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Preferred IUPAC name
9H-Xanthen-9-ol | |
Other names
Xanthanol, 9-Hydroxyxanthene, 9-Xanthydrol, Xanthen-9-ol, 9-Xanthenol, Xanthydrol solution
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Identifiers | |
3D model (JSmol)
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10395 | |
ChemSpider | |
ECHA InfoCard | 100.001.815 |
EC Number |
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PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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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: | |
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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
[edit]Xanthydrol can be produced by the reduction of xanthone.
See also
[edit]References
[edit]- ^ 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) - ^ "9H-Xanthen-9-ol". pubchem.ncbi.nlm.nih.gov.
- ^ 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.