Xanthene

{{Short description|Chemical compound used to make dyes}}

{{Distinguish|xanthine}}

{{Chembox

| Verifiedfields = changed

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| verifiedrevid = 412200450

| ImageFile = Xanthen.svg

| ImageSize =

| ImageAlt = Skeletal formula

| ImageFile1 = Xanthene-3D-balls.png

| ImageSize1 = 220

| ImageAlt1 = Ball-and-stick model

| PIN = 9H-Xanthene{{cite book |author=International Union of Pure and Applied Chemistry |date=2014 |title=Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013 |publisher=The Royal Society of Chemistry |pages=213 |doi=10.1039/9781849733069 |isbn=978-0-85404-182-4}}

| OtherNames = Dibenzo[a,e]pyran
10H-9-Oxaanthracene

|Section1={{Chembox Identifiers

| Abbreviations =

| CASNo = 92-83-1

| CASNo_Ref = {{cascite|correct|CAS}}

| Beilstein = 133939

| ChEBI_Ref = {{ebicite|correct|EBI}}

| ChEBI = 10057

| ChEMBL_Ref = {{ebicite|correct|EBI}}

| ChEMBL = 486760

| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}

| ChemSpiderID = 6840

| EINECS = 202-194-4

| Gmelin = 83576

| KEGG_Ref = {{keggcite|changed|kegg}}

| KEGG = C01464

| PubChem = 7107

| RTECS =

| MeSHName =

| UNII_Ref = {{fdacite|correct|FDA}}

| UNII = A762Z8101Y

| InChI = 1/C13H10O/c1-3-7-12-10(5-1)9-11-6-2-4-8-13(11)14-12/h1-8H,9H2

| InChIKey = GJCOSYZMQJWQCA-UHFFFAOYAO

| StdInChI_Ref = {{stdinchicite|changed|chemspider}}

| StdInChI = 1S/C13H10O/c1-3-7-12-10(5-1)9-11-6-2-4-8-13(11)14-12/h1-8H,9H2

| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}

| StdInChIKey = GJCOSYZMQJWQCA-UHFFFAOYSA-N

| SMILES = O1c2ccccc2Cc3ccccc31

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|Section2={{Chembox Properties

| C=13 | H=10 | O=1

| Appearance = Yellow solid

| Density =

| MeltingPtC = 101 to 102

| MeltingPt_ref = [http://www.sigmaaldrich.com/catalog/product/aldrich/x201 Xanthene] at Sigma-Aldrich

| BoilingPtC = 310 to 312

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|Section6={{Chembox Pharmacology

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|Section7={{Chembox Hazards

| MainHazards =

| NFPA-H =

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| Hazards_ref={{cite web |title=Xanthene 99% |url=https://www.sigmaaldrich.com/AU/en/product/aldrich/x201 |publisher=Sigma Aldrich}}

| GHSPictograms = {{GHS07}}

| GHSSignalWord = Warning

| HPhrases = {{H-phrases|317}}

| PPhrases = {{P-phrases|280}}

| FlashPt =

| AutoignitionPt =

| ExploLimits =

| PEL =

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Xanthene (9H-xanthene, 10H-9-oxaanthracene) is the organic compound with the formula CH2[C6H4]2O. It is a yellow solid that is soluble in common organic solvents. Xanthene itself is an obscure compound, but many of its derivatives are useful dyes.{{Ullmann's | last1 = Gessner | first1 = Thomas | last2 = Mayer | first2 = Udo | title = Triarylmethane and Diarylmethane Dyes | year = 2000 | doi = 10.1002/14356007.a27_179}}

Xanthene dyes

Image:Rhodamine skeleton.svgs are commercial dyes with xanthene cores.]]

Dyes that contain a xanthene core include bikaverin, fluorescein, eosins, and rhodamines. Xanthene dyes tend to be fluorescent, yellow to pink to bluish red, brilliant dyes. Many xanthene dyes can be prepared by condensation of derivates of phthalic anhydride with derivates of resorcinol or 3-aminophenol.

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Further reading

  • {{cite book|chapter=Photochemistry of the Xanthene Dyes|author1=Neckers, Douglas C. |author2=Valdes-Aguilera Oscar M. |title=Advances in Photochemistry|series=|year=1993|volume=18|pages=315–94|doi=10.1002/9780470133491.ch4|isbn=9780470133491}}

See also

References