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Revision as of 04:47, 17 February 2012 editBeetstra (talk | contribs)Edit filter managers, Administrators172,031 edits Saving copy of the {{chembox}} taken from revid 476656548 of page Alizarine_Yellow_R for the Chem/Drugbox validation project (updated: 'CASNo').  Latest revision as of 09:17, 27 September 2024 edit JWBE (talk | contribs)Extended confirmed users10,126 edits removed Category:Nitrobenzene derivatives; added Category:4-Nitrophenyl compounds using HotCat 
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{{ambox | text = This page contains a copy of the infobox ({{tl|chembox}}) taken from revid of page ] with values updated to verified values.}}
{{chembox {{chembox
| Verifiedfields = changed
⚫ | verifiedrevid = 421637880
| Watchedfields = changed
⚫ | Name = Alizarine Yellow R
⚫ | verifiedrevid = 477314571
⚫ | ImageFile1 = Alizarin-yellow-R-1718-34-9-sodium-salt-2D-skeletal.png
⚫ | Name = Alizarine Yellow R
⚫ | ImageSize1 = 220px
| ImageName1 = Alizarin Yellow R (sodium salt) | ImageFile1 = Alizarin-yellow-R-1718-34-9-sodium-salt-2D-skeletal.png
⚫ | ImageSize1 = 220px
| ImageFile2 = Alizarin-yellow-R-2243-76-7-acid-2D-skeletal.png
| ImageName1 = Alizarin Yellow R (sodium salt)
⚫ | ImageSize2 = 200px
| ImageName2 = Alizarin Yellow R (acid) | ImageFile2 = Alizarine-Yellow-R-sodium-3D-spacefill.png
| ImageAlt2 = Space-filling model of Alizarine Yellow R as a sodium salt
| IUPACName =
⚫ | ImageFile3 = Alizarin-yellow-R-2243-76-7-acid-2D-skeletal.png
⚫ | OtherNames = 5-salicylic acid sodium salt <br /> Chrome Orange <br /> Mordant Orange 1 <br /> C.I. 14030
⚫ | ImageSize3 = 200px
| ImageName3 = Alizarin Yellow R (acid)
| IUPACName = Sodium 2-hydroxy-5-benzoate
⚫ | OtherNames = 5-salicylic acid sodium salt<br />Chrome orange<br />Mordant orange 1<br />C.I. 14030
| Section1 = {{Chembox Identifiers | Section1 = {{Chembox Identifiers
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 17215762 | ChemSpiderID = 17215762
| InChI = 1/C13H9N3O5.Na/c17-12-6-3-9(7-11(12)13(18)19)15-14-8-1-4-10(5-2-8)16(20)21;/h1-7,17H,(H,18,19);/q;+1/p-1/b15-14+; | InChI = 1/C13H9N3O5.Na/c17-12-6-3-9(7-11(12)13(18)19)15-14-8-1-4-10(5-2-8)16(20)21;/h1-7,17H,(H,18,19);/q;+1/p-1/b15-14+;
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| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = HXKKTXMJSVFQSL-WPDLWGESSA-M | StdInChIKey = HXKKTXMJSVFQSL-WPDLWGESSA-M
| CASNo_Ref = {{cascite|correct|??}} | CASNo_Ref = {{cascite|correct|CAS}}
| CASNo = <!-- blanked - oldvalue: 1718-34-9 --> | CASNo = 1718-34-9
| CASNo_Comment =(Na salt)
| CASOther = &nbsp;(Na salt)<br />2243-76-7 (acid)<ref name="CRC">{{ cite book | title = CRC Handbook of Chemistry and Physics, 89th Edition | last = Lide | first = David R. | year = 2008 | publisher = ] | isbn = 978-0-8493-0488-0 | pages = 3–10}}</ref>
| CASNo2_Ref = {{cascite|correct|CAS}}
⚫ | SMILES = .O=C()c1cc(ccc1O)/N=N/c2ccc(cc2)()=O
| CASNo2 = 2243-76-7
| CASNo2_Comment = (acid)<ref name="CRC">{{cite book|title=CRC Handbook of Chemistry and Physics, 88th Edition|url=https://books.google.com/books?id=SdW_QgAACAAJ|url-access =limited|last=Lide|first=David R.|date=25 June 2007|publisher=]|oclc=1024315229|isbn=9780849304880|pages=–10}}</ref>
| PubChem = 6504724
| PubChem_Comment =(Na salt)
| EC_number = 209-536-1
| UNII1_Ref = {{fdacite|correct|FDA}}
| UNII1 = R1T3O0G585
| UNII1_Comment = (Na salt)
| UNII2_Ref = {{fdacite|correct|FDA}}
| UNII2 = OBF2VZO457
| UNII2_Comment = (acid)

⚫ | SMILES = .O=C()c1cc(ccc1O)/N=N/c2ccc(cc2)()=O
}} }}
| Section2 = {{Chembox Properties | Section2 = {{Chembox Properties
| Formula = C<sub>13</sub>H<sub>8</sub>N<sub>3</sub>NaO<sub>5</sub> (Na salt)<br />C<sub>13</sub>H<sub>9</sub>N<sub>3</sub>O<sub>5</sub> (acid) | Formula = C<sub>13</sub>H<sub>8</sub>N<sub>3</sub>NaO<sub>5</sub> (Na salt)<br />C<sub>13</sub>H<sub>9</sub>N<sub>3</sub>O<sub>5</sub> (acid)
| MolarMass = 309.21 g mol<sup>−1</sup> (Na salt) <br /> 287.23 g mol<sup>−1</sup> (acid) | MolarMass = 309.21 g mol<sup>−1</sup> (Na salt) <br /> 287.23 g mol<sup>−1</sup> (acid)
| Density = | Density =
| MeltingPt = | MeltingPt =
| BoilingPt = | BoilingPt =
}} }}
| Section3 = {{Chembox Hazards | Section3 = {{Chembox Hazards
| FlashPt =
| MainHazards = Harmful
| FlashPt = | AutoignitionPt =
| GHSPictograms = {{GHS exclamation mark}}
| Autoignition =

| GHSSignalWord = Warning

| HPhrases = {{H-phrases|H302|H319}}

| PPhrases = {{P-phrases|P264|P270|P280|P301+P312|P305+P351+P338|P330|P337+P313|P501}}
| Hazards_ref = {{Sigma-Aldrich|id=R320897|name=ALIZARINE YELLOW R|accessdate=09 April 2023}}
}} }}
}} }}
{{pH indicator template|indicator_name=Alizarine Yellow R|low_pH=10.1|high_pH=12.0|low_pH_color=yellow|high_pH_color=red|high_pH_text=white}}
'''Alizarine Yellow R''' is a ] colored ] made by the ] ]. It is usually commercially available as a sodium salt. In its pure form, it is a rust-colored solid.<ref>{{cite web|url=http://msds.chem.ox.ac.uk/AL/alizarin_yellow_R.html|url-status=dead|title=Safety Datasheet (MSDS) for alizarin yellow R|archive-url=https://web.archive.org/web/20110319233005/http://msds.chem.ox.ac.uk/AL/alizarin_yellow_R.html|date=2005|access-date=11 October 2008|archive-date=19 March 2011|publisher=Department of Chemistry, University of Oxford}}</ref> It is mainly used as a ].

==Preparation==
Alizarine Yellow R is produced by ] of salicylic ] and diazonium derivative of ]

]

==References==
{{Reflist}}

==External links==
*

]
]
]
]

{{organic-compound-stub}}