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Revision as of 16:03, 16 February 2012 editBeetstra (talk | contribs)Edit filter managers, Administrators172,084 edits Saving copy of the {{chembox}} taken from revid 473851287 of page 1,2,3,5-Tetrahydroxybenzene for the Chem/Drugbox validation project (updated: 'CASNo').  Latest revision as of 17:34, 13 December 2023 edit 2a02:8109:b588:4500:f9dd:a390:52b:a110 (talk) topTags: Mobile edit Mobile app edit Android app edit 
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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
| Watchedfields = changed | Watchedfields = changed
| verifiedrevid = 444252614 | verifiedrevid = 477202283
| Name = 1,2,3,5-Tetrahydroxybenzene | Name = 1,2,3,5-Tetrahydroxybenzene
| ImageFileL1 = 1,2,3,5-tetrahydroxybenzene.PNG | ImageFileL1 = 1,2,3,5-tetrahydroxybenzene.svg
| ImageSizeL1 = 130px | ImageSizeL1 = 130px
| ImageNameL1 = Chemical structure of 1,2,3,5-tetrahydroxybenzene | ImageNameL1 = Chemical structure of 1,2,3,5-tetrahydroxybenzene
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| ImageSizeR1 = 115px | ImageSizeR1 = 115px
| ImageNameR1 = Ball-and-stick model | ImageNameR1 = Ball-and-stick model
| IUPACName = Benzene-1,2,3,5-tetrol | PIN = Benzene-1,2,3,5-tetrol
| OtherNames = 1,2,3,5-Benzenetetrol | OtherNames = 1,2,3,5-Benzenetetrol
|Section1= {{Chembox Identifiers |Section1={{Chembox Identifiers
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChEBI_Ref = {{ebicite|correct|EBI}} | ChEBI_Ref = {{ebicite|correct|EBI}}
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| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = RDJUHLUBPADHNP-UHFFFAOYSA-N | StdInChIKey = RDJUHLUBPADHNP-UHFFFAOYSA-N
| CASNo = <!-- blanked - oldvalue: 634-94-6 --> | CASNo = 634-94-6
| CASNo_Ref = {{cascite|correct|??}}= | CASNo_Ref = {{cascite|changed|??}}=
| CASOther = | CASNoOther =
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = 6KQM6GV7J9
| PubChem = 12 <!-- SID 582616 --> | PubChem = 12 <!-- SID 582616 -->
| SMILES = Oc1cc(O)cc(O)c1O | SMILES = Oc1cc(O)cc(O)c1O
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| MeSHName = | MeSHName =
}} }}
|Section2= {{Chembox Properties |Section2={{Chembox Properties
| C=6|H=6|O=4 | C=6 | H=6 | O=4
| ExactMass = 142.02660866 u
| Appearance = | Appearance =
| Density = | Density =
| MeltingPt = <!-- °C --> | MeltingPt =
| BoilingPt = <!-- °C --> | BoilingPt =
| Solubility = | Solubility =
}} }}
}} }}

'''1,2,3,5-Tetrahydroxybenzene''' is a ].

It is a metabolite in the degradation of ] (gallic acid) by '']''.<ref>{{cite journal | url= | title = Initial steps in the anaerobic degradation of 3,4,5-trihydroxybenzoate by Eubacterium oxidoreducens: characterization of mutants and role of 1,2,3,5-tetrahydroxybenzene | author = J D Haddock, and J G Ferry | journal = J. Bacteriol. | year = 1993 | volume = 175 | issue = 3 | pages = 669–673 | doi = 10.1128/jb.175.3.669-673.1993 | pmid = 8423143 | pmc = 196204}}</ref>

The enzyme ] uses 1,2,3,5-tetrahydroxybenzene and 1,2,3-trihydroxybenzene (]), whereas its two products are 1,3,5-trihydroxybenzene (]) and 1,2,3,5-tetrahydroxybenzene.<ref> at www.uniprot.org</ref>

== Uses ==

1,2,3,5-Tetrahydroxybenzene, also known as pyrogallol, has various uses. It is used in the production of certain dyes, photographic developers, and hair dyes. Additionally, pyrogallol has been employed in traditional medicine and some cosmetic formulations due to its antioxidant properties.

== See also ==
* ]
* ]

== References ==
{{reflist}}

{{DEFAULTSORT:Tetrahydroxybenzene, 1,2,3,5-}}
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{{phenol-stub}}
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