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Revision as of 15:32, 18 April 2011 by CheMoBot (talk | contribs) (Updating {{chembox}} (no changed fields - added verified revid - updated 'UNII_Ref', 'ChemSpiderID_Ref', 'StdInChI_Ref', 'StdInChIKey_Ref', 'ChEMBL_Ref', 'KEGG_Ref') per Chem/Drugbox validation ()(diff) ← Previous revision | Latest revision (diff) | Newer revision → (diff)This article does not cite any sources. Please help improve this article by adding citations to reliable sources. Unsourced material may be challenged and removed. Find sources: "Gallacetophenone" – news · newspapers · books · scholar · JSTOR (July 2009) (Learn how and when to remove this message) |
Names | |
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IUPAC name 1-(2,3,4-trihydroxyphenyl)ethanone | |
Other names Alizarin Yellow C; Galloacetophenone; 2',3',4'-Trihydroxyacetophenone | |
Identifiers | |
CAS Number | |
3D model (JSmol) | |
ECHA InfoCard | 100.007.665 |
PubChem CID | |
CompTox Dashboard (EPA) | |
SMILES
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Properties | |
Chemical formula | C8H8O4 |
Molar mass | 168.15 g/mol |
Melting point | 171-172 C |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Y verify (what is ?) Infobox references |
Gallacetophenone is the acetyl derivative of pyrogallol. It is synthesized from pyrogallol using zinc chloride and acetic anhydride.
Properties and Uses
Antiseptic; skin affections (psoriasis, etc.), in 10 p. c. solutions or ointments, being a good substitute for pyrogallol, as it does not stain nor poison so easily.
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