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| | 2,3,4-Trihydroxybenzophenone Basic information |
| Product Name: | 2,3,4-Trihydroxybenzophenone | | Synonyms: | 2,3,4-Trihydroxybenzophenon;(2,3,4-Trihydroxyphenyl) phenylmethanone;alizarin yellow A;2,3,4-Trihydroxybenzophenone(Bp-20);4-BENZOYL PYROGALLOL;Gallobenzophenone;2,3,4-TRIHYDROXYBENZOPHENONE GR 99.5%;Alizarine Yellow A | | CAS: | 1143-72-2 | | MF: | C13H10O4 | | MW: | 230.22 | | EINECS: | 214-540-1 | | Product Categories: | RAW material for Photo Active Compounds;Industrial/Fine Chemicals;C13 to C14;Carbonyl Compounds;Ketones;Building Blocks;C13 to C14;Carbonyl Compounds;Chemical Synthesis;Organic Building Blocks;Aromatic Benzophenones & Derivatives (substituted) | | Mol File: | 1143-72-2.mol |  |
| | 2,3,4-Trihydroxybenzophenone Chemical Properties |
| Melting point | 139-141 °C (lit.) | | Boiling point | 439.7±45.0 °C(Predicted) | | density | 1.413±0.06 g/cm3(Predicted) | | vapor pressure | 0Pa at 20℃ | | storage temp. | Sealed in dry,Room Temperature | | solubility | ethanol: soluble2%, clear, yellow to very dark yellow-orange | | form | powder to crystal | | pka | 7.51±0.40(Predicted) | | color | Light yellow to Yellow to Orange | | PH | 6-7 (H2O) | | Water Solubility | 13.22g/L(24.99 ºC) | | BRN | 2697065 | | InChIKey | HTQNYBBTZSBWKL-UHFFFAOYSA-N | | LogP | 2.8 at 23℃ | | CAS DataBase Reference | 1143-72-2(CAS DataBase Reference) | | EPA Substance Registry System | Methanone, phenyl(2,3,4-trihydroxyphenyl)- (1143-72-2) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36 | | WGK Germany | 1 | | TSCA | Yes | | HS Code | 29145090 |
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ALFA
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| | 2,3,4-Trihydroxybenzophenone Usage And Synthesis |
| Uses | 2,3,4-Trihydroxybenzophenone is used in manufacturing method of electrophotographic photosensitive member containing styrene acrylic resin particle and melamine formaldehyde resin particle. | | Definition | ChEBI: 2,3,4-trihydroxbenzophenone is a benzenetriol that is benzophenone in which one of the phenyl groups is substituted by hydroxy groups at positions 2, 3, and 4. It is a redox mediator. It has a role as a quorum sensing inhibitor, an EC 1.14.18.1 (tyrosinase) inhibitor, a human urinary metabolite, a rat metabolite and a drug metabolite. It is a hydroxybenzophenone and a benzenetriol. | | Preparation | Preparation by reaction of benzoic acid with pyrogallol,
in the presence of zinc chloride during 3 h at 145°;
in the presence of Amberlyst-15 (a strongly acid ion exchanger) in chlorobenzene during 10 h at 131–132° (60%);
in the presence of Amberlite IR-120 or Zeokarb 225 (cation exchange resins, sulfonic acid type) during 3 h at 160° (14%);
in the presence of boron trifluoride in ethyl ether at 0° (44%). | | General Description | 2,3,4-Trihydroxybenzophenone is a hydroxylated benzophenone UV filter and has been quantitated in sea water samples by dispersive liquid-liquid microextraction followed by GC-MS. Estrogenic activity of 2,3,4-trihydroxybenzophenone has been tested by yeast-two hybrid assay. | | Flammability and Explosibility | Not classified |
| | 2,3,4-Trihydroxybenzophenone Preparation Products And Raw materials |
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