2-Hydroxybenzophenone
2-Hydroxybenzophenone
  • CAS No.:117-99-7
Other grades of this product :
2-Hydroxybenzophenone Basic information
Product Name:2-Hydroxybenzophenone
Synonyms:(2-Hydroxy-phenyl)-phenylmethanon;2-Hydroxybenzophenone99%;2-HYDROXYBENZOPHENONE 99%;2-Hydroxybenzophenone, 99% 1GR;2-Hydroxybenzophenone, 99% 25GR;(2-hydroxyphenyl)phenyl-methanon;(2-hydroxyphenyl)phenylmethanone;(2-Hydroxy-phenyl)-phenylmethanone
CAS:117-99-7
MF:C13H10O2
MW:198.22
EINECS:204-226-2
Product Categories:Aromatic Benzophenones & Derivatives (substituted);API intermediates;Linkers for Solid Phase Synthesis;C13 to C14;Carbonyl Compounds;Ketones
Mol File:117-99-7.mol
2-Hydroxybenzophenone Chemical Properties
Melting point 37-39 °C (lit.)
Boiling point 171-173 °C/12 mmHg (lit.)
density 1.1184 (rough estimate)
refractive index 1.5954 (estimate)
Fp >230 °F
storage temp. Sealed in dry,2-8°C
pka8.07±0.30(Predicted)
form Crystalline Powder
color Yellow
Water Solubility insoluble
BRN 1638174
CAS DataBase Reference117-99-7(CAS DataBase Reference)
NIST Chemistry ReferenceMethanone, (2-hydroxyphenyl)phenyl-(117-99-7)
EPA Substance Registry SystemMethanone, (2-hydroxyphenyl)phenyl- (117-99-7)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-37/39-36
WGK Germany 3
TSCA Yes
HazardClass IRRITANT
HS Code 29145000
MSDS Information
ProviderLanguage
2-Hydroxybenzophenone English
ACROS English
SigmaAldrich English
ALFA English
2-Hydroxybenzophenone Usage And Synthesis
Chemical Propertiesyellow crystalline powder
UsesUV absorber in plastics.
Uses2-Hydroxybenzophenone was used to quantify the metabolites of unmethylated extracts from the supernatants of Pseudomonas acidovorans cultures grown on 1,1-diphenylethylene.
Application2-Hydroxybenzophenone was used to quantify the metabolites of unmethylated extracts from the supernatants of Pseudomonas acidovorans cultures grown on 1,1-diphenylethylene.2-Hydroxybenzophenone forms copolymer 2-hydroxy, 3-allyl, 4,4′-dimethoxybenzophenone with methyl methacrylate.It forms photostabilizer compounds with 2,2,6,6-tetramethylpiperidine under phase transfer catalysis conditions.It reacts with 3-aminophenyl boronic acid to form macrocyclic boronates.
PreparationPreparation by Friedel–Crafts acylation of benzene in the presence of aluminium chloride, ? with 2-hydroxybenzoyl chloride (salicylic acid chloride), (52%), (39%), at temperature <60°; ? with o-anisoyl chloride. Demethylation occurred during the Friedel–Crafts acylation, especially in the presence of ferric chloride at 130–140°; ? with 2-ethoxybenzoyl chloride in a boiling water bath (42%).
Synthesis Reference(s)Journal of the American Chemical Society, 76, p. 5469, 1954 DOI: 10.1021/ja01650a062The Journal of Organic Chemistry, 32, p. 3844, 1967 DOI: 10.1021/jo01287a027
General Description
  • 2-Hydroxybenzophenone forms copolymer 2-hydroxy, 3-allyl, 4,4′-dimethoxybenzophenone with methyl methacrylate.
  • It forms photostabilizer compounds with 2,2,6,6-tetramethylpiperidine under phase transfer catalysis conditions.
  • It reacts with 3-aminophenyl boronic acid to form macrocyclic boronates.

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