Name | 2-hydroxy-1-phenylethan-1-one |
Synonyms | Glycolophenone Methanol, benzoyl- 2-HYDROXYACETOPHENONE Acetophenone, 2-hydroxy- omega-Hydroxyacetophenone 2-Hydroxy-1-phenylethanone 2-hydroxy-1-phenyl-ethanon 2-hydroxy-1-phenylethanone 2-Hydroxyethylphenyl ketone Acetophenone, alpha-hydroxy- Ethanone, 2-hydroxy-1-phenyl- 2-hydroxy-1-phenylethan-1-one |
CAS | 582-24-1 |
EINECS | 209-480-8 |
InChI | InChI=1/C8H8O2/c9-6-8(10)7-4-2-1-3-5-7/h1-5,9H,6H2 |
Molecular Formula | C8H8O2 |
Molar Mass | 136.15 |
Density | 1.0963 |
Melting Point | 86-89 °C (lit.) |
Boling Point | 126 °C / 12mmHg |
Flash Point | 100.4°C |
Water Solubility | Soluble in water, ether, ethanol, chloroform. |
Vapor Presure | 0.0161mmHg at 25°C |
Appearance | Orange powder |
Color | Slightly yellow to orange |
pKa | 13.09±0.10(Predicted) |
Storage Condition | Sealed in dry,Room Temperature |
Sensitive | Air & Moisture Sensitive |
Refractive Index | 1.5470 (estimate) |
MDL | MFCD00041829 |
Hazard Symbols | Xi - Irritant |
Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. S37/39 - Wear suitable gloves and eye/face protection |
WGK Germany | 3 |
TSCA | Yes |
HS Code | 29144000 |
NIST chemical information | information provided by: webbook.nist.gov (external link) |
EPA chemical substance information | information provided by: ofmpeb.epa.gov (external link) |
Use | 2-hydroxyacetophenone can be used for the preparation of benzoylformic acid, which is an intermediate for the preparation of pharmaceuticals and pesticides, by complexing with metal elements, it is found that it can be used as a sensitizer for fluorescent materials and a catalyst for organic oxidation reactions, which has attracted more attention. |
preparation | Add 20mmol of 48% hydrobromic acid at room temperature to a ML three-necked flask with 20mmol of styrene and ml of water, 200mmol 30% hydrogen peroxide was slowly added dropwise, controlled dropwise addition time was 30min, stirred at room temperature for 30min, heated to 80 ℃, and reacted for 10H. The organic phase and the aqueous phase were separated by standing. The organic phase containing 2-bromoacetophenone was added to a reactor containing 150ml of water , hydrolysis was completed under microwave acceleration, and the organic phase and the aqueous phase were allowed to stand to separate to obtain a 2-hydroxyacetophenone solution. |