3'-hydroxyacetophenone
acetophenone, 3'-hydroxy-
Identification
| Name | 3'-hydroxyacetophenone |
| CAS Number | 121-71-1 |
| EINECS | 204-494-0 |
| FDA UNII | UV3GO1D90J |
| Molecular Formula | C8 H8 O2 |
| Molecular Weight | 136.15016000 |
| MDL Number | MFCD00002298 |
| Nikkaji Number | J60.314G |
| Beilstein | 2040676 |
| XlogP3 | 1.40 (est) |
Regulatory
Physical Properties
| Appearance | white to tan crystalline powder (est) |
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Specific Gravity | 1.10000 @ 25.00 °C. |
| Melting Point | 96.00 °C. @ 760.00 mm Hg |
| Boiling Point | 296.00 °C. @ 760.00 mm Hg, 153.00 °C. @ 5.00 mm Hg |
| Vapor Pressure | 0.003000 mmHg @ 25.00 °C. (est) |
| Flash Point | 240.00 °F. TCC ( 115.80 °C. ) (est) |
| logP (o/w) | 1.390 |
| Soluble in | alcohol |
| Insoluble in | water |
No sensory data available
Safety Information
| Preferred SDS | View |
| Oral/Parenteral Toxicity | Not determined |
| Dermal Toxicity | Not determined |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']
Safety in Use
| Category | natural substances and extractives |
| Recommendation for 3'-hydroxyacetophenone usage levels up to | not for fragrance use. |
| Recommendation for 3'-hydroxyacetophenone flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
Synonyms
acetophenone, 3-hydroxy-
acetophenone, 3'-hydroxy-
3-
acetyl phenol
1-
acetyl-3-hydroxybenzene
3-
acetylphenol
m-
acetylphenol
ethanone, 1-(3-hydroxyphenyl)-
1-(3-
hydroxy-phenyl)-ethanone
3-
hydroxyacetophenone
1-(3-
hydroxyphenyl)ethan-1-one
1-(3-
hydroxyphenyl)ethanon
1-(3-
hydroxyphenyl)ethanone
Google Patents:
Process for producing m-hydroxyacetophenone
PubMed:
Controlling Dissociation of Alkyl Phenyl Ketone Radical Cations in the Strong-Field Regime through Hydroxyl Substitution Position.
PubMed:
Isolation and characterization of a novel Rhodococcus strain with switchable carbonyl reductase and para-acetylphenol hydroxylase activities.
PubMed:
Chemoenzymatic synthesis of rivastigmine via dynamic kinetic resolution as a key step.
PubMed:
Studies on some iridium(III) complexes with Schiff bases derived from amino carboxylic acids.