Propan-2-one oxime structure 
             | 
        Common Name | Propan-2-one oxime | ||
|---|---|---|---|---|
| CAS Number | 127-06-0 | Molecular Weight | 73.094 | |
| Density | 0.9±0.1 g/cm3 | Boiling Point | 135.0±0.0 °C at 760 mmHg | |
| Molecular Formula | C3H7NO | Melting Point | 60-63 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 45.2±8.0 °C | |
| Name | acetone oxime | 
|---|---|
| Synonym | More Synonyms | 
| Density | 0.9±0.1 g/cm3 | 
|---|---|
| Boiling Point | 135.0±0.0 °C at 760 mmHg | 
| Melting Point | 60-63 °C(lit.) | 
| Molecular Formula | C3H7NO | 
| Molecular Weight | 73.094 | 
| Flash Point | 45.2±8.0 °C | 
| Exact Mass | 73.052765 | 
| PSA | 32.59000 | 
| LogP | 0.12 | 
| Vapour Pressure | 4.7±0.5 mmHg at 25°C | 
| Index of Refraction | 1.410 | 
| Water Solubility | 330 g/L (20 ºC) | 
                                    CHEMICAL IDENTIFICATION
 
 
 
 
 
 
 
 
 HEALTH HAZARD DATAACUTE TOXICITY DATA
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
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| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter | 
|---|---|
| Hazard Codes | Xn:Harmful; | 
| Safety Phrases | S22-S24/25 | 
| RIDADR | UN1325 | 
| WGK Germany | 3 | 
| RTECS | AL6825000 | 
| Packaging Group | III | 
| Hazard Class | 4.1 | 
| HS Code | 2928000090 | 
| Precursor 10 | |
|---|---|
| DownStream 10 | |
| HS Code | 2928000090 | 
|---|---|
| Summary | 2928000090 other organic derivatives of hydrazine or of hydroxylamine VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0% | 
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                                    Slow oxidation of acetoxime and methylethyl ketoxime to the corresponding nitronates and hydroxy nitronates by liver microsomes from rats, mice, and humans.
                                    
                                    
                                     Toxicol. Sci. 47(2) , 144-50, (1999) Acetoxime and methylethyl ketoxime (MEKO) are tumorigenic in rodents, inducing liver tumors in male animals. The mechanisms of tumorigenicity for these compounds are not well defined. Oxidation of the...  | 
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                                    Synthesis and anticancer evaluation of benzyloxyurea derivatives.
                                    
                                    
                                     Chem. Pharm. Bull. 62(9) , 898-905, (2014) A series of novel benzyloxyurea derivatives was designed, synthesized by substituting different benzyls or phenyls on N,N'-positions of the hydroxyurea (HU). These target compounds were evaluated for ...  | 
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                                    Reversion of structure-activity relationships of antitumor platinum complexes by acetoxime but not hydroxylamine ligands.
                                    
                                    
                                     Mol. Pharmacol. 71(1) , 357-65, (2007) The presence of cis-configured exchangeable ligands has long been considered a prerequisite for antitumor activity of platinum complexes, but over the past few years, several examples violating this s...  | 
                                
| N-Hydroxypropan-2-imine | 
| Acetone, oxime | 
| β-Isonitrosopropane | 
| MFCD00002118 | 
| Acetone oxime | 
| 2-Propanone, oxime | 
| Acetoxime | 
| EINECS 204-820-1 | 
| b-Isonitrosopropane | 
| N-Hydroxy-2-propanimine | 
| N-propan-2-ylidenehydroxylamine | 
| propan-2-one oxime |