Pinacolone structure
|
Common Name | Pinacolone | ||
|---|---|---|---|---|
| CAS Number | 75-97-8 | Molecular Weight | 100.159 | |
| Density | 0.8±0.1 g/cm3 | Boiling Point | 104.9±8.0 °C at 760 mmHg | |
| Molecular Formula | C6H12O | Melting Point | -52.5 °C | |
| MSDS | Chinese USA | Flash Point | 23.9±0.0 °C | |
| Symbol |
GHS02, GHS07 |
Signal Word | Danger | |
Use of PinacolonePinacolin is a metabolite of soman. |
| Name | 3,3-Dimethyl-2-butanone |
|---|---|
| Synonym | More Synonyms |
| Density | 0.8±0.1 g/cm3 |
|---|---|
| Boiling Point | 104.9±8.0 °C at 760 mmHg |
| Melting Point | -52.5 °C |
| Molecular Formula | C6H12O |
| Molecular Weight | 100.159 |
| Flash Point | 23.9±0.0 °C |
| Exact Mass | 100.088814 |
| PSA | 17.07000 |
| LogP | 1.07 |
| Vapour Pressure | 30.3±0.2 mmHg at 25°C |
| Index of Refraction | 1.394 |
| Stability | Stable. Incompatible with strong oxidizing agents. Flammable. |
| Water Solubility | 2.44 g/100 mL (15 ºC) |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
|
| Symbol |
GHS02, GHS07 |
|---|---|
| Signal Word | Danger |
| Hazard Statements | H225-H302 |
| Precautionary Statements | P210 |
| Personal Protective Equipment | Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter |
| Hazard Codes | F:Flammable |
| Risk Phrases | R11;R22 |
| Safety Phrases | S9-S16-S29-S33-S20/21 |
| RIDADR | UN 1224 3/PG 2 |
| WGK Germany | 2 |
| RTECS | EL7700000 |
| Packaging Group | II |
| Hazard Class | 3 |
| HS Code | 29141990 |
| Precursor 9 | |
|---|---|
| DownStream 10 | |
| HS Code | 29141990 |
|---|
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A novel carbonyl reductase with anti-Prelog stereospecificity from Acetobacter sp. CCTCC M209061: purification and characterization.
PLoS ONE 9(4) , e94543, (2014) A novel carbonyl reductase (AcCR) catalyzing the asymmetric reduction of ketones to enantiopure alcohols with anti-Prelog stereoselectivity was found in Acetobacter sp. CCTCC M209061 and enriched 27.5... |
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Isolation and characterization of 4-tert-butylphenol-utilizing Sphingobium fuliginis strains from Phragmites australis rhizosphere sediment.
Appl. Environ. Microbiol. 76(20) , 6733-40, (2010) We isolated three Sphingobium fuliginis strains from Phragmites australis rhizosphere sediment that were capable of utilizing 4-tert-butylphenol as a sole carbon and energy source. These strains are t... |
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Enhancement of hepatic microsomal esterase activity following soman pretreatment in guinea pigs.
Biochem. Pharmacol. 46(11) , 2083-92, (1993) Soman (pinacolyl methylphosphonofluoridate), a highly toxic organophosphate compound, has been found to be a strong inhibitor of hepatic microsomal carboxylesterase in vitro, but an enhancer of carbox... |
| 3,3-dimethylbutan-2-on |
| EINECS 200-920-4 |
| tert-Butyl methyl ketone |
| Pinacolone |
| MFCD00008846 |
| CH3COC(CH3)3 |
| α,α,α-Trimethylacetone |
| 3,3-dimethylbutan-2-one |
| 2-Butanone, 3,3-dimethyl- |
| 3,3-Dimethyl-2-butanone |
| tert-butylmethyl ketone |
| UNII-3U1AAG3528 |