出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2016/09/16 13:20:28」(JST)
| Names | |
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| IUPAC name
Epoxypropane
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| Other names
Propylene oxide; Epoxypropane; Propylene epoxide; 1,2-Propylene oxide; Methyl oxirane; 1,2-Epoxypropane; Propene oxide; Methyl ethylene oxide; Methylethylene oxide; PPO; PO
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| Identifiers | |
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CAS Number
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75-56-9 Y |
| ChEBI | CHEBI:38685 N |
| EC Number | 200-879-2 |
| Jmol 3D model | Interactive image |
| KEGG | C15508 N |
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SMILES
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| Properties | |
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Chemical formula
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C3H6O |
| Molar mass | 58.08 g·mol−1 |
| Appearance | Colorless liquid |
| Odor | benzene-like[1] |
| Density | 0.830 g/cm3 |
| Melting point | −112 °C (−170 °F; 161 K) |
| Boiling point | 34 °C (93 °F; 307 K) |
|
Solubility in water
|
41% (20°C)[1] |
| Vapor pressure | 445 mmHg (20°C)[1] |
| Hazards | |
| Main hazards | Extremely flammable |
| Safety data sheet | Oxford MSDS |
| GHS pictograms | |
| GHS signal word | DANGER! |
| R-phrases | R45, R46, R12, R20/21/22, R36/37/38 |
| S-phrases | S53, S45 |
| NFPA 704 |
4
3
2
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| Flash point | −37 °C (−35 °F; 236 K) |
|
Autoignition
temperature |
747 °C (1,377 °F; 1,020 K) |
| Explosive limits | 2.3-36%[1] |
| Lethal dose or concentration (LD, LC): | |
|
LD50 (median dose)
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660 mg/kg (guinea pig, oral) 380 mg/kg (rat, oral) |
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LC50 (median concentration)
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1740 ppm (mouse, 4 hr) 4000 ppm (rat, 4 hr)[2] |
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LCLo (lowest published)
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2005 ppm (dog, 4 hr) 4000 ppm (guinea pig, 4 hr)[2] |
| US health exposure limits (NIOSH): | |
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PEL (Permissible)
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TWA 100 ppm (240 mg/m3)[1] |
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REL (Recommended)
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Ca[1] |
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IDLH (Immediate danger)
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Ca [400 ppm][1] |
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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| N verify (what is YN ?) | |
| Infobox references | |
Propylene oxide is an organic compound with the molecular formula CH3CHCH2O. This colourless volatile liquid is produced on a large scale industrially, its major application being its use for the production of polyether polyols for use in making polyurethane plastics. It is a chiral epoxide, although it is commonly used as a racemic mixture.
This compound is sometimes called 1,2-propylene oxide to distinguish it from its isomer 1,3-propylene oxide, better known as oxetane.
Industrial production of propylene oxide starts from propylene. Two general approaches are employed, one involving hydrochlorination and the other involving oxidation.[5] In 2005, about half of the world production was through chlorohydrin technology and one half via oxidation routes. The latter approach is growing in importance.
The traditional route proceeds via the conversion of propylene to chloropropanols:
The reaction produces a mixture of 1-chloro-2-propanol and 2-chloro-1-propanol, which is then dehydrochlorinated. For example:
Lime is often used as a chlorine absorber.
The other general route to propylene oxide involves co-oxidation of the organic chemicals isobutane or ethylbenzene. In the presence of catalyst, air oxidation occurs as follows:
The coproducts of these reactions, t-butyl alcohol or styrene, are useful feedstock for other products. For example, t-butyl alcohol reacts with methanol to give MTBE, an additive for gasoline. Before the current US ban of MTBE, propylene/isobutane was one of the most important production process.
In April 2003, Sumitomo Chemical commercialized the first PO-only plant in Japan, which produces propylene oxide from oxidation of cumene without significant production of other products.[6] This method is a variant of the POSM process (co-oxidation) that uses cumene hydroperoxide instead of ethylbenzene hydroperoxide and recycles the coproduct (alpha-hydroxycumene) via dehydration and hydrogenation back to cumene.
In March 2009, BASF and Dow Chemical started up their new HPPO plant in Antwerp.[7] In the HPPO-Process, propylene is oxidized with hydrogen peroxide:
In this process no side products other than water are generated.[8]
Between 60 and 70% of all propylene oxide is converted to polyether polyols for the production of polyurethane plastics.[9] About 20% of propylene oxide is hydrolyzed into propylene glycol, via a process which is accelerated by acid or base catalysis. Other major products are polypropylene glycol, propylene glycol ethers, and propylene carbonate.
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Propylene oxide was once used as a racing fuel, but that usage is now prohibited under the US NHRA rules for safety reasons. It has also been used in glow fuel for model aircraft and surface vehicles, typically combined in small percentages of around 2% as an additive to the typical methanol, nitromethane, and oil mix. It is also used in thermobaric weapons, and microbial fumigation.
The United States Food and Drug Administration has approved the use of propylene oxide to pasteurize raw almonds beginning on September 1, 2007, in response to two incidents of contamination by Salmonella in commercial orchards, one incident occurring in Canada and one in the United States.[10][11] Pistachio nuts can also be subjected to propylene oxide to control Salmonella.
Propylene oxide is commonly used in the preparation of biological samples for electron microscopy, to remove residual ethanol previously used for dehydration. In a typical procedure, the sample is first immersed in a mixture of equal volumes of ethanol and propylene oxide for 5 minutes, and then four times in pure oxide, 10 minutes each.
Propylene oxide is a probable human carcinogen,[12] and listed as an IARC Group 2B carcinogen.[13]
In 2016 it was reported that propylene oxide was detected in Sagittarius B2, a cloud of gas in the Milky Way weighing three million solar masses. It is the first chiral molecule to be detected in space.[14]
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| リンク元 | 「プロピレンオキシド」 |
| 関連記事 | 「oxide」「propylene」 |