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| TRIMETHYLENE OXIDE Basic information |
| TRIMETHYLENE OXIDE Chemical Properties |
| Melting point | -97°C | | Boiling point | 50 °C(lit.) | | density | 0.893 g/mL at 25 °C(lit.) | | vapor pressure | 5.09 psi ( 20 °C) | | refractive index | n20/D 1.392(lit.) | | Fp | −19 °F | | storage temp. | 2-8°C | | solubility | 1000g/l | | form | Liquid | | color | Clear colorless | | Odor | agreeable odor | | explosive limit | 2.4%(V) | | Water Solubility | Soluble in water. | | Merck | 14,9715 | | BRN | 102382 | | CAS DataBase Reference | 503-30-0(CAS DataBase Reference) | | EPA Substance Registry System | Oxetane (503-30-0) |
| TRIMETHYLENE OXIDE Usage And Synthesis |
| Chemical Properties | CLEAR COLOURLESS LIQUID | | Uses | Trimethylene oxide useful for the synthesis of 3-substituted propanols by reaction with Grignards or organolithiums in the presence of CuBr. | | Definition | ChEBI: A saturated organic heteromonocyclic parent that is a four-membered ring comprising of three carbon atoms and an oxygen atom. | | General Description | Clear, colorless liquid with an agreeable aromatic odor. | | Air & Water Reactions | Highly flammable. Water soluble. | | Reactivity Profile | TRIMETHYLENE OXIDE reacts with Grignard reagents and organolithium compounds. TRIMETHYLENE OXIDE is also incompatible with oxidizing agents and strong acids. . An explosion occurred when propylene oxide was added to epoxy resin. Polymerization was catalyzed by amine accelerator in the resin [Bretherick 1995]. Propylene oxide and sodium hydroxide base-catalyzed the polymerization of the former, causing ignition and explosion of a drum of the crude product. [Combust Sci. Technol., 1983]. | | Fire Hazard | TRIMETHYLENE OXIDE is flammable. | | Safety Profile | Moderately toxic by subcutaneous route. May be narcotic in high concentrations. Questionable carcinogen with experimental tumorigenic data. Mutation data reported. When heated to decomposition it emits acrid smoke and irritating fumes | | Purification Methods | Distil oxetane twice from sodium metal and then fractionate it through a small column at atmospheric pressure, b 47.0-47.2o. It can also be purified by preparative gas chromatography using a 2m silica gel column. Alternatively, add KOH pellets (50g for 100g of oxetane) and distil it through an efficient column or a column packed with 1/4in Berl Saddles with the main portion boiling at 45-50o being collected and redistilled over fused KOH. [Noller Org Synth Coll Vol III 835 1955, Dittmer et al. J Am Chem Soc 79 4431 1957, Beilstein 17 H 6, 17 I 3, 17 II 12, 17 III/IV 13, 17/1 V 11.] |
| TRIMETHYLENE OXIDE Preparation Products And Raw materials |
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