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TRIMETHYLENE OXIDE

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TRIMETHYLENE OXIDE Basic information

Product Name:
TRIMETHYLENE OXIDE
Synonyms:
  • 1,3-PROPYLENE OXIDE
  • 1,3-TRIMETHYLENE OXIDE
  • 1,3-EPOXYPROPAN
  • 1,3-EPOXYPROPANE
  • OXETANE
  • TRIMETHYLENE OXIDE
  • alpha,gamma-Propane oxide
  • alpha,gamma-propaneoxide
CAS:
503-30-0
MF:
C3H6O
MW:
58.08
EINECS:
207-964-3
Product Categories:
  • Asymmetric Synthesis
  • Building Blocks
  • Heterocyclic Compounds
  • Chemical Synthesis
  • Chiral Building Blocks
  • Heterocyclic Building Blocks
  • Oxetanes
  • Simple 4-Membered Ring Compounds
  • Other Products
Mol File:
503-30-0.mol
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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.)
Flash point:
−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)
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Safety Information

Hazard Codes 
F,Xn
Risk Statements 
11-20/21/22
Safety Statements 
9-16-26-29
RIDADR 
UN 1993 3/PG 2
WGK Germany 
1
RTECS 
RQ6825000
3-10-23
TSCA 
Yes
HazardClass 
3
PackingGroup 
II
HS Code 
29329990
Hazardous Substances Data
503-30-0(Hazardous Substances Data)
Toxicity
mmo-sat 3333 mg/plate EMMUEG 11(Suppl 12),1,88

MSDS

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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

Preparation Products

TRIMETHYLENE OXIDESupplier

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