Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Empirical Formula (Hill Notation):
C3H6O
CAS Number:
Molecular Weight:
58.08
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-964-3
Beilstein/REAXYS Number:
102382
MDL number:
Product Name
Trimethylene oxide, 97%
InChI
1S/C3H6O/c1-2-4-3-1/h1-3H2
InChI key
AHHWIHXENZJRFG-UHFFFAOYSA-N
SMILES string
C1COC1
vapor pressure
5.09 psi ( 20 °C)
assay
97%
refractive index
n20/D 1.388-1.396
n20/D 1.392 (lit.)
bp
50 °C (lit.)
density
0.893 g/mL at 25 °C (lit.)
storage temp.
2-8°C
Quality Level
Looking for similar products? Visit Product Comparison Guide
Application
- Trimethylene oxide is a strained cyclic ether which can be used to replace carbonyl / gem-dimethyl groups during molecular modelling of bioactive molecules.
- It can be incorporated in various bioactive molecule and drug substances for its improved physicochemical properties, via novel C-H activation methods.
- Trimethylene oxide can also be used in the synthesis of poly(trimethylene oxide) and related polymer electrolytes.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Flam. Liq. 2
Storage Class
3 - Flammable liquids
wgk
WGK 1
flash_point_f
-4.0 °F - closed cup
flash_point_c
-20 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Synthesis and characterization of high molecular weight poly (trimethylene oxide).
Qureshi MY and Ochel M
Eur. Polymer J., 32(6), 691-693 (1996)
Cross-linked poly (oxetane) matrix for polymer electrolyte containing lithium ions.
Tsutsumi H, et al.
Solid State Ionics, 262, 761-764 (2014)
Role of polar side chains in Li+ coordination and transport properties of polyoxetane-based polymer electrolytes.
Sai R, et al.
Physical Chemistry Chemical Physics, 19(7), 5185-5194 (2017)
Photocatalytic Synthesis of Oxetane Derivatives by Selective C-H Activation.
Ravelli D, et al.
Advanced Synthesis & Catalysis, 356(13), 2781-2786 (2014)
Radical ?-C? H Hydroxyalkylation of Ethers and Acetal.
Yoshimitsu T, et al.
The Journal of Organic Chemistry, 70(6), 2342-2345 (2005)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service
