grade
technical grade
Quality Level
form
viscous liquid
eq. wt.
138-154 (perchloric acid method)
mol wt
226.70 g/mol
refractive index
n20/D 1.477 (lit.)
viscosity
120-180 cP(25 °C, Ubbelohde)(lit.)
density
1.157 g/mL at 25 °C (lit.)
SMILES string
ClCC1OC1.OCC(CO)(CC)CO
InChI
InChI=1S/C6H14O3.C3H5ClO/c1-2-6(3-7,4-8)5-9;4-1-3-2-5-3/h7-9H,2-5H2,1H3;3H,1-2H2
InChI key
HNCWRXZORGVRPD-UHFFFAOYSA-N
General description
(2-Ethyl-2-(hydroxymethyl)-1,3-propanediol polymer with (chloromethyl)oxirane has a trifunctional aliphatic glycidyl ether epoxide monomer mainly used as a crosslinking agent which provides chemical and mechanical resistance.
Application
(2-Ethyl-2-(hydroxymethyl)-1,3-propanediol polymer with (chloromethyl)oxirane is used in the synthesis of azidated trimethylolpropane triglycidyl ether for the preparation of polyether polyol based hyperbranched polyurethanes. It can be coated on polycarbonated chips for improving chemical resistance from different organic solvents. Cross-linking of (2-Ethyl-2-(hydroxymethyl)-1,3-propanediol polymer with (chloromethyl)oxirane can be done with poly(4-venylphenol) (PVP) for the preparation of organic field effect transistors (OFETs).
Additive in fast-setting adhesives, low temperature curing coatings and hard, abrasion resistant castings and decoupage systems.
Features and Benefits
Reduces viscosity but retains high epoxide level, imparts hardness and toughness to epoxide polymers. Improves solubility/compatibility characteristics of highly aromatic epoxy systems.
signalword
Danger
Hazard Classifications
Aquatic Chronic 2 - Carc. 2 - Eye Dam. 1 - Muta. 2 - Repr. 2 - Skin Corr. 1B - Skin Sens. 1
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Improved cardanol derived epoxy coatings.
Darroman E, et al.
Progress in Organic Coatings, 91(16), 9-16 (2016)
Synthesis and characterization of triazole rich polyether polyols using click chemistry for highly branched polyurethanes.
Sarath PS, et al.
Reactive and Functional Polymers, 73(12), 1597-1605 (2013)
Photocurable Organic Gate Insulator for the Fabrication of High-Field Effect Mobility Organic Transistors by Low Temperature and Solution Processing.
Lee TW, et al.
Advanced Materials, 19(18), 2702-2706 (2007)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 430269-1L | 04061832107851 |
| 430269-250ML | 04061832107868 |



