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About This Item
Linear Formula:
C2H5C(CH2OCH2CH=CH2)2CH2OH
CAS Number:
Molecular Weight:
214.30
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12162002
EC Number:
211-661-1
MDL number:
InChI key
BDKDHWOPFRTWPP-UHFFFAOYSA-N
InChI
1S/C12H22O3/c1-4-7-14-10-12(6-3,9-13)11-15-8-5-2/h4-5,13H,1-2,6-11H2,3H3
SMILES string
CCC(CO)(COCC=C)COCC=C
assay
90%
form
liquid
refractive index
n20/D 1.458 (lit.)
bp
135 °C/13 mmHg (lit.)
density
0.955 g/mL at 25 °C (lit.)
Quality Level
Related Categories
General description
Trimethylolpropane diallyl ether (TMPAE) is an unsaturated allyl ether that can be synthesized by Williamson esterification reaction in the presence of trimethylolpropane, sodium hydroxide, and allyl chloride as starting materials.
Application
TMPAE can be used in the synthesis of isophorone diisocyanate (IPDI) based tetracene monomers which can further be used in the formation of polymer dispersed liquid crystals. It can also be used in the synthesis of allyl ether based dendrimers that find potential usage in coatings.
Other Notes
remainder monoethers and triethers
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
244.4 °F - closed cup
flash_point_c
118 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Thermal and Mechanical Properties of Cross-Linked Photopolymers Based on Multifunctional Thiol- Urethane Ene Monomers
Senyurt AF, et al.
Macromolecules, 40(9), 3174-3182 (2007)
Synthesis and thiol-ene photopolymerization of allyl-ether functionalized dendrimers
Nilsson C, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 46(4), 1339-1348 (2008)
Optimization of Synthetical Technology for Trimethylolpropane Diallyl Ether by Response Surface Method
ZHANG JT, et al.
Shanghai Kou Qiang yi Xue = Shanghai Journal of Stomatology, 2(25), 7671-7678 (2010)
Visible light induced polymerization of maleimide-vinyl and maleimide-allyl ether based systems
Burget D, et al.
Polymer, 44(25), 7671-7678 (2003)
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