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| | Trimethylolpropane diallyl ether Basic information |
| Product Name: | Trimethylolpropane diallyl ether | | Synonyms: | 1,1,1-TRIMETHYLOLPROPANE DIALLYL ETHER;1,1,1-(TRIHYDROXYMETHYL)PROPANE DIALLYL ETHER;2-ETHYL-2-(HYDROXYMETHYL)-1 3-PROPANEDIOL DIALLYL ETHER;2,2-BIS(ALLYLOXYMETHYL)-1-BUTANOL;TRIMETHYLOLPROPANE DIALLYL ETHER;1-Butanol,2,2-bis[(2-propenyloxy)methyl]-;2,2-bis[(2-propenyloxy)methyl]-1-butano;2,2-bis[(2-propenyloxy)methyl]-1-Butanol | | CAS: | 682-09-7 | | MF: | C12H22O3 | | MW: | 214.3 | | EINECS: | 211-661-1 | | Product Categories: | | | Mol File: | 682-09-7.mol |  |
| | Trimethylolpropane diallyl ether Chemical Properties |
| Boiling point | 135 °C/13 mmHg (lit.) | | density | 0.955 g/mL at 25 °C (lit.) | | vapor pressure | 0.17-0.23Pa at 25℃ | | refractive index | n20/D 1.458(lit.) | | Fp | >230 °F | | Water Solubility | Practically insoluble in water | | form | Viscous | | pka | 14.62±0.10(Predicted) | | color | Colorless to Light yellow | | Specific Gravity | 0.955 | | 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 | | InChIKey | BDKDHWOPFRTWPP-UHFFFAOYSA-N | | SMILES | CCC(CO)(COCC=C)COCC=C | | LogP | 1.4-3 at 20-25℃ | | Surface tension | 50mN/m at 1g/L and 20℃ | | CAS DataBase Reference | 682-09-7(CAS DataBase Reference) | | EPA Substance Registry System | Trimethylolpropane diallyl ether (682-09-7) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36 | | WGK Germany | 2 | | RTECS | TY6667000 | | TSCA | TSCA listed | | HS Code | 29094990 | | Storage Class | 10 - Combustible liquids |
| | Trimethylolpropane diallyl ether Usage And Synthesis |
| Uses | 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. | | 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. |
| | Trimethylolpropane diallyl ether Preparation Products And Raw materials |
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