| Identification | Back Directory | [Name]
BENZYL GLYCIDYL ETHER | [CAS]
89616-40-0 | [Synonyms]
692
XY692
VITAS-BB TBB000194
LS-692 benzyl ether
BENZYL GLYCIDYL ETHER
Benzyl glycidol ether
Benzyl glycidin ether
Epoxy Reactive Diluent
BENZYL GLYCIDYL ETHER 692
Benzyl glycidyl ether ,99%
2-(BENZYLOXYMETHYL)OXIRANE
692 (Benzyl Glycidyl Ether)
1-BENZYLOXY-2,3-EPOXYPROPANE
3-BENZYLOXY-1,2-EPOXYPROPANE
TIANFUCHEM--89616-40-0--High purity BENZYL GLYCIDYL ETHER factory price | [EINECS(EC#)]
220-899-5 | [Molecular Formula]
C10H12O2 | [MDL Number]
MFCD00068664 | [MOL File]
89616-40-0.mol | [Molecular Weight]
164.2 |
| Chemical Properties | Back Directory | [Boiling point ]
70-73 °C11 mm Hg(lit.) | [density ]
1.077 g/mL at 25 °C(lit.) | [refractive index ]
n20/D 1.5170(lit.) | [Fp ]
>230 °F | [InChI]
InChI=1S/C10H12O2/c1-2-4-9(5-3-1)6-11-7-10-8-12-10/h1-5,10H,6-8H2 | [InChIKey]
QNYBOILAKBSWFG-UHFFFAOYSA-N | [SMILES]
O(CC1=CC=CC=C1)CC1OC1 |
| Hazard Information | Back Directory | [Uses]
Benzyl Glycidyl Ether is widely used in electrical apparatus electromechanics and the machinery industry. Low viscosity can greatly lower the viscosity of epoxy resin. Decrease the viscosity of epoxy resin. | [Synthesis]
Synthesis of benzyl glycidyl ether: To a stirred mixture of epichlorohydrin (2.0 g, 21.6 mmol), benzyl alcohol (2.12 g, 19.6 mmol) and tetrabutylam monium hydrogen sulphate (290 mg, 0.86 mmol) were added to 50% (w/v) aqueous NaOH (10 ml) drop wise at 0 °C and the reaction mixture was allowed to stir for 30 min at the same temperature. The stirring was con tinued for additional 4 h after which the mixture was extracted with diethyl ether. The ether-extract was washed with brine (2 × 10 ml), dried over anhydrous sodium sulfate and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel using a mixture of hexane: ether (6:1) as eluent to obtain an overall yield of 2.0 g (65%)[1]. | [References]
[1] Neeraj Bala. (2011). Bioresolution of benzyl glycidyl ether using whole cells of Bacillus alcalophilus. Journal of Basic Microbiology, 52 4, 383–389. https://doi.org/10.1002/jobm.201100204 |
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