Epichlorhydrin ethylene-propylene

Ethylene propylene (Nordel) Epichlorhydrin (Hydrin) Fluoroelastomers (Viton)... 

SYNS 1-CHLOOR-2.3-EPOXY-PROPAAN (DUTCH) 1-CHLOR-2,3 -EPOXY-PROPAN (GERiMAN) 1-CHLORO-2,3-EPOXYPROPANE 3-CHLORO-l,2-EPOXYPRO-PANE epi-CHLOROHYTDRIN (CHLOROMETHYL)-ETHYLENE OXIDE CHLOROMETHYLOXIRANE 2-(CHLOROMETHYL)OXIRANE CHLOROPROPYLENE OXIDE t-CHLOROPROPYLENE OXIDE 3-CHLORO-1,2-PROPYLENE OXIDE l-CLORO-2,3-EPOSSIPROPANO (ITALIAN) ECH EPICHLOOR-HYDRINE. DUTCH) EPICHLORHYDRIN (GERMAN)... 

Jones and Savill ( 6) have described the very rapid catalytic effect upon trimerization of isocyanates by ethylene oxide, propylene oxide, styrene oxide, or epichlorhydrin when a trace of pyridine is present. No reaction occurs in the absence of pyridine. They express the opinion that the function of the tertiary base is to open the epoxide ring and that the catalytic action is believed due to initial formation of... 

Al, aluminum oxide BA, boric acid C, cellulose CW, Carbowax 4(X) DEAE, diethylaminoethyl DMF, dimethylformamide DMSO, dimethylsulfoxide ECTEOLA, ethanolomine-epichlorhydrin EG, ethylene glycol F, formamide KC, Whatman KC reversed phase plates KG, kieselguhr OA, oxalic acid P, polyamide PEG, polyethylene glycol 4(X) PEI, polyethyleneimine PG, propylene glycol PO, paraffin oil POEG, polyoxyethylene glycol 1000 SG, silica gel SO, silicone oil TD, tetradecane Un, undecane. 

Synonyms 1-Chloro-2,3-epoxypropane 3-Chloro-1,2-epoxypropane (Chloromethyl) ethylene oxide Chloromethyloxirane 2-(Chloromethyl) oxirane Chloropropylene oxide 3-Chloro-1,2-propylene oxide j-Chloropropylene oxide ECU a-Epichlorohydrin 1,2-Epoxy-3-chloropropane 2,3-Epoxypropyl chloride Glycerol epichlorhydrin Classification Chlorinated epoxide Empirical C3H5CIO... 

The hydroformylation of ethylene oxide gives acrolein in very low yields, which is not surprising in view of its extraordinary reactivity in the main, resinous products are obtained. The reactions of ethylene oxide, propylene oxide, cyclohexene oxide, styrene oxide and epichlorhydrin were studied by Takegami et al. [297] at normal conditions. They found that generally internal and conjugated olefin oxides were more reactive than terminal ones and established the following order of reactivity cyclohexene oxide (appr. 5) > styrene oxide > propylene oxide (1) > ethylene oxide epichlorhydrin (1/20-1/10) (the numbers give the relative reactivity). 

Propylene oxide has also been copolymerized with beta-propiolactone, epichlorohydrin, and methyl methacrylate using the alkaline earth/aluminum compound-type initiators (151). Terpolymers from ethylene oxide or propylene oxide, epichlorohydrin, and epsilon-caprolactone, as well as from epichlorhydrin, epsilon-caprolactone, and 2,2-bis(chloromethyl)oxetane,... 

The absence of reports of the presence in the environment of vinyl chloride, vinylidene chloride, methylene chloride, ethylene dichloride, propylene dichloride, allyl chloride, epichlorhydrin and chloroprene, and any of the more polar intermediate degradation products found in laboratory studies, suggest that the natural degradation processes of these compounds proceed at higher rates than inputs. 

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