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Bis 2-chloroisopropyl ether

Bhmingham Metal Company Ltd., 207 Bis(2-chloroisopropyl) ether, 25 Bis(chloromethyl) ether, 25 Bis(chloromethyl) ketone, 25 Bis(2-EthyUiexyl) phthalate, 25 Bismuth and Bismuth Compounds, 25 Bismuth Institute, 256 Bismuth telluride, 26 Bisphenol-A, 26 Bithionol, 26 Bitmac Ltd., 207, 236 Bitoscanate, 26 Bitoumina SA, 167... [Pg.324]

Chlorophenyl phenyl ether 4-Bromophenyl phenyl ether Bis(2-chloroisopropyl)ether Bis(2-chloroethoxy)methane Methylene chloride (dichloromethane)... [Pg.385]

Note Technical grade bis(2-chloroisopropyl) ether contains the isomer 2-chloro-l-methylethyl(2-chloropropyl) ether (< 30 wt %). [Pg.179]

Biological. When bis(2-chloroisopropyl) ether (5 and 10 mg/L) was statically incubated in the dark at 25 °C with yeast extract and settled domestic wastewater inoculum, complete biodegradation was achieved after 14 d (Tabak et ah, 1981). [Pg.180]

Chemical/Physical. Kollig (1993) reported that bis(2-chloroisopropyl) ether is subject to hydrolysis forming HCl and the intermediate (2-hydroxyisopropyl-2-chloroisopropyl) ether. The intermediate compound undergoes hydrolysis yielding bis(2-hydroxyisopropyl) ether. Van Duuren et al. (1972) reported a hydrolysis half-life of 21 h at 25 °C and pH 7. [Pg.180]

Bis(p-chloroethyl) ether, see Bis(2-chloroethyl) ether Bis(2-chloroethyl)formal, see Bis(2-chloroethoxy)methane Bis(p-chloroethyl)formal, see Bis(2-chloroethoxy)methane Bis(p-chloroisopropyl) ether, see Bis(2-chloroisopropyl) ether... [Pg.1463]

Chloro-3-hydrox34oluene, see p-Chloro-ro-cresol 2-Chloroisopropyl ether, see Bis(2-chloroisopropyl) ether p-Chloroisopropyl ether, see Bis(2-chloroisopropyl) ether Chloromethane, see Methyl chloride (Chloromethyl)benzene, see Benzyl chloride Chloromethyl bromide, see Bromochloromethane Chloromethyl ether, see sym-Dichloromethyl ether (Chloromethyl)ethylene oxide, see Epichlorohydrin (2-Chloro-l-methylethyl) ether, see Bis(2-chloroisoprop-yl)... [Pg.1472]

DCE, see 1,2-Dichloroethane DCEE, see Bis(2-chloroethyl) ether DCIP, see Bis(2-chloroisopropyl) ether... [Pg.1474]

Dichlorohydroxybenzene, see 2,4-Dichlorophenol 4,6-Dichlorohydroxybenzene, see 2,4-Dichlorophenol Dichloroisopropyl ether, see Bis(2-chloroisopropyl) ether 2,2 -Dichloroisopropyl ether, see Bis(2-chloroisopropyl)... [Pg.1476]

EINECS 203-468-6, see Ethylenediamine EINECS 203-470-7, see Allyl alcohol EINECS 203-472-8, see Chloroacetaldehyde EINECS 203-481-7, see Methyl formate EINECS 203-523-4, see 2-Methylpentane EINECS 203-528-1, see 2-Pentanone EINECS 203-544-9, see 1-Nitropropane EINECS 203-545-4, see Vinyl acetate EINECS 203-548-0, see 2,4-Dimethylpentane EINECS 203-550-1, see 4-Methyl-2-pentanone EINECS 203-558-5, see Diisopropylamine EINECS 203-560-6, see Isopropyl ether EINECS 203-561-1, see Isopropyl acetate EINECS 203-564-8, see Acetic anhydride EINECS 203-571-6, see Maleic anhydride EINECS 203-576-3, see m-Xylene EINECS 203-598-3, see Bis(2-chloroisopropyl) ether EINECS 203-604-4, see 1,3,5-Trimethylbenzene EINECS 203-608-6, see 1,3,5-Trichlorobenzene EINECS 203-620-1, see Diisobutyl ketone EINECS 203-621-7, see sec-Hexyl acetate EINECS 203-623-8, see Bromobenzene EINECS 203-624-3, see Methylcyclohexane EINECS 203-625-9, see Toluene EINECS 203-628-5, see Chlorobenzene EINECS 203-630-6, see Cyclohexanol EINECS 203-632-7, see Phenol EINECS 203-686-1, see Propyl acetate EINECS 203-692-4, see Pentane EINECS 203-694-5, see 1-Pentene EINECS 203-695-0, see cis-2-Pentene EINECS 203-699-2, see Butylamine EINECS 203-713-7, see Methyl cellosolve EINECS 203-714-2, see Methylal EINECS 203-716-3, see Diethylamine EINECS 203-721-0, see Ethyl formate EINECS 203-726-8, see Tetrahydrofuran EINECS 203-729-4, see Thiophene EINECS 203-767-1, see 2-Heptanone EINECS 203-772-9, see Methyl cellosolve acetate EINECS 203-777-6, see Hexane EINECS 203-799-6, see 2-Chloroethyl vinyl ether EINECS 203-804-1, see 2-Ethoxyethanol EINECS 203-806-2, see Cyclohexane EINECS 203-807-8, see Cyclohexene EINECS 203-809-9, see Pyridine EINECS 203-815-1, see Morpholine EINECS 203-839-2, see 2-Ethoxyethyl acetate EINECS 203-870-1, see Bis(2-chloroethyl) ether EINECS 203-892-1, see Octane EINECS 203-893-7, see 1-Octene EINECS 203-905-0, see 2-Butoxyethanol EINECS 203-913-4, see Nonane EINECS 203-920-2, see Bis(2-chloroethoxy)methane EINECS 203-967-9, see Dodecane EINECS 204-066-3, see 2-Methylpropene EINECS 204-112-2, see Triphenyl phosphate EINECS 204-211-0, see Bis(2-ethylhexyl) phthalate EINECS 204-258-7, see l,3-Dichloro-5,5-dimethylhydantoin... [Pg.1482]

Bis(2-chloroisopropyl) ether Chloromethyl formate, see sjm-Dichloromethyl ether 1 Chloro-2-methylnaphthalene, see 2-Methylnaphthalene... [Pg.1522]

Hydracrylic acid, see p-Propiolactone Hydrazobenzene, see Aniline Hydriodic acid, see Methyl iodide Hydrobromic acid, see Bromodichloromethane, Bromoform, Methyl bromide, Metobromuron Hydrochloric acid, see Alachlor. Aldrin, Benzyl chloride, a-BHC, p-BHC, Bis (2-chloroethyl) ether, Bis(2-chloroisopropyl) ether, Bromacil. Bromodichloromethane, Carbon tetrachloride, Chloroethane, Chloroform, o-Chloronitrobenzene. Chloropicrin, Chloroprene, p-Chloronitrobenzene, 2,4-D, see Dalanon-sodium. p.p -DDD, p,p -DDT, Dicamba. 1,1-Dichloroethane, 1,1-Dichloroethylene, fratts-l,2-Dichloroethylene, s/m-Dichloromethyl ether, 2.3-Dichloronitrobenzene. 3.4-Dichloronitrobenzene. 1,2-Dichloropropane, cis-1,3-... [Pg.1531]

Proposed neutral hydrolysis pathway for bis(2-chloroisopropyl)ether. [Pg.350]

Chlorohydrins are compounds characterized by alpha halo-alpha alkoxy groups bound to a common carbon atom. These compounds undergo rapid hydrolysis at this shared carbon atom. Bis(2-chloroisopropyl)ether, a chlorohydrin, has two such carbon atoms, and both react very rapidly with water. In fact, the reactions are so fast that acid and alkaline contributions have not been determined. It is likely, however, that base accelerates the reaction kinetics. The proposed reaction pathway for this compound is based on the reported pathway for bis(chloroethyl)ether (Figure 13.4). The reported rate constant for bis(chlorome-thyl)ether, of 0.23 sec-1 was based on an observed half-life of a few minutes. Similarly, for bis(2-chloroisopropyl)ether, both of the chloro substituents are reactive, and a half-life of a few minutes can be assigned to this compound, as well. [Pg.350]

See other pages where Bis 2-chloroisopropyl ether is mentioned: [Pg.223]    [Pg.227]    [Pg.2211]    [Pg.25]    [Pg.272]    [Pg.355]    [Pg.480]    [Pg.159]    [Pg.180]    [Pg.1190]    [Pg.1450]    [Pg.1454]    [Pg.1458]    [Pg.1461]    [Pg.1461]    [Pg.1463]    [Pg.1465]    [Pg.1469]    [Pg.1471]    [Pg.1492]    [Pg.1497]    [Pg.1498]    [Pg.1498]    [Pg.1499]    [Pg.1505]    [Pg.1515]    [Pg.1532]    [Pg.25]    [Pg.1269]    [Pg.334]    [Pg.350]    [Pg.350]   


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Bis Ether

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