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Ethylene chlorohydrin 2-Chloroethanol

Ethylene chlorohydrin (2-chloroethanol) Cloperastine Defosfamide Metronidazole Oxypendyl Ethylenediamine Clonidine HCI Edetate disodium Indanazoline Lofexidine HCI Naphazoline Oxymetazoline HCI Penicillin G Benzathine Tetrahydrozoline HCI Tolazoline Tolonidine nitrate Xylometazoline HCI Ethylene dibromide... [Pg.1633]

ETHYLENE CHLOROHYDRIN 2-Chloroethanol, 2-Chlorethanol, 2-Chloroethyl Alcohol, Glycol Chlorohydrin Poison, Class B, II 3 2 0... [Pg.101]

Ethylene chlorohydrin (2-chloroethanol (CAS 107-07-3)) Irritating to eyes upon direct contact. Skin contact is extremely hazardous because it is not irritating and absorption is rapid. Vapors irritating to eyes and respiratoiy tract puimonary edema has been reported. Systemic effects inciude CNS depression, myocardiopathy, shock, and liverand kidney damage. [Pg.572]

Reppe was also working on the preparation of ethylene oxide. The first step was the reaction of ethylene with chlorine and water to form ethylene chlorohydrin (2-chloroethanol). He was able to convert the unsatisfactory batch process, which had been used for indigo manufacture, into a continuous process. This was called the tower process (Turm-Verfahren), because a mixture of ethylene and a carefully controlled amount of chlorine was driven up a tower filled with water. The dilute solution of ethylene chlorohydrin was drawn off at the top and then heated, without being isolated, with lime water to form ethylene oxide. Ethylene oxide was chiefly converted into the glycol by adding water, but it could also be used to make diethylene glycoF (diglycol). [Pg.97]

Preparation by reaction of ethylene chlorohydrin (2-chloroethanol) with resbenzophenone,... [Pg.102]

Elastin reservoir molding Copolymer from styrene and butadiene, polymerized in emulsion Environmental stress cracking Environmental stress cracking resistance Epoxidized soy bean oil (DIN, ISO) Ethylene poly sulfide Ethylene chlorohydrine 2-chloroethanol Copolymer of ethylene and tetrafluor-oethylene (ASTM)... [Pg.2252]

Ethylene chlorohydrin [107-07-3J, HOCH2CH2CI, is the simplest chlorohydrin. It may also be called 2-chloroethanol, 2-chloroethyl alcohol, or glycol chlorohydrin. Ethylene chlorohydrin is ahquid at 15°C and 101.3 kPa (1 atm) (Table 1). This polar compound is miscible with water [7732-18-5] and ethanol [64-17-5] and is slightly soluble in ethyl ether [60-29-7] (5). [Pg.70]

Ethylene oxide [75-21-8] was first prepared in 1859 by Wurt2 from 2-chloroethanol (ethylene chlorohydrin) and aqueous potassium hydroxide (1). He later attempted to produce ethylene oxide by direct oxidation but did not succeed (2). Many other researchers were also unsuccesshil (3—6). In 1931, Lefort achieved direct oxidation of ethylene to ethylene oxide using a silver catalyst (7,8). Although early manufacture of ethylene oxide was accompHshed by the chlorohydrin process, the direct oxidation process has been used almost exclusively since 1940. Today about 9.6 x 10 t of ethylene oxide are produced each year worldwide. The primary use for ethylene oxide is in the manufacture of derivatives such as ethylene glycol, surfactants, and ethanolamines. [Pg.450]

Chloroethanol (ethylene chlorohydrin) [107-07-3] M 80.5, b 51.0 /31mm, 128.6 /760mm, d 1.201, n 1.444. Dried with, then distd from, CaS04 in the presence of a little Na2C03 to remove traces of acid. [Pg.163]

Chloroethanol, see Ethylene chlorohydrin Chloroethylene, see Vinyl chloride... [Pg.154]

Chloroethane, see Ethyl chloride Chloroethanol, see Ethylene chlorohydrin... [Pg.203]

Chloro-1 -nitropropane Chloroacetaldehyde a-Chloroacetophenone Chlorobenzene (monochlorobenzene) o-Chlorobenzylidine malononitrile Chlorobromomethane Chlorodiphenyl (42% chlorine) Chlorodiphenyl (54% chlorine) 2-Chloroethanol (ethylene chlorohydrin) Chloroform... [Pg.366]

Chloro-2,3-epoxypropane, see Epichlorohydrin Chloroethane, see Ethyl chloride Chloroethanol, see Ethylene chlorohydrin Chloromethane, see Methyl chloride Chloronaphthalene 1.19 5.6 132 >558... [Pg.120]

Chloro,2,3,-Epoxypropane, see Epichlorohydrin 2- Chloroethanol, see Ethylene chlorohydrin Chloroethylene, see Vinyl chloride Chloroform (trichloromethane) 13.0... [Pg.237]

McCann J, Simmon Streitwieser D, et al Mutagenicity of chloroacetaldehyde, a possible metabolic product of 1,2-dichloroethane (ethylene dichloride), chloroethanol (ethylene chlorohydrin), and cyclophosphamide. Proc Natl Acad Sci USA 72 3190-3193, 1975... [Pg.143]

Ethylene Chlorohydrin. See Chloroethanol or Chloro Ethyl Alcohol in Vol 3, p C254. Its Nitrite, Nitrate, 2 Nitro- and 2-Nitro-niixaterderivs are described on p C255... [Pg.107]

Several addition reactions have been or are currently used on a large scale in industrial chemical plants. For example, an older method for the preparation of ethylene oxide employed the addition of chlorine to ethylene in water to form ethylene chlorohydrin or 2-chloroethanol. (In industry, ethene is almost always called ethylene.) Treatment of the chlorohydrin with calcium hydroxide results in the formation of ethylene oxide, which is an important intermediate in the manufacture of ethylene glycol and other products (see the Focus On box on page 375). However, this method is wasteful of... [Pg.421]

See other pages where Ethylene chlorohydrin 2-Chloroethanol is mentioned: [Pg.112]    [Pg.367]    [Pg.242]    [Pg.367]    [Pg.249]    [Pg.242]    [Pg.109]    [Pg.101]    [Pg.72]    [Pg.115]    [Pg.116]    [Pg.72]    [Pg.2173]    [Pg.924]    [Pg.112]    [Pg.367]    [Pg.162]    [Pg.81]    [Pg.242]    [Pg.367]    [Pg.664]    [Pg.248]    [Pg.249]    [Pg.318]    [Pg.34]    [Pg.214]    [Pg.214]    [Pg.662]    [Pg.37]    [Pg.47]    [Pg.1306]    [Pg.47]    [Pg.1306]    [Pg.241]    [Pg.242]    [Pg.109]   


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Chlorohydrination

Chlorohydrins

Ethylene Chlorohydrine

Ethylene chlorohydrin

Ethylene chlorohydrination

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