P-Aminoethyl alcohol

Synonyms AI3-24219 2-Aminoethanol p-Aminoethyl alcohol BRN 0505944 Caswell No. 426 CCRIS 6260 Colamine EINECS 205-483-3 EPA pesticide chemicai code 011601 P-Ethanolamine Ethylolamine Glycinol 2-Hydroxyethylamine p-Hydroxyethylamine MEA Monoethanolamine Olamine Thiofalco M-50 UN 2491 USAF EK-1597. [Pg.548]

Aminoethanol, see Ethanolamine Aminoethene, see Ethylenimine p-Aminoethyl alcohol, see Ethanolamine p-Aminoethylamine, see Ethylenediamine Aminoethylene, see Ethylenimine Aminogen 11, see p-Phenylenediamine Aminomethane, see Methylamine l-Amino-2-methoxybenzene, see o-Anisidine l-Amino-4-methoxybenzene, see p-Anisidine 4-Aminomethoxybenzene, see p-Anisidine p-Aminomethoxybenzene, see p-Anisidine... [Pg.1460]

Synonym p-aminoethyl alcohol, ethylolamine, 2-hydroxyethylamine, p-hydroxyethylamine, monoethanolamine, MEA... [Pg.49]

PYRIDAZINYL)BENZENESULFONAMIDE see SNJIOO a-AMINOETHYL ALCOHOL see AAG500 P-AMINOETHYL ALCOHOL see EEC600... [Pg.1507]

P-Aminoethyl alcohol colamine ethylolamine P-hydroxy-ethylamine 2-hydroxyethylamine. [Pg.478]

Synonyms/Trade Names 2-Aminoethanol, p-Aminoethyl alcohol, Ethylolamine, 2-Hydroxyethylamine,... [Pg.129]

Synonyms 2-Ami noethanol 2-Ami noethyl alcohol p-Aminoethyl alcohol p-Ethanolamine Ethylolamine Glycinol 2-Hydroxyethylamine p-Hydroxyethylamine MEA MELA Monoethanolamine Classification Aliphatic amino alcohol alkanolamine Empirical C2H7NO Formula NH2CH2CH2OH Properties Colorless clear mod. vise, liq. ammoniacal odor misc. with water, alcohol, acetone, glycerin sol. in chloroform si. sol. in benzene m.w. 61.10 dens. 1.012 vapor pressure 0.26 mm Hg m.p. 10.5 C b.p. 170 C flash pt. 93 C autoignition temp. 410 C ref. index 1.4540 pH 12.1 surf. tens. 48.89 dynes/cm dielec, const. 37.72... [Pg.1665]

Monoethanolainine, 2-aminoethyl alcohol, 2-hydroxyelhy amine, HOCH2CH2NH2. M.p. 10-5°Q b.p. 17UC. [Pg.164]

The Wenker aziridine synthesis entails the treatment of a P-amino alcohol 1 with sulfuric acid to give P-aminoethyl sulfate ester 2 which is subsequently treated with base to afford aziridine 3. Before the discovery of the Mitsunobu reaction, wbicb transforms an amino alcohol into an aziridine in one step under very mild conditions, the Wenker reaction was one of the most convenient methods for aziridine synthesis. However, due to the involvement of strong acid and then strong base, its utility has been limited to substrates without labile functionalities. [Pg.63]

A solution of 27 g of co-chloroacetopyrocatechol in 150 ml of ethyl alcohol is added dropwise within 2 hours into a stirred and refluxed solution of 81 g of 7-(p-aminoethyl)theophylline in 200 ml of a 60% aqueous ethyl alcohol. Following this, boiling is continued for another 3.5 hours while passing through nitrogen, and the precipitated product is separated by suction filtration, washed with water and dried. The product is suspended in alcohol, admixed with alcoholic hydrochloric acid while heating until an acid reaction is observed and subjected to suction filtration after cooling. Obtained in this manner are 37 g of 7-[p-(P -3,4-dihydroxyphenyl-p -... [Pg.3188]

BIS(p-AMINOETHYL)AMINE (111-40-0) Combustible liquid (flash point 208°F/98°C oc). An organic base. Ignites spontaneously with cellulose nitrate, and possibly other nitrogen compounds. Silver, cobalt, or chromium compounds may cause explosions. Contact with nitromethane forms a heat-, friction-, and shock-sensitive explosive. Incompatible with acids, acrylates, aldehydes, alcohols, alkylene oxides, caprolactam solution, cresols, organic anhydrides, substituted allyls, epichlorohydrin, glycols, halogenated compounds, isocyanates, ketones, mercury, phenols, strong oxidizers, vinyl acetate. Attacks aluminum, copper, cobalt, lead, tin. zinc, and their alloys. [Pg.182]

HYDRACRYLIC ACID, P-LACTONE (57-57-8) Combustible liquid (flash point 165°F/74°C). Able to polymerizes in elevated temperatures and decomposes at room temp>er-ature, forming unstable peroxides stable below 41°F/5°C. Violent reaction with strong oxidizers, strong acids, alkalis, aniline, chlorosulfonic acid, 1,2-ethanediamine, ethanolamine, ethyleneimine, pyridine, sodium hydroxide. Incompatible with 2-aminoethyl alcohol, ammonium hydroxide. Hydrolyzes in fresh water, forming hydracrylic acid in salt water reacts with the chloride, forming 3-chloropropionic acid. [Pg.627]

Chloro-1-(3-ethoxy4-nitrophenoxy)-4-(trifluoromethyl) benzene. See Ox luorfen 2-Chloroethyl alcohol p-Chloroethyl alcohol. See Ethylene chlorohydrin 2-Chloroethylamine hydrochloride CAS 870-24-6 EINECS/ELINCS 212-793-2 Synonyms 2-Aminoethyl chloride hydrochloride p-Chloroethylamine hydrochloride 2-Chloroethylammonium chloride... [Pg.889]

Aziridine synthesis via treatment of a -amino alcohol with sulfuric acid to give P-aminoethyl sulfuric acid, which is subsequently treated with base. [Pg.431]

Synonyms 2-Aminoethanol 2-Aminoethyl alcohol P-Amlnoethyl alcohol 3-Etha-nolamlne Ethylolamlne Glycinol 2-Hydroxyethylamlne P-Hydroxyethylamlne MEA MELA Monoethanolamlne Classification Aliphatic amino alcohol alkanolamlne Empirical CjM NO Formula NHjCHjCHjOH... [Pg.2116]

Aminoethylpolyvinyl Alcohol(AEPVA) and Its Perchlorote(AEPVAP). Treatment of PVAC Elvanol ) with ethyleneimine in a bomb reactor at 100° as indicated in Rept No 2,p 37, produced AEPVA with as high as 26.8% N. Treatment of the dry product with 70% perchloric acid in the manner used for am inoethyIcel lulos e perchlorate(A ECP) yielded the perchlorate(AEPVAP) with 20.3% Cl and 10.8% N(See also Aminoethylation)... [Pg.205]

SYN S 2-AMINO-l -(2,5-DIMETHOXYPHENYL)-l -PROPANOL HYDROCHLORIDE a-(l-AMINOETHYL)-2,5-DIMETHOXYBENZYL ALCOHOL HYDROCHLORIDE p-(2,5-DIMETHOX1THENYL)-p-HYDROXYISO-PROPYL.AMINE HYDROCHLORIDE p-HYDROXY-P-(2,5-DIMETHOXYPHENYL)-ISOPROPYLAi nNE HYDROCHLORIDE PRESSOMIN HYDROCHLORIDE VASO-XINE VASOXINE HYDROCHLORIDE VASOXYL HYDROCHLORIDE... [Pg.888]

SYNS a-(l-AMINOETHYL)BENZENEMETHANOL HYDROCHLORIDE a-(l-AMINOETHYL)BENZYL ALCOHOL HYDROCHLORIDE ( )-2-AMINO-l-PHENYL-l-PROPANOL HYDROCHLORIDE O-HYDROXY-P-AMINOPROPYLBENZENE HYDROCHLORIDE MONHYDRIN MUCORAMA MYDRIATINE dl-NOREPHEDRINE HYDROCHLORIDE dl-l-PHENYL-2-AMINO-l-PROPANOL MONOHYDROCHLORIDE PHENYLPROPANOLAMINE HYDROCHLORIDE... [Pg.1176]

AMINO-4-ETHYLBENZENE see EGLOOO P-AMINOETHYLBENZENE see PDE250 a-(l-AMINOETHYL)BENZENEMETHANOL HYDROCHLORIDE see PMJ500 a-(l-AMINOETHYL)-BENZYL ALCOHOL see NNMOOO a-(l-AMINOETHYL)BENZYL ALCOHOL HYDROCHLORIDE see PMJ500... [Pg.1507]

Anhydrous piperazine is a white solid which is obtained as leaflets when crystallised from alcohol, m.p. 106°C (b.p. 145-146 C). Piperazine may be prepared by several methods [40], However, industrially it is best prepared by cyclodehydration of 2-hydroxyethylamine (34) or N-(2-aminoethyl)-2-hydroxyethylamine (35) at high temperatures in the presence of a catalyst like Ra-Ni and habdes of Zn, Fe, A1 or Mg [41-43]. Catalytic deamination of diethylenetriamine (36) in the presence of Ra-Ni catalyst in an autoclave at 150°C also gives piperazine. Another useful method to prepare piperazine involves reduction of pyrazine (37) by sodium and ethanol [40] (Scheme 1). [Pg.154]

Methylenebis (3-chloro-2,6-diethylaniline) 4,4 -Methylenebis 2,6-diethylaniline curing agent, epoxies Adipic acid dihydrazide 1-[(2-Aminoethyl) aminol-2-propanol Aminoethylpiperazine Aniline 3,3, 4,4 -Benzophenone tetracarboxylic dianhydride Benzyl alcohol N-Benzyidimethylamine Bis (p-aminocyclohexyl) methane Bis-hexamethylenetriamine Boron trifluoride 1-(2-Cyanoethyl)-2-ethyl-4-methylimidazole 1,2-Diaminocyclohexane 3,4-Diaminotoluene Diazabicycloundecene Didecyl methylamine... [Pg.5047]

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