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Mono-n-butylamine

Chemical Designations - Synonyms 1-Aminobutane Butylamine Mono-n-butylamine Norvalamine Chemical Formula CH3(CHj)3NH4. [Pg.60]

Mole-nots, see Strychnine Mollan 0, see Bis(2-ethylhexyl) phthalate Mondur TD, see 2,4-Toluene diisocyanate Mondur TD-80, see 2,4-Toluene diisocyanate Mondur TDS, see 2,4-Toluene diisocyanate Monobromobenzene, see Bromobenzene Monobromobenzol, see Bromobenzene Monobromoethane, see Ethyl bromide Monobromomethane, see Methyl bromide Monobromotrifluoromethane, see Bromotrifluoromethane Monobutylamine, see Butylamine Mono-n-butylamine, see Butylamine Monobutyl ethylene glycol ether, see 2-Butoxyethanol Monochlorbenzene, see Chlorobenzene Monochlorethane, see Chloroethane Monochloroacetaldehyde, see Chloroacetaldehyde Monochlorobenzene, see Chlorobenzene Monochlorodibromomethane, see Dibromochloromethane Monochlorodiphenyl oxide, see 4-Chlorophenyl phenyl ether... [Pg.1496]

SYNS l-AMINO-BUTAAN pUTCH) 1-AMINOBUTAN (GERMAN) 1-AMINOBUTANE 1-BUTANAMINE n-BUTILAMINA (ITALIAN) n-BUTYLAMIN (GERMAN) BUTYLAMINE (OSHA) MONOBUTILAAflNA MONOBUTYLAMINE MONO-n-BUTYLAMINE NORVALAMINE... [Pg.229]

N-Butylamine 1-Aminobutane Butlamine Mono-N- Butylamine Norvalamine ... [Pg.233]

AI3-24197 Amine-C4 1-Amino-butaan 1-Aminobutan 1-Aminobutane 1-Butanamine n-Butiiamina n-Butylamin Butylamine n-Butylamine CCRIS 4756 EINECS 203-699-2 FEMA Number 3130 HSDB 515 Mono-n-butylamine Monobutilamina Monobutylamine Norvalamine NSC 8029 UN1125. Chemical intermediate. Liquid mp = -49.1° bp = 77,0°, d = 0.7414 freely soluble in H2O, soluble in EtOH, Et20 LD50 (rat ort) = 366 mg/kg. Akzo Nobel Chemicals Inc Akzo Nobel. [Pg.90]

CAS 109-73-9 EINECS/ELINCS 203-699-2 UN 1125 (DOT) FEMA 3130 Synonyms Amine C4 1-Aminobutane 1-Butanamine Butylamine MNBA Monobutylamine Mono-n-butylamine Classification Saturated aliphatic amine Empirical C4H11N Formula CH3(CH2)3NH2... [Pg.601]

Monobenzone. See Hydroquinone benzyl ether Monobenzylamine. See N-Benzylamine Monobenzyl ether hydroquinone Monobenzyl hydroquinone. See Hydroquinone benzyl ether Monobromobenzene. See Bromobenzene Monobromodichloromethane. See Bromodichloromethane Monobromoethane. See Ethyl bromide Monobromomethane. See Methyl bromide Monobutylamine Mono-n-butylamine. See n-Butylamine... [Pg.2729]

Monobutylamine Mono-n-butylamine Classification Saturated aliphatic amine Empirical CjH-.N Formula CH3(CH2)3NH2... [Pg.2002]

Mono (2-aminoethyl) sulfate. See Amlnoethyl sulfate Monobasic sodium phosphate. See Sodium phosphate Monobutylamine Mono-n-butylamine. See n-Butylamine Monobutyl glycol ether. See Butoxyethanol Mono-t-butyl hydroquinone. See t-Butyl hydroquinone Monocalcium carbonate. See Calcium carbonate Monocalcium dihydrogen diphosphate. See Calcium dihydrogen pyrophosphate Calcium dihydrogen diphosphate Monocalcium orthophosphate monohydrate Monocalcium phosphate monohydrate. See Calcium phosphate monobasic monohydrate Monocaprin. See Glyceryl caprate... [Pg.2221]

Synonyms AI3-24197 1-Aminobutane BRN 0605269 Butan-l-amine 1-Butanamine n-Butylamine CCRIS 4756 EINECS-203-699-2 FEMA No. 3130 Monobutylamine Mono-/3-but-ylamine Norralamine Norvalamine NSC 8029 Tutane UN 1125. [Pg.232]

Magadiite apart from pentasil phases can be found in zeolites synthesized with mono-n-methy1-, -ethyl-, -propyl- or -butylamine, with di-n-methyl-, -ethyl- or -propylamine, with tri-n-methyl- or -ethylamine and with tetramethylammonium iodide. Table IV shows that the zeolite content increases with the number of carbon atoms per group and with the number of alkyl groups. [Pg.280]

With 1,3-pcntadiyne and primary amines it is possible to obtain either the mono-or diadduct. Thus, refluxing a solution of the diyne in excess n-propylamine produces cw-l-propylamine-l-penten-3-yne (132, R = Pr), whereas healing at 90-100 °C in THF yields the diadduct 134 (R = Pr) presumably by prototropic rearrangement of the initially formed diadduct 133 Analogous behaviour is found for n-butylamine. [Pg.69]

Synonyms 1-butylamine 1-butanamine 1-aminobntane mono-n-bntylamine... [Pg.239]

The data arising from the kinetics of the reaction of three n-butylamines (mono, di, tri-substituted amines) with methyl p-nitrobenezene sulfonate in a variety of... [Pg.280]

Finally, as an example of regioselective aminolysis, a recent report by Conde and Lopez-Serrano deserves to be cited. They used CalB for the regioselective mono-amidation of N-protected aspartic acid diethyl esters with butylamine [96]. [Pg.160]


See other pages where Mono-n-butylamine is mentioned: [Pg.67]    [Pg.280]    [Pg.287]    [Pg.296]    [Pg.992]    [Pg.44]    [Pg.154]    [Pg.451]    [Pg.204]    [Pg.67]    [Pg.280]    [Pg.287]    [Pg.296]    [Pg.992]    [Pg.44]    [Pg.154]    [Pg.451]    [Pg.204]    [Pg.82]    [Pg.137]    [Pg.148]    [Pg.89]    [Pg.360]    [Pg.197]    [Pg.845]    [Pg.536]    [Pg.576]    [Pg.405]   
See also in sourсe #XX -- [ Pg.60 ]

See also in sourсe #XX -- [ Pg.60 ]




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