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2-Aminobutane

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

See related ALKYLMETALS, ALKYLSILANES j1723. Butylamine (1-Aminobutane)... [Pg.572]

Aminobenzenethiol, a297 Aminobenzyl cyanide, a255 1-Aminobutane, b509... [Pg.85]

Abstract Titration of weak bases in non-aqueous solvents can provide valuable information about these weak bases. Some primary amines 1-aminobutane, 1-aminopropane, 2-aminoheptane, aminocyclohexane, 3-amino-l-phenylbutane were titrated with hydrochloric acid in toluene solvent. All the primary amines gave very well-shaped potentiometric titration curves. The same titrations were done with hydrochloric acid in methanol solvent to show the effect of amphiprotic solvent in the titrations with hydrochloric acid. [Pg.327]

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]

Amarthol fast orange R base, see 3-Nitroaniline Amatin, see Hexachlorobenzene Ameisenatod, see Lindane Ameisenmittel merck, see Lindane American Cyanamid 3422, see Parathion American Cyanamid 4049, see Malathion Amerstat 274, see Ethylenediamine Amfol, see Ammonia Amidox, see 2,4-D Amine 2,4,5-T for rice, see 2,4,5-T Aminic acid, see Formic acid 2-Aminoacetylfluorene, see 2-Acetylaminofluorene 4-Aminoaniline, see / Phenylenediamine p-Aminoaniline, see / Phenylenediamine 2-Aminoanisole, see oAnisidine 4-Aminoanisole, see p-Anisidine oAminoanisole, see oAnisidine joAminoanisole, see p-Anisidine Aminobenzene, see Aniline p-Aminobiphenyl, see 4-Aminobiphenyl 1-Aminobutane, see Butylamine l-Amino-4-chloroaniline, see 4-Chloroaniline l-Amino-4-chlorobenzene, see 4-Chloroaniline 1-Amino-p-chlorobenzene, see 4-Chloroaniline 4-Aminochlorobenzene, see 4-Chloroaniline p-Aminochlorobenzene, see 4-Chloroaniline 4-Aminodiphenyl, see 4-Aminobiphenyl... [Pg.1459]

Synonyms 1-Aminobutane -butylamine Physical Form. Colorless liquid... [Pg.103]

O-H-O bonds are stronger than N-H - N bonds, which explains the order of the last two compounds. No hydrogen bonding is possible in the first two compounds, but C-O bonds are polar, giving the ether a higher boiling point than the alkane. The actual boiling points are pentane, 36°C methyl propyl ether, 39°C 1-aminobutane, 78°C and 1-butanol, 118°C. [Pg.223]

These diastereomerically and enantiomerically enriched compounds are useful as intermediates for a variety of interesting building blocks such as 1-aminobutanes, nonprotected homoallylamines, [3-amino acids, and y-amino alcohols (Figure 25.5). The conversion to 1-aminobutanes and homoallylamines will be described. [Pg.492]

This was the basis of the approach by Chessick et al. (1954, 1955) and Zettlemoyer etal. (1958), which involved the use of a series of immersion liquids such as butyl derivatives differing only in their polar groups 1-butanol, 2-butanol, butanal, 1-aminobutane, 1-chlorobutane, butanoic acid. With the polar surfaces studied (rutile, CaF2, Aerosil, alumina), an approximately linear relation was found between the energy of immersion and the dipole moment. The slope gave directly the average field strength (for instance, 820 V//rm 1 on a rutile titanium (tv) oxide) and the... [Pg.135]

Synonyms and trade names 1-aminobutane, 1-butanamine, butylamine, mono- -butylamine (MNBA), monobutylamine... [Pg.57]

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]

What information does the name 1-aminobutane provide about the structure of this organic compound ... [Pg.723]

Recognizing Cause and Effect Arrange the following compounds in order of increasing boiling point, butanol, butane, 1-aminobutane, ethyl ether... [Pg.772]

The monomers A-methacryloyl-l-aminopropane (9), A-methacryloyl-1-aminobutane (10), A-methacryl-oyl-l-aminopentane (11), and A-methacryloyl-1-aminohexane (12) are synthesized directly from the corresponding amine and methacrylic acid by microwave irradiation [50], or classically by the treatment of amines with methacryloyl chloride (Fig. 17). [Pg.189]

See other pages where 2-Aminobutane is mentioned: [Pg.821]    [Pg.589]    [Pg.590]    [Pg.401]    [Pg.1090]    [Pg.1302]    [Pg.20]    [Pg.294]    [Pg.618]    [Pg.651]    [Pg.566]    [Pg.606]    [Pg.656]    [Pg.2043]    [Pg.33]    [Pg.223]    [Pg.381]    [Pg.383]    [Pg.47]    [Pg.47]    [Pg.487]    [Pg.493]    [Pg.493]    [Pg.217]    [Pg.377]    [Pg.501]    [Pg.1506]    [Pg.1506]    [Pg.360]   
See also in sourсe #XX -- [ Pg.60 ]

See also in sourсe #XX -- [ Pg.103 ]

See also in sourсe #XX -- [ Pg.60 ]



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1 - -4-aminobutan

2- Methyl-3-aminobutane

2-Aminobutane, oxidation

3- Methyl-l-aminobutane

4- aminobutan-l-ol

4-aminobutanal

4-aminobutanal

L-Phenyl-3-aminobutane

Phenyl-3-aminobutane

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