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Amino-2-Methyl-1 -Propanol

Does the C NMR spectrum shown in Figure 22.10 correspond to that of l-amino-2-methyl-2-propanol or to 2-amino-2-methyl-1-propanol Could this compound be prepared by reaction of an epoxide with ammonia ... [Pg.970]

Amino 2 deoxy d glucose, conversion of hydrochloride to 2 acetamido-2 deoxy d glucose, 46, 2 l-(Ammomcthyl) cycloheptanol, 46, 31 2 Amino 2 methyl 1 propanol in isolation of levopimanc acid 45, 64 c-Amino p nitrobiphenyl, by nitration of o aminobiphenyl, 46, 86 from o,p dimtrobiphenyl, 46, 88 Amino 2 propanone, semicarbazone... [Pg.120]

Amino,2-methyl,1-propanol (AMP), also known as Isobutanolamine (IBA), (CH3)2CNH2CH2OH, MW = 89. Available as a 95% solution (AMP-95 ) from Angus Chemical Company. Sp. gr. = 0.942. Flash point = 87 °C/188 °F (PMCC). Boiling point = 329 °F. Suitable for short to medium steam-condensate pipe runs provided the operating pressure is at least 75 psig. A safe replacement for morpholine. Reasonable thermal stability. [Pg.518]

Dimethoxybenzoyl chloride Benzoyl chloride, 2,3-dimethoxy- (9) (7169-06-4) 2-Amino-2-methyl-1-propanol 1-Propanol, 2-amino-2-methyl- (8,9) (124-68-5) 2,2 -Dimethoxy-6-(4 ,4 -dimethyloxazolinyl)biphenyl Oxazole, 2-(2 ,6-dimethoxy[1,1-biphenyl]-2-yl)-4,5-dihydro-4,4-dimethyl- (9) (57698-39-7)... [Pg.195]

Amino-2-methyl-1 -propanol [124-68-5] 194B I(3)425D, N(1)294B UA5950000... [Pg.1050]

Pine oleoresin [1 kg. containing 260 g. (0.86 mole) of levo-pimaric acid] (Notes 1 and 2) is dissolved in 2 1. of acetone in a 4-1. beaker. A solution of 200 g. (2.2 moles) of 2-amino-2-methyl-1-propanol (Note 3) in 200 ml. of acetone is added as rapidly as possible with stirring. The pasty precipitate which forms almost immediately is collected by suction filtration and is pressed as dry as possible using a rubber dam (Note 4). The crude moist precipitate is returned to a 2-1. beaker and is dissolved in the minimum volume ( 1 1.) of boiling methanol. The methanolic solution is cooled to 5° in a refrigerator and stirred occasionally to expedite crystallization. When the crystallization is completed, the solid is collected by suction filtration. The precipitate is redissolved in a minimum volume of boiling methanol ( l 1.) (Note 5), the solution concentrated to two-thirds its original volume (Note 6), cooled to 5°, and the amine salt allowed to... [Pg.33]

The maximum observed rotation for the 2-amino-2-methyl-1-propanol salt of levopimaric acid is [a] n —218°. Methanol and ethanol solutions give the same specific rotations, but methanol is the preferred solvent because the time required to effect solution in ethanol is longer. If pure levopimaric acid, m.p. 151-153°, [a] D —276° is desired, the salt with —210° rotation should be dissolved in 8 parts of boiling methanol, the solution concentrated to the point of incipient crystallization, cooled, and filtered. The yield in this recrystallization is about 70%. [Pg.34]

Davis, R.A. and Pogainis, B.J. Solubility of nitrous oxide in aqneons blends of TV-methyldiethanolamine and 2-amino-2-methyl-1-propanol, J. Chem. Eng. Data, 40(6) 1249-1251, 1995. [Pg.1648]

Can be prepd from 2-amino-2-methyl- 1-propanol according to the reactions given in Ref 2, as follows ... [Pg.233]

N- Carboethoxy- 2- amino—2—methyl-1 - propanol N- Carboethoxy- 2- amino—2—methyl- 1- hydroxy-propane or 1- Hydroxy-2,2 - dimethyl- 2- urethane... [Pg.447]

A. 2,2-Dimethylethylenimine. A cold mixture of 110 g. (60 ml., 1.06 moles) of concentrated sulfuric acid and 200 ml. of water is added in portions, with shaking, to a solution of 100 g. (107 ml., 1.12 moles) of 2-amino-2-methyl-1-propanol in 200 ml. of water contained in a 1-1. round-bottomed flask (Note 1). The flask is fitted with a thermometer extending into the liquid and a short still head carrying a downward condenser. [Pg.7]

C4H11NO 2-amino-2-methyl-1-propanol 124-68-5 20.00 0.9340 1 4278 C5H4CI2N2 3,6-dichloro-4-methylpyridazine 19064-64-3 25.00 1.4259 2... [Pg.215]

Enteric polymers can be coated from aqueous latexes or from aqueous solutions that are produced by solubilizing the polymer via pH neutralization with the addition of an alkali or organic base. Typical neutralizing agents used to create aqueous solutions of enteric polymers include ammonia sodium hydroxide, triethanolamine 2-amino-2-methyl-1-propanol and ammonium hydrogen carbonate. In most cases acid preireal-ment is required to convert the enteric polymer from its salt state back to the neural state to achieve enteric functionality of the polymer however, it has been reported that acid... [Pg.388]


See other pages where Amino-2-Methyl-1 -Propanol is mentioned: [Pg.855]    [Pg.938]    [Pg.16]    [Pg.328]    [Pg.1613]    [Pg.781]    [Pg.783]    [Pg.985]    [Pg.188]    [Pg.55]    [Pg.192]    [Pg.1124]    [Pg.1207]    [Pg.89]    [Pg.27]    [Pg.108]    [Pg.111]    [Pg.135]    [Pg.101]    [Pg.793]    [Pg.650]    [Pg.164]    [Pg.239]    [Pg.78]    [Pg.657]    [Pg.14]    [Pg.118]    [Pg.321]    [Pg.425]    [Pg.603]    [Pg.698]    [Pg.398]   
See also in sourсe #XX -- [ Pg.963 ]




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1- Amino-2-methyl-2-propanol, N-alkyl

1- Amino-2-methyl-2-propanol, N-alkyl derivatives

1- Amino-2-propanol

2 Methyl 2 propanol

2- Amino-2-methyl-l-propanol

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