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124-68-5 - 2-Amino-2-methyl-1-propanol, 95%, may cont. ca 5% water - AMP - Isobutanolamine - A17814 - Alfa Aesar

A17814 2-Amino-2-methyl-1-propanol, 95%, may cont. ca 5% water

Número CAS
124-68-5
Nombre Alternativo
AMP
Isobutanolamine

Tamaño Precio ($) Cantidad Disponibilidad
100ml 18,30
500ml 28,70
2500ml 92,60
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2-Amino-2-methyl-1-propanol, 95%, may cont. ca 5% water

MDL
MFCD00008051
EINECS
204-709-8

Propiedades químicas

Fórmula
C4H11NO
Peso molecular
89.14
Punto de fusión
24-28°
Punto de ebullición
164-166°
Punto de inflamabilidad
67°(152°F)
Densidad
0.934
Índice de refracción
1.4455
Solubilidad
Immiscible with water. Miscible with alcohols.

Aplicaciones

2-Amino-2-methyl-1-propanol is used for the preparation of buffer solution and in cosmetics. It is also used in ATR-FTIR spectroscopic investigation of the carbon monoxide absorption characteristics of a series of heterocyclic diamines.

Notas

Incompatible withoxidizing agents, strong acids, copper, brass and aluminum.

Referencias documentales

Buffer and phosphate acceptor in assay of phosphatases: Methods of Enzymatic Analysis, 3rd ed., H. U. Bergmeyer, Ed., Verlag Chemie, Weinheim (1984), vol. 4, p76.

Precursor of 2-substituted-4,4-dimethyl-2-oxazoline derivatives of carboxylic acids: J. Org. Chem., 39, 2787 (1974), developed by Meyers. The oxazoline, which is readily formed with the acid chloride and thionyl chloride, is stable to base, organometallic reagents, etc., but readily cleaved by dilute acid. For further information on the reactivity of these derivatives, see 2,4,4-Trimethyl-2-oxazoline, L00181.

2-Aryl-4,4-dimethyl-2-oxazolines are activated towards ortho-lithiation: J. Org. Chem., 40, 3058 (1975). Methoxy- or fluoro-substituents in the ortho-position are readily substitutied by organolithiums or Grignards, providing a versatile route to biaryls: J. Am. Chem. Soc ., 97, 7383 (1975). For examples, see: Org. Synth. Coll., 9, 258 (1998). The oxazoline can also be converted to an aldehyde by methylation and borohydride reduction.

For reviews of the use of oxazolines in synthesis, see: Angew. Chem. Int. Ed., 15, 270 (1976); Tetrahedron, 41, 837 (1985); 50, 2297 (1994).

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Conway, W.; Bruggink, S.; Beyad, Y.; Luo, W.; Cabrera, I. M., Puxty, G.; Feron, P. CO2 absorption into aqueous amine blended solutions containing monoethanolamine (MEA), N, N-dimethylethanolamine (DMEA), N, N-diethylethanolamine (DEEA) and 2-amino-2-methyl-1-propanol (AMP) for post-combustion capture processes. Chem. Eng. Sci. 2015, 126, 446-454.

Halim, H. N. A.; Shariff, A. M.; Bustam, M. A. High pressure CO2 absorption from natural gas using piperazine promoted 2-amino-2-methyl-1-propanol in a packed absorption column. Sep. Purif. Technol. 2015, 152, 87-93.

Indicaciones de peligro y de precaución del GHS

Indicaciones de peligro (UE): H315-H319

Causes skin irritation. Causes serious eye irritation.

Indicaciones de precaución: P273-P280g-P305+P351+P338-P337+P313

Avoid release to the environment. Wear protective gloves. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. If eye irritation persists: Get medical advice/attention.

Otras referencias

Merck
14,449
Beilstein
505979
Código de tarifa arancelaria unificado
2922.19
TSCA
Yes
RTECS
UA5950000

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