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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

CAS-Nummer
124-68-5
Synonyme
AMP
Isobutanolamine

Größe Preis ($) Menge Verfügbarkeit
100ml 18,30
500ml 28,70
2500ml 92,60
Zum Warenkorb hinzufügen Zur Angebotsanfrage hinzufügen Artikel anzeigen

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

MDL
MFCD00008051
EINECS
204-709-8

Chemische Eigenschaften

Formel
C4H11NO
Molmasse
89.14
Schmelzpunkt
24-28°
Siedepunkt
164-166°
Flammpunkt
67°(152°F)
Dichte
0.934
Brechungsindex
1.4455
Löslichkeit
Immiscible with water. Miscible with alcohols.

Anwendungen

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.

Bemerkungen

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

Literaturverweise

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).

/

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.

GHS Gefahren- und Sicherheitshinweise

Gefahrenhinweise (EU): H315-H319

Causes skin irritation. Causes serious eye irritation.

Sicherheitshinweise: P260u-P201-P280-P303+P361+P353-P305+P351+P338-P301+P330+P331-P304+P340-P310a-P405-P501a

Obtain special instructions before use. Wear protective gloves/protective clothing/eye protection/face protection. IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.

Weitere Referenzen

Merck
14,449
Beilstein
505979
Harmonized Tariff Code
2922.19
TSCA
Yes
RTECS
UA5950000

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