777625
1-Amino-2-methyl-2-propanol
95% anhydrous basis
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Synonym(s):
1-Amino-2-methylpropan-2-ol, 1,1-Dimethylethanolamine, 2-Amino-α,α-dimethylethanol, 2-Hydroxy-2-methyl-1-propylamine, 2-Hydroxyisobutylamine, 2-Methyl-2-hydroxypropylamine, 3-Amino-2-methyl-2-propanol, NSC 17697
Empirical Formula (Hill Notation):
C4H11NO
CAS Number:
Molecular Weight:
89.14
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
95% anhydrous basis
form
liquid
refractive index
n20/D 1.448
density
0.957 g/mL at 25 °C
storage temp.
2-8°C
SMILES string
CC(C)(O)CN
InChI
1S/C4H11NO/c1-4(2,6)3-5/h6H,3,5H2,1-2H3
InChI key
LXQMHOKEXZETKB-UHFFFAOYSA-N
Related Categories
Other Notes
May contain up to 10% water.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
WGK
WGK 3
Flash Point(F)
closed cup
Flash Point(C)
closed cup
Regulatory Information
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Sandi A Kwee et al.
Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 55(6), 905-910 (2014-03-29)
This study investigated the prognostic significance of metabolically active tumor volume (MATV) measurements applied to (18)F-fluorocholine PET/CT in castration-resistant prostate cancer (CRPC). (18)F-fluorocholine PET/CT imaging was performed on 30 patients with CRPC. Metastatic disease was quantified on the basis of
Ernst Pittenauer et al.
Analytical and bioanalytical chemistry, 407(17), 5079-5089 (2015-01-31)
A new type of low-mass substituted 4-oxazolin product ions of [M + H](+) precursor ions of aminophospholipids (glycerophosphatidylethanolamine, glycerophosphatidyl-N-methylethanolamine, glycerophosphatidyl-N,N-dimethylethanolamine, glycerophosphatidylserine) resulting from high-energy collision-induced dissociation (matrix-assisted laser desorption/ionization time-of-flight/reflectron time-of-flight mass spectrometry) and low-energy collision-induced dissociation (e.g., electrospray ionization
Alexander R Parent et al.
Dalton transactions (Cambridge, England : 2003), 43(33), 12501-12513 (2014-07-09)
Iron tris(2-methylpyridyl)amine (TPA) and iron 1-(bis(2-methylpyridyl)amino)-2-methyl-2-propanoate (BPyA) salts are characterized as water oxidation catalysts (WOCs) using sodium periodate. Under the conditions used, these complexes serve as homogeneous WOCs as demonstrated via kinetic analysis and dynamic light scattering (DLS). The Fe(BPyA)
Anita Aranyi et al.
Journal of chromatography. A, 1387, 123-133 (2015-02-18)
The direct separation of the enantiomers of 1-(α-aminoarylmethyl)-2-naphthol, 1-(α-aminoalkyl)-2-naphthol, 2-(α-aminoarylmethyl)-1-naphthol analogues and 2-(1-amino-2-methylpropyl)-1-naphthol) was investigated in supercritical fluid chromatography. Five commercially available chiral stationary phases based on immobilized polysaccharide chiral selectors (Chiralpak IA, IB, IC, ID and IE) were evaluated.
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