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Merck
CN

777625

1-Amino-2-methyl-2-propanol

95% anhydrous basis

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

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About This Item

Empirical Formula (Hill Notation):
C4H11NO
CAS Number:
2854-16-2
Molecular Weight:
89.14
NACRES:
NA.22
PubChem Substance ID:
329767916
UNSPSC Code:
12352100
MDL number:
MFCD01697283

Key Documents

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Product Name

1-Amino-2-methyl-2-propanol, 95% anhydrous basis

InChI

1S/C4H11NO/c1-4(2,6)3-5/h6H,3,5H2,1-2H3

SMILES string

CC(C)(O)CN

InChI key

LXQMHOKEXZETKB-UHFFFAOYSA-N

assay

95% anhydrous basis

form

liquid

refractive index

n20/D 1.448

density

0.957 g/mL at 25 °C

functional group

amine
hydroxyl

storage temp.

2-8°C

Quality Level

100

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Other Notes

May contain up to 10% water.

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

164.8 °F - closed cup

flash_point_c

73.8 °C - closed cup

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Certificates of Analysis (COA)

Lot/Batch Number
MKCG3639
MKBT8037V
MKBQ0990V

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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
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)
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
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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