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About This Item
Linear Formula:
NH2C(CH3)2CH2OH · HCl
CAS Number:
Molecular Weight:
125.60
EC Number:
221-713-5
UNSPSC Code:
12161700
PubChem Substance ID:
Beilstein/REAXYS Number:
3668007
MDL number:
InChI key
PMZIUAOBHNJYQT-UHFFFAOYSA-N
InChI
1S/C4H11NO.ClH/c1-4(2,5)3-6;/h6H,3,5H2,1-2H3;1H
SMILES string
Cl.CC(C)(N)CO
assay
≥98% (titration)
form
crystalline
useful pH range
9.0-10.5
pKa (25 °C)
9.7
solubility
water: 0.5 g/mL, clear, colorless
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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K Lewandrowski et al.
Clinical chemistry, 38(11), 2286-2294 (1992-11-11)
We evaluated N-methyl-D-glucamine (MEG) as a buffer for assay of alkaline phosphatase (ALP; EC 3.1.3.1) and compared the MEG-based assay with the current International Federation of Clinical Chemistry Reference Method for ALP (IFCC/RM/ALP), in which 2-amino-2-methyl-1-propanol (AMP) is the pH
C Cipolla et al.
Arhiv za higijenu rada i toksikologiju, 48(2), 205-209 (1997-06-01)
The authors described two cases of airborne contact dermatitis caused by 2-amino-2-methyl-1-propanol (AMP 100) in two subjects with periorbital erythema and itching skin. The AMP 100 has been used to replace ammonia as a hair dye component in the cosmetic
Shakil A Saghir et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 46(2), 678-687 (2007-10-27)
This study determined the oral and dermal ADME of 2-amino-2-methyl-1-propanol (AMP), a substituted aliphatic alcohol used in a number of industrial and consumer products. Groups of 4 male Fischer 344 rats received either a single bolus oral or dermal dose
Shia-Chung Chen et al.
Journal of hazardous materials, 179(1-3), 692-700 (2010-04-15)
In this study, the recovery of carbon dioxide using an absorbent composed of 2-amino-2-methyl-l-propanol (AMP)+monoethanolamine (MEA)+piperazine (PZ) in polytetrafluoroethylene (PTFE) membrane contactors was investigated. Experiments were conducted using various gas flow rates, liquid flow rates, absorbent blends, and pore size
M Lamberto et al.
Analytical biochemistry, 230(2), 224-228 (1995-09-20)
The effect of derivatization with 2-amino-2-methyl-propanol on trans-3-hexadecenoic acid was investigated as part of the identification of the trans-3-hexadecenoic acid in two Nova Scotian seaweeds. After the extraction of the total fatty acids and their methylation, the monoenoic trans fraction
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