423041
2-Dimethylamino-2-methylpropanol solution
80% in H2O, technical grade
Synonym(s):
DMAMP-80™
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About This Item
Linear Formula:
(CH3)2C(CH2OH)N(CH3)2
CAS Number:
Molecular Weight:
117.19
Beilstein/REAXYS Number:
1732837
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
grade
technical grade
Quality Level
form
liquid
concentration
80% in H2O
refractive index
n20/D 1.44
bp
61 °C/20 mmHg
density
0.91 g/mL at 25 °C
SMILES string
CN(C)C(C)(C)CO
InChI
1S/C6H15NO/c1-6(2,5-8)7(3)4/h8H,5H2,1-4H3
InChI key
XRIBIDPMFSLGFS-UHFFFAOYSA-N
Related Categories
General description
2-Dimethylamino-2-methylpropanol solution (DMAMP-80™) is a propanol amine derivative. It is applicable as synthetic intermediate, emulsifying amine and vapor phase corrosion inhibitor. It shows low volatility and higher catalytic activity which makes it a viable alternative to DMEA (dimethylethanolamine) owing in the foam formulation process. It is a non-lachrymator, shows low toxicity profile and has been approved by FDA for indirect food contact. 2-Dimethylamino-2-methyl-1-propanol (DMAMP) has been reported to show good antimicrobial properties against a mixed flora of fungi and bacteria in cutting fluids. The photocatalytic degradation of DMAMP in the presence of TiO2 particles and UV-A (λ = 365nm) radiation has been investigated.
Legal Information
DMAMP-80 is a trademark of Angus Chemie GmbH
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1
wgk_germany
WGK 1
flash_point_f
152.6 °F
flash_point_c
67 °C
Certificates of Analysis (COA)
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Chung-Shin Lu et al.
Journal of hazardous materials, 165(1-3), 306-316 (2008-11-18)
The present study deals with the photocatalytic degradation of the alkanolamine, 2-dimethylamino-2-methyl-1-propanol (DMAMP), in the presence of TiO(2) particles and UV-A (lambda=365 nm) radiation. The obtained results show complete oxidation of DMAMP after 20h, and a little over 90% of
Antimicrobial properties of butanolamines and propanolamines in metal working fluids.
Bennett EO, et al.
The Journal of General and Applied Microbiology, 25(2), 63-69 (1979)
M Sandin et al.
Antimicrobial agents and chemotherapy, 34(3), 491-493 (1990-03-01)
The antimicrobial effects of diethanolamine, dimethylamino-methyl-propanol, and butylethanolamine are greatly enhanced at high pH. Their antimicrobial activities are closely correlated with their uncharged forms, indicating that diffusion through cell membrane(s) is rate limiting for the antimicrobial action. Since these compounds
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