所有图片(2)
About This Item
线性分子式:
(CH3)2C(CH2OH)N(CH3)2
CAS号:
分子量:
117.19
Beilstein:
1732837
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
等级
technical grade
质量水平
形式
liquid
浓度
80% in H2O
折射率
n20/D 1.44
bp
61 °C/20 mmHg
密度
0.91 g/mL at 25 °C
SMILES字符串
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
一般描述
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.
法律信息
DMAMP-80 is a trademark of Angus Chemie GmbH
警示用语：
Danger
危险声明
危险分类
Eye Dam. 1 - Skin Corr. 1
WGK
WGK 1
闪点(°F)
152.6 °F
闪点(°C)
67 °C
法规信息
新产品
Api Api
API Polyurethanes Expo 2001, 552-554 (2001)
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)
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
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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