推荐产品
等級
technical grade
形狀
liquid
濃度
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 字串
CN(C)C(C)(C)CO
InChI
1S/C6H15NO/c1-6(2,5-8)7(3)4/h8H,5H2,1-4H3
InChI 密鑰
XRIBIDPMFSLGFS-UHFFFAOYSA-N
一般說明
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.
法律資訊
DMAMP-80 is a trademark of Angus Chemie GmbH
訊號詞
Danger
危險聲明
危險分類
Eye Dam. 1 - Skin Corr. 1
儲存類別代碼
8A - Combustible corrosive hazardous materials
水污染物質分類(WGK)
WGK 1
閃點(°F)
152.6 °F - Tag closed cup
閃點(°C)
67 °C - Tag closed cup
其他客户在看
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
API Polyurethanes Expo 2001, 552-554 (2001)
Antimicrobial properties of butanolamines and propanolamines in metal working fluids.
The Journal of General and Applied Microbiology, 25(2), 63-69 (1979)
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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