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Sigma-Aldrich

2-Dimethylamino-2-methylpropanol solution

80% in H2O, technical grade

Sinônimo(s):

DMAMP-80

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About This Item

Fórmula linear:
(CH3)2C(CH2OH)N(CH3)2
Número CAS:
Peso molecular:
117.19
Beilstein:
1732837
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22

grau

technical grade

forma

liquid

concentração

80% in H2O

índice de refração

n20/D 1.44

pb

61 °C/20 mmHg

densidade

0.91 g/mL at 25 °C

cadeia de caracteres SMILES

CN(C)C(C)(C)CO

InChI

1S/C6H15NO/c1-6(2,5-8)7(3)4/h8H,5H2,1-4H3

chave InChI

XRIBIDPMFSLGFS-UHFFFAOYSA-N

Descrição geral

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.

Informações legais

DMAMP-80 is a trademark of Angus Chemie GmbH

Pictogramas

Corrosion

Palavra indicadora

Danger

Frases de perigo

Classificações de perigo

Eye Dam. 1 - Skin Corr. 1

Código de classe de armazenamento

8A - Combustible corrosive hazardous materials

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

152.6 °F - Tag closed cup

Ponto de fulgor (°C)

67 °C - Tag closed cup


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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
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)
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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