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Merck
CN

423041

2-二甲胺基-2-甲基丙醇 溶液

80% in H2O, technical grade

别名:

DMAMP-80

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关于此项目

线性分子式:
(CH3)2C(CH2OH)N(CH3)2
化学文摘社编号:
分子量:
117.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1732837
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产品名称

2-二甲胺基-2-甲基丙醇 溶液, 80% in H2O, technical grade

InChI

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

SMILES string

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

InChI key

XRIBIDPMFSLGFS-UHFFFAOYSA-N

grade

technical grade

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

functional group

amine
hydroxyl

Quality Level

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

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1

存储类别

8A - Combustible corrosive hazardous materials

wgk

WGK 1

flash_point_f

152.6 °F - Tag closed cup

flash_point_c

67 °C - Tag closed cup


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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)
Api Api
API Polyurethanes Expo 2001, 552-554 (2001)
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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