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Merck
CN

240044

2-(Diethylamino)ethanol

≥99%

Synonym(s):

N,N-Diethylethanolamine, DEAE, DEEA

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About This Item

Linear Formula:
(C2H5)2NCH2CH2OH
CAS Number:
Molecular Weight:
117.19
Beilstein:
741863
EC Number:
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
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vapor density

4.04 (vs air)

vapor pressure

1 mmHg ( 20 °C)

Assay

≥99%

expl. lim.

11.7 %

refractive index

n20/D 1.441 (lit.)

bp

161 °C (lit.)

density

0.884 g/mL at 25 °C (lit.)

SMILES string

CCN(CC)CCO

InChI

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

InChI key

BFSVOASYOCHEOV-UHFFFAOYSA-N

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Peter H Otto et al.
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Rotaviruses (RVs) are a major cause of neonatal diarrhoea in humans and animals worldwide. In this study, 425 faecal samples were collected between 1999 and 2013 from diarrhoeic livestock and companion animals at different locations in Germany and tested for
Rachel Kerwin et al.
eLife, 4 (2015-04-14)
Natural populations persist in complex environments, where biotic stressors, such as pathogen and insect communities, fluctuate temporally and spatially. These shifting biotic pressures generate heterogeneous selective forces that can maintain standing natural variation within a species. To directly test if
Stephen P Miller et al.
Chembiochem : a European journal of chemical biology, 15(8), 1145-1153 (2014-05-07)
An active site lysine essential to catalysis in isocitrate dehydrogenase (IDH) is absent from related enzymes. As all family members catalyze the same oxidative β-decarboxylation at the (2R)-malate core common to their substrates, it seems odd that an amino acid
Ryota Mizushima et al.
PloS one, 9(6), e98554-e98554 (2014-06-06)
MutL is a multi-domain protein comprising an N-terminal ATPase domain (NTD) and C-terminal dimerization domain (CTD), connected with flexible linker regions, that plays a key role in DNA mismatch repair. To expand understanding of the regulation mechanism underlying MutL endonuclease
Mariya S Spasova et al.
Experimental biology and medicine (Maywood, N.J.), 239(6), 724-736 (2014-04-15)
Inter-alpha inhibitor proteins (IAIPs) found in relatively high concentrations in human plasma are important in inflammation. IAIPs attenuate brain damage in young and adult subjects, decrease during sepsis and necrotizing enterocolitis in premature infants, and attenuate sepsis-related inflammation in newborn

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