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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
EC Number:
202-845-2
UNSPSC Code:
12352200
PubChem Substance ID:
Beilstein/REAXYS Number:
741863
MDL number:
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InChI key

BFSVOASYOCHEOV-UHFFFAOYSA-N

InChI

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

SMILES string

CCN(CC)CCO

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.)

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Ryota Mizushima et al.
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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
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
Peter H Otto et al.
Veterinary microbiology, 179(3-4), 168-176 (2015-08-01)
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
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
Elizabeth C Schramm et al.
Blood, 125(15), 2359-2369 (2015-01-23)
The pathogenesis of atypical hemolytic uremic syndrome (aHUS) is strongly linked to dysregulation of the alternative pathway of the complement system. Mutations in complement genes have been identified in about two-thirds of cases, with 5% to 15% being in C3.

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