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Key Documents

38990

Sigma-Aldrich

2-Dimethylaminoethanol

purum, ≥98.0% (GC)

Synonym(s):

Deanol, N,N-Dimethyl-2-hydroxyethylamine, N,N-Dimethylethanolamine, Jeffcat DMEA

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About This Item

Linear Formula:
(CH3)2NCH2CH2OH
CAS Number:
Molecular Weight:
89.14
Beilstein:
1209235
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor pressure

100 mmHg ( 55 °C)
6.12 mmHg ( 20 °C)

Quality Level

grade

purum

Assay

≥98.0% (GC)

refractive index

n20/D 1.4294 (lit.)
n20/D 1.430

bp

134-136 °C (lit.)

mp

−70 °C (lit.)

solubility

H2O: soluble

density

0.886 g/mL at 20 °C (lit.)

functional group

amine

SMILES string

CN(C)CCO

InChI

1S/C4H11NO/c1-5(2)3-4-6/h6H,3-4H2,1-2H3

InChI key

UEEJHVSXFDXPFK-UHFFFAOYSA-N

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Application

2-Dimethylaminoethanol (Deanol) can be used to functionalize the sensitizers in dye-sensitized solar cells to prevent aggregation and to increase the dye adsorption density. It is used in the synthesis of NNO-tridentate Schiff base ligands to prepare zinc alkoxide complexes that catalyze ring-opening polymerization of L-lactide. It is also used in the preparation of ionic liquids.

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

104.0 °F - Seta closed cup

Flash Point(C)

40 °C - Seta closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Molecular engineering of zinc phthalocyanine sensitizers for efficient dye-sensitized solar cells.
Ikeuchi, Takuro et al.
Chemical Communications (Cambridge, England), 50(16), 1941-1943 (2014)
Dual functions of N, N-dimethylethanolamnium-based ionic liquids for the Knoevenagel reactions at room temperature.
Zhu, Anlian et al.
Catalysis Today, 200(11), 17-23 (2013)
Ring-opening polymerization of lactides initiated by zinc alkoxides derived from NNO-tridentate ligands.
Chen H Y, et al.
Macromolecules, 39(11), 3745-3752 (2006)
Ouassila Amiri-Attou et al.
Molecules (Basel, Switzerland), 10(3), 545-551 (2007-11-17)
We report herein the synthesis of substituted 2-(6-nitrobenzo[1,3]dioxol-5-yl)-1- aryl ethanols and 2-(6-nitrobenzo[1,3]dioxol-5-yl)-propionic acid ethyl esters from the reaction of 5-chloromethyl-6-nitrobenzo[1,3]dioxole with various aromatic carbonyl and alpha- carbonyl ester derivatives using the tetrakis(dimethylamino)ethylene (TDAE) methodology.
Zhifeng Fu et al.
Analytica chimica acta, 638(2), 220-224 (2009-03-31)
Numerous drugs are carboxylic acid derivatives containing amino group, and hydrolysis reaction of these agents often generates toxic amines. Thus, the detection of amine impurity is of great importance in drug quality control of these amino group-containing ester and amide.

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