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About This Item
Linear Formula:
(C2H5)2NCH2N(C2H5)2
CAS Number:
Molecular Weight:
158.28
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
97%
refractive index
n20/D 1.426 (lit.)
bp
166-169 °C (lit.)
density
0.811 g/mL at 25 °C (lit.)
functional group
amine
SMILES string
CCN(CC)CN(CC)CC
InChI
1S/C9H22N2/c1-5-10(6-2)9-11(7-3)8-4/h5-9H2,1-4H3
InChI key
UNEXJVCWJSHFNN-UHFFFAOYSA-N
Related Categories
Application
N,N,N′,N′-Tetraethylmethanediamine has been used to study the tertiary amine catalytic activities in the reaction of phenyl isocyanate with 1-butanol in toluene.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
107.6 °F - closed cup
Flash Point(C)
42 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Tertiary Amine Catalysis of the Reaction of Phenyl Isocyanate with Alcohols.
BURKUS J
The Journal of Organic Chemistry, 26(3), 779-782 (1961)
Abdullah Alzahrani et al.
Organic & biomolecular chemistry, 16(22), 4108-4116 (2018-05-19)
The traditional thermal Mannich reaction is unsuitable for preparing polymerizable N-methylene amino substituted acrylamides and methacrylamides. Herein we provide a facile multi-gram high yield synthesis of these monomeric precursors to stimuli-responsive polymers by the addition of acrylamides and methacrylamides onto
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