270032
N,N′-Dimethylethylenediamine
85%
Synonym(s):
1,2-Bis(methylamino)ethane
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All Photos(2)
About This Item
Linear Formula:
CH3NHCH2CH2NHCH3
CAS Number:
Molecular Weight:
88.15
Beilstein:
878142
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
85%
form
liquid
refractive index
n20/D 1.431 (lit.)
bp
119 °C (lit.)
density
0.819 g/mL at 20 °C (lit.)
functional group
amine
SMILES string
CNCCNC
InChI
1S/C4H12N2/c1-5-3-4-6-2/h5-6H,3-4H2,1-2H3
InChI key
KVKFRMCSXWQSNT-UHFFFAOYSA-N
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Application
N,N′-Dimethylethylenediamine was used to enhance CO2 adsorption. It was incorporated into H3[(Cu4Cl)3(BTTri)8 (CuBTTri; H3BTTri = 1,3,5-tri(1H-1,2,3-triazol-4-yl)benzene), a water-stable, triazolate-bridged framework, to form a metal–organic framework for CO2 separation.
Other Notes
remainder N-Methylethylenediamine
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)
78.8 °F - closed cup
Flash Point(C)
26 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Enhanced carbon dioxide capture upon incorporation of N, N?-dimethylethylenediamine in the metal?organic framework CuBTTri.
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PEGylated polyamidoamine (PAA) polymers were investigated for the production of sterically stabilised DNA delivery systems. Comparison of a PEGylated polymer (NG47) with a non-PEGylated polymer (NG49) showed similar binding of co-polymer to DNA by displacement of ethidium bromide (EB) and
Takenao Odagami et al.
Chemical & pharmaceutical bulletin, 57(2), 211-213 (2009-02-03)
The deprotection of the indole (N(ind))-formyl (For) group on Trp was achieved in a 95% yield using N,N'-dimethylethylendiamine (DMEDA) (1.5, 2.0, 3.0 eq) in water at room temperature. A new reagent was successfully applied to the deprotection of a model
J G Qian et al.
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Chandi C Malakar et al.
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Water makes it possible: The Cu(2)O-catalyzed reaction between easily available o-bromobenzylbromides and benzamidines by using Cs(2)CO(3) as the base and N,N'-dimethylethylenediamine (DMEDA) as the additive in water as the solvent gives access to substituted quinazolines in a single step with
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