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447005

Sigma-Aldrich

N,N′-Di-tert-butylethylenediamine

98%

Synonym(s):

1,2-Bis(tert-butylamino)ethane

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About This Item

Linear Formula:
(CH3)3CNHCH2CH2NHC(CH3)3
CAS Number:
4062-60-6
Molecular Weight:
172.31
Beilstein:
1738432
EC Number:
223-769-6
MDL number:
MFCD00014996
UNSPSC Code:
12352100
PubChem Substance ID:
24868313
NACRES:
NA.22

Quality Level

100

Assay

98%

form

liquid

refractive index

n20/D 1.43 (lit.)

bp

196-198 °C (lit.)

density

0.799 g/mL at 25 °C (lit.)

SMILES string

CC(C)(C)NCCNC(C)(C)C

InChI

1S/C10H24N2/c1-9(2,3)11-7-8-12-10(4,5)6/h11-12H,7-8H2,1-6H3

InChI key

KGHYGBGIWLNFAV-UHFFFAOYSA-N

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Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

143.6 °F - closed cup

Flash Point(C)

62 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Silylene and Germylene Intermediates in the Reactions of Silole and Germole Dianions with N,N'-Di-tert-butylethylenediimine.
Toulokhonova IS, et al.
European Journal of Inorganic Chemistry, 14, 2344-2349 (2008)
Aluminium amides derived from metallation of N,N'-di-tert-butylethylenediamine.
Gardiner MG, et al.
J. Chem. Soc., Dalton Trans., 22, 4163-4169 (1996)
Michael G. Gardiner et al.
Inorganic chemistry, 35(13), 4047-4059 (1996-06-19)
The lithiation of N,N'-di-tert-butylethylenediamine by MeLi in benzene has been shown by (1)H NMR spectroscopy to proceed via the partially lithiated species [cis-{Li[&mgr;-N(t-Bu)CH(2)CH(2)N(H)t-Bu]}(2)], 2, and [{Li[N(t-Bu)CH(2)CH(2)N(H)t-Bu]}(2)Li{N(t-Bu)CH(2)CH(2)Nt-Bu}Li], 3, prior to the formation of the dilithiated species {Li[N(t-Bu)CH(2)CH(2)Nt-Bu]Li}, 4. The solid state
New chemistry from the reaction of N, N'-disubstituted ethylenediamines with glyoxal: synthesis of 2-imidazolidinecarboxaldehydes and 1, 4, 6, 9-tetraalkyl-1, 4, 6, 9-tetraaza-5, 10-dioxaperhydroanthracenes.
Willer RL, et al.
The Journal of Organic Chemistry, 50(13), 2368-2372 (1985)
Meishan Chen et al.
Molecules (Basel, Switzerland), 24(8) (2019-04-21)
In recent years, polyureas with dynamic hindered urea bonds (HUBs), a class of promising biomedical polymers, have attracted wide attention as a result of their controlled hydrolytic properties. The effect of the chemical structures on the properties of polyureas and
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