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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.)

functional group

amine

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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Related Categories

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 2 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

447005-BULK:
447005-5ML:
447005-VAR:
447005-25ML:

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Certificates of Analysis (COA)

Lot/Batch Number
MKBF5169V
13628PN
16914JN
03525LO
50921006

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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)
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)
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
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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Global Trade Item Number

SKUGTIN
447005-5ML4061836826970
447005-25ML4061836826963

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