86545
N,N,N′,N′-Tetraacetylethylenediamine
technical, ≥90% (CHN)
Sinónimos:
TAED, N,N′-Ethylenebis(diacetamide)
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About This Item
Fórmula empírica (notación de Hill):
C10H16N2O4
Número de CAS:
Peso molecular:
228.25
Beilstein/REAXYS Number:
1795711
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Productos recomendados
grade
technical
Quality Level
assay
≥90% (CHN)
form
crystals
functional group
amide
imide
SMILES string
CC(=O)N(CCN(C(C)=O)C(C)=O)C(C)=O
InChI
1S/C10H16N2O4/c1-7(13)11(8(2)14)5-6-12(9(3)15)10(4)16/h5-6H2,1-4H3
InChI key
BGRWYDHXPHLNKA-UHFFFAOYSA-N
Categorías relacionadas
Application
N, N, N′, N′-Tetraacetylethylenediamine (TAED) can be used as a reagent:
It can also be used as a peroxide bleach activator in laundry detergents and in textile chemistry applications.
- Along with sodium perborate and sodium bicarbonate for the oxidation of primary aliphatic amines to aliphatic C-nitroso compounds.
- In combination with sodium percarbonate to deliver peracetic acid in situ for Baeyer-Villiger oxidation.
It can also be used as a peroxide bleach activator in laundry detergents and in textile chemistry applications.
Storage Class
11 - Combustible Solids
wgk_germany
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Los clientes también vieron
N,N,N',N'-Tetraacetylethylenediamin and sodium percarbonate reagents as an in situ produsing of peracetic acid for Baeyer-Villiger oxidation of ketones.
M.Hashemi, Mohammed and Khezri, S.Hadi
Organic Chemistry: An Indian Journal, 2(4), 56-59 (2006)
Kinetics of the hydrolysis and perhydrolysis of tetraacetylethylenediamine, a peroxide bleach activator.
Martin
Journal of the Chemical Society, 696(10), 1549-1552 (1991)
Kinetics of the hydrolysis and perhydrolysis of tetraacetylethylenediamine, a peroxide bleach activator
Martin D, et al.
J. Chem. Soc. Perkin Trans. II, 2(10), 1549-1552 (1991)
Oxidation of primary aliphatic amines with sodium perborate
Zajac Jr WW, et al.
Tetrahedron Letters, 30(47), 6495-6496 (1989)
Muhammad Naveed Khan et al.
International journal of biological macromolecules, 153, 72-78 (2020-03-07)
In the current study, cellulose was extracted from the plant dunchi fiber by using an ecofriendly method followed by preparation of nanocellulose. The procedure involved an alkali treatment and chlorine-free bleaching for removal of lignin and hemicelluloses from material. Fourier
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