Basic Description

Synonyms	EC 234-123-8 \| AKOS005207256 \| J-001421 \| N-Acetyl-N-[2-(diacetylamino)ethyl]acetamide \| D92422 \| N,N,N',N'-Tetraacetylethylenediamine, technical, >=90% (CHN) \| SCHEMBL20390 \| Tetraacetylethylenediamine \| UNII-P411ED0N2B \| n,n,n',n'-tetraacetyl ethylenedi
Specifications & Purity	92-94 %
Shipped In	Normal
Product Description	application： N, N, N′, N′-Tetraacetylethylenediamine (TAED) can be used as a reagent: 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.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic acids and derivatives
  - Class Carboxylic acids and derivatives
    - Subclass Carboxylic acid derivatives
      - Level5 Carboxylic acid imides
        Level6 N-substituted carboxylic acid imides

Kingdom	Organic compounds
Superclass	Organic acids and derivatives
Class	Carboxylic acids and derivatives
Subclass	Carboxylic acid derivatives
Intermediate Tree Nodes	Carboxylic acid imides
Direct Parent	N-substituted carboxylic acid imides
Alternative Parents	Dicarboximides Acetamides Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aliphatic acyclic compounds
Substituents	Carboxylic acid imide, n-substituted - Acetamide - Dicarboximide - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as n-substituted carboxylic acid imides. These are compounds comprising an N-substituted carboxylic acid imide group, with the general structure R1N(C(R2)=O)C(R3)=O (R2,R3=H, alkyl, aryl; R1=Anything but H).
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Names and Identifiers

Pubchem Sid	488183784
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488183784
IUPAC Name	N-acetyl-N-[2-(diacetylamino)ethyl]acetamide
INCHI	InChI=1S/C10H16N2O4/c1-7(13)11(8(2)14)5-6-12(9(3)15)10(4)16/h5-6H2,1-4H3
InChIKey	BGRWYDHXPHLNKA-UHFFFAOYSA-N
Smiles	CC(=O)N(CCN(C(=O)C)C(=O)C)C(=O)C
Isomeric SMILES	CC(=O)N(CCN(C(=O)C)C(=O)C)C(=O)C
WGK Germany	1
PubChem CID	66347
Molecular Weight	228.25
Beilstein	1795711
Reaxy-Rn	1795711

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

9 results found

Lot Number	Certificate Type	Date	Item
D2122029	Certificate of Analysis	Feb 11, 2025	T115334
D2122028	Certificate of Analysis	Feb 07, 2025	T115334
G2415020	Certificate of Analysis	Apr 26, 2024	T115334
L2410041	Certificate of Analysis	Apr 26, 2024	T115334
D2509106	Certificate of Analysis	Apr 26, 2024	T115334
C1906100	Certificate of Analysis	Dec 12, 2022	T115334
B2314078	Certificate of Analysis	Aug 13, 2021	T115334
L2410030	Certificate of Analysis	Aug 13, 2021	T115334
J2312095	Certificate of Analysis	Aug 13, 2021	T115334

Chemical and Physical Properties

Solubility	Soluble in chloroform and methylenechloride. Slightly soluble in water and acetone.
Melt Point(°C)	152°C
Molecular Weight	228.240 g/mol
XLogP3	-1.200
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	4
Rotatable Bond Count	3
Exact Mass	228.111 Da
Monoisotopic Mass	228.111 Da
Topological Polar Surface Area	74.800 Å²
Heavy Atom Count	16
Formal Charge	0
Complexity	265.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Yuan-Bin Zheng, Jian-Xin Jia, Wei Shi, Jia-Jie Long. (2021) A sustainable one-step pretreatment of cotton gray fabric with 18-crown-6 as phase transfer in supercritical carbon dioxide. JOURNAL OF SUPERCRITICAL FLUIDS, 175 (105269).
2. Weiming Wang, Meng Xu, Jiahao Lou, Aixue Dong. (2020) Changes in physicomechanical properties and structures of jute fibers after tetraacetylethylenediamine activated hydrogen peroxide treatment. Journal of Materials Research and Technology-JMR&T, 9 (15412).
3. Wang Xiaoyan, Fu Jiangpeng, Gu Fuyang, Du Jinmei, Xiao Guowei, Jiang Yang, Shao Dongyan, Xu Changhai. (2024) Roles of Electrostatic Interactions in the Peroxide System for Bleaching of Cotton Fabric. FIBERS AND POLYMERS, (1-10).

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SKU	Size	Availability	Price
T115334-10g	10g	2	$34.90
T115334-25g	25g	1	$65.90
T115334-50g	50g	3	$117.90
T115334-100g	100g	3	$255.90
T115334-250g	250g	4	$574.90
T115334-500g	500g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$1,034.90

N,N,N,N-Tetraacetylethylenediamine - 92-94 %, high purity , CAS No.10543-57-4