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

CAS: 10543-57-4 Cat. No.: T115334 Peso molecular: 228.25 Beilstein Registry Number: 1795711 Número EC: 234-123-8 PubChem CID: 66347

GRADE & PURITY 92-94 %

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

Storage

Room temperature

Shipped In

Normal

Descripción general

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.

Specifications

Sinónimos

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

Especificaciones y pureza

92-94 %

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Nombres e identificadores

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

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase 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
• Clase: 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
• Descripción: 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

Data sources

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

Propiedades químicas y físicas

• Solubilidad: Soluble in chloroform and methylenechloride. Slightly soluble in water and acetone.
• Punto de fusión (°C): 152°C
• Peso molecular: 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 Ų
• 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

Referencias

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,      [PMID:] [10.1016/j.supflu.2021.105269]

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,      [PMID:] [10.1016/j.jmrt.2020.10.096]

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,      [PMID:] [10.1007/s12221-024-00628-y]