Grundinformationen
- Standard-SMILES
CC(=O)N(CCN(C(C)=O)C(C)=O)C(C)=O- InChIKey
BGRWYDHXPHLNKA-UHFFFAOYSA-N- Summenformel
- C10H16N2O4
- Durchschnittliche Molmasse
- 228,24 g/mol
- Monoisotopische Masse
- 228,11100699
Überblick
Tetraacetylethylenediamine is a dicarboximide.
Namen und Bezeichner
- Bevorzugter Name
- Tetraacetylethylenediamine
- IUPAC
- N-acetyl-N-[2-(diacetylamino)ethyl]acetamide
- Lokaler Name
- N,N'-Ethylenbis[N-acetylacetamid]
- Englischer Name
- Tetraacetylethylenediamine
- Summenformel
- C10H16N2O4
- Molmasse
- 228.24
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
10543-57-4- PubChem CID
- 66347
- DTXSID
DTXSID5040752- ChEBI
CHEBI:166456- UNII
- P411ED0N2B
- EC Number
- 234-123-8
- Nikkaji
- J150.345F
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- -1,2
- Polarare Oberfläche (TPSA)
- 74,8 Ų
- H-Brücken-Donoren
- 0
- H-Brücken-Akzeptoren
- 4
- Frei drehbare Bindungen
- 3
- Schwere Atome
- 16
- Formalladung
- 0
- Komplexität
- 265
Experimentelle und physikochemische Eigenschaften
Physical Description
Large Crystals; Dry Powder; Other Solid
Solid
Physikochemische Eigenschaften
- Schmelzpunkt
- 149 · 149-154 °C
- Siedepunkt
- 140 °C · 140 °C (1.5002 mmHg)
- Dichte
- 0.9 · 0.9
- Brechungsindex
- 1.455 · 1.4550 (estimate)
- Flammpunkt
- 140 °C · 140 °C
- pka
- -1.23 · -1.23±0.70(Predicted)
- Aggregatzustand
- Granular Powder
- Farbe
- Off-white to beige
- Wasserlöslichkeit
- slightly soluble
- Merck
- 14 · 14,9028
- BRN
- 1795711 · 1795711
- Kosmetik-Inhaltsstoffe Funktionen
- BLEACHING
- 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(C)=O)C(C)=O)C(C)=O
- CAS Datenbank
- 10543 · 10543-57-4(CAS DataBase Reference)
- NIST chemische Informationen
- N,n,n',n'-tetraacetylethylenediamine(10543-57-4)
- EPA chemische Informationen
- Tetraacetylethylenediamine (10543-57-4)
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
This chemical does not meet GHS hazard criteria for 100% (435 of 435) of all reports.
Not Classified
Aggregated GHS information provided per 435 reports by companies from 1 notifications to the ECHA C&L Inventory.
Gefahrenhinweise
Regulatory Information
Chemical: Acetamide, N,N'-1,2-ethanediylbis[N-acetyl-
Acetamide, N,N'-1,2-ethanediylbis[N-acetyl- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Acetamide, N,N'-1,2-ethanediylbis[N-acetyl- are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)
Status: Active Update: 11-04-2014 https://echa.europa.eu/registration-dossier/-/registered-dossier/14315
Tetraacetyl ethylenediamine: Does not have an individual approval but may be used under an appropriate group standard
Sicherheitsdaten
- wgk
- 1
- tsca
- TSCA listed
- hs_code
- 29241900
- safety_code
- 22-24/25
- Speicherklasse
- 11 - Combustible Solids
Chemie und Industrie
Pharmakologische Informationen
Verwendung und Herstellung
Use Classification
EPA Safer Chemical Functional Use Classes -> Oxidants and Oxidant Stabilizers
Safer Chemical Classes -> Yellow triangle - The chemical has met Safer Choice Criteria for its functional ingredient-class, but has some hazard profile issues
Cosmetics -> Bleaching
General Manufacturing Information
Wholesale and Retail Trade
Acetamide, N,N'-1,2-ethanediylbis[N-acetyl-: ACTIVE
Anwendungen
VerwendenTetraacetylethylenediamine (TAED) is a bleaching activator which is mainly used in detergents and additives for laundry washing and dishwashing. Typical concentrations of TAED range between 1.4% and 13% in these products. A small amount of the produced TAED is also used in bleaching of paper, textiles and for the generation of Peracetic acid. Peroxide bleach activator for household detergents, paper pulp.
Darstellung
synthetischeTetraacetylethylenediamine (TAED) is produced in a two stage process from ethylenediamine (ED) and acetic anhydride (Ac2O). ED is first diacetylated to DAED. In the second step DAED is subsequently converted with Ac2O via TriAED into TAED (Clariant, 1999). TAED is crystallized out of the reaction mixture, filtered, washed and dried, and if necessary also granulated. The raw materials used occur almost quantitatively in the product. Byproducts are not formed. TAED was prepared by acetylation of diacetylethylenediamine (DAED) with acetic anhydride in a 5 L reactor coupled with a packed distillation column, 2.5 cm in inside diameter and 1 m in length. The reaction temperature was set at 135 °C and the reflux ratio at 6. The molar ratio of acetic anhydride to DAED was varied from 3 to 5. A TAED yield as high as 80% was obtained, higher by 15% than in the absence of distillation.
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