Show legend Show as text

Structure type: polymer chemical repeating unit ; 32500
Compound class: glucuronoxylan
Contained glycoepitopes: IEDB_114701,IEDB_115136,IEDB_140630,IEDB_167188,IEDB_174332

• Article ID: 11341
  Ebringerova A, Srokova I, Talaba P, Kačuráková M, Hromádková Z "Amphiphilic beechwood glucuronoxylan derivatives" - Journal of Applied Polymer Science 97(9) (1998) 1523-1530
  

  Long alkyl chains (C-12) have been introduced onto glucuronoxylan and its sulfoethyl derivative via O-alkylation using 1-bromododecane in dimethylsulfoxide. The new amphiphilic xylan derivatives were characterized by chemical, elemental, and spectral analyses. They reduce the surface tension and exhibit remarkable emulsifying and protein foam-stabilizing properties. The results indicate that the development of new biopolymeric surfactants may be based on heteroxylans that are abundant in hardwoods and annual plants, and represent an unexploited renewable polysaccharide resource.

  structure, surface tension, beechwood glucuronoxylan, amphiphilic derivative, foamability, emulsifying efficiency

  Publication DOI: 10.1002/(SICI)1097-4628(19980228)67:9<1523::AID-APP3>3.0.CO;2-F
  Journal NLM ID: 9891577
  Publisher: Wiley
  Institutions: Institute of Chemistry, Slovak Academy of Sciences, Bratislava, Slovak Republic, Department of Fibres and Textile, Faculty of Chemical Technology, Slovak Technical University, Bratislava, Slovak Republic
  Methods: 13C NMR, 1H NMR, elemental analysis, HPGPC, DEPT, determination of surface tension, FT-IR, titration
  
   
  
  (Fagaceae)
  CSDB ID 61347 (all data & tools)

Show legend Show as text

Structure type: polymer chemical repeating unit ; 30000
Compound class: glucuronoxylan
Contained glycoepitopes: IEDB_114701,IEDB_115136,IEDB_140630,IEDB_167188,IEDB_174332

• Article ID: 11341
  Ebringerova A, Srokova I, Talaba P, Kačuráková M, Hromádková Z "Amphiphilic beechwood glucuronoxylan derivatives" - Journal of Applied Polymer Science 97(9) (1998) 1523-1530
  

  Long alkyl chains (C-12) have been introduced onto glucuronoxylan and its sulfoethyl derivative via O-alkylation using 1-bromododecane in dimethylsulfoxide. The new amphiphilic xylan derivatives were characterized by chemical, elemental, and spectral analyses. They reduce the surface tension and exhibit remarkable emulsifying and protein foam-stabilizing properties. The results indicate that the development of new biopolymeric surfactants may be based on heteroxylans that are abundant in hardwoods and annual plants, and represent an unexploited renewable polysaccharide resource.

  structure, surface tension, beechwood glucuronoxylan, amphiphilic derivative, foamability, emulsifying efficiency

  Publication DOI: 10.1002/(SICI)1097-4628(19980228)67:9<1523::AID-APP3>3.0.CO;2-F
  Journal NLM ID: 9891577
  Publisher: Wiley
  Institutions: Institute of Chemistry, Slovak Academy of Sciences, Bratislava, Slovak Republic, Department of Fibres and Textile, Faculty of Chemical Technology, Slovak Technical University, Bratislava, Slovak Republic
  Methods: 13C NMR, 1H NMR, elemental analysis, HPGPC, DEPT, determination of surface tension, FT-IR, titration
  
   
  
  (Fagaceae)
  CSDB ID 61348 (all data & tools)

Show legend Show as text

Structure type: polymer chemical repeating unit ; 29500
Compound class: glucuronoxylan
Contained glycoepitopes: IEDB_114701,IEDB_115136,IEDB_140630,IEDB_167188,IEDB_174332

• Article ID: 11341
  Ebringerova A, Srokova I, Talaba P, Kačuráková M, Hromádková Z "Amphiphilic beechwood glucuronoxylan derivatives" - Journal of Applied Polymer Science 97(9) (1998) 1523-1530
  

  Long alkyl chains (C-12) have been introduced onto glucuronoxylan and its sulfoethyl derivative via O-alkylation using 1-bromododecane in dimethylsulfoxide. The new amphiphilic xylan derivatives were characterized by chemical, elemental, and spectral analyses. They reduce the surface tension and exhibit remarkable emulsifying and protein foam-stabilizing properties. The results indicate that the development of new biopolymeric surfactants may be based on heteroxylans that are abundant in hardwoods and annual plants, and represent an unexploited renewable polysaccharide resource.

  structure, surface tension, beechwood glucuronoxylan, amphiphilic derivative, foamability, emulsifying efficiency

  Publication DOI: 10.1002/(SICI)1097-4628(19980228)67:9<1523::AID-APP3>3.0.CO;2-F
  Journal NLM ID: 9891577
  Publisher: Wiley
  Institutions: Institute of Chemistry, Slovak Academy of Sciences, Bratislava, Slovak Republic, Department of Fibres and Textile, Faculty of Chemical Technology, Slovak Technical University, Bratislava, Slovak Republic
  Methods: 13C NMR, 1H NMR, elemental analysis, HPGPC, DEPT, determination of surface tension, FT-IR, titration
  
   
  
  (Fagaceae)
  CSDB ID 61349 (all data & tools)

Show legend Show as text

Structure type: polymer chemical repeating unit ; 31800
Compound class: glucuronoxylan
Contained glycoepitopes: IEDB_114701,IEDB_115136,IEDB_140630,IEDB_167188,IEDB_174332

• Article ID: 11341
  Ebringerova A, Srokova I, Talaba P, Kačuráková M, Hromádková Z "Amphiphilic beechwood glucuronoxylan derivatives" - Journal of Applied Polymer Science 97(9) (1998) 1523-1530
  

  Long alkyl chains (C-12) have been introduced onto glucuronoxylan and its sulfoethyl derivative via O-alkylation using 1-bromododecane in dimethylsulfoxide. The new amphiphilic xylan derivatives were characterized by chemical, elemental, and spectral analyses. They reduce the surface tension and exhibit remarkable emulsifying and protein foam-stabilizing properties. The results indicate that the development of new biopolymeric surfactants may be based on heteroxylans that are abundant in hardwoods and annual plants, and represent an unexploited renewable polysaccharide resource.

  structure, surface tension, beechwood glucuronoxylan, amphiphilic derivative, foamability, emulsifying efficiency

  Publication DOI: 10.1002/(SICI)1097-4628(19980228)67:9<1523::AID-APP3>3.0.CO;2-F
  Journal NLM ID: 9891577
  Publisher: Wiley
  Institutions: Institute of Chemistry, Slovak Academy of Sciences, Bratislava, Slovak Republic, Department of Fibres and Textile, Faculty of Chemical Technology, Slovak Technical University, Bratislava, Slovak Republic
  Methods: 13C NMR, 1H NMR, elemental analysis, HPGPC, DEPT, determination of surface tension, FT-IR, titration
  
   
  
  (Fagaceae)
  CSDB ID 61350 (all data & tools)