GB990390A - Polyurethane polymers and process for their preparation - Google Patents

Polyurethane polymers and process for their preparation

Info

Publication number
GB990390A
GB990390A GB690962A GB690962A GB990390A GB 990390 A GB990390 A GB 990390A GB 690962 A GB690962 A GB 690962A GB 690962 A GB690962 A GB 690962A GB 990390 A GB990390 A GB 990390A
Authority
GB
United Kingdom
Prior art keywords
reacting
alkyl
derivative
diamine
alkyl glucoside
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB690962A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Unilever Bestfoods North America
Original Assignee
Unilever Bestfoods North America
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Unilever Bestfoods North America filed Critical Unilever Bestfoods North America
Publication of GB990390A publication Critical patent/GB990390A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H15/00Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
    • C07H15/02Acyclic radicals, not substituted by cyclic structures
    • C07H15/04Acyclic radicals, not substituted by cyclic structures attached to an oxygen atom of the saccharide radical
    • C07H15/08Polyoxyalkylene derivatives
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/48Polyethers
    • C08G18/487Polyethers containing cyclic groups
    • C08G18/4883Polyethers containing cyclic groups containing cyclic groups having at least one oxygen atom in the ring

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Biochemistry (AREA)
  • Biotechnology (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Molecular Biology (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Polyethers (AREA)
  • Saccharide Compounds (AREA)

Abstract

A polyurethane is obtained by reacting a polyoxalkylene alkyl glocoside with an organic polyisocyanate. The alkyl glucoside may be the methyl, ethyl, propyl or butyl derivative and preferably 2-90 mols. of ethylene oxide or propylene oxide is used per mol. of alkyl glucoside at a temperature of 200-400 DEG F. in the presence of an alkaline catalyst, to give a derivative having a molecular weight of 300 and 5000. Specified polyisocyanates are the toluene and tolylene disocyanates. A cellular product may be obtained by reacting in the presence a blowing agent, such as trichlorofluoromethane, an amine catalyst such as tetramethyl butane 1,4-diamine, or triethylene diamine, together with stannous octoate. A silicone emulsifier, lecithin and N-ethylmopholine may also be used.
GB690962A 1961-03-01 1962-02-22 Polyurethane polymers and process for their preparation Expired GB990390A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US9271861A 1961-03-01 1961-03-01
US9498161A 1961-03-13 1961-03-13

Publications (1)

Publication Number Publication Date
GB990390A true GB990390A (en) 1965-04-28

Family

ID=26785967

Family Applications (1)

Application Number Title Priority Date Filing Date
GB690962A Expired GB990390A (en) 1961-03-01 1962-02-22 Polyurethane polymers and process for their preparation

Country Status (5)

Country Link
BE (1) BE614434A (en)
CH (1) CH395046A (en)
DE (1) DE1443556A1 (en)
GB (1) GB990390A (en)
NL (1) NL275362A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4629768A (en) * 1986-05-02 1986-12-16 Olin Corporation Thermally stable polyurethane elastomers containing glycoside polyols and a method of producing them
GB8829033D0 (en) * 1988-12-13 1989-01-25 Univ Manchester Formation of polyether polyols

Also Published As

Publication number Publication date
DE1443556A1 (en) 1969-03-20
NL275362A (en)
BE614434A (en)
CH395046A (en) 1965-07-15

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