GB1187560A - Modified Amino Formaldehyde Compositions - Google Patents

Modified Amino Formaldehyde Compositions

Info

Publication number
GB1187560A
GB1187560A GB2465468A GB2465468A GB1187560A GB 1187560 A GB1187560 A GB 1187560A GB 2465468 A GB2465468 A GB 2465468A GB 2465468 A GB2465468 A GB 2465468A GB 1187560 A GB1187560 A GB 1187560A
Authority
GB
United Kingdom
Prior art keywords
alcohol
formaldehyde
resin
isobutoxymethyl
heated
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
GB2465468A
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.)
Scado Archer Daniels N V
Original Assignee
Scado Archer Daniels N V
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 Scado Archer Daniels N V filed Critical Scado Archer Daniels N V
Publication of GB1187560A publication Critical patent/GB1187560A/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G12/00—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
    • C08G12/02—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes
    • C08G12/40—Chemically modified polycondensates
    • C08G12/42—Chemically modified polycondensates by etherifying
    • C08G12/421—Chemically modified polycondensates by etherifying of polycondensates based on acyclic or carbocyclic compounds
    • C08G12/422—Chemically modified polycondensates by etherifying of polycondensates based on acyclic or carbocyclic compounds based on urea or thiourea
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G12/00—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
    • C08G12/02—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes
    • C08G12/40—Chemically modified polycondensates
    • C08G12/42—Chemically modified polycondensates by etherifying
    • C08G12/424—Chemically modified polycondensates by etherifying of polycondensates based on heterocyclic compounds
    • C08G12/425—Chemically modified polycondensates by etherifying of polycondensates based on heterocyclic compounds based on triazines

Landscapes

  • Chemical & Material Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Phenolic Resins Or Amino Resins (AREA)

Abstract

1,187,560. Etherified amine-formaldehyde condensates. SCADO - ARCHER - DANIELS N.V. 23 May, 1968 [23 May, 1967], No. 24654/68. Heading C3R. An etherified amine-formaldehyde condensate is prepared by etherifying less than one methylol group per amino group of an amineformaldehyde condensate with a C 1-5 alcohol then subjecting the product to ether-interchange with a hydroxyl compound less volatile than the first alcohol, in the presence of a boron halide catalyst. Suitable less volatile alcohols are C 8-22 alcohols; glycols, polyglycols and ethylene or propylene oxide condensates; and glycerol partial esters. In examples, an MF resin having on average 2À3 isobutoxymethyl groups per molecule of melamine is heated in the presence of BF 3 etherate with (1) octadecyl alcohol, (2) diethylene glycol, (3) pentaerythritol dilinoleate, and (4) an oil alkyd resin containing 52% oil and 35% phthalic anhydride and having a hydroxyl number above 40, and stearyl alcohol is also heated with (5) a UF resin having 0À55 methylol and 0À53 isobutoxymethyl groups per urea residue, and (6) a benzoguanamine resin containing 4 formaldehyde residues, 1À35 of them butoxymethyl groups, per residue of benzoguanamine. The products are useful in lacquers.
GB2465468A 1967-05-23 1968-05-23 Modified Amino Formaldehyde Compositions Expired GB1187560A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
NL6707091A NL131745C (en) 1967-05-23 1967-05-23

Publications (1)

Publication Number Publication Date
GB1187560A true GB1187560A (en) 1970-04-08

Family

ID=19800190

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2465468A Expired GB1187560A (en) 1967-05-23 1968-05-23 Modified Amino Formaldehyde Compositions

Country Status (5)

Country Link
BE (1) BE715487A (en)
DE (1) DE1770475A1 (en)
FR (1) FR1566965A (en)
GB (1) GB1187560A (en)
NL (1) NL131745C (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3814292A1 (en) * 1988-04-28 1989-11-09 Basf Ag AGENT FOR DRINKING FIBER FABRICS CONTAINING CELLULOSE

Also Published As

Publication number Publication date
NL6707091A (en) 1968-11-25
FR1566965A (en) 1969-05-09
DE1770475A1 (en) 1971-10-28
BE715487A (en) 1968-10-16
NL131745C (en)

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Legal Events

Date Code Title Description
PS Patent sealed
PLNP Patent lapsed through nonpayment of renewal fees