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1,2,6-Thiadiazine-3,5-dione-1,1-dioxides and their use as polymerization accelerators

Assignee: Abitz Morf Gritschneder
•
Filing: 1982-02-18
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Granted: 1984-04-17
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Expires: 2002-02-18
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Abstract

Abstract 1,2,6-Thiadiazine-3,5-dione-1,1-dioxides of the general formula ##STR1## wherein each R and R 3 independently may be substituted or unsubstituted alkyl, alkenyl or substituted cycloalkyl are described. These compounds, as well as those wherein the R substituents additionally may be cycloalkyl or substituted or unsubstituted aryl, are useful as accelerators for the peroxidic polymerization of ethylenically unsaturated compounds, such as methacrylic acid compounds, and have particular utility in dental compositions.

Inventors

  • 👤 Werner Schmitt
  • 👤 Robert Purrmann
  • 👤 Peter Jochum
  • 👤 Heinz-Joachim Hubner
  • 👤 Bernd Burger

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-08 11:12
CPC Classifications
C; C07; C07D; C07D285/00; C07D285/15; C07D285/16; A; A61; A61K; A61K6/00; A61K6/80; A61K6/884; A61K6/887; C08; C08F; C08F2/00; C08F2/38; C08F2/40

Claims Analysis

Total Claims: 8
Claim 1
Independent Claim 98 words
In a method for the peroxidic polymerization of ethylenically unsaturated compounds selected from the group consisting of acrylic and methacrylic acid compounds useful in the formation of dental type molded articles including the steps of mixing such ethylenically unsaturated compounds with a peroxidic initiator and accelerator and polymerizing the resulting mixture in a mold, the improvement comprising use of a compound of the formula ##STR6## wherein R 4 and R 5 independently are alkyl, substituted alkyl, alkenyl, cycloalkyl, substituted cycloalkyl, aryl, or substituted aryl, and R 3 is alkyl, substituted alkyl, alkenyl, or substituted cycloalkyl, as an accelerator.
Claim 2
Dependent Claim 98 words
In a method for the peroxidic polymerization of ethylenically unsaturated compounds selected from the group consisting of acrylic and methacrylic acid compounds useful in the formation of dental type molded articles including the steps of mixing such ethylenically unsaturated compounds with a peroxidic initiator and accelerator and polymerizing the resulting mixture in a mold, the improvement comprising use of a compound of the formula ##STR6## wherein R 4 and R 5 independently are alkyl, substituted alkyl, alkenyl, cycloalkyl, substituted cycloalkyl, aryl, or substituted aryl, and R 3 is alkyl, substituted alkyl, alkenyl, or substituted cycloalkyl, as an accelerator.
Claim 3
Dependent Claim 28 words
The method of claim 1 wherein the accelerator compound is present in an amount from 0.1 to 15% by weight based upon the ethylenically unsaturated compound being polymerized.
Claim 4
Dependent Claim 21 words
The method of claim 1 wherein the peroxo catalyst is selected from the group consisting of benzoyl peroxide and lauroyl peroxide.
Claim 5
Dependent Claim 34 words
The method of claim 1 wherein the polymerization is effected in the presence of 1 to 200 ppm heavy metal compound and 0.01 to 1% by weight ionic halogen or pseudohalogen as additional accelerators.
Claim 6
Dependent Claim 17 words
The method of claim 4 wherein the heavy metal is copper and the ionic halogen is chloride.
Claim 7
Dependent Claim 13 words
The method of claim 1 wherein the methacrylic acid compound is an ester.
Claim 8
Dependent Claim 26 words
The method of claim 1 wherein the ethylenically unsaturated compounds and the accelerator are mixed and are polymerized in a mold to form a dental device.

References Cited (Backward Citations)

US2956997A Cited
US3347954A Cited
US4302381A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1987-04-17 1987-10-17 1988-04-17 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1991-04-17 1991-10-17 1992-04-17 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1995-04-17 1995-10-17 1996-04-17 $7700.00 Window Closed / Lapsed

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