Synergistic combination of fungicides to protect wood and wood-based products and wood treated by such combination as well as methods of making the same 机翻标题: 暂无翻译,请尝试点击翻译按钮。

公开号/公开日
CA2513755 A1 2004-08-12 [CA2513755]CA2513755 C 2011-07-19 [CA2513755] / 2004-08-122011-07-19
申请号/申请日
2004CA-2513755 / 2004-01-23
发明人
MARKS BRIAN;ROSS ALAN S;WARD HANS A;
申请人
KOP COAT;
主分类号
IPC分类号
A01N-043/64B27K-003/50
摘要
(CA2513755) A wood treatment composition having a synergistic combination of fungicides which may include two or more compounds.  These combinations are shown to be especially effective in providing resistance to decay, mold and mildew when wood is treated with these combinations.  Also provided is wood treated by these combinations, and a method of treatment for composite wood.
机翻摘要
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地址
代理人
代理机构
;
优先权号
2003US-10351021 2003-01-24 2004WO-US01829 2004-01-23
主权利要求
(CA2513755)  CLAIMS: 1. A fungicidal wood treatment composition in concentrate form comprising from about 0.1 to 10% by weight of an azole compound, about 0.1 to 10% by weight of a halopropynyl compound, about 0.1 to 10% by weight of diiodomethyl-p-tolylsulfone, and about 5 to 90% by weight of an amine oxide, based upon 100% by weight of the total wood treatment composition. 2. The composition of claim 1, wherein the azole compound is a 1,2,4-triazole. 3. The composition of claim 2, wherein the azole is selected from the group consisting of triadimefon, triazbutil, propiconazole, cyproconazole, difenoconazole, fluquinoconazole, tebuconazole, flusiazole, uniconazole, diniconazole, bitertanol, hexaconazole, azaconazole, flutriafol, epoxiconazole, tetraconazole, penconazole, and mixtures thereof. 4. The composition of claim 3, wherein the azole is propiconazole. 5. The composition of claim 3, wherein the azole is selected from the group consisting of azaconazole and hexaconazole. 6. The composition of any one of claims 1 to 5, wherein the halopropynyl compound is represented by the formula: and R is selected from the group consisting of hydrogen, substituted and unsubstituted alkyl groups having from 1 to 20 carbon atoms, substituted and unsubstituted aryl, alkyl aryl, and aralkyl groups having from 6 to 20 carbon atoms and from substituted and unsubstituted cycloalkyl and cycloalkenyl groups of 3 to 10 carbon atoms, and m and n are independently integers from 1 to 3. 7. The composition of claim 6, wherein the halopropynyl compound is selected from the group consisting of 3-iodo-2-propynyl propyl carbamate, 3-iodo-2-propynyl butyl carbamate, 3-iodo-2-propynyl hexyl carbamate, 3-iodo-2-propynyl cyclohexyl carbamate, 3-iodo-2-propynyl phenyl carbamate, and mixtures thereof. 8. The composition of claim 7, wherein the halopropynyl compound is 3-iodo-2-propynyl butyl carbamate. 9. The composition of any one of claims 1 to 8, wherein the amine oxide compound is represented by the formula: where.  R1, R2 and R3 are independent and can be linear, branched, cyclic, aromatic or any combination thereof of saturated or unsaturated Cl to C20 group and any C2-C20 carbon atom can be replaced with a heteroatom selected from the group consisting of O, S and N. 10. The composition of claim 9, wherein the amine oxide compound is selected from the group consisting of decyl dimethyl amine oxide, lauryl dimethyl amine oxide, isoalkyl dimethyl amine oxide, myristyl dimethyl amine oxide, cetyl dimethyl amine oxide, stearyl dimethyl amine oxide, octyl dimethyl amine oxide, N-alkyl(C12-C16)-N,N-dimethylamine oxide and mixtures thereof. 11. The composition of claim 10, wherein the amine oxide compound is N-alkyl(C12-C16)-N,N-dimethylamine oxide. 12. The composition of claim 1, wherein the azole is propiconazole, the halopropynyl compound is 3-iodo-2-propynyl-n-butylcarbamate, and the amine oxide compound is N-alkyl(C12-C16)-N,N-dimethylamine oxide. 13. The composition of any one of claims 1 to 12, further comprising a solvent. 14. The composition of claim 13, wherein the solvent is selected from the group consisting of alcohols, glycols, esters, ethers, polyethers, and mixtures thereof. 15. The composition of any one of claims 1 to 12, further comprising water. 16. The composition of any one of claims 1 to 15, further comprising an additive. 17. The composition of claim 16, wherein the additive is selected from the group consisting of a corrosion inhibitor, iron stain inhibitor, wetting agent, colorant, adhesive, emulsifier, filler, carrier, viscosity regulator, pH regulator, binder, tackifier, and mixtures thereof. 18. A fungicidal wood treatment composition in treating solution form comprising from about 0.001 to 10% by weight of an azole compound, about 0.001 to 10% by weight of a halopropynyl compound, about 0.001 to 10% by weight of diiodomethyl-p-tolylsulfone, and about 0.01 to 90% by weight of an amine oxide, based upon 100% by weight of the total wood treatment composition. 19. The composition of claim 18, wherein the azole compound is a 1,2,4-triazole. 20. The composition of claim 19, wherein the azole is selected from the group consisting of triadimefon, triazbutil, propiconazole, cyproconazole, difenoconazole, fluquinoconazole, tebuconazole, flusiazole, uniconazole, diniconazole, bitertanol, hexaconazole, azaconazole, flutriafol, epoxiconazole, tetraconazole, penconazole, and mixtures thereof. 21. The composition of claim 20, wherein the azole is propiconazole. 22. The composition of claim 20, wherein the azole is selected from the group consisting of azaconazole and hexaconazole. 23. The composition of any one of claims 18 to 22, wherein the halopropynyl compound is represented by the formula: and R is selected from the group consisting of hydrogen, substituted and unsubstituted alkyl groups having from 1 to 20 carbon atoms, substituted and unsubstituted aryl, alkyl aryl, and aralkyl groups having from 6 to 20 carbon atoms and from substituted and unsubstituted cycloalkyl and cycloalkenyl groups of 3 to 10 carbon atoms, and m and n are independently integers from 1 to 3. 24. The composition of claim 23, wherein the halopropynyl compound is selected from the group consisting of 3-iodo-2-propynyl propyl carbamate, 3-iodo-2-propynyl butyl carbamate, 3-iodo-2-propynyl hexyl carbamate, 3-iodo-2-propynyl cyclohexyl carbamate, 3-iodo-2-propynyl phenyl carbamate, and mixtures thereof. 25. The composition of claim 24, wherein the halopropynyl compound is 3-iodo-2-propynyl butyl carbamate. 26. The composition of any one of claims 18 to 25, wherein the amine oxide compound is represented by the formula: where R1, R2 and R3 are independent and can be linear, branched, cyclic, aromatic or any combination thereof of saturated or unsaturated C1 to C20 group and any C2-C20 carbon atom can be replaced with a heteroatom selected from the group consisting of 0, S and N. 27. The composition of claim 26, wherein the amine oxide compound is selected from the group consisting of decyl dimethyl amine oxide, lauryl dimethyl amine oxide, isoalkyl dimethyl amine oxide, myristyl dimethyl amine oxide, cetyl dimethyl amine oxide, stearyl dimethyl amine oxide, octyl dimethyl amine oxide, N-alkyl(C12-C16)-N,N-dimethylamine oxide and mixtures thereof. 28. The composition of claim 27, wherein the amine oxide compound is N-alkyl(C12-C16)-N,N-dimethylamine oxide. 29. The composition of claim 18, wherein the azole is propiconazole, the halopropynyl compound is 3-iodo-2-propynyl-n-butylcarbamate, and the amine oxide compound is N-alkyl(C12-C16)-N,N-dimethylamine oxide. 30. The composition of any one of claims 18 to 29, further comprising a solvent. 31. The composition of claim 30, wherein the solvent is selected from the group consisting of alcohols, glycols, esters, ethers, polyethers, and mixtures thereof. 32. The composition of any one of claims 18 to 29, further comprising water. 33. The composition of any one of claims 18 to 32, further comprising an additive. 34. The composition of claim 33, wherein the additive is selected from the group consisting of a corrosion inhibitor, iron stain inhibitor, wetting agent, colorant, adhesive, emulsifier, filler, carrier, viscosity regulator, pH regulator, binder, tackifier, and mixtures thereof. 35. A fungicide treated wood comprising wood treated with a composition in concentrate form comprising from about 0.1 to 10% by weight of an azole compound, about 0.1 to 10% by weight of a halopropynyl compound, about 0.1 to 10% by weight of diiodomethyl-p-tolylsulfone, and about 5 to 90% by weight of an amine oxide, based upon 100% by weight of the total wood treatment composition. 36. The wood of claim 35, wherein the azole compound is a 1,2,4-triazole. 37. The wood of claim 36, wherein the azole is selected from the group consisting of triadimefon, triazbutil, propiconazole, cyproconazole, difenoconazole, fluquinoconazole, tebuconazole, flusiazole, uniconazole, diniconazole, bitertanol, hexaconazole, azaconazole, flutriafol, epoxiconazole, tetraconazole, penconazole, and mixtures thereof. 38. The wood of claim 37, wherein the azole is propiconazole. 39. The wood of claim 37, wherein the azole is selected from the group consisting of azaconazole and hexaconazole. 40. The wood of any one of claims 35 to 39, wherein the halopropynyl compound is represented by the formula: and R is selected from the group consisting of hydrogen, substituted and unsubstituted alkyl groups having from 1 to 20 carbon atoms, substituted and unsubstituted aryl, alkylaryl, and aralkyl groups having from 6 to 20 carbon atoms and from substituted and unsubstituted cycloalkyl and cycloalkenyl groups of 3 to 10 carbon atoms, and m and n are independently integers from 1 to 3. 41. The wood of claim 40, wherein the halopropynyl compound is selected from the group consisting of 3-iodo-2-propynyl propyl carbamate, 3-iodo-2-propynyl butyl carbamate, 3-iodo-2-propynyl hexyl carbamate, 3-iodo-2-propynyl cyclohexyl carbamate, 3-iodo-2-propynyl phenyl carbamate, and mixtures thereof. 42. The wood of claim 41, wherein the halopropynyl compound is 3-iodo-2-propynyl butyl carbamate. 43. The wood of any one of claims 35 to 42, wherein the amine oxide compound is represented by the formula: where R1, R2 and R3 are independent and can be linear, branched, cyclic, aromatic or any combination thereof of saturated or unsaturated C1 to C20 group and any C2-C20 carbon atom can be replaced with a heteroatom selected from the group consisting of 0, S and N. 44. The wood of claim 43, wherein the amine oxide compound is selected from the group consisting of decyl dimethyl amine oxide, lauryl dimethyl amine oxide, isoalkyl dimethyl amine oxide, myristyl dimethyl amine oxide, cetyl dimethyl amine oxide, stearyl dimethyl amine oxide, octyl dimethyl amine oxide, N-alkyl(C12-C16)-N,N-dimethylamine oxide and mixtures thereof. 45. The wood of claim 44, wherein the amine oxide compound is N-alkyl(C12-C16)-N,N-dimethylamine oxide. 46. The wood of claim 35, wherein the azole is propiconazole, the halopropynyl compound is 3-iodo-2-propynyl-n-butylcarbamate, the amine oxide compound is N-alkyl(C12-C16)-N,N-dimethylamine oxide, and the iodo-sulfone is diiodomethyl-p-tolylsulfone. 47. The wood of any one of claims 35 to 46, wherein the composition further comprises a solvent. 48. The wood of claim 47, wherein the solvent is selected from the group consisting of alcohols, glycols, esters, ethers, polyethers, and mixtures thereof. 49. The wood of any one of claims 35 to 46, wherein the composition further comprises water. 50. The wood of any one of claims 35 to 49, wherein the composition further comprises an additive. 51. The wood of claim 50, wherein the additive is selected from the group consisting of a corrosion inhibitor, iron stain inhibitor, wetting agent, colorant, adhesive, emulsifier, filler, carrier, viscosity regulator, pH regulator, binder, tackifier, and mixtures thereof. 52. The wood of any one of claims 35 to 51, wherein the wood is engineered wood. 53. A fungicide treated wood comprising wood treated with a wood treatment composition in treating solution form comprising from about 0.001 to 10% by weight of an azole compound, about 0.001 to 10% by weight of a halopropynyl compound, about 0.001 to 10% by weight of an iodo-sulfone, and about 0.01 to 90% by weight of an amine oxide, based upon 100% by weight of the total wood treatment composition. 54. The wood of claim 53, wherein the azole compound is a 1,2,4-triazole. 55. The wood of claim 54, wherein the azole is selected from the group consisting of triadimefon, triazbutil, propiconazole, cyproconazole, difenoconazole, fluquinoconazole, tebuconazole, flusiazole, uniconazole, diniconazole, bitertanol, hexaconazole, azaconazole, flutriafol, epoxiconazole, tetraconazole, penconazole, and mixtures thereof. 56. The wood of claim 55, wherein the azole is propiconazole. 57. The wood of claim 55, wherein the azole is selected from the group consisting of azaconazole and hexaconazole. 58. The wood of any one of claims 53 to 57, wherein the halopropynyl compound is represented by the formula: and R is selected from the group consisting of hydrogen, substituted and unsubstituted alkyl groups having from 1 to 20 carbon atoms, substituted and unsubstituted aryl, alkylaryl, and aralkyl groups having from 6 to 20 carbon atoms and from substituted and unsubstituted cycloalkyl and cycloalkenyl groups of 3 to 10 carbon atoms, and m and n are independently integers from 1 to 3. 59. The wood of claim 58, wherein the halopropynyl compound is selected from the group consisting of 3-iodo-2-propynyl propyl carbamate, 3-iodo-2-propynyl butyl carbamate, 3-iodo-2-propynyl hexyl carbamate, 3-iodo-2-propynyl cyclohexyl carbamate, 3-iodo-2-propynyl phenyl carbamate, and mixtures thereof. 60. The wood of claim 59, wherein the halopropynyl compound is 3-iodo-2-propynyl butyl carbamate. 61. The wood of any one of claims 53 to 60, wherein the amine oxide compound is represented by the formula: where R1, R2 and R3 are independent and can be linear, branched, cyclic, aromatic or any combination thereof of saturated or unsaturated C1 to C20 group and any C2-C20 carbon atom can be replaced with a heteroatom selected from the group consisting of 0, S and N. 62. The wood of claim 61, wherein the amine oxide compound is selected from the group consisting of decyl dimethyl amine oxide, lauryl dimethyl amine oxide, isoalkyl dimethyl amine oxide, myristyl dimethyl amine oxide, cetyl dimethyl amine oxide, stearyl dimethyl amine oxide, octyl dimethyl amine oxide, N-alkyl(C12-C16)-N,N-dimethylamine oxide and mixtures thereof. 63. The wood of claim 62, wherein the amine oxide compound is N-alkyl(C12-C16)-N,N-dimethylamine oxide. 64. The wood of claim 53, wherein the azole is propiconazole, the halopropynyl compound is 3-iodo-2-propynyl-n-butylcarbamate, the amine oxide compound is N-alkyl(C12-C16)-N,N-dimethylamine oxide, and the iodo-sulfone is diiodomethyl-p-tolylsulfone. 65. The wood of any one of claims 53 to 64, wherein the composition further comprises a solvent. 66. The wood of claim 65, wherein the solvent is selected from the group consisting of alcohols, glycols, esters, ethers, polyethers, and mixtures thereof. 67. The wood of any one of claims 53 to 64, wherein the composition further comprises water. 68. The wood of any one of claims 53 to 67, wherein the composition further comprises an additive. 69. The wood of claim 68, wherein the additive is selected from the group consisting of a corrosion inhibitor, iron stain inhibitor, wetting agent, colorant, adhesive, emulsifier, filler, carrier, viscosity regulator, pH regulator, binder, tackifier, and mixtures thereof. 70. The wood of any one of claims 53 to 69, wherein the wood is engineered wood. 71. A method of treating wood comprising treating wood with a composition in concentrate form comprising from about 0.1 to 10% by weight of an azole compound, about 0.1 to 10% by weight of a halopropynyl compound, about 0.1 to 10% by weight of diiodomethyl-p-tolylsulfone, and about 5 to 90% by weight of an amine oxide, based upon 100% by weight of the total wood treatment composition. 72. The method of claim 71, wherein the azole compound is a 1,2,4-triazole. 73. The method of claim 72, wherein the azole is selected from the group consisting of triadimefon, triazbutil, propiconazole, cyproconazole, difenoconazole, fluquinoconazole, tebuconazole, flusiazole, uniconazole, diniconazole, bitertanol, hexaconazole, azaconazole, flutriafol, epoxiconazole, tetraconazole, penconazole, and mixtures thereof. 74. The method of claim 73, wherein the azole is propiconazole. 75. The method of claim 73, wherein the azole is selected from the group consisting of azaconazole and hexaconazole. 76. The method of any one of claims 71 to 75, wherein the halopropynyl compound is represented by the formula: and R is selected from the group consisting of hydrogen, substituted and unsubstituted alkyl groups having from 1 to 20 carbon atoms, substituted and unsubstituted aryl, alkyl aryl, and aralkyl groups having from 6 to 20 carbon atoms and from substituted and unsubstituted cycloalkyl and cycloalkenyl groups of 3 to 10 carbon atoms, and m and n are independently integers from 1 to 3. 77. The method of claim 76, wherein the halopropynyl compound is selected from the group consisting of 3-iodo-2-propynyl propyl carbamate, 3-iodo-2-propynyl butylcarbamate, 3-iodo-2-propynyl hexyl carbamate, 3-iodo-2-propynyl cyclohexyl carbamate, 3-iodo-2-propynyl phenyl carbamate, and mixtures thereof. 78. The method of claim 77, wherein the halopropynyl compound is 3-iodo-2-propynyl butyl carbamate. 79. The method of any one of claims 71 to 78, wherein the amine oxide compound is represented by the formula: where R1, R2 and R3 are independent and can be linear, branched, cyclic, aromatic or any combination thereof of saturated or unsaturated C1 to C20 group and any C2-C20 carbon atom can be replaced with a heteroatom selected from the group consisting of 0, S and N. 80. The method of claim 79, wherein the amine oxide compound is selected from the group consisting of decyl dimethyl amine oxide, lauryl dimethyl amine oxide, isoalkyl dimethyl amine oxide, myristyl dimethyl amine oxide, cetyl dimethyl amine oxide, stearyl dimethyl amine oxide, octyl dimethyl amine oxide, N-alkyl(C12-C16)-N,N-dimethylamine oxide and mixtures thereof. 81. The method of claim 80, wherein the amine oxide compound is N-alkyl(C12-C16)-N,N-dimethylamine oxide. 82. The method of claim 71, wherein the azole is propiconazole, the halopropynyl compound is 3-iodo-2-propynyl-n-butylcarbamate, and the amine oxide compound is N-alkyl(C12-C16)-N,N-dimethylamine oxide. 83. The method of any one of claims 71 to 82, wherein the composition further comprises a solvent. 84. The method of claim 83, wherein the solvent is selected from the group consisting of alcohols, glycols, esters, ethers, polyethers, and mixtures thereof. 85. The method of any one of claims 71 to 82, wherein the composition further comprises water. 86. The method of any one of claims 71 to 85, wherein the composition further comprises an additive. 87. The method of claim 86, wherein the additive is selected from the group consisting of a corrosion inhibitor, iron stain inhibitor, wetting agent, colorant, adhesive, emulsifier, filler, carrier, viscosity regulator, pH regulator, binder, tackifier, and mixtures thereof. 88. A method of treating wood comprising treating the wood with a wood treatment composition in treating solution form comprising from about 0.001 to 10% by weight of an azole compound, about 0.001 to 10% by weight of a halopropynyl compound, about 0.001 to 10% by weight of diiodomethyl-p-tolylsulfone, and about 0.01 to 90% by weight of an amine oxide, based upon 100% by weight of the total wood treatment composition. 89. The method of claim 88, wherein the azole compound is a 1,2,4-triazole. 90. The method of claim 89, wherein the azole is selected from the group consisting of triadimefon, triazbutil, propiconazole, cyproconazole, difenoconazole, fluquinoconazole, tebuconazole, flusiazole, uniconazole, diniconazole, bitertanol, hexaconazole, azaconazole, flutriafol, epoxiconazole, tetraconazole, penconazole, and mixtures thereof. 91. The method of claim 90, wherein the azole is propiconazole. 92. The method of claim 90, wherein the azole is selected from the group consisting of azaconazole and hexaconazole. 93. The method of any one of claims 88 to 92, wherein the halopropynyl compound is represented by the formula: and R is selected from the group consisting of hydrogen, substituted and unsubstituted alkyl groups having from 1 to 20 carbon atoms, substituted and unsubstituted aryl, alkyl aryl, and aralkyl groups having from 6 to 20 carbon atoms and from substituted and unsubstituted cycloalkyl and cycloalkenyl groups of 3 to 10 carbon atoms, and m and n are independently integers from 1 to 3. 94. The method of claim 93, wherein the halopropynyl compound is selected from the group consisting of 3-iodo-2-propynyl propyl carbamate, 3-iodo-2-propynyl butylcarbamate, 3-iodo-2-propynyl hexyl carbamate, 3-iodo-2-propynyl cyclohexyl carbamate, 3-iodo-2-propynyl phenyl carbamate, and mixtures thereof. 95. The method of claim 94, wherein the halopropynyl compound is 3-iodo-2-propynyl butyl carbamate. 96. The method of any one of claims 88 to 95, wherein the amine oxide compound is represented by the formula: where R1, R2 and R3 are independent and can be linear, branched, cyclic, aromatic or any combination thereof of saturated or unsaturated C1 to C20 group and any C2-C20 carbon atom can be replaced with a heteroatom selected from the group consisting of 0, S and N. 97. The method of claim 96, wherein the amine oxide compound is selected from the group consisting of decyl dimethyl amine oxide, lauryl dimethyl amine oxide, isoalkyl dimethyl amine oxide, myristyl dimethyl amine oxide, cetyl dimethyl amine oxide, stearyl dimethyl amine oxide, octyl dimethyl amine oxide, N-alkyl(C12-C16)-N,N-dimethylamine oxide and mixtures thereof. 98. The method of claim 97, wherein the amine oxide compound is N-alkyl(C12-C16)-N,N-dimethylamine oxide. 99. The method of claim 88, wherein the azole is propiconazole, the halopropynyl compound is 3-iodo-2-propynyl-n-butylcarbamate, and the amine oxide compound is N-alkyl(C12-C16)-N,N-dimethylamine oxide. 100. The method of any one of claims 88 to 99, wherein the composition further comprises a solvent. 101. The method of claim 100, wherein the solvent is selected from the group consisting of alcohols, glycols, esters, ethers, polyethers, and mixtures thereof. 102. The method of any one of claims 88 to 99, wherein the composition further comprises water. 103. The method of any one of claims 88 to 102, the composition further comprises an additive. 104. The method of claim 103, wherein the additive is selected from the group consisting of a corrosion inhibitor, iron stain inhibitor, wetting agent, colorant, adhesive, emulsifier, filler, carrier, viscosity regulator, pH regulator, binder, tackifier, and mixtures thereof. 105. A fungicidal wood treatment composition in concentrate form comprising from about 0.1 to 10% by weight of a halopropynyl compound, about 0.1 to 10% by weight of diiodomethyl-p-tolylsulfone, and about 5 to 90% by weight of an amine oxide, based upon 100% by weight of the total wood treatment composition. 106. The composition of claim 105, wherein the halopropynyl compound is represented by the formula: and R is selected from the group consisting of hydrogen, substituted and unsubstituted alkyl groups having from 1 to 20 carbon atoms, substituted and unsubstituted aryl, alkyl aryl, and aralkyl groups having from 6 to 20 carbon atoms and from substituted and unsubstituted cycloalkyl and cycloalkenyl groups of 3 to 10 carbon atoms, and m and n are independently integers from 1 to 3. 107. The composition of claim 106, wherein the halopropynyl compound is selected from the group consisting of 3-iodo-2-propynyl propyl carbamate, 3- iodo-2- propynyl butyl carbamate, 3-iodo-2-propynyl hexyl carbamate, 3-iodo-2-propynyl cyclohexyl carbamate, 3-iodo-2-propynyl phenyl carbamate, and mixtures thereof. 108. The composition of claim 107, wherein the halopropynyl compound is 3- iodo-2-propynyl butyl carbamate. 109. The composition of any one of claims 105 to 108, wherein the amine oxide compound is represented by the formula: where R1, R2 and R3 are independent and can be linear, branched, cyclic, aromatic or any combination thereof of saturated or unsaturated C, to C20 group and any C2- C20 carbon atom can be replaced with a heteroatom selected from the group consisting of 0, S and N. 110. The composition of claim 109, wherein the amine oxide compound is selected from the group consisting of decyl dimethyl amine oxide, lauryl dimethyl amine oxide, isoalkyl dimethyl amine oxide, myristyl dimethyl amine oxide, cetyl dimethyl amine oxide, stearyl dimethyl amine oxide, octyl dimethyl amine oxide, N-alkyl(C12-C16)-N,N-dimethylamine oxide and mixtures thereof. 111. The composition of claim 110, wherein the amine oxide compound is N- alkyl(C12-C16)-N,N-dimethylamine oxide. 112. The composition of any one of claims 105 to 111, further comprising a solvent. 113. The composition of claim 112, wherein the solvent is selected from the group consisting of alcohols, glycols, esters, ethers, polyethers, and mixtures thereof. 114. The composition of any one of claims 105 to 111, further comprising water. 115. The composition of any one of claims 105 to 114, further comprising an additive. 116. The composition of claim 115, wherein the additive is selected from the group consisting of a corrosion inhibitor, iron stain inhibitor, wetting agent, colorant, adhesive, emulsifier, filler, carrier, viscosity regulator, pH regulator, binder, tackifier, and mixtures thereof.
法律状态
(CA2513755) LEGAL DETAILS FOR CA2513755  Actual or expected expiration date=2024-01-23    Legal state=ALIVE    Status=GRANTED     Event publication date=2004-01-23  Event code=CA/APP  Event indicator=Pos  Event type=Examination events  Application details  Application country=CA CA2513755  Application date=2004-01-23  Standardized application number=2004CA-2513755     Event publication date=2004-08-12  Event code=CA/A1  Event type=Examination events  Application laid open  Publication country=CA  Publication number=CA2513755  Publication stage Code=A1  Publication date=2004-08-12  Standardized publication number=CA2513755     Event publication date=2008-09-04  Event code=CA/EEER  Event indicator=Pos  Event type=Examination events  Examination request    Event publication date=2011-07-19  Event code=CA/C  Event indicator=Pos  Event type=Event indicating In Force  Patent (second level)  Publication country=CA  Publication number=CA2513755  Publication stage Code=C  Publication date=2011-07-19  Standardized publication number=CA2513755
专利类型码
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