CH619730A5 - Surface-coating composition - Google Patents
Surface-coating composition Download PDFInfo
- Publication number
- CH619730A5 CH619730A5 CH98275A CH98275A CH619730A5 CH 619730 A5 CH619730 A5 CH 619730A5 CH 98275 A CH98275 A CH 98275A CH 98275 A CH98275 A CH 98275A CH 619730 A5 CH619730 A5 CH 619730A5
- Authority
- CH
- Switzerland
- Prior art keywords
- composition according
- hydroxymethyl
- aza
- octane
- biocidal
- Prior art date
Links
- 239000008199 coating composition Substances 0.000 title abstract description 24
- 230000003115 biocidal effect Effects 0.000 claims abstract description 51
- 239000000203 mixture Substances 0.000 claims abstract description 50
- 150000001875 compounds Chemical class 0.000 claims abstract description 25
- -1 hydroxymethoxymethyl Chemical group 0.000 claims abstract description 25
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 14
- 239000011230 binding agent Substances 0.000 claims abstract description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 11
- 229920000642 polymer Polymers 0.000 claims abstract description 10
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims abstract description 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 7
- 125000005059 halophenyl group Chemical group 0.000 claims abstract description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 6
- 239000000178 monomer Substances 0.000 claims abstract description 3
- 125000004965 chloroalkyl group Chemical group 0.000 claims abstract 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 claims description 23
- 241000894006 Bacteria Species 0.000 claims description 21
- 125000005704 oxymethylene group Chemical group [H]C([H])([*:2])O[*:1] 0.000 claims description 19
- 241000233866 Fungi Species 0.000 claims description 10
- 239000011248 coating agent Substances 0.000 claims description 9
- 238000000576 coating method Methods 0.000 claims description 9
- 229920002689 polyvinyl acetate Polymers 0.000 claims description 8
- 239000011118 polyvinyl acetate Substances 0.000 claims description 8
- GUQMDNQYMMRJPY-UHFFFAOYSA-N 4,4-dimethyl-1,3-oxazolidine Chemical compound CC1(C)COCN1 GUQMDNQYMMRJPY-UHFFFAOYSA-N 0.000 claims description 7
- BFHKYHMIVDBCPC-UHFFFAOYSA-N 1,3,5,7-tetrahydro-[1,3]oxazolo[3,4-c][1,3]oxazol-7a-ylmethanol Chemical compound C1OCN2COCC21CO BFHKYHMIVDBCPC-UHFFFAOYSA-N 0.000 claims description 6
- 125000004429 atom Chemical group 0.000 claims description 2
- 239000008601 oleoresin Substances 0.000 claims description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 2
- 229910052799 carbon Inorganic materials 0.000 claims 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims 1
- CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical group O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 claims 1
- 235000019256 formaldehyde Nutrition 0.000 abstract description 11
- 239000003973 paint Substances 0.000 description 53
- 239000003921 oil Substances 0.000 description 50
- 235000019198 oils Nutrition 0.000 description 50
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 42
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 31
- 239000003139 biocide Substances 0.000 description 26
- 239000007864 aqueous solution Substances 0.000 description 22
- 239000000243 solution Substances 0.000 description 22
- 150000002917 oxazolidines Chemical class 0.000 description 19
- 230000000694 effects Effects 0.000 description 17
- 239000000047 product Substances 0.000 description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- 125000001424 substituent group Chemical group 0.000 description 10
- 235000001674 Agaricus brunnescens Nutrition 0.000 description 9
- WYNCHZVNFNFDNH-UHFFFAOYSA-N Oxazolidine Chemical compound C1COCN1 WYNCHZVNFNFDNH-UHFFFAOYSA-N 0.000 description 9
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- 239000004816 latex Substances 0.000 description 9
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- 239000007788 liquid Substances 0.000 description 8
- 238000001035 drying Methods 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- 238000010422 painting Methods 0.000 description 6
- 229920001817 Agar Polymers 0.000 description 5
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 5
- 150000001299 aldehydes Chemical class 0.000 description 5
- 239000008098 formaldehyde solution Substances 0.000 description 5
- 239000012456 homogeneous solution Substances 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 230000035899 viability Effects 0.000 description 5
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 4
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- 238000005481 NMR spectroscopy Methods 0.000 description 4
- 229930040373 Paraformaldehyde Natural products 0.000 description 4
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 4
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- 230000000052 comparative effect Effects 0.000 description 4
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- 244000005700 microbiome Species 0.000 description 4
- 239000005012 oleoresinous Substances 0.000 description 4
- 229920002866 paraformaldehyde Polymers 0.000 description 4
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 4
- 229920002554 vinyl polymer Polymers 0.000 description 4
- GOPUCFKUFOFEIC-UHFFFAOYSA-N 2-methyl-1,3-oxazolidine Chemical compound CC1NCCO1 GOPUCFKUFOFEIC-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 230000006866 deterioration Effects 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 239000000944 linseed oil Substances 0.000 description 3
- 235000021388 linseed oil Nutrition 0.000 description 3
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 3
- 125000002950 monocyclic group Chemical group 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 239000002966 varnish Substances 0.000 description 3
- WSUSUJZHSLPJQA-UHFFFAOYSA-N (4,4-dimethyl-1,3-oxazolidin-3-yl)methanol Chemical compound OCN1COCC1(C)C WSUSUJZHSLPJQA-UHFFFAOYSA-N 0.000 description 2
- 125000006176 2-ethylbutyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(C([H])([H])*)C([H])([H])C([H])([H])[H] 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 241000206672 Gelidium Species 0.000 description 2
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- 241000589517 Pseudomonas aeruginosa Species 0.000 description 2
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000008272 agar Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 229920000180 alkyd Polymers 0.000 description 2
- 239000002518 antifoaming agent Substances 0.000 description 2
- 230000001580 bacterial effect Effects 0.000 description 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
- 125000002619 bicyclic group Chemical group 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000004587 chromatography analysis Methods 0.000 description 2
- 150000001923 cyclic compounds Chemical class 0.000 description 2
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 2
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 2
- 230000005764 inhibitory process Effects 0.000 description 2
- 238000002955 isolation Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- 239000004408 titanium dioxide Substances 0.000 description 2
- 108010050327 trypticase-soy broth Proteins 0.000 description 2
- MTWBDLVHLHCQCE-UHFFFAOYSA-N (4-methyl-1,3-oxazolidin-4-yl)methanol Chemical compound OCC1(C)COCN1 MTWBDLVHLHCQCE-UHFFFAOYSA-N 0.000 description 1
- CZGIIMXACFKZDB-UHFFFAOYSA-N (4-methyl-2-phenyl-1,3-oxazolidin-4-yl)methanol Chemical compound N1C(C)(CO)COC1C1=CC=CC=C1 CZGIIMXACFKZDB-UHFFFAOYSA-N 0.000 description 1
- GYJLXDVQKAHKAO-UHFFFAOYSA-N (4-methyl-3-phenyl-1,3-oxazolidin-4-yl)methanol Chemical compound C1(=CC=CC=C1)N1COCC1(CO)C GYJLXDVQKAHKAO-UHFFFAOYSA-N 0.000 description 1
- ZXTMLKYJGBZOSK-UHFFFAOYSA-N (5-methyl-1,3,5,7-tetrahydro-[1,3]oxazolo[3,4-c][1,3]oxazol-7a-yl)oxymethanol Chemical compound C1OCN2C(C)OCC21OCO ZXTMLKYJGBZOSK-UHFFFAOYSA-N 0.000 description 1
- AEBWATHAIVJLTA-UHFFFAOYSA-N 1,2,3,3a,4,5,6,6a-octahydropentalene Chemical compound C1CCC2CCCC21 AEBWATHAIVJLTA-UHFFFAOYSA-N 0.000 description 1
- LOOVHMYLQJKYRI-UHFFFAOYSA-N 1,3,5,7-tetrahydro-[1,3]oxazolo[3,4-c][1,3]oxazol-7a-ylmethoxymethanol Chemical compound C1OCN2COCC21COCO LOOVHMYLQJKYRI-UHFFFAOYSA-N 0.000 description 1
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 1
- 229940035437 1,3-propanediol Drugs 0.000 description 1
- VSHIRTNKIXRXMI-UHFFFAOYSA-N 2,2-dimethyl-1,3-oxazolidine Chemical compound CC1(C)NCCO1 VSHIRTNKIXRXMI-UHFFFAOYSA-N 0.000 description 1
- YSFBEAASFUWWHU-UHFFFAOYSA-N 2,4-dichlorobenzaldehyde Chemical compound ClC1=CC=C(C=O)C(Cl)=C1 YSFBEAASFUWWHU-UHFFFAOYSA-N 0.000 description 1
- HCGKZMQZAFUBJD-UHFFFAOYSA-N 2-(2,4-dichlorophenyl)-4,4-dipropyl-1,3-oxazolidine Chemical compound ClC1=C(C=CC(=C1)Cl)C1OCC(N1)(CCC)CCC HCGKZMQZAFUBJD-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- UNNGUFMVYQJGTD-UHFFFAOYSA-N 2-Ethylbutanal Chemical compound CCC(CC)C=O UNNGUFMVYQJGTD-UHFFFAOYSA-N 0.000 description 1
- UXFQFBNBSPQBJW-UHFFFAOYSA-N 2-amino-2-methylpropane-1,3-diol Chemical compound OCC(N)(C)CO UXFQFBNBSPQBJW-UHFFFAOYSA-N 0.000 description 1
- QSKPIOLLBIHNAC-UHFFFAOYSA-N 2-chloro-acetaldehyde Chemical compound ClCC=O QSKPIOLLBIHNAC-UHFFFAOYSA-N 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- QHINYJQPBCMLCJ-UHFFFAOYSA-N 3,3a,4,5,6,6a-hexahydro-2h-cyclopenta[b]furan Chemical compound C1COC2CCCC21 QHINYJQPBCMLCJ-UHFFFAOYSA-N 0.000 description 1
- YGRCLLQIAOXAHD-UHFFFAOYSA-N 3,5,7,7a-tetrahydro-1h-[1,3]oxazolo[3,4-c][1,3]oxazole Chemical compound C1OCC2COCN21 YGRCLLQIAOXAHD-UHFFFAOYSA-N 0.000 description 1
- KSKIZBJQFUMCKS-UHFFFAOYSA-N 4,4-dimethyl-1,3-oxazolidine-2-carbaldehyde Chemical compound CC1(C)COC(C=O)N1 KSKIZBJQFUMCKS-UHFFFAOYSA-N 0.000 description 1
- AVPYQKSLYISFPO-UHFFFAOYSA-N 4-chlorobenzaldehyde Chemical compound ClC1=CC=C(C=O)C=C1 AVPYQKSLYISFPO-UHFFFAOYSA-N 0.000 description 1
- ZUAQJBUBRVFDNQ-UHFFFAOYSA-N 4-hexyl-4-methyl-1,3-oxazolidine Chemical compound CCCCCCC1(C)COCN1 ZUAQJBUBRVFDNQ-UHFFFAOYSA-N 0.000 description 1
- MBYNWOKUWYKNQS-UHFFFAOYSA-N 5-methyl-1,3,5,7-tetrahydro-[1,3]oxazolo[3,4-c][1,3]oxazol-7a-ol Chemical compound C1OCN2C(C)OCC21O MBYNWOKUWYKNQS-UHFFFAOYSA-N 0.000 description 1
- YWIJBUYJSIQULU-UHFFFAOYSA-N 7a-methyl-1,3,5,7-tetrahydro-[1,3]oxazolo[3,4-c][1,3]oxazole Chemical compound C1OCN2COCC21C YWIJBUYJSIQULU-UHFFFAOYSA-N 0.000 description 1
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- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 1
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- RYZCLUQMCYZBJQ-UHFFFAOYSA-H lead(2+);dicarbonate;dihydroxide Chemical compound [OH-].[OH-].[Pb+2].[Pb+2].[Pb+2].[O-]C([O-])=O.[O-]C([O-])=O RYZCLUQMCYZBJQ-UHFFFAOYSA-H 0.000 description 1
- GIWKOZXJDKMGQC-UHFFFAOYSA-L lead(2+);naphthalene-2-carboxylate Chemical compound [Pb+2].C1=CC=CC2=CC(C(=O)[O-])=CC=C21.C1=CC=CC2=CC(C(=O)[O-])=CC=C21 GIWKOZXJDKMGQC-UHFFFAOYSA-L 0.000 description 1
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- 150000004668 long chain fatty acids Chemical class 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- SGGOJYZMTYGPCH-UHFFFAOYSA-L manganese(2+);naphthalene-2-carboxylate Chemical compound [Mn+2].C1=CC=CC2=CC(C(=O)[O-])=CC=C21.C1=CC=CC2=CC(C(=O)[O-])=CC=C21 SGGOJYZMTYGPCH-UHFFFAOYSA-L 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 125000000160 oxazolidinyl group Chemical group 0.000 description 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000008363 phosphate buffer Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000012262 resinous product Substances 0.000 description 1
- 235000005713 safflower oil Nutrition 0.000 description 1
- 239000003813 safflower oil Substances 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 235000015096 spirit Nutrition 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 239000001974 tryptic soy broth Substances 0.000 description 1
- 239000002383 tung oil Substances 0.000 description 1
- HGBOYTHUEUWSSQ-UHFFFAOYSA-N valeric aldehyde Natural products CCCCC=O HGBOYTHUEUWSSQ-UHFFFAOYSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/02—Emulsion paints including aerosols
- C09D5/024—Emulsion paints including aerosols characterised by the additives
- C09D5/025—Preservatives, e.g. antimicrobial agents
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N35/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
- A01N35/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical at least one of the bonds to hetero atoms is to nitrogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/04—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/14—Paints containing biocides, e.g. fungicides, insecticides or pesticides
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Plant Pathology (AREA)
- General Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Health & Medical Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Dispersion Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Paints Or Removers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US44304474A | 1974-02-15 | 1974-02-15 | |
| US447797A US3890264A (en) | 1974-03-04 | 1974-03-04 | Surface-coating compositions containing polyoxymethyleneoxazolidines |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH619730A5 true CH619730A5 (en) | 1980-10-15 |
Family
ID=27033373
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH98275A CH619730A5 (en) | 1974-02-15 | 1975-01-28 | Surface-coating composition |
Country Status (14)
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3019356A1 (de) * | 1980-05-21 | 1981-11-26 | Sika AG, vorm. Kaspar Winkler & Co., 8048 Zürich | Neue, adimin- und oxazolidingruppen aufweisende verbindungen sowie verfahren zu deren herstellung und ihre verwendung als haerter fuer polyisocyanate |
| BR112013014873B8 (pt) * | 2010-12-17 | 2019-08-06 | Angus Chemical | método para inibir o crescimento ou a propagação de microrganismos, exterminar microorganismos, desinfectar e/ou evitar o crescimento de novos microorganismos em um sistema aquoso ou contendo água, e, composto |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2448890A (en) * | 1948-09-07 | Condensation products of polyht | ||
| US3062710A (en) * | 1959-02-18 | 1962-11-06 | Dow Chemical Co | Treating compositions containing nitrogenous condensation products |
| US3759942A (en) * | 1970-06-08 | 1973-09-18 | Sun Chemical Corp | Crosslinking monomers containing the 1-aza-3,7-dioxabicyclo {8 3.3.0{9 {11 octane structure |
| US3773730A (en) * | 1971-03-06 | 1973-11-20 | Comm Solvents Corp | Polymers from oxazolidines and urea |
| US3738992A (en) * | 1972-02-07 | 1973-06-12 | Commercial Solvents Corp | 1-aza-5-hydroxymethyl-3,7-dioxabicyclo-(3.3.0)-octann |
| DE2218417A1 (de) * | 1972-04-15 | 1973-10-25 | Henkel & Cie Gmbh | Verwendung substituierter oxazolidine als antimikrobielle wirkstoffe |
| DE2218348A1 (de) * | 1972-04-15 | 1973-10-31 | Henkel & Cie Gmbh | Verwendung bicyclischer oxazolidine als antimikrobielle wirkstoffe |
| DE2337755B2 (de) * | 1973-07-25 | 1976-10-07 | Schülke & Mayr GmbH, 2000 Norderstedt | Konservierungs- und desinfektionsmittel |
| DE2454740A1 (de) * | 1974-11-19 | 1976-05-20 | Bayer Ag | Neue n-phenylcarbamate |
-
1975
- 1975-01-28 CH CH98275A patent/CH619730A5/fr not_active IP Right Cessation
- 1975-01-31 CA CA219,138A patent/CA1045972A/en not_active Expired
- 1975-02-03 IL IL46544A patent/IL46544A/xx unknown
- 1975-02-07 BR BR832/75A patent/BR7500832A/pt unknown
- 1975-02-12 AT AT102975A patent/AT342734B/de not_active IP Right Cessation
- 1975-02-12 IT IT48142/75A patent/IT1029706B/it active
- 1975-02-12 MX MX100227U patent/MX3134E/es unknown
- 1975-02-13 SE SE7713651A patent/SE434051B/xx not_active IP Right Cessation
- 1975-02-13 SE SE7501609A patent/SE414940B/xx not_active IP Right Cessation
- 1975-02-14 DE DE19752506310 patent/DE2506310A1/de active Granted
- 1975-02-14 JP JP50018069A patent/JPS5927321B2/ja not_active Expired
- 1975-02-14 NO NO75750490A patent/NO143029C/no unknown
- 1975-02-14 ES ES434734A patent/ES434734A1/es not_active Expired
- 1975-02-14 NL NLAANVRAGE7501762,A patent/NL178084C/xx not_active IP Right Cessation
- 1975-02-14 FR FR7504730A patent/FR2279737A1/fr active Granted
- 1975-10-20 FR FR7532027A patent/FR2283138A1/fr active Granted
- 1975-10-20 FR FR7532028A patent/FR2279828A1/fr active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| IL46544A0 (en) | 1975-04-25 |
| FR2283138A1 (fr) | 1976-03-26 |
| AU7750075A (en) | 1976-07-22 |
| SE434051B (sv) | 1984-07-02 |
| BR7500832A (pt) | 1975-12-02 |
| NO750490L (enrdf_load_stackoverflow) | 1975-08-18 |
| NL178084C (nl) | 1986-01-16 |
| NO143029B (no) | 1980-08-25 |
| FR2279828B1 (enrdf_load_stackoverflow) | 1978-10-06 |
| CA1045972A (en) | 1979-01-09 |
| NL7501762A (nl) | 1975-08-19 |
| JPS5927321B2 (ja) | 1984-07-05 |
| SE414940B (sv) | 1980-08-25 |
| FR2279828A1 (fr) | 1976-02-20 |
| SE7501609L (enrdf_load_stackoverflow) | 1975-08-18 |
| FR2279737A1 (fr) | 1976-02-20 |
| DE2506310A1 (de) | 1975-08-21 |
| ATA102975A (de) | 1977-08-15 |
| FR2279737B1 (enrdf_load_stackoverflow) | 1979-04-13 |
| IT1029706B (it) | 1979-03-20 |
| FR2283138B1 (enrdf_load_stackoverflow) | 1979-06-22 |
| IL46544A (en) | 1978-06-15 |
| MX3134E (es) | 1980-04-28 |
| DE2506310C2 (enrdf_load_stackoverflow) | 1989-12-28 |
| SE7713651L (sv) | 1977-12-01 |
| JPS50116641A (enrdf_load_stackoverflow) | 1975-09-12 |
| AT342734B (de) | 1978-04-25 |
| NO143029C (no) | 1980-12-03 |
| ES434734A1 (es) | 1977-04-01 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PUE | Assignment |
Owner name: NUODEX INC. |
|
| PL | Patent ceased | ||
| PL | Patent ceased |