NL8401969A - Gestabiliseerd 2-mercaptopyridine-1-oxide en derivaten daarvan. - Google Patents
Gestabiliseerd 2-mercaptopyridine-1-oxide en derivaten daarvan. Download PDFInfo
- Publication number
- NL8401969A NL8401969A NL8401969A NL8401969A NL8401969A NL 8401969 A NL8401969 A NL 8401969A NL 8401969 A NL8401969 A NL 8401969A NL 8401969 A NL8401969 A NL 8401969A NL 8401969 A NL8401969 A NL 8401969A
- Authority
- NL
- Netherlands
- Prior art keywords
- oxide
- mercaptopyridine
- benzotriazole
- hydroxy
- biocide
- Prior art date
Links
- YBBJKCMMCRQZMA-UHFFFAOYSA-N pyrithione Chemical compound ON1C=CC=CC1=S YBBJKCMMCRQZMA-UHFFFAOYSA-N 0.000 title claims description 16
- 239000000203 mixture Substances 0.000 claims description 24
- WPZSJJJTNREFSV-UHFFFAOYSA-N [Zn].[O-][N+]1=CC=CC=C1S Chemical compound [Zn].[O-][N+]1=CC=CC=C1S WPZSJJJTNREFSV-UHFFFAOYSA-N 0.000 claims description 18
- 239000012964 benzotriazole Substances 0.000 claims description 18
- -1 benzotriazole compound Chemical class 0.000 claims description 17
- 230000003115 biocidal effect Effects 0.000 claims description 17
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 claims description 16
- 230000000845 anti-microbial effect Effects 0.000 claims description 15
- 239000003381 stabilizer Substances 0.000 claims description 15
- 229920000642 polymer Polymers 0.000 claims description 14
- 239000003139 biocide Substances 0.000 claims description 13
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 claims description 10
- 229940113120 dipropylene glycol Drugs 0.000 claims description 10
- 150000002903 organophosphorus compounds Chemical class 0.000 claims description 9
- HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 claims description 9
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 6
- CAKYHYXDPFZAKC-UHFFFAOYSA-N [N+]=1(C(=CC=CC1)S)[O-].[Sn] Chemical compound [N+]=1(C(=CC=CC1)S)[O-].[Sn] CAKYHYXDPFZAKC-UHFFFAOYSA-N 0.000 claims description 6
- 239000004599 antimicrobial Substances 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- 229910021626 Tin(II) chloride Inorganic materials 0.000 claims description 3
- 229910052751 metal Chemical class 0.000 claims description 3
- 239000002184 metal Chemical class 0.000 claims description 3
- RMSGQZDGSZOJMU-UHFFFAOYSA-N 1-butyl-2-phenylbenzene Chemical group CCCCC1=CC=CC=C1C1=CC=CC=C1 RMSGQZDGSZOJMU-UHFFFAOYSA-N 0.000 claims description 2
- BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 claims description 2
- DIHRARMZJFMJHO-UHFFFAOYSA-N [Ca].SC1=[N+](C=CC=C1)[O-] Chemical compound [Ca].SC1=[N+](C=CC=C1)[O-] DIHRARMZJFMJHO-UHFFFAOYSA-N 0.000 claims description 2
- PFVFLPBQVZNQHU-UHFFFAOYSA-N [N+]=1(C(=CC=CC1)S)[O-].[Cd] Chemical compound [N+]=1(C(=CC=CC1)S)[O-].[Cd] PFVFLPBQVZNQHU-UHFFFAOYSA-N 0.000 claims description 2
- XDILZEPJCPEDLT-UHFFFAOYSA-N [Na].[O-][N+]1=CC=CC=C1S Chemical compound [Na].[O-][N+]1=CC=CC=C1S XDILZEPJCPEDLT-UHFFFAOYSA-N 0.000 claims description 2
- ZANLKRASLWUSFW-UHFFFAOYSA-N [Sb].[O-][N+]1=CC=CC=C1S Chemical compound [Sb].[O-][N+]1=CC=CC=C1S ZANLKRASLWUSFW-UHFFFAOYSA-N 0.000 claims description 2
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 claims description 2
- 235000011150 stannous chloride Nutrition 0.000 claims description 2
- AXZWODMDQAVCJE-UHFFFAOYSA-L tin(II) chloride (anhydrous) Chemical compound [Cl-].[Cl-].[Sn+2] AXZWODMDQAVCJE-UHFFFAOYSA-L 0.000 claims description 2
- 229940125782 compound 2 Drugs 0.000 claims 2
- ZAHDWFQLTZUDAL-UHFFFAOYSA-N 2-(2H-benzotriazol-4-yl)-4,6-bis(2-phenylpropan-2-yl)phenol Chemical compound C=1C(C=2C=3N=NNC=3C=CC=2)=C(O)C(C(C)(C)C=2C=CC=CC=2)=CC=1C(C)(C)C1=CC=CC=C1 ZAHDWFQLTZUDAL-UHFFFAOYSA-N 0.000 claims 1
- MXSYTUFGOMKSBW-UHFFFAOYSA-N 2h-benzotriazole;2-tert-butyl-6-(5-chlorobenzotriazol-2-yl)-4-methylphenol Chemical compound C1=CC=CC2=NNN=C21.CC(C)(C)C1=CC(C)=CC(N2N=C3C=C(Cl)C=CC3=N2)=C1O MXSYTUFGOMKSBW-UHFFFAOYSA-N 0.000 claims 1
- 229920000388 Polyphosphate Polymers 0.000 claims 1
- CSKVRPUNTIHCGS-UHFFFAOYSA-N SC1=[N+](C=CC=C1)[O-].C1(=CC=CC=C1)[Sn](C1=CC=CC=C1)C1=CC=CC=C1 Chemical compound SC1=[N+](C=CC=C1)[O-].C1(=CC=CC=C1)[Sn](C1=CC=CC=C1)C1=CC=CC=C1 CSKVRPUNTIHCGS-UHFFFAOYSA-N 0.000 claims 1
- 239000001205 polyphosphate Substances 0.000 claims 1
- 235000011176 polyphosphates Nutrition 0.000 claims 1
- 229920001944 Plastisol Polymers 0.000 description 17
- 239000004999 plastisol Substances 0.000 description 17
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- FGVVTMRZYROCTH-UHFFFAOYSA-N pyridine-2-thiol N-oxide Chemical compound [O-][N+]1=CC=CC=C1S FGVVTMRZYROCTH-UHFFFAOYSA-N 0.000 description 4
- 230000015556 catabolic process Effects 0.000 description 3
- 238000006731 degradation reaction Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- VOQFZENYFWLTBF-UHFFFAOYSA-N 2,4-ditert-butyl-6-(5-chloro-2H-benzotriazol-4-yl)phenol Chemical compound CC(C)(C)c1cc(c(O)c(c1)C(C)(C)C)-c1c(Cl)ccc2[nH]nnc12 VOQFZENYFWLTBF-UHFFFAOYSA-N 0.000 description 2
- JQDJSFVRBAXBCM-UHFFFAOYSA-N 2-tert-butyl-6-(5-chloro-2H-benzotriazol-4-yl)-4-methylphenol Chemical compound CC(C)(C)C1=CC(C)=CC(C=2C=3N=NNC=3C=CC=2Cl)=C1O JQDJSFVRBAXBCM-UHFFFAOYSA-N 0.000 description 2
- JSVDMQKVGLGYCM-UHFFFAOYSA-N 5,5-dimethyl-2-phenoxy-1,3,2-dioxaphosphinane Chemical compound O1CC(C)(C)COP1OC1=CC=CC=C1 JSVDMQKVGLGYCM-UHFFFAOYSA-N 0.000 description 2
- 239000007983 Tris buffer Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- ZJIPHXXDPROMEF-UHFFFAOYSA-N dihydroxyphosphanyl dihydrogen phosphite Chemical class OP(O)OP(O)O ZJIPHXXDPROMEF-UHFFFAOYSA-N 0.000 description 2
- 238000002845 discoloration Methods 0.000 description 2
- MCPKSFINULVDNX-UHFFFAOYSA-N drometrizole Chemical compound CC1=CC=C(O)C(N2N=C3C=CC=CC3=N2)=C1 MCPKSFINULVDNX-UHFFFAOYSA-N 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- XZZWOTQMUOIIFX-UHFFFAOYSA-N 1-(2-diphenoxyphosphanyloxypropoxy)propan-2-yl diphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC(C)COCC(C)OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 XZZWOTQMUOIIFX-UHFFFAOYSA-N 0.000 description 1
- GFRYVFGLHNRJRY-UHFFFAOYSA-N 1-[3-(2H-benzotriazol-4-yl)-5-pentylphenyl]pentan-2-ol Chemical compound OC(CC=1C=C(C=C(C1)C1=CC=CC=2NN=NC21)CCCCC)CCC GFRYVFGLHNRJRY-UHFFFAOYSA-N 0.000 description 1
- JRRSZPBVIHXNBS-UHFFFAOYSA-N 2-(2H-benzotriazol-4-yl)-4-(2,4,4-trimethylpentan-2-yl)phenol Chemical compound CC(C)(C)CC(C)(C)c1ccc(O)c(c1)-c1cccc2[nH]nnc12 JRRSZPBVIHXNBS-UHFFFAOYSA-N 0.000 description 1
- LHPPDQUVECZQSW-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4,6-ditert-butylphenol Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC(N2N=C3C=CC=CC3=N2)=C1O LHPPDQUVECZQSW-UHFFFAOYSA-N 0.000 description 1
- 241000228245 Aspergillus niger Species 0.000 description 1
- TXSWGTOCTHQLJU-UHFFFAOYSA-N CCCCCCCCCC(C=C1)=C(CCCCCCCCC)C(CCCCCCCCC)=C1P(O)(O)O Chemical compound CCCCCCCCCC(C=C1)=C(CCCCCCCCC)C(CCCCCCCCC)=C1P(O)(O)O TXSWGTOCTHQLJU-UHFFFAOYSA-N 0.000 description 1
- MVWXFHWWDOEOPF-UHFFFAOYSA-N OP(O)OP(O)O.OCCOCCOCCO Chemical compound OP(O)OP(O)O.OCCOCCOCCO MVWXFHWWDOEOPF-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical class [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 150000001565 benzotriazoles Chemical class 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- AMVRSVDNRZHJAR-UHFFFAOYSA-N dihydroxyphosphanyl dihydrogen phosphite 1,1,2,3-tetrakis(2-nonylphenyl)propane-1,2-diol Chemical compound OP(O)OP(O)O.CCCCCCCCCC1=CC=CC=C1CC(O)(C(O)(C=1C(=CC=CC=1)CCCCCCCCC)C=1C(=CC=CC=1)CCCCCCCCC)C1=CC=CC=C1CCCCCCCCC AMVRSVDNRZHJAR-UHFFFAOYSA-N 0.000 description 1
- OKXAFOJPRGDZPB-UHFFFAOYSA-N dioctadecoxy(oxo)phosphanium Chemical compound CCCCCCCCCCCCCCCCCCO[P+](=O)OCCCCCCCCCCCCCCCCCC OKXAFOJPRGDZPB-UHFFFAOYSA-N 0.000 description 1
- XMQYIPNJVLNWOE-UHFFFAOYSA-N dioctyl hydrogen phosphite Chemical compound CCCCCCCCOP(O)OCCCCCCCC XMQYIPNJVLNWOE-UHFFFAOYSA-N 0.000 description 1
- KUMNEOGIHFCNQW-UHFFFAOYSA-N diphenyl phosphite Chemical compound C=1C=CC=CC=1OP([O-])OC1=CC=CC=C1 KUMNEOGIHFCNQW-UHFFFAOYSA-N 0.000 description 1
- XHWQYYPUYFYELO-UHFFFAOYSA-N ditridecyl phosphite Chemical compound CCCCCCCCCCCCCOP([O-])OCCCCCCCCCCCCC XHWQYYPUYFYELO-UHFFFAOYSA-N 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 238000009533 lab test Methods 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 230000002906 microbiologic effect Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- CBFCDTFDPHXCNY-UHFFFAOYSA-N octyldodecane Natural products CCCCCCCCCCCCCCCCCCCC CBFCDTFDPHXCNY-UHFFFAOYSA-N 0.000 description 1
- UWJJYHHHVWZFEP-UHFFFAOYSA-N pentane-1,1-diol Chemical compound CCCCC(O)O UWJJYHHHVWZFEP-UHFFFAOYSA-N 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- NVTPMUHPCAUGCB-UHFFFAOYSA-L pentyl phosphate Chemical compound CCCCCOP([O-])([O-])=O NVTPMUHPCAUGCB-UHFFFAOYSA-L 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000008301 phosphite esters Chemical class 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000003223 protective agent Substances 0.000 description 1
- ILVXOBCQQYKLDS-UHFFFAOYSA-N pyridine N-oxide Chemical compound [O-][N+]1=CC=CC=C1 ILVXOBCQQYKLDS-UHFFFAOYSA-N 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000011885 synergistic combination Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000003017 thermal stabilizer Substances 0.000 description 1
- 150000007970 thio esters Chemical class 0.000 description 1
- IVIIAEVMQHEPAY-UHFFFAOYSA-N tridodecyl phosphite Chemical compound CCCCCCCCCCCCOP(OCCCCCCCCCCCC)OCCCCCCCCCCCC IVIIAEVMQHEPAY-UHFFFAOYSA-N 0.000 description 1
- SUXIKHBBPQWLHO-UHFFFAOYSA-N trihydroxy-(8-methylnonyl)-(8-methyl-1-phenylnonyl)-lambda5-phosphane Chemical compound CC(C)CCCCCCCP(O)(O)(O)C(CCCCCCC(C)C)C1=CC=CC=C1 SUXIKHBBPQWLHO-UHFFFAOYSA-N 0.000 description 1
- CNUJLMSKURPSHE-UHFFFAOYSA-N trioctadecyl phosphite Chemical compound CCCCCCCCCCCCCCCCCCOP(OCCCCCCCCCCCCCCCCCC)OCCCCCCCCCCCCCCCCCC CNUJLMSKURPSHE-UHFFFAOYSA-N 0.000 description 1
- DECPGQLXYYCNEZ-UHFFFAOYSA-N tris(6-methylheptyl) phosphite Chemical compound CC(C)CCCCCOP(OCCCCCC(C)C)OCCCCCC(C)C DECPGQLXYYCNEZ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H02—GENERATION; CONVERSION OR DISTRIBUTION OF ELECTRIC POWER
- H02K—DYNAMO-ELECTRIC MACHINES
- H02K1/00—Details of the magnetic circuit
- H02K1/06—Details of the magnetic circuit characterised by the shape, form or construction
-
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/22—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing ingredients stabilising the active ingredients
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3412—Heterocyclic compounds having nitrogen in the ring having one nitrogen atom in the ring
- C08K5/3432—Six-membered rings
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3472—Five-membered rings
- C08K5/3475—Five-membered rings condensed with carbocyclic rings
-
- H—ELECTRICITY
- H02—GENERATION; CONVERSION OR DISTRIBUTION OF ELECTRIC POWER
- H02K—DYNAMO-ELECTRIC MACHINES
- H02K29/00—Motors or generators having non-mechanical commutating devices, e.g. discharge tubes or semiconductor devices
- H02K29/06—Motors or generators having non-mechanical commutating devices, e.g. discharge tubes or semiconductor devices with position sensing devices
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Plant Pathology (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Dentistry (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Toxicology (AREA)
- Power Engineering (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/506,764 US4474760A (en) | 1983-06-22 | 1983-06-22 | Stabilized 2-mercaptopyridene-1-oxide and derivatives |
| US50676483 | 1983-06-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NL8401969A true NL8401969A (nl) | 1985-01-16 |
Family
ID=24015917
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NL8401969A NL8401969A (nl) | 1983-06-22 | 1984-06-21 | Gestabiliseerd 2-mercaptopyridine-1-oxide en derivaten daarvan. |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US4474760A (pt) |
| EP (1) | EP0132301A1 (pt) |
| JP (1) | JPS6013705A (pt) |
| KR (1) | KR850000188A (pt) |
| AU (1) | AU2956584A (pt) |
| BR (1) | BR8403032A (pt) |
| DK (1) | DK302984A (pt) |
| IL (1) | IL72207A0 (pt) |
| NL (1) | NL8401969A (pt) |
| ZA (1) | ZA844699B (pt) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4891391A (en) * | 1985-01-03 | 1990-01-02 | Morton Thiokol, Inc. | Compositions containing antimicrobial agents in combination with stabilizers |
| US4624679A (en) * | 1985-01-03 | 1986-11-25 | Morton Thiokol, Inc. | Compositions containing antimicorbial agents in combination with stabilizers |
| US5227156A (en) * | 1992-04-14 | 1993-07-13 | Amway Corporation | Use of zinc compounds to stabilize a thiazolinone preservative in an anti-dandruff shampoo |
| US5928671A (en) | 1995-04-25 | 1999-07-27 | Winthrop University Hospital | Method and composition for inhibiting bacteria |
| US6086921A (en) * | 1995-04-25 | 2000-07-11 | Wintrop-University Hospital | Metal/thiol biocides |
| DE19725017A1 (de) * | 1997-06-13 | 1998-12-17 | Bayer Ag | Verwendung von 2-Mercapto-pyridin-N-oxid |
| ATE249142T1 (de) * | 1999-03-17 | 2003-09-15 | Api Corp | Beschichtetes bis(2-pyridinthiol 1-oxid) kupfersalz |
| WO2001000720A1 (de) * | 1999-06-24 | 2001-01-04 | Sanitized Ag | Antimikrobielle ausrüstung von schäumen aus polyurethan durch einsatz von zink-bis-(2-pyridinthiol-1-oxid) zusammen mit anderen wirkstoffen |
| US6525117B1 (en) | 2000-06-08 | 2003-02-25 | Akzo Nobel N.V. | Stabilized zinc pyrithione for vinyl chloride polymers |
| EP1761595A1 (de) * | 2004-06-16 | 2007-03-14 | Sanitized AG | Verfahren zur stabilisierung von mit zinkpyrithion antimikrobiell ausgerüstetem polyvinylchlorid |
| US7659326B2 (en) * | 2006-01-09 | 2010-02-09 | Beyond Technologies Australia Pty Ltd. | Antimicrobial paint |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2686786A (en) * | 1953-01-09 | 1954-08-17 | Olin Mathieson | Nu-hydroxy-2-pyridinethiones and method of preparing same |
| US2809971A (en) * | 1955-11-22 | 1957-10-15 | Olin Mathieson | Heavy-metal derivatives of 1-hydroxy-2-pyridinethiones and method of preparing same |
| NL251248A (pt) * | 1959-05-04 | |||
| US3393990A (en) * | 1965-07-15 | 1968-07-23 | Plant Products Corp | Stabilized pesticide compositions and methods for making same |
| US3533993A (en) * | 1968-06-18 | 1970-10-13 | Olin Mathieson | Vinyl chloride resins stabilized with 2 - mercaptopyridine - 1 - oxide and derivatives |
| US3940482A (en) * | 1971-04-21 | 1976-02-24 | Colgate-Palmolive Company | Solubilization of the zinc salt of 1-hydroxy-2-pyridinethione |
| GB1592691A (en) * | 1976-10-05 | 1981-07-08 | Ici Australia Ltd | Stabilised tickicidal compositions |
| US4161526A (en) * | 1978-07-20 | 1979-07-17 | Sterling Drug Inc. | Zinc salt prevention or removal of discoloration in pyrithione, pyrithione salt and dipyrithione compositions |
| US4363663A (en) * | 1979-06-20 | 1982-12-14 | Hill Nicholas J | Antimicrobial solution |
-
1983
- 1983-06-22 US US06/506,764 patent/US4474760A/en not_active Expired - Fee Related
-
1984
- 1984-06-20 BR BR8403032A patent/BR8403032A/pt unknown
- 1984-06-20 AU AU29565/84A patent/AU2956584A/en not_active Abandoned
- 1984-06-21 ZA ZA844699A patent/ZA844699B/xx unknown
- 1984-06-21 NL NL8401969A patent/NL8401969A/nl not_active Application Discontinuation
- 1984-06-21 KR KR1019840003503A patent/KR850000188A/ko not_active Withdrawn
- 1984-06-21 EP EP84304207A patent/EP0132301A1/en not_active Withdrawn
- 1984-06-21 JP JP59126589A patent/JPS6013705A/ja active Pending
- 1984-06-21 DK DK302984A patent/DK302984A/da not_active Application Discontinuation
- 1984-06-22 IL IL72207A patent/IL72207A0/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP0132301A1 (en) | 1985-01-30 |
| BR8403032A (pt) | 1985-05-28 |
| DK302984A (da) | 1984-12-23 |
| AU2956584A (en) | 1985-01-03 |
| IL72207A0 (en) | 1984-11-30 |
| DK302984D0 (da) | 1984-06-21 |
| JPS6013705A (ja) | 1985-01-24 |
| US4474760A (en) | 1984-10-02 |
| ZA844699B (en) | 1985-05-29 |
| KR850000188A (ko) | 1985-02-26 |
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Legal Events
| Date | Code | Title | Description |
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| BV | The patent application has lapsed |