NO855096L - Preparat inneholdende antimikrobiale stoffer i kombinasjon med stabilisatorer. - Google Patents
Preparat inneholdende antimikrobiale stoffer i kombinasjon med stabilisatorer. Download PDFInfo
- Publication number
- NO855096L NO855096L NO855096A NO855096A NO855096L NO 855096 L NO855096 L NO 855096L NO 855096 A NO855096 A NO 855096A NO 855096 A NO855096 A NO 855096A NO 855096 L NO855096 L NO 855096L
- Authority
- NO
- Norway
- Prior art keywords
- butyl
- composition
- hydroxyphenyl
- antimicrobial agent
- bis
- Prior art date
Links
- 230000000845 anti-microbial effect Effects 0.000 title claims description 21
- 239000003381 stabilizer Substances 0.000 title description 16
- 239000000126 substance Substances 0.000 title description 6
- 238000002360 preparation method Methods 0.000 title description 5
- 239000000203 mixture Substances 0.000 claims description 96
- 239000004599 antimicrobial Substances 0.000 claims description 77
- 239000003963 antioxidant agent Substances 0.000 claims description 48
- 239000000835 fiber Substances 0.000 claims description 39
- VCRZAKVGPJFABU-UHFFFAOYSA-N 10-phenoxarsinin-10-yloxyphenoxarsinine Chemical group C12=CC=CC=C2OC2=CC=CC=C2[As]1O[As]1C2=CC=CC=C2OC2=CC=CC=C21 VCRZAKVGPJFABU-UHFFFAOYSA-N 0.000 claims description 34
- 230000003078 antioxidant effect Effects 0.000 claims description 27
- 239000011347 resin Substances 0.000 claims description 20
- 229920005989 resin Polymers 0.000 claims description 20
- -1 3,5-di-t-butyl-4-hydroxyhydrocinnamic acid triester Chemical class 0.000 claims description 19
- 238000000034 method Methods 0.000 claims description 18
- 150000001875 compounds Chemical class 0.000 claims description 15
- 229920001169 thermoplastic Polymers 0.000 claims description 13
- 239000004416 thermosoftening plastic Substances 0.000 claims description 13
- 230000015556 catabolic process Effects 0.000 claims description 11
- 238000006731 degradation reaction Methods 0.000 claims description 11
- 150000003751 zinc Chemical class 0.000 claims description 11
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 10
- 229920002292 Nylon 6 Polymers 0.000 claims description 9
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 9
- 238000011282 treatment Methods 0.000 claims description 9
- 239000004952 Polyamide Substances 0.000 claims description 8
- 229920002647 polyamide Polymers 0.000 claims description 8
- 239000004800 polyvinyl chloride Substances 0.000 claims description 8
- 239000011342 resin composition Substances 0.000 claims description 8
- UDQCDDZBBZNIFA-UHFFFAOYSA-N 4-methyl-1,3-dihydrobenzimidazole-2-thione Chemical compound CC1=CC=CC2=C1NC(=S)N2 UDQCDDZBBZNIFA-UHFFFAOYSA-N 0.000 claims description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 7
- 230000000813 microbial effect Effects 0.000 claims description 7
- 229910052760 oxygen Inorganic materials 0.000 claims description 7
- 239000001301 oxygen Substances 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- 238000010128 melt processing Methods 0.000 claims description 6
- 229910052757 nitrogen Inorganic materials 0.000 claims description 6
- 229920005992 thermoplastic resin Polymers 0.000 claims description 6
- CWIYBOJLSWJGKV-UHFFFAOYSA-N 5-methyl-1,3-dihydrobenzimidazole-2-thione Chemical compound CC1=CC=C2NC(S)=NC2=C1 CWIYBOJLSWJGKV-UHFFFAOYSA-N 0.000 claims description 5
- 239000004743 Polypropylene Substances 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 5
- 229910052759 nickel Inorganic materials 0.000 claims description 5
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 claims description 5
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 claims description 5
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 claims description 5
- 229920001155 polypropylene Polymers 0.000 claims description 5
- 229910052717 sulfur Inorganic materials 0.000 claims description 5
- 150000007970 thio esters Chemical class 0.000 claims description 5
- JKIJEFPNVSHHEI-UHFFFAOYSA-N Phenol, 2,4-bis(1,1-dimethylethyl)-, phosphite (3:1) Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C JKIJEFPNVSHHEI-UHFFFAOYSA-N 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 239000002952 polymeric resin Substances 0.000 claims description 4
- 229920003002 synthetic resin Polymers 0.000 claims description 4
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M thiocyanate group Chemical group [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 claims description 4
- XYXJKPCGSGVSBO-UHFFFAOYSA-N 1,3,5-tris[(4-tert-butyl-3-hydroxy-2,6-dimethylphenyl)methyl]-1,3,5-triazinane-2,4,6-trione Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C)=C1CN1C(=O)N(CC=2C(=C(O)C(=CC=2C)C(C)(C)C)C)C(=O)N(CC=2C(=C(O)C(=CC=2C)C(C)(C)C)C)C1=O XYXJKPCGSGVSBO-UHFFFAOYSA-N 0.000 claims description 3
- YHMYGUUIMTVXNW-UHFFFAOYSA-N 1,3-dihydrobenzimidazole-2-thione Chemical compound C1=CC=C2NC(S)=NC2=C1 YHMYGUUIMTVXNW-UHFFFAOYSA-N 0.000 claims description 3
- 150000003923 2,5-pyrrolediones Chemical class 0.000 claims description 3
- 125000005393 dicarboximide group Chemical group 0.000 claims description 3
- 150000002367 halogens Chemical group 0.000 claims description 3
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 claims description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
- 150000008442 polyphenolic compounds Chemical class 0.000 claims description 3
- 235000013824 polyphenols Nutrition 0.000 claims description 3
- 235000012424 soybean oil Nutrition 0.000 claims description 3
- 239000003549 soybean oil Substances 0.000 claims description 3
- 125000004434 sulfur atom Chemical group 0.000 claims description 3
- VUWCWMOCWKCZTA-UHFFFAOYSA-N 1,2-thiazol-4-one Chemical class O=C1CSN=C1 VUWCWMOCWKCZTA-UHFFFAOYSA-N 0.000 claims description 2
- LLZHXQRNOOAOFF-UHFFFAOYSA-N 1,3-dihydrobenzimidazole-2-thione;zinc Chemical compound [Zn].C1=CC=C2NC(S)=NC2=C1 LLZHXQRNOOAOFF-UHFFFAOYSA-N 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 150000004982 aromatic amines Chemical class 0.000 claims description 2
- 238000004043 dyeing Methods 0.000 claims description 2
- 239000007800 oxidant agent Substances 0.000 claims description 2
- 150000002989 phenols Chemical class 0.000 claims description 2
- 239000011593 sulfur Chemical group 0.000 claims description 2
- ZTHYODDOHIVTJV-UHFFFAOYSA-N Propyl gallate Chemical compound CCCOC(=O)C1=CC(O)=C(O)C(O)=C1 ZTHYODDOHIVTJV-UHFFFAOYSA-N 0.000 claims 10
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 claims 9
- WPMYUUITDBHVQZ-UHFFFAOYSA-N 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoic acid Chemical compound CC(C)(C)C1=CC(CCC(O)=O)=CC(C(C)(C)C)=C1O WPMYUUITDBHVQZ-UHFFFAOYSA-N 0.000 claims 8
- 239000007983 Tris buffer Substances 0.000 claims 6
- JVKWTDRHWOSRFT-UHFFFAOYSA-N n-(4-hydroxyphenyl)dodecanamide Chemical compound CCCCCCCCCCCC(=O)NC1=CC=C(O)C=C1 JVKWTDRHWOSRFT-UHFFFAOYSA-N 0.000 claims 5
- VQLURHRLTDWRLX-UHFFFAOYSA-N n-(4-hydroxyphenyl)nonanamide Chemical compound CCCCCCCCC(=O)NC1=CC=C(O)C=C1 VQLURHRLTDWRLX-UHFFFAOYSA-N 0.000 claims 5
- SSDSCDGVMJFTEQ-UHFFFAOYSA-N octadecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SSDSCDGVMJFTEQ-UHFFFAOYSA-N 0.000 claims 5
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims 4
- KESXDDATSRRGAH-UHFFFAOYSA-N n-(4-hydroxyphenyl)butanamide Chemical compound CCCC(=O)NC1=CC=C(O)C=C1 KESXDDATSRRGAH-UHFFFAOYSA-N 0.000 claims 4
- BPXVHIRIPLPOPT-UHFFFAOYSA-N 1,3,5-tris(2-hydroxyethyl)-1,3,5-triazinane-2,4,6-trione Chemical compound OCCN1C(=O)N(CCO)C(=O)N(CCO)C1=O BPXVHIRIPLPOPT-UHFFFAOYSA-N 0.000 claims 3
- 150000005208 1,4-dihydroxybenzenes Chemical class 0.000 claims 3
- MQQKTNDBASEZSD-UHFFFAOYSA-N 1-(octadecyldisulfanyl)octadecane Chemical compound CCCCCCCCCCCCCCCCCCSSCCCCCCCCCCCCCCCCCC MQQKTNDBASEZSD-UHFFFAOYSA-N 0.000 claims 3
- VMZVBRIIHDRYGK-UHFFFAOYSA-N 2,6-ditert-butyl-4-[(dimethylamino)methyl]phenol Chemical compound CN(C)CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 VMZVBRIIHDRYGK-UHFFFAOYSA-N 0.000 claims 3
- WKTJXDHLMJKSGI-UHFFFAOYSA-N 3,9-di(cyclohex-3-en-1-yl)-2,4,8,10-tetraoxaspiro[5.5]undecane Chemical compound C1C=CCCC1C1OCC2(COC(OC2)C2CC=CCC2)CO1 WKTJXDHLMJKSGI-UHFFFAOYSA-N 0.000 claims 3
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 claims 3
- 229930185605 Bisphenol Natural products 0.000 claims 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims 3
- 150000001412 amines Chemical class 0.000 claims 3
- 229940111121 antirheumatic drug quinolines Drugs 0.000 claims 3
- 229910052791 calcium Inorganic materials 0.000 claims 3
- 239000011575 calcium Substances 0.000 claims 3
- 125000005266 diarylamine group Chemical group 0.000 claims 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims 3
- 239000002184 metal Substances 0.000 claims 3
- 229910052751 metal Inorganic materials 0.000 claims 3
- YCBUXHNUQAZVSS-UHFFFAOYSA-L n,n-bis(2-methylpropyl)carbamodithioate;nickel(2+) Chemical compound [Ni+2].CC(C)CN(C([S-])=S)CC(C)C.CC(C)CN(C([S-])=S)CC(C)C YCBUXHNUQAZVSS-UHFFFAOYSA-L 0.000 claims 3
- BLCKKNLGFULNRC-UHFFFAOYSA-L n,n-dimethylcarbamodithioate;nickel(2+) Chemical compound [Ni+2].CN(C)C([S-])=S.CN(C)C([S-])=S BLCKKNLGFULNRC-UHFFFAOYSA-L 0.000 claims 3
- 150000005002 naphthylamines Chemical class 0.000 claims 3
- 150000004989 p-phenylenediamines Chemical class 0.000 claims 3
- 235000010388 propyl gallate Nutrition 0.000 claims 3
- 150000003248 quinolines Chemical class 0.000 claims 3
- VFBJXXJYHWLXRM-UHFFFAOYSA-N 2-[2-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]ethylsulfanyl]ethyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCCSCCOC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 VFBJXXJYHWLXRM-UHFFFAOYSA-N 0.000 claims 2
- HPOWMHUJHHIQGP-UHFFFAOYSA-L n,n-dibutylcarbamodithioate;nickel(2+) Chemical compound [Ni+2].CCCCN(C([S-])=S)CCCC.CCCCN(C([S-])=S)CCCC HPOWMHUJHHIQGP-UHFFFAOYSA-L 0.000 claims 2
- 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 2
- ZLFHNCHMEGLFKL-UHFFFAOYSA-N 3,3-bis(3-tert-butyl-4-hydroxyphenyl)butanoic acid Chemical compound C1=C(O)C(C(C)(C)C)=CC(C(C)(CC(O)=O)C=2C=C(C(O)=CC=2)C(C)(C)C)=C1 ZLFHNCHMEGLFKL-UHFFFAOYSA-N 0.000 claims 1
- XMIIGOLPHOKFCH-UHFFFAOYSA-N 3-phenylpropionic acid Chemical compound OC(=O)CCC1=CC=CC=C1 XMIIGOLPHOKFCH-UHFFFAOYSA-N 0.000 claims 1
- 240000007594 Oryza sativa Species 0.000 claims 1
- 235000007164 Oryza sativa Nutrition 0.000 claims 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims 1
- DNSISZSEWVHGLH-UHFFFAOYSA-N butanamide Chemical compound CCCC(N)=O DNSISZSEWVHGLH-UHFFFAOYSA-N 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- BQHTWZRFOSRCCH-UHFFFAOYSA-L nickel(2+);dicarbamodithioate Chemical compound [Ni+2].NC([S-])=S.NC([S-])=S BQHTWZRFOSRCCH-UHFFFAOYSA-L 0.000 claims 1
- XPNWIWHUGHAVLC-UHFFFAOYSA-N octadecyl 3-[(3-octadecoxy-3-oxopropyl)disulfanyl]propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCSSCCC(=O)OCCCCCCCCCCCCCCCCCC XPNWIWHUGHAVLC-UHFFFAOYSA-N 0.000 claims 1
- KZAUOCCYDRDERY-UHFFFAOYSA-N oxamyl Chemical compound CNC(=O)ON=C(SC)C(=O)N(C)C KZAUOCCYDRDERY-UHFFFAOYSA-N 0.000 claims 1
- PLIKAWJENQZMHA-UHFFFAOYSA-N p-hydroxyphenylamine Natural products NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 claims 1
- 229920006122 polyamide resin Polymers 0.000 claims 1
- 235000009566 rice Nutrition 0.000 claims 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 229910052725 zinc Inorganic materials 0.000 claims 1
- 239000011701 zinc Substances 0.000 claims 1
- 235000006708 antioxidants Nutrition 0.000 description 34
- 101100188540 Candida albicans (strain SC5314 / ATCC MYA-2876) OBPA gene Proteins 0.000 description 26
- 239000000463 material Substances 0.000 description 11
- 229920001778 nylon Polymers 0.000 description 10
- 238000012360 testing method Methods 0.000 description 10
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- 239000000654 additive Substances 0.000 description 8
- 238000012545 processing Methods 0.000 description 8
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000004677 Nylon Substances 0.000 description 6
- 238000000354 decomposition reaction Methods 0.000 description 6
- SELUFQBSYXBQEB-UHFFFAOYSA-N 10H-phenoxarsinine Chemical class C1=CC=C2OC3=CC=CC=C3[AsH]C2=C1 SELUFQBSYXBQEB-UHFFFAOYSA-N 0.000 description 5
- 230000008901 benefit Effects 0.000 description 5
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- 239000007864 aqueous solution Substances 0.000 description 3
- 230000004071 biological effect Effects 0.000 description 3
- 239000012141 concentrate Substances 0.000 description 3
- PWWSSIYVTQUJQQ-UHFFFAOYSA-N distearyl thiodipropionate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCCCCCCCC PWWSSIYVTQUJQQ-UHFFFAOYSA-N 0.000 description 3
- 235000019305 distearyl thiodipropionate Nutrition 0.000 description 3
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- 229920001817 Agar Polymers 0.000 description 2
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 2
- APQHKWPGGHMYKJ-UHFFFAOYSA-N Tributyltin oxide Chemical compound CCCC[Sn](CCCC)(CCCC)O[Sn](CCCC)(CCCC)CCCC APQHKWPGGHMYKJ-UHFFFAOYSA-N 0.000 description 2
- QKDLQFSLLCQTOH-UHFFFAOYSA-N Trichodonin Natural products C1C(O)C2C3(COC(=O)C)C(C=O)C(C)(C)CCC3OC(=O)C22C(=O)C(=C)C1C2 QKDLQFSLLCQTOH-UHFFFAOYSA-N 0.000 description 2
- XEFQLINVKFYRCS-UHFFFAOYSA-N Triclosan Chemical compound OC1=CC(Cl)=CC=C1OC1=CC=C(Cl)C=C1Cl XEFQLINVKFYRCS-UHFFFAOYSA-N 0.000 description 2
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 2
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- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
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- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 2
- RTXFDQZPYZIUDD-UHFFFAOYSA-N phenylperoxyarsonic acid Chemical compound O[As](O)(=O)OOC1=CC=CC=C1 RTXFDQZPYZIUDD-UHFFFAOYSA-N 0.000 description 2
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- OKYPBVCIBXLADD-UHFFFAOYSA-N 1,2,4,10-tetrachlorophenoxarsinine Chemical compound C1=C(Cl)C(Cl)=C2[As](Cl)C3=CC=CC=C3OC2=C1Cl OKYPBVCIBXLADD-UHFFFAOYSA-N 0.000 description 1
- LXEINDTXUULHRQ-UHFFFAOYSA-N 1,3,10-trichlorophenoxarsinine Chemical compound ClC1=CC(Cl)=C2[As](Cl)C3=CC=CC=C3OC2=C1 LXEINDTXUULHRQ-UHFFFAOYSA-N 0.000 description 1
- MEZJQXVOMGUAMP-UHFFFAOYSA-N 1-(2-methylnaphthalen-1-yl)pyrrole-2,5-dione Chemical compound CC1=CC=C2C=CC=CC2=C1N1C(=O)C=CC1=O MEZJQXVOMGUAMP-UHFFFAOYSA-N 0.000 description 1
- DMYOHQBLOZMDLP-UHFFFAOYSA-N 1-[2-(2-hydroxy-3-piperidin-1-ylpropoxy)phenyl]-3-phenylpropan-1-one Chemical compound C1CCCCN1CC(O)COC1=CC=CC=C1C(=O)CCC1=CC=CC=C1 DMYOHQBLOZMDLP-UHFFFAOYSA-N 0.000 description 1
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 1
- KLOXBDFIXJLJQB-UHFFFAOYSA-N 1-n'-(trichloromethylsulfanyl)cyclohex-2-ene-1,1-dicarboxamide Chemical compound ClC(Cl)(Cl)SNC(=O)C1(C(=O)N)CCCC=C1 KLOXBDFIXJLJQB-UHFFFAOYSA-N 0.000 description 1
- SDMIOFRAYIQSKO-UHFFFAOYSA-N 10-(5h-phenarsazinin-10-yloxy)-5h-phenarsazinine Chemical compound C12=CC=CC=C2NC2=CC=CC=C2[As]1O[As]1C2=CC=CC=C2NC2=CC=CC=C21 SDMIOFRAYIQSKO-UHFFFAOYSA-N 0.000 description 1
- FMJJAEOAECZCSG-UHFFFAOYSA-N 10-(5h-phenarsazinin-10-ylsulfanyl)-5h-phenarsazinine Chemical compound C12=CC=CC=C2NC2=CC=CC=C2[As]1S[As]1C2=CC=CC=C2NC2=CC=CC=C21 FMJJAEOAECZCSG-UHFFFAOYSA-N 0.000 description 1
- IQROBNCNQUQVHM-UHFFFAOYSA-N 10-bromophenoxarsinine Chemical compound C1=CC=C2[As](Br)C3=CC=CC=C3OC2=C1 IQROBNCNQUQVHM-UHFFFAOYSA-N 0.000 description 1
- POHAAYQYRRLSNT-UHFFFAOYSA-N 10-chloro-1,4-dimethylphenoxarsinine Chemical compound Cl[As]1C2=CC=CC=C2OC2=C1C(C)=CC=C2C POHAAYQYRRLSNT-UHFFFAOYSA-N 0.000 description 1
- DRNURBALDVSCDX-UHFFFAOYSA-N 10-chloro-4-methylphenoxarsinine Chemical compound Cl[As]1C2=CC=CC=C2OC2=C1C=CC=C2C DRNURBALDVSCDX-UHFFFAOYSA-N 0.000 description 1
- RUZFPOBOXIDMSZ-UHFFFAOYSA-N 10-chlorophenoxarsinine Chemical compound C1=CC=C2[As](Cl)C3=CC=CC=C3OC2=C1 RUZFPOBOXIDMSZ-UHFFFAOYSA-N 0.000 description 1
- VVVJRIDLCFKHBP-UHFFFAOYSA-N 10-iodophenoxarsinine Chemical compound C1=CC=C2[As](I)C3=CC=CC=C3OC2=C1 VVVJRIDLCFKHBP-UHFFFAOYSA-N 0.000 description 1
- OPIAKPHPSGNHLC-UHFFFAOYSA-N 10-phenoxarsinin-10-ylsulfanylphenoxarsinine Chemical compound C12=CC=CC=C2OC2=CC=CC=C2[As]1S[As]1C2=CC=CC=C2OC2=CC=CC=C21 OPIAKPHPSGNHLC-UHFFFAOYSA-N 0.000 description 1
- JTMIZPDDFNGWEE-UHFFFAOYSA-N 2,10-dichloro-8-methylphenoxarsinine Chemical compound C1=C(Cl)C=C2[As](Cl)C3=CC(C)=CC=C3OC2=C1 JTMIZPDDFNGWEE-UHFFFAOYSA-N 0.000 description 1
- JHPTWFGJOWLZEV-UHFFFAOYSA-N 2,6,10-trichlorophenoxarsinine Chemical compound C1=CC=C2[As](Cl)C3=CC(Cl)=CC=C3OC2=C1Cl JHPTWFGJOWLZEV-UHFFFAOYSA-N 0.000 description 1
- VDUHWWPWPBGUPJ-UHFFFAOYSA-N 2,8,10-trichlorophenoxarsinine Chemical compound C1=C(Cl)C=C2[As](Cl)C3=CC(Cl)=CC=C3OC2=C1 VDUHWWPWPBGUPJ-UHFFFAOYSA-N 0.000 description 1
- OLFNXLXEGXRUOI-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4,6-bis(2-phenylpropan-2-yl)phenol Chemical compound C=1C(N2N=C3C=CC=CC3=N2)=C(O)C(C(C)(C)C=2C=CC=CC=2)=CC=1C(C)(C)C1=CC=CC=C1 OLFNXLXEGXRUOI-UHFFFAOYSA-N 0.000 description 1
- VYFCWUVTRWLLFW-UHFFFAOYSA-N 2-n-(trichloromethylsulfanyl)cyclohex-4-ene-1,2-dicarboxamide Chemical compound NC(=O)C1CC=CCC1C(=O)NSC(Cl)(Cl)Cl VYFCWUVTRWLLFW-UHFFFAOYSA-N 0.000 description 1
- CDVCTBMEYGRMLK-UHFFFAOYSA-N 2-tert-butyl-10-chlorophenoxarsinine Chemical compound C1=CC=C2[As](Cl)C3=CC(C(C)(C)C)=CC=C3OC2=C1 CDVCTBMEYGRMLK-UHFFFAOYSA-N 0.000 description 1
- CDIJOYCNNFLOAX-UHFFFAOYSA-N 4-(trichloromethylsulfanyl)isoindole-1,3-dione Chemical compound ClC(Cl)(Cl)SC1=CC=CC2=C1C(=O)NC2=O CDIJOYCNNFLOAX-UHFFFAOYSA-N 0.000 description 1
- 239000004604 Blowing Agent Substances 0.000 description 1
- 239000005745 Captan Substances 0.000 description 1
- IVHVNMLJNASKHW-UHFFFAOYSA-M Chlorphonium chloride Chemical compound [Cl-].CCCC[P+](CCCC)(CCCC)CC1=CC=C(Cl)C=C1Cl IVHVNMLJNASKHW-UHFFFAOYSA-M 0.000 description 1
- 241000156978 Erebia Species 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- DCXXMTOCNZCJGO-UHFFFAOYSA-N Glycerol trioctadecanoate Natural products CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 description 1
- OKOBUGCCXMIKDM-UHFFFAOYSA-N Irganox 1098 Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)NCCCCCCNC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 OKOBUGCCXMIKDM-UHFFFAOYSA-N 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 241000191967 Staphylococcus aureus Species 0.000 description 1
- 229920001079 Thiokol (polymer) Polymers 0.000 description 1
- 239000013504 Triton X-100 Substances 0.000 description 1
- 229920004890 Triton X-100 Polymers 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 239000003124 biologic agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229940117949 captan Drugs 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000007380 fibre production Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 239000001963 growth medium Substances 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 230000002779 inactivation Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 238000002074 melt spinning Methods 0.000 description 1
- 239000001964 microbiological growth medium Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 238000011369 optimal treatment Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000010525 oxidative degradation reaction Methods 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- DOIRQSBPFJWKBE-UHFFFAOYSA-N phthalic acid di-n-butyl ester Natural products CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000307 polymer substrate Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- PICXIOQBANWBIZ-UHFFFAOYSA-N zinc;1-oxidopyridine-2-thione Chemical compound [Zn+2].[O-]N1C=CC=CC1=S.[O-]N1C=CC=CC1=S PICXIOQBANWBIZ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F1/00—General methods for the manufacture of artificial filaments or the like
- D01F1/02—Addition of substances to the spinning solution or to the melt
- D01F1/10—Other agents for modifying properties
- D01F1/103—Agents inhibiting growth of microorganisms
-
- 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
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/005—Stabilisers against oxidation, heat, light, ozone
-
- 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
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0058—Biocides
-
- 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
- C08K5/59—Arsenic- or antimony-containing compounds
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/907—Resistant against plant or animal attack
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Organic Chemistry (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Textile Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biodiversity & Conservation Biology (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Artificial Filaments (AREA)
- Food Preservation Except Freezing, Refrigeration, And Drying (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/688,490 US4624679A (en) | 1985-01-03 | 1985-01-03 | Compositions containing antimicorbial agents in combination with stabilizers |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO855096L true NO855096L (no) | 1986-07-04 |
Family
ID=24764633
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO855096A NO855096L (no) | 1985-01-03 | 1985-12-17 | Preparat inneholdende antimikrobiale stoffer i kombinasjon med stabilisatorer. |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US4624679A (da) |
| EP (1) | EP0218768A3 (da) |
| JP (1) | JPS61165304A (da) |
| AU (1) | AU582609B2 (da) |
| BR (1) | BR8506583A (da) |
| DK (1) | DK986A (da) |
| ES (2) | ES8800301A1 (da) |
| NO (1) | NO855096L (da) |
| ZA (1) | ZA859539B (da) |
Families Citing this family (45)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4789692A (en) * | 1986-08-12 | 1988-12-06 | Morton Thiokol, Inc. | Resin-immobilized biocides |
| JPS63158713A (ja) * | 1986-12-19 | 1988-07-01 | 日立電線株式会社 | 防▲ばい▼性電線・ケ−ブル |
| JPS63158712A (ja) * | 1986-12-19 | 1988-07-01 | 日立電線株式会社 | 防▲ばい▼性電線・ケ−ブル |
| US4761247A (en) * | 1987-03-06 | 1988-08-02 | Morton Thiokol, Inc. | Phenol-stabilized microbiocidal compositions |
| JPS63265958A (ja) * | 1987-04-22 | 1988-11-02 | Shinagawa Nenryo Kk | 抗菌性樹脂組成物 |
| US4769268A (en) * | 1987-08-19 | 1988-09-06 | Basf Corporation | Thermoplastic compositions containing stabilized antimicrobial agents |
| US4797511A (en) * | 1987-09-25 | 1989-01-10 | Uniroyal Chemical Company, Inc. | Polyethylene stabilized by mixture of hindered phenol and amine antioxidants |
| US4947785A (en) * | 1988-01-07 | 1990-08-14 | International Paint Public Limited Company | Improvements in or relating to boat hulls |
| US4842932A (en) * | 1988-03-08 | 1989-06-27 | Basf Corporation | Fiber-containing yarn possessing antimicrobial activity |
| EP0357559B1 (de) * | 1988-09-02 | 1994-10-19 | AgrEvo UK Limited | Wässrige Formulierungen und deren Verwendung |
| US5279813A (en) * | 1989-10-26 | 1994-01-18 | Colgate-Palmolive Company | Plaque inhibition with antiplaque oral composition dispensed from container having polymeric material in contact and compatible with the composition |
| IL96820A (en) * | 1990-12-28 | 1995-06-29 | Bromine Compounds Ltd | Stabilized formulations of isothiazolinone |
| US6585843B2 (en) | 1992-01-10 | 2003-07-01 | Super Sack Mfg. Corp. | Anti-static, anti-corrosion, and/or anti-microbial films, fabrics, and articles |
| US6592702B2 (en) | 1992-01-10 | 2003-07-15 | Super Sack Mfg. Corp. | Anti-static, anti-corrosion, and/or anti-microbial films, fabrics, and articles |
| US5236652A (en) * | 1992-02-11 | 1993-08-17 | E. I. Du Pont De Nemours And Company | Process for making polyamide fiber useful as staple for papermaking machine felt |
| US5543110A (en) * | 1993-03-16 | 1996-08-06 | Westvaco Corporation | Tall oil deodorization process |
| US5554373A (en) * | 1993-11-05 | 1996-09-10 | Seabrook; Samuel G. | Compositions containing anti-microbial agents and methods for making and using same |
| US5562874A (en) * | 1993-12-17 | 1996-10-08 | Dowbrands L.P. | Multilayered antioxidant film |
| US6300395B1 (en) * | 1994-12-07 | 2001-10-09 | Nikon Parkerizing, Co., Ltd. | Aqueous hydrophilization treatment composition and method for aluminum-containing metal material |
| US5906825A (en) * | 1997-10-20 | 1999-05-25 | Magellan Companies, Inc. | Polymers containing antimicrobial agents and methods for making and using same |
| US6207290B1 (en) | 1998-04-07 | 2001-03-27 | Burlington Bio-Medical & Scientific Corp. | Antifoulant compositions and methods of treating wood |
| US5962562A (en) * | 1998-09-01 | 1999-10-05 | The Goodyear Tire & Rubber Company | Rubber compositions containing N-(4-hydroxyphenyl) stearamide |
| AU3436499A (en) * | 1999-04-15 | 2000-11-02 | Plasticisers Limited | Polyolefin fibres |
| US6723428B1 (en) * | 1999-05-27 | 2004-04-20 | Foss Manufacturing Co., Inc. | Anti-microbial fiber and fibrous products |
| US6627676B1 (en) | 1999-08-27 | 2003-09-30 | Richard George | Antimicrobial biocidic fiber-plastic composite and method of making same |
| GB0004437D0 (en) * | 2000-02-25 | 2000-04-12 | Clariant Int Ltd | Synergistic combinations of phenolic antioxidants |
| DE10010072A1 (de) * | 2000-03-02 | 2001-09-06 | Rheinchemie Rheinau Gmbh | Biozid-Batche auf Basis vernetzter Öle, Verfahren zu ihrer Gerstellung und ihre Verwendung in thermoplastischen Formmassen |
| US6444737B1 (en) | 2000-04-05 | 2002-09-03 | 3M Innovative Properties Company | Water-dispersed polymer stabilizer |
| US7101624B2 (en) | 2000-06-22 | 2006-09-05 | Cello-Foil Products, Inc. | Laminate antioxidant film |
| DE10043072A1 (de) * | 2000-09-01 | 2002-03-14 | Bosch Gmbh Robert | Verfahren zur Gemischadaption bei Verbrennungsmotoren mit Benzindirekteinspritzung |
| DE10134327A1 (de) * | 2001-07-14 | 2002-02-28 | Raschig Gmbh | Antioxidantien für Polyamide |
| US6666185B1 (en) * | 2002-05-30 | 2003-12-23 | Caterpillar Inc | Distributed ignition method and apparatus for a combustion engine |
| WO2004024278A2 (en) * | 2002-09-16 | 2004-03-25 | Triosyn Holding, Inc. | Electrostatically charged filter media incorporating an active agent |
| US7569526B2 (en) * | 2003-04-08 | 2009-08-04 | Crompton Corporation | Anti-oxidants in soluble oil base for metal working fluids |
| CN101056926B (zh) * | 2004-11-09 | 2011-11-23 | 西巴特殊化学品控股有限公司 | 具有改善抗褪色性抗微生物聚合物组合物 |
| JP4950583B2 (ja) * | 2006-07-28 | 2012-06-13 | 大日精化工業株式会社 | 抗菌性樹脂組成物及びその製造方法、抗菌性樹脂成形品、並びに抗菌性物品 |
| US9555167B2 (en) | 2006-12-11 | 2017-01-31 | 3M Innovative Properties Company | Biocompatible antimicrobial compositions |
| MX2008001141A (es) * | 2007-02-09 | 2009-02-24 | Rohm & Haas | Metodo para reducir el olor en pinturas de latex. |
| US20080295843A1 (en) * | 2007-06-01 | 2008-12-04 | Haas Marci B | Self sanitizing face masks and method of manufacture |
| JP5388326B2 (ja) * | 2008-05-12 | 2014-01-15 | 住化スタイロンポリカーボネート株式会社 | 抗菌性に優れた透明熱可塑性樹脂組成物およびそれからなる成形品 |
| JP5170762B2 (ja) * | 2008-08-27 | 2013-03-27 | 住化スタイロンポリカーボネート株式会社 | 抗菌性熱可塑性樹脂組成物からなる把手部品 |
| US20110233810A1 (en) * | 2010-03-25 | 2011-09-29 | W. M. Barr & Company | Antimicrobial plastic compositions and methods for preparing same |
| US20130025456A1 (en) * | 2011-07-25 | 2013-01-31 | Chapman Rick L | Air cleaning filter media |
| US9382448B2 (en) * | 2014-08-29 | 2016-07-05 | Prc-Desoto International, Inc. | Polythioether sealants with enhanced thermal resistance |
| US10299954B2 (en) * | 2015-02-13 | 2019-05-28 | Enma Troutner | Therapeutic cushioning pants |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2371618A (en) * | 1941-02-20 | 1945-03-20 | Dow Chemical Co | Preservation of textile materials |
| US2689837A (en) * | 1951-03-02 | 1954-09-21 | Monsanto Chemicals | Fungi and bacteria resistant polyvinyl halide compositions |
| US2802811A (en) * | 1953-11-02 | 1957-08-13 | Vanderbilt Co R T | Chloroprene stabilized with a mixture of zinc dimethyl dithiocarbamate and the zinc salt of mercaptobenzothiazole |
| US3096183A (en) * | 1959-03-12 | 1963-07-02 | Bayer Ag | Bacteria-resistant plastic materials |
| FR1293695A (fr) * | 1961-04-29 | 1962-05-18 | Procédé de protection temporaire des surfaces sensibles par revêtements filmogènes en contact direct | |
| US3223547A (en) * | 1961-06-07 | 1965-12-14 | Geigy Chem Corp | Antimicrobic compositions and use thereof |
| US3105060A (en) * | 1961-09-22 | 1963-09-24 | Dow Chemical Co | Microbiocidal resinous compositions |
| US3133072A (en) * | 1962-01-16 | 1964-05-12 | Hollichem Corp | Quaternary ammonium cyclic imides |
| US3288674A (en) * | 1965-03-15 | 1966-11-29 | Scient Chemicals Inc | Phenoxarsine compounds incorporated into resins with phenols |
| US3360431A (en) * | 1965-03-15 | 1967-12-26 | Scient Chemicals Inc | Compositions and method for incorporating microbiocidal amounts of arsenosobenzene into resins |
| NL6911454A (da) * | 1969-07-25 | 1969-10-27 | ||
| US3567119A (en) * | 1969-10-06 | 1971-03-02 | Godfrey Wilbert | Enhanced diffusion of odor vapor from polymers |
| US3833520A (en) * | 1973-01-05 | 1974-09-03 | Tenneco Chem | Method of controlling microbial growth in polyvinyl halide resin compositions |
| US4049822A (en) * | 1975-08-04 | 1977-09-20 | Ventron Corporation | Microbiocidal compositions comprising a solution of a phenoxarsine compound |
| US4086297A (en) * | 1975-11-28 | 1978-04-25 | Ventron Corporation | Method of making polymeric compositions and compositions therefor |
| US4474760A (en) * | 1983-06-22 | 1984-10-02 | Excalibur, Inc. | Stabilized 2-mercaptopyridene-1-oxide and derivatives |
| ATE43471T1 (de) * | 1983-11-17 | 1989-06-15 | Akzo Nv | Antimikrobielle mischungen. |
| AU4799185A (en) * | 1984-09-02 | 1986-04-10 | Wellcome Foundation Limited, The | Animal pour-on formulations stabilized by carbodiimide derivatives |
-
1985
- 1985-01-03 US US06/688,490 patent/US4624679A/en not_active Expired - Fee Related
- 1985-12-11 EP EP85309016A patent/EP0218768A3/en not_active Withdrawn
- 1985-12-11 AU AU51107/85A patent/AU582609B2/en not_active Expired - Fee Related
- 1985-12-12 ZA ZA859539A patent/ZA859539B/xx unknown
- 1985-12-17 NO NO855096A patent/NO855096L/no unknown
- 1985-12-27 JP JP60299726A patent/JPS61165304A/ja active Pending
- 1985-12-30 BR BR8506583A patent/BR8506583A/pt unknown
-
1986
- 1986-01-02 DK DK986A patent/DK986A/da not_active Application Discontinuation
- 1986-01-02 ES ES550639A patent/ES8800301A1/es not_active Expired
-
1987
- 1987-05-28 ES ES557567A patent/ES8802172A1/es not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| ES550639A0 (es) | 1987-11-01 |
| ES8800301A1 (es) | 1987-11-01 |
| EP0218768A3 (en) | 1988-08-24 |
| AU582609B2 (en) | 1989-04-06 |
| EP0218768A2 (en) | 1987-04-22 |
| ES8802172A1 (es) | 1988-04-01 |
| US4624679A (en) | 1986-11-25 |
| DK986D0 (da) | 1986-01-02 |
| BR8506583A (pt) | 1986-09-09 |
| JPS61165304A (ja) | 1986-07-26 |
| DK986A (da) | 1986-07-04 |
| AU5110785A (en) | 1986-07-17 |
| ES557567A0 (es) | 1988-04-01 |
| ZA859539B (en) | 1986-11-26 |
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