IL100290A - Preparations for the eradication of bacteria, fungi and algae containing 3-isothiazolones - Google Patents

Preparations for the eradication of bacteria, fungi and algae containing 3-isothiazolones

Info

Publication number: IL100290A
Authority: IL; Israel
Prior art keywords: copper; isothiazolone; carbon atoms; composition; substituted
Prior art date: 1990-12-10

Application number

IL10029091A

Other languages

English (en)

Hebrew (he)

Other versions

IL100290A0 (en

Original Assignee

Rohm & Haas

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1990-12-10

Filing date

1991-12-09

Publication date

1995-08-31

1991-12-09 Application filed by Rohm & Haas filed Critical Rohm & Haas

1992-09-06 Publication of IL100290A0 publication Critical patent/IL100290A0/xx

1995-08-31 Publication of IL100290A publication Critical patent/IL100290A/en

Links

239000000203 mixture Substances 0.000 title claims abstract description 48
MGIYRDNGCNKGJU-UHFFFAOYSA-N isothiazolinone Chemical class O=C1C=CSN1 MGIYRDNGCNKGJU-UHFFFAOYSA-N 0.000 title claims abstract description 11
241000894006 Bacteria Species 0.000 title claims description 3
241000195493 Cryptophyta Species 0.000 title claims description 3
241000233866 Fungi Species 0.000 title claims description 3
JLHMJWHSBYZWJJ-UHFFFAOYSA-N 1,2-thiazole 1-oxide Chemical compound O=S1C=CC=N1 JLHMJWHSBYZWJJ-UHFFFAOYSA-N 0.000 claims abstract description 40
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 39
239000010949 copper Substances 0.000 claims abstract description 36
-1 3-isothiazolone compound Chemical class 0.000 claims abstract description 21
229910052802 copper Inorganic materials 0.000 claims abstract description 21
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims abstract description 20
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims abstract description 12
239000003208 petroleum Substances 0.000 claims abstract description 10
WHMUWYOLIAEORL-UHFFFAOYSA-N copper;1,4-dioctoxy-1,4-dioxobutane-2-sulfonic acid Chemical compound [Cu].CCCCCCCCOC(=O)CC(S(O)(=O)=O)C(=O)OCCCCCCCC WHMUWYOLIAEORL-UHFFFAOYSA-N 0.000 claims abstract description 9
OUNVHRVEZKVXQB-UHFFFAOYSA-N copper;dodecyl benzenesulfonate Chemical compound [Cu].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 OUNVHRVEZKVXQB-UHFFFAOYSA-N 0.000 claims abstract description 9
239000003960 organic solvent Substances 0.000 claims abstract description 6
125000004432 carbon atom Chemical group C* 0.000 claims description 21
239000003381 stabilizer Substances 0.000 claims description 17
239000003973 paint Substances 0.000 claims description 15
125000000217 alkyl group Chemical group 0.000 claims description 13
239000002904 solvent Substances 0.000 claims description 12
239000005749 Copper compound Substances 0.000 claims description 10
150000001880 copper compounds Chemical class 0.000 claims description 10
125000001475 halogen functional group Chemical group 0.000 claims description 8
125000003710 aryl alkyl group Chemical group 0.000 claims description 6
238000000034 method Methods 0.000 claims description 6
238000002144 chemical decomposition reaction Methods 0.000 claims description 5
230000003641 microbiacidal effect Effects 0.000 claims description 5
229940124561 microbicide Drugs 0.000 claims description 5
PORQOHRXAJJKGK-UHFFFAOYSA-N 4,5-dichloro-2-n-octyl-3(2H)-isothiazolone Chemical compound CCCCCCCCN1SC(Cl)=C(Cl)C1=O PORQOHRXAJJKGK-UHFFFAOYSA-N 0.000 claims description 4
125000003118 aryl group Chemical group 0.000 claims description 4
125000004104 aryloxy group Chemical group 0.000 claims description 4
229910052739 hydrogen Inorganic materials 0.000 claims description 4
239000001257 hydrogen Substances 0.000 claims description 4
230000000087 stabilizing effect Effects 0.000 claims description 4
150000002431 hydrogen Chemical class 0.000 claims description 3
125000000041 C6-C10 aryl group Chemical class 0.000 claims description 2
230000002411 adverse Effects 0.000 claims description 2
125000003545 alkoxy group Chemical group 0.000 claims description 2
125000003282 alkyl amino group Chemical group 0.000 claims description 2
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
125000004663 dialkyl amino group Chemical group 0.000 claims description 2
239000003995 emulsifying agent Substances 0.000 claims description 2
229910052736 halogen Inorganic materials 0.000 claims description 2
150000002367 halogens Chemical class 0.000 claims description 2
230000002401 inhibitory effect Effects 0.000 claims description 2
JPMIIZHYYWMHDT-UHFFFAOYSA-N octhilinone Chemical group CCCCCCCCN1SC=CC1=O JPMIIZHYYWMHDT-UHFFFAOYSA-N 0.000 claims description 2
125000000547 substituted alkyl group Chemical group 0.000 claims description 2
239000002519 antifouling agent Substances 0.000 claims 2
239000011248 coating agent Substances 0.000 claims 2
238000000576 coating method Methods 0.000 claims 2
239000012530 fluid Substances 0.000 claims 2
238000005555 metalworking Methods 0.000 claims 2
239000003171 wood protecting agent Substances 0.000 claims 2
JRQLZCFSWYQHPI-UHFFFAOYSA-N 4,5-dichloro-2-cyclohexyl-1,2-thiazol-3-one Chemical compound O=C1C(Cl)=C(Cl)SN1C1CCCCC1 JRQLZCFSWYQHPI-UHFFFAOYSA-N 0.000 claims 1
125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
125000004093 cyano group Chemical group *C#N 0.000 claims 1
125000004356 hydroxy functional group Chemical group O* 0.000 claims 1
239000002855 microbicide agent Substances 0.000 claims 1
150000001879 copper Chemical class 0.000 abstract description 14
239000012141 concentrate Substances 0.000 abstract description 2
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 57
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 15
239000000243 solution Substances 0.000 description 14
JJLJMEJHUUYSSY-UHFFFAOYSA-L Copper hydroxide Chemical compound [OH-].[OH-].[Cu+2] JJLJMEJHUUYSSY-UHFFFAOYSA-L 0.000 description 13
239000005750 Copper hydroxide Substances 0.000 description 13
229910001956 copper hydroxide Inorganic materials 0.000 description 13
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 12
150000003839 salts Chemical class 0.000 description 10
230000006641 stabilisation Effects 0.000 description 8
238000011105 stabilization Methods 0.000 description 8
229910052751 metal Inorganic materials 0.000 description 7
239000002184 metal Substances 0.000 description 7
NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 6
229920001429 chelating resin Polymers 0.000 description 6
239000008367 deionised water Substances 0.000 description 6
229910021641 deionized water Inorganic materials 0.000 description 6
238000000605 extraction Methods 0.000 description 6
238000009472 formulation Methods 0.000 description 6
239000003456 ion exchange resin Substances 0.000 description 6
229920003303 ion-exchange polymer Polymers 0.000 description 6
239000002808 molecular sieve Substances 0.000 description 6
239000012508 resin bead Substances 0.000 description 6
URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 6
239000000463 material Substances 0.000 description 5
239000007787 solid Substances 0.000 description 5
150000001735 carboxylic acids Chemical class 0.000 description 4
238000000921 elemental analysis Methods 0.000 description 4
229920000126 latex Polymers 0.000 description 4
239000000047 product Substances 0.000 description 4
238000011084 recovery Methods 0.000 description 4
WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
239000006185 dispersion Substances 0.000 description 3
229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 3
239000004816 latex Substances 0.000 description 3
DAFHKNAQFPVRKR-UHFFFAOYSA-N (3-hydroxy-2,2,4-trimethylpentyl) 2-methylpropanoate Chemical compound CC(C)C(O)C(C)(C)COC(=O)C(C)C DAFHKNAQFPVRKR-UHFFFAOYSA-N 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
150000001336 alkenes Chemical class 0.000 description 2
230000003115 biocidal effect Effects 0.000 description 2
150000001805 chlorine compounds Chemical class 0.000 description 2
238000005345 coagulation Methods 0.000 description 2
230000015271 coagulation Effects 0.000 description 2
239000000084 colloidal system Substances 0.000 description 2
230000000052 comparative effect Effects 0.000 description 2
150000004696 coordination complex Chemical class 0.000 description 2
230000007797 corrosion Effects 0.000 description 2
238000005260 corrosion Methods 0.000 description 2
YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical compound CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 description 2
150000002334 glycols Chemical class 0.000 description 2
235000019447 hydroxyethyl cellulose Nutrition 0.000 description 2
239000004615 ingredient Substances 0.000 description 2
229910001960 metal nitrate Inorganic materials 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
HFQQZARZPUDIFP-UHFFFAOYSA-M sodium;2-dodecylbenzenesulfonate Chemical compound [Na+].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O HFQQZARZPUDIFP-UHFFFAOYSA-M 0.000 description 2
239000012265 solid product Substances 0.000 description 2
239000000126 substance Substances 0.000 description 2
125000001424 substituent group Chemical group 0.000 description 2
229940104261 taurate Drugs 0.000 description 2
125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
QWOZZTWBWQMEPD-UHFFFAOYSA-N 1-(2-ethoxypropoxy)propan-2-ol Chemical compound CCOC(C)COCC(C)O QWOZZTWBWQMEPD-UHFFFAOYSA-N 0.000 description 1
NFGXHKASABOEEW-UHFFFAOYSA-N 1-methylethyl 11-methoxy-3,7,11-trimethyl-2,4-dodecadienoate Chemical compound COC(C)(C)CCCC(C)CC=CC(C)=CC(=O)OC(C)C NFGXHKASABOEEW-UHFFFAOYSA-N 0.000 description 1
RNAMYOYQYRYFQY-UHFFFAOYSA-N 2-(4,4-difluoropiperidin-1-yl)-6-methoxy-n-(1-propan-2-ylpiperidin-4-yl)-7-(3-pyrrolidin-1-ylpropoxy)quinazolin-4-amine Chemical compound N1=C(N2CCC(F)(F)CC2)N=C2C=C(OCCCN3CCCC3)C(OC)=CC2=C1NC1CCN(C(C)C)CC1 RNAMYOYQYRYFQY-UHFFFAOYSA-N 0.000 description 1
229940109696 4,5-dichloro-2-octyl-3-isothiazolone Drugs 0.000 description 1
DFDBVSYZLJCHQG-UHFFFAOYSA-N 4,5-dichloro-3-octyl-1,2-thiazole 1-oxide Chemical class CCCCCCCCC1=NS(=O)C(Cl)=C1Cl DFDBVSYZLJCHQG-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
XTEGARKTQYYJKE-UHFFFAOYSA-M Chlorate Chemical class [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
241000784732 Lycaena phlaeas Species 0.000 description 1
ZVXSESPJMKNIQA-YXMSTPNBSA-N Lys-Thr-Pro-Pro Chemical compound NCCCC[C@H](N)C(=O)N[C@@H]([C@H](O)C)C(=O)N1CCC[C@H]1C(=O)N1[C@H](C(O)=O)CCC1 ZVXSESPJMKNIQA-YXMSTPNBSA-N 0.000 description 1
229910002651 NO3 Inorganic materials 0.000 description 1
NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
229920013802 TRITON CF-10 Polymers 0.000 description 1
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
229910052787 antimony Inorganic materials 0.000 description 1
WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
230000008901 benefit Effects 0.000 description 1
239000003139 biocide Substances 0.000 description 1
150000001721 carbon Chemical group 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
XTVVROIMIGLXTD-UHFFFAOYSA-N copper(II) nitrate Chemical compound [Cu+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O XTVVROIMIGLXTD-UHFFFAOYSA-N 0.000 description 1
RJHOEBMKVFIBNW-UHFFFAOYSA-N copper;1,2-thiazole 1-oxide Chemical compound [Cu].O=S1C=CC=N1 RJHOEBMKVFIBNW-UHFFFAOYSA-N 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 description 1
SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
235000019262 disodium citrate Nutrition 0.000 description 1
239000002526 disodium citrate Substances 0.000 description 1
YHAIUSTWZPMYGG-UHFFFAOYSA-L disodium;2,2-dioctyl-3-sulfobutanedioate Chemical compound [Na+].[Na+].CCCCCCCCC(C([O-])=O)(C(C([O-])=O)S(O)(=O)=O)CCCCCCCC YHAIUSTWZPMYGG-UHFFFAOYSA-L 0.000 description 1
CEYULKASIQJZGP-UHFFFAOYSA-L disodium;2-(carboxymethyl)-2-hydroxybutanedioate Chemical compound [Na+].[Na+].[O-]C(=O)CC(O)(C(=O)O)CC([O-])=O CEYULKASIQJZGP-UHFFFAOYSA-L 0.000 description 1
229940071161 dodecylbenzenesulfonate Drugs 0.000 description 1
238000001035 drying Methods 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
230000003993 interaction Effects 0.000 description 1
239000003446 ligand Substances 0.000 description 1
210000004072 lung Anatomy 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000011707 mineral Substances 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
238000002156 mixing Methods 0.000 description 1
238000006386 neutralization reaction Methods 0.000 description 1
150000002823 nitrates Chemical class 0.000 description 1
239000012457 nonaqueous media Substances 0.000 description 1
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
229920000620 organic polymer Polymers 0.000 description 1
VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical class OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 1
229920005862 polyol Polymers 0.000 description 1
150000003077 polyols Chemical class 0.000 description 1
231100000683 possible toxicity Toxicity 0.000 description 1
230000008569 process Effects 0.000 description 1
238000000926 separation method Methods 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
235000015096 spirit Nutrition 0.000 description 1
238000003756 stirring Methods 0.000 description 1
238000003860 storage Methods 0.000 description 1
239000000758 substrate Substances 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
231100000606 suspected carcinogen Toxicity 0.000 description 1
230000002195 synergetic effect Effects 0.000 description 1
239000011885 synergistic combination Substances 0.000 description 1
XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 1
229910052723 transition metal Inorganic materials 0.000 description 1
150000003624 transition metals Chemical class 0.000 description 1
GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
239000002023 wood Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc Substances 0.000 description 1

Classifications

- 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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
- 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
- C09D5/16—Antifouling paints; Underwater paints
- C09D5/1606—Antifouling paints; Underwater paints characterised by the anti-fouling agent
- C09D5/1612—Non-macromolecular compounds
- C09D5/1625—Non-macromolecular compounds organic
- 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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B23/00—Re-forming shaped glass
- C03B23/02—Re-forming glass sheets
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B23/00—Re-forming shaped glass
- C03B23/02—Re-forming glass sheets
- C03B23/023—Re-forming glass sheets by bending
- C03B23/025—Re-forming glass sheets by bending by gravity
- C03B23/0252—Re-forming glass sheets by bending by gravity by gravity only, e.g. sagging
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B23/00—Re-forming shaped glass
- C03B23/02—Re-forming glass sheets
- C03B23/023—Re-forming glass sheets by bending
- C03B23/03—Re-forming glass sheets by bending by press-bending between shaping moulds
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B23/00—Re-forming shaped glass
- C03B23/02—Re-forming glass sheets
- C03B23/023—Re-forming glass sheets by bending
- C03B23/035—Re-forming glass sheets by bending using a gas cushion or by changing gas pressure, e.g. by applying vacuum or blowing for supporting the glass while bending
- C03B23/0352—Re-forming glass sheets by bending using a gas cushion or by changing gas pressure, e.g. by applying vacuum or blowing for supporting the glass while bending by suction or blowing out for providing the deformation force to bend the glass sheet
- C03B23/0357—Re-forming glass sheets by bending using a gas cushion or by changing gas pressure, e.g. by applying vacuum or blowing for supporting the glass while bending by suction or blowing out for providing the deformation force to bend the glass sheet by suction without blowing, e.g. with vacuum or by venturi effect
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B27/00—Tempering or quenching glass products
- C03B27/04—Tempering or quenching glass products using gas
- C03B27/0417—Controlling or regulating for flat or bent glass sheets
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B27/00—Tempering or quenching glass products
- C03B27/04—Tempering or quenching glass products using gas
- C03B27/044—Tempering or quenching glass products using gas for flat or bent glass sheets being in a horizontal position
- C03B27/048—Tempering or quenching glass products using gas for flat or bent glass sheets being in a horizontal position on a gas cushion
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B29/00—Reheating glass products for softening or fusing their surfaces; Fire-polishing; Fusing of margins
- C03B29/04—Reheating glass products for softening or fusing their surfaces; Fire-polishing; Fusing of margins in a continuous way
- C03B29/06—Reheating glass products for softening or fusing their surfaces; Fire-polishing; Fusing of margins in a continuous way with horizontal displacement of the products
- C03B29/08—Glass sheets
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B35/00—Transporting of glass products during their manufacture, e.g. hot glass lenses, prisms
- C03B35/14—Transporting hot glass sheets or ribbons, e.g. by heat-resistant conveyor belts or bands
- C03B35/145—Transporting hot glass sheets or ribbons, e.g. by heat-resistant conveyor belts or bands by top-side transfer or supporting devices, e.g. lifting or conveying using suction
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B35/00—Transporting of glass products during their manufacture, e.g. hot glass lenses, prisms
- C03B35/14—Transporting hot glass sheets or ribbons, e.g. by heat-resistant conveyor belts or bands
- C03B35/16—Transporting hot glass sheets or ribbons, e.g. by heat-resistant conveyor belts or bands by roller conveyors
- C03B35/163—Drive means, clutches, gearing or drive speed control means
- C03B35/164—Drive means, clutches, gearing or drive speed control means electric or electronicsystems therefor, e.g. for automatic control
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B35/00—Transporting of glass products during their manufacture, e.g. hot glass lenses, prisms
- C03B35/14—Transporting hot glass sheets or ribbons, e.g. by heat-resistant conveyor belts or bands
- C03B35/20—Transporting hot glass sheets or ribbons, e.g. by heat-resistant conveyor belts or bands by gripping tongs or supporting frames
- C03B35/202—Transporting hot glass sheets or ribbons, e.g. by heat-resistant conveyor belts or bands by gripping tongs or supporting frames by supporting frames
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B35/00—Transporting of glass products during their manufacture, e.g. hot glass lenses, prisms
- C03B35/14—Transporting hot glass sheets or ribbons, e.g. by heat-resistant conveyor belts or bands
- C03B35/22—Transporting hot glass sheets or ribbons, e.g. by heat-resistant conveyor belts or bands on a fluid support bed, e.g. on molten metal
- C03B35/24—Transporting hot glass sheets or ribbons, e.g. by heat-resistant conveyor belts or bands on a fluid support bed, e.g. on molten metal on a gas support bed
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
- C07C303/32—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of salts of sulfonic acids
- 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
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B2225/00—Transporting hot glass sheets during their manufacture
- C03B2225/02—Means for positioning, aligning or orientating the sheets during their travel, e.g. stops

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Life Sciences & Earth Sciences (AREA)
Materials Engineering (AREA)
Wood Science & Technology (AREA)
Plant Pathology (AREA)
Dentistry (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Health & Medical Sciences (AREA)
Environmental Sciences (AREA)
General Health & Medical Sciences (AREA)
Zoology (AREA)
Thermal Sciences (AREA)
Physics & Mathematics (AREA)
Microelectronics & Electronic Packaging (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Thiazole And Isothizaole Compounds (AREA)
Plural Heterocyclic Compounds (AREA)
Paints Or Removers (AREA)
Chemical And Physical Treatments For Wood And The Like (AREA)
Lubricants (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Preventing Corrosion Or Incrustation Of Metals (AREA)

IL10029091A 1990-12-10 1991-12-09 Preparations for the eradication of bacteria, fungi and algae containing 3-isothiazolones IL100290A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US07/625,269 US5108500A (en)	1990-12-10	1990-12-10	Stabilization of water insoluble 3-isothiazolones

Publications (2)

Publication Number	Publication Date
IL100290A0 IL100290A0 (en)	1992-09-06
IL100290A true IL100290A (en)	1995-08-31

Family

ID=24505302

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL10029091A IL100290A (en)	1990-12-10	1991-12-09	Preparations for the eradication of bacteria, fungi and algae containing 3-isothiazolones

Country Status (13)

Country	Link
US (1)	US5108500A (de)
EP (1)	EP0490565B1 (de)
JP (1)	JP3176674B2 (de)
KR (1)	KR100218057B1 (de)
AT (1)	ATE199148T1 (de)
AU (1)	AU659113B2 (de)
CA (1)	CA2056632C (de)
DE (1)	DE69132534T2 (de)
ES (1)	ES2153819T3 (de)
HU (1)	HU208470B (de)
IL (1)	IL100290A (de)
MY (1)	MY107685A (de)
SG (1)	SG66265A1 (de)

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US5252223A (en) *	1992-11-23	1993-10-12	Nalco Chemical Company	Reduction of copper discharge to waste streams contaminated with isothiazolone biocides
US5373016A (en) *	1993-05-28	1994-12-13	Zeneca, Inc.	Protection of isothiazolinone biocides from free radicals
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EP0669364A1 (de) *	1993-12-24	1995-08-30	Marubishi Oil Chemical Co., Ltd.	Modifikator für Harze und Kautschuk
JP3393909B2 (ja) *	1993-12-27	2003-04-07	中国塗料株式会社	有害水中生物防除剤および防汚塗料
US5461150A (en) *	1994-12-14	1995-10-24	Rohm And Haas Company	Stabilization of 3-isothiazolone solutions
DE19534532C2 (de) *	1995-09-08	1999-04-08	Schuelke & Mayr Gmbh	Additivmischungen für Kühlschmiermittelprodukte und deren Verwendung
US6299622B1 (en)	1999-08-19	2001-10-09	Fox Hollow Technologies, Inc.	Atherectomy catheter with aligned imager
US7713279B2 (en)	2000-12-20	2010-05-11	Fox Hollow Technologies, Inc.	Method and devices for cutting tissue
US7708749B2 (en)	2000-12-20	2010-05-04	Fox Hollow Technologies, Inc.	Debulking catheters and methods
US8328829B2 (en)	1999-08-19	2012-12-11	Covidien Lp	High capacity debulking catheter with razor edge cutting window
US6255331B1 (en) *	1999-09-14	2001-07-03	Rohm And Haas Company	Stable biocidal compositions
US6403533B2 (en) *	2000-01-27	2002-06-11	Rohm And Haas Company	Stabilized microbicide formulation
ATE499054T1 (de)	2000-12-20	2011-03-15	Fox Hollow Technologies Inc	Verkleinerungskatheter
EP1421852B1 (de) *	2002-11-22	2006-06-07	Rohm And Haas Company	Wässrige Dispersion von organischen Feststoffen mit niedrigem Schmelzpunkt
US8246640B2 (en)	2003-04-22	2012-08-21	Tyco Healthcare Group Lp	Methods and devices for cutting tissue at a vascular location
JP2005068125A (ja) *	2003-08-21	2005-03-17	Rohm & Haas Co	殺生物剤配合物の調製方法
US20070276419A1 (en)	2006-05-26	2007-11-29	Fox Hollow Technologies, Inc.	Methods and devices for rotating an active element and an energy emitter on a catheter
US8784440B2 (en)	2008-02-25	2014-07-22	Covidien Lp	Methods and devices for cutting tissue
US8414604B2 (en)	2008-10-13	2013-04-09	Covidien Lp	Devices and methods for manipulating a catheter shaft
AU2010241801B2 (en)	2009-04-29	2013-04-11	Covidien Lp	Methods and devices for cutting and abrading tissue
EP2429423B1 (de)	2009-05-14	2015-11-11	Covidien LP	Leicht zu reinigende atherektomiekatheter
BR112012013389A2 (pt)	2009-12-02	2018-03-06	Tyco Healthcare	métodos e dispositivos para o corte de um tecido
CN102695463B (zh)	2009-12-11	2015-01-14	泰科保健集团有限合伙公司	具有提高的材料捕获效率的材料去除装置及使用方法
BR112012031907A2 (pt)	2010-06-14	2020-08-04	Covidien Lp	dispositivo de remoção de material.
CN103200886B (zh)	2010-10-28	2015-07-29	科维蒂恩有限合伙公司	物质移除装置和使用方法
JP5688160B2 (ja)	2010-11-11	2015-03-25	コヴィディエンリミテッドパートナーシップ	撮像を伴う可撓性減量カテーテル、および、その使用および製造方法
JP5806407B2 (ja)	2011-09-01	2015-11-10	コヴィディエンリミテッドパートナーシップ	螺旋駆動軸を有するカテーテルおよび製造方法
US9579157B2 (en)	2012-09-13	2017-02-28	Covidien Lp	Cleaning device for medical instrument and method of use
US9943329B2 (en)	2012-11-08	2018-04-17	Covidien Lp	Tissue-removing catheter with rotatable cutter
WO2015200702A1 (en)	2014-06-27	2015-12-30	Covidien Lp	Cleaning device for catheter and catheter including the same
US10314667B2 (en)	2015-03-25	2019-06-11	Covidien Lp	Cleaning device for cleaning medical instrument
US10292721B2 (en)	2015-07-20	2019-05-21	Covidien Lp	Tissue-removing catheter including movable distal tip
EP3340797B1 (de) *	2015-08-11	2020-02-12	Dow Global Technologies LLC	Verfahren zur herstellung einer stabilen isothiazolonformulierung
US10314664B2 (en)	2015-10-07	2019-06-11	Covidien Lp	Tissue-removing catheter and tissue-removing element with depth stop

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US3452034A (en) *	1967-03-09	1969-06-24	American Cyanamid Co	Substituted 2-(1,3,4-thiadiazol-2-yl)-4(5)-nitroimidazoles
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US4150026A (en) *	1971-05-12	1979-04-17	Rohm And Haas Company	Metal salt complexes of 3-isothiazolones
US3870795A (en) *	1973-02-28	1975-03-11	Rohm & Haas	Stabilization of solutions of 3-isothiazolones employing certain metal nitrates and nitrites
AR207229A1 (es) *	1973-08-20	1976-09-22	Rohm & Haas	Composicion de recubrimiento estabilizada con formaldehido y metodo para su preparacion
US4067878A (en) *	1976-03-05	1978-01-10	Rohm And Haas Company	Stabilization of solutions of 3-isothiazolones
US4165318A (en) *	1977-09-06	1979-08-21	Rohm And Haas Company	Formaldehyde stabilized coating compositions
US4608183A (en) *	1985-01-14	1986-08-26	Board Of Governors Of Wayne State University	Synergistic antimicrobial or biocidal mixtures including isothiazolones
US4783221A (en) *	1986-12-12	1988-11-08	Mooney Chemicals, Inc.	Compositions and process for preserving wood
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US5073582A (en)	1989-07-11	1991-12-17	Rohm And Haas Company	Mildew resistant paint compositions comprising an isothiazolone and a water-insoluble copper compound, articles, and methods

1990
- 1990-12-10 US US07/625,269 patent/US5108500A/en not_active Expired - Lifetime
1991
- 1991-11-29 CA CA002056632A patent/CA2056632C/en not_active Expired - Lifetime
- 1991-12-04 AT AT91311269T patent/ATE199148T1/de not_active IP Right Cessation
- 1991-12-04 ES ES91311269T patent/ES2153819T3/es not_active Expired - Lifetime
- 1991-12-04 DE DE69132534T patent/DE69132534T2/de not_active Expired - Lifetime
- 1991-12-04 EP EP91311269A patent/EP0490565B1/de not_active Expired - Lifetime
- 1991-12-04 SG SG1996006095A patent/SG66265A1/en unknown
- 1991-12-04 MY MYPI91002243A patent/MY107685A/en unknown
- 1991-12-06 AU AU88894/91A patent/AU659113B2/en not_active Expired
- 1991-12-09 KR KR1019910022444A patent/KR100218057B1/ko not_active Expired - Lifetime
- 1991-12-09 IL IL10029091A patent/IL100290A/en not_active IP Right Cessation
- 1991-12-10 JP JP35004891A patent/JP3176674B2/ja not_active Expired - Lifetime
- 1991-12-10 HU HU913881A patent/HU208470B/hu unknown

Also Published As

Publication number	Publication date
US5108500A (en)	1992-04-28
HU208470B (en)	1993-11-29
JP3176674B2 (ja)	2001-06-18
CA2056632A1 (en)	1992-06-11
DE69132534T2 (de)	2001-06-07
AU659113B2 (en)	1995-05-11
DE69132534D1 (de)	2001-03-22
ATE199148T1 (de)	2001-02-15
SG66265A1 (en)	1999-07-20
HUT60102A (en)	1992-08-28
JPH0565206A (ja)	1993-03-19
ES2153819T3 (es)	2001-03-16
KR920011359A (ko)	1992-07-24
EP0490565B1 (de)	2001-02-14
CA2056632C (en)	2002-05-14
HU913881D0 (en)	1992-02-28
KR100218057B1 (ko)	1999-10-01
AU8889491A (en)	1992-06-11
MY107685A (en)	1996-05-30
EP0490565A1 (de)	1992-06-17
IL100290A0 (en)	1992-09-06

Legal Events

Date	Code	Title	Description
1998-04-05	KB	Patent renewed
2002-08-14	MM9K	Patent not in force due to non-payment of renewal fees

Publication	Publication Date	Title
EP0490565B1 (de)	2001-02-14	Stabilisierung wasserunlöslicher 3-Isothiazolonen
EP0880892B1 (de)	2002-12-18	Zusammensetzungen mit kontrollierter Wirkstoffabgabe
EP0686347A2 (de)	1995-12-13	Zusammensetzung enthaltend 3-Isothiazolen und Stabilisator
US4906274A (en)	1990-03-06	Organic stabilizers
US5073582A (en)	1991-12-17	Mildew resistant paint compositions comprising an isothiazolone and a water-insoluble copper compound, articles, and methods
DE60103582T2 (de)	2005-07-07	Zusammensetzungen mit kontrollierter Freisetzung
EP0658180B1 (de)	1998-10-28	Verfahren zur erzeugung von kupferpyrithione in-situ in farben
EP1225804B1 (de)	2003-11-12	Bei niedrigen temperaturen stabile konservierungsmittel
US9420791B2 (en)	2016-08-23	Biocidal compositions
HUT54870A (en)	1991-04-29	Compositions comprising stabilized 3-isothiazolone derivatives and process for stabilizing 3-isothiazolones
KR0139060B1 (ko)	1998-04-30	항생작용을 하는 조성물 및 이들의 용도
US5242893A (en)	1993-09-07	Use of hexamethylenetetramine as a stabilizer for 3-isothiazolones
KR0179359B1 (ko)	1999-04-01	안정화된 3-이소티아졸론 조성물
US20210204548A1 (en)	2021-07-08	Stabilized Biocide Composition
EP0606986B1 (de)	1998-05-20	Eisen-Stabilisatoren für 3-Isothiazolone
US5208272A (en)	1993-05-04	Mildew resistant paint compositions comprising an isothiazolone and a water-insoluble zinc compound, articles, and methods
EP1514473A1 (de)	2005-03-16	Salzarme bzw. salzfreie microbizide Zusammensetzung auf Basis von Isothiazolon-Derivaten und Pyriondisulfid
KR20010050093A (ko)	2001-06-15	이소티아졸론 농축물
JP2834219B2 (ja)	1998-12-09	工業用殺菌・静菌組成物の安定化方法
IE901985L (en)	1990-12-02	Mildew resistant paint compositions
EP0686346A1 (de)	1995-12-13	Zusammensetzung, die 3-Isothiazolone und Stabilisatoren enthält