IL100291A - Compositions comprising 3-isothiazolones and a solid carrier and a method for their preparation - Google Patents

Compositions comprising 3-isothiazolones and a solid carrier and a method for their preparation

Info

Publication number: IL100291A
Authority: IL; Israel
Prior art keywords: carrier; isothiazolone; composition according; polymers; alkyl
Prior art date: 1990-12-10

Application number

IL10029191A

Other languages

English (en)

Other versions

IL100291A0 (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 IL100291A0 publication Critical patent/IL100291A0/xx

1995-08-31 Publication of IL100291A publication Critical patent/IL100291A/en

Links

MGIYRDNGCNKGJU-UHFFFAOYSA-N isothiazolinone Chemical class O=C1C=CSN1 MGIYRDNGCNKGJU-UHFFFAOYSA-N 0.000 title claims abstract description 20
239000007787 solid Substances 0.000 title claims abstract description 14
239000000203 mixture Substances 0.000 title claims description 29
238000000034 method Methods 0.000 title claims description 9
238000002360 preparation method Methods 0.000 title description 2
229920000642 polymer Polymers 0.000 claims abstract description 18
239000001913 cellulose Substances 0.000 claims abstract description 7
229920002678 cellulose Polymers 0.000 claims abstract description 7
238000002144 chemical decomposition reaction Methods 0.000 claims abstract description 7
229920002635 polyurethane Polymers 0.000 claims abstract description 7
239000004814 polyurethane Substances 0.000 claims abstract description 7
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims abstract description 4
230000002209 hydrophobic effect Effects 0.000 claims abstract description 4
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims abstract description 4
XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 claims abstract description 4
229920001282 polysaccharide Polymers 0.000 claims abstract description 4
239000005017 polysaccharide Substances 0.000 claims abstract description 4
SQAINHDHICKHLX-UHFFFAOYSA-N 1-naphthaldehyde Chemical compound C1=CC=C2C(C=O)=CC=CC2=C1 SQAINHDHICKHLX-UHFFFAOYSA-N 0.000 claims abstract description 3
229920002845 Poly(methacrylic acid) Polymers 0.000 claims abstract description 3
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims abstract description 3
229920001577 copolymer Polymers 0.000 claims abstract description 3
150000004676 glycans Chemical class 0.000 claims abstract description 3
239000012141 concentrate Substances 0.000 claims abstract 2
-1 3-isothiazolone compound Chemical class 0.000 claims description 13
JLHMJWHSBYZWJJ-UHFFFAOYSA-N 1,2-thiazole 1-oxide Chemical compound O=S1C=CC=N1 JLHMJWHSBYZWJJ-UHFFFAOYSA-N 0.000 claims description 9
238000002156 mixing Methods 0.000 claims description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 7
125000000217 alkyl group Chemical group 0.000 claims description 6
239000003381 stabilizer Substances 0.000 claims description 6
125000003545 alkoxy group Chemical group 0.000 claims description 5
125000004104 aryloxy group Chemical group 0.000 claims description 4
229910052736 halogen Inorganic materials 0.000 claims description 4
150000002367 halogens Chemical class 0.000 claims description 4
150000003839 salts Chemical class 0.000 claims description 4
239000003795 chemical substances by application Substances 0.000 claims description 3
238000001704 evaporation Methods 0.000 claims description 3
230000008020 evaporation Effects 0.000 claims description 3
125000001475 halogen functional group Chemical group 0.000 claims description 3
230000000087 stabilizing effect Effects 0.000 claims description 3
241000894006 Bacteria Species 0.000 claims description 2
125000004399 C1-C4 alkenyl group Chemical group 0.000 claims description 2
241000195493 Cryptophyta Species 0.000 claims description 2
241000233866 Fungi Species 0.000 claims description 2
230000002411 adverse Effects 0.000 claims description 2
125000003282 alkyl amino group Chemical group 0.000 claims description 2
125000004414 alkyl thio group Chemical group 0.000 claims description 2
125000000304 alkynyl group Chemical group 0.000 claims description 2
125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims description 2
239000004599 antimicrobial Substances 0.000 claims description 2
125000003710 aryl alkyl group Chemical group 0.000 claims description 2
125000001769 aryl amino group Chemical group 0.000 claims description 2
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
125000004093 cyano group Chemical group *C#N 0.000 claims description 2
125000006310 cycloalkyl amino group Chemical group 0.000 claims description 2
125000000753 cycloalkyl group Chemical group 0.000 claims description 2
239000002781 deodorant agent Substances 0.000 claims description 2
125000005265 dialkylamine group Chemical group 0.000 claims description 2
239000002270 dispersing agent Substances 0.000 claims description 2
239000000975 dye Substances 0.000 claims description 2
239000003205 fragrance Substances 0.000 claims description 2
125000004438 haloalkoxy group Chemical group 0.000 claims description 2
150000002431 hydrogen Chemical class 0.000 claims description 2
229910052739 hydrogen Inorganic materials 0.000 claims description 2
239000001257 hydrogen Substances 0.000 claims description 2
125000004356 hydroxy functional group Chemical group O* 0.000 claims description 2
230000002401 inhibitory effect Effects 0.000 claims description 2
238000000465 moulding Methods 0.000 claims description 2
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
239000003960 organic solvent Substances 0.000 claims description 2
239000000546 pharmaceutical excipient Substances 0.000 claims description 2
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
239000003352 sequestering agent Substances 0.000 claims description 2
239000002002 slurry Substances 0.000 claims description 2
239000002904 solvent Substances 0.000 claims description 2
238000001694 spray drying Methods 0.000 claims description 2
239000004094 surface-active agent Substances 0.000 claims description 2
230000003641 microbiacidal effect Effects 0.000 abstract description 2
229940124561 microbicide Drugs 0.000 abstract description 2
239000002855 microbicide agent Substances 0.000 abstract description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
OQMBBFQZGJFLBU-UHFFFAOYSA-N Oxyfluorfen Chemical compound C1=C([N+]([O-])=O)C(OCC)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 OQMBBFQZGJFLBU-UHFFFAOYSA-N 0.000 description 3
239000005590 Oxyfluorfen Substances 0.000 description 3
239000000969 carrier Substances 0.000 description 3
DHNRXBZYEKSXIM-UHFFFAOYSA-N chloromethylisothiazolinone Chemical compound CN1SC(Cl)=CC1=O DHNRXBZYEKSXIM-UHFFFAOYSA-N 0.000 description 3
BEGLCMHJXHIJLR-UHFFFAOYSA-N methylisothiazolinone Chemical compound CN1SC=CC1=O BEGLCMHJXHIJLR-UHFFFAOYSA-N 0.000 description 3
230000000717 retained effect Effects 0.000 description 3
229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
230000000845 anti-microbial effect Effects 0.000 description 2
238000001816 cooling Methods 0.000 description 2
229940117927 ethylene oxide Drugs 0.000 description 2
238000009472 formulation Methods 0.000 description 2
238000003756 stirring Methods 0.000 description 2
241000416162 Astragalus gummifer Species 0.000 description 1
229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
229920000569 Gum karaya Polymers 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
229920003105 Methocel™ A15 LV Polymers 0.000 description 1
229920003094 Methocel™ K4M Polymers 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
241000934878 Sterculia Species 0.000 description 1
229920001615 Tragacanth Polymers 0.000 description 1
239000000654 additive Substances 0.000 description 1
230000032683 aging Effects 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
239000001768 carboxy methyl cellulose Substances 0.000 description 1
235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
239000008112 carboxymethyl-cellulose Substances 0.000 description 1
239000012050 conventional carrier Substances 0.000 description 1
230000009977 dual effect Effects 0.000 description 1
239000000945 filler Substances 0.000 description 1
239000012530 fluid Substances 0.000 description 1
UPBDXRPQPOWRKR-UHFFFAOYSA-N furan-2,5-dione;methoxyethene Chemical compound COC=C.O=C1OC(=O)C=C1 UPBDXRPQPOWRKR-UHFFFAOYSA-N 0.000 description 1
239000008187 granular material Substances 0.000 description 1
239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 1
235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 1
229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 1
UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 description 1
235000010494 karaya gum Nutrition 0.000 description 1
239000000231 karaya gum Substances 0.000 description 1
229940039371 karaya gum Drugs 0.000 description 1
230000014759 maintenance of location Effects 0.000 description 1
239000000463 material Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
239000012768 molten material Substances 0.000 description 1
PSZYNBSKGUBXEH-UHFFFAOYSA-M naphthalene-1-sulfonate Chemical compound C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-M 0.000 description 1
231100000344 non-irritating Toxicity 0.000 description 1
JPMIIZHYYWMHDT-UHFFFAOYSA-N octhilinone Chemical compound CCCCCCCCN1SC=CC1=O JPMIIZHYYWMHDT-UHFFFAOYSA-N 0.000 description 1
239000002245 particle Substances 0.000 description 1
239000008188 pellet Substances 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
235000010408 potassium alginate Nutrition 0.000 description 1
239000000737 potassium alginate Substances 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000013557 residual solvent Substances 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
239000000126 substance Substances 0.000 description 1
229920001059 synthetic polymer Polymers 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
- 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

Landscapes

Life Sciences & Earth Sciences (AREA)
Wood Science & Technology (AREA)
Environmental Sciences (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Pest Control & Pesticides (AREA)
General Health & Medical Sciences (AREA)
Zoology (AREA)
Agronomy & Crop Science (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Paints Or Removers (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Plural Heterocyclic Compounds (AREA)
Indole Compounds (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

IL10029191A 1990-12-10 1991-12-09 Compositions comprising 3-isothiazolones and a solid carrier and a method for their preparation IL100291A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US62526590A	1990-12-10	1990-12-10

Publications (2)

Publication Number	Publication Date
IL100291A0 IL100291A0 (en)	1992-09-06
IL100291A true IL100291A (en)	1995-08-31

Family

ID=24505286

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL10029191A IL100291A (en)	1990-12-10	1991-12-09	Compositions comprising 3-isothiazolones and a solid carrier and a method for their preparation

Country Status (22)

Country	Link
US (2)	US5703105A (fr)
EP (1)	EP0492843B1 (fr)
JP (1)	JP3248589B2 (fr)
KR (1)	KR100225270B1 (fr)
CN (1)	CN1038979C (fr)
AT (1)	ATE126419T1 (fr)
AU (1)	AU656746B2 (fr)
BR (1)	BR9105131A (fr)
CA (1)	CA2055380A1 (fr)
DE (1)	DE69112193T2 (fr)
DK (1)	DK0492843T3 (fr)
ES (1)	ES2077185T3 (fr)
FI (1)	FI97268C (fr)
GR (1)	GR3017149T3 (fr)
HU (1)	HU207786B (fr)
IE (1)	IE68952B1 (fr)
IL (1)	IL100291A (fr)
MX (1)	MX9102485A (fr)
NO (1)	NO179962C (fr)
NZ (1)	NZ240893A (fr)
PT (1)	PT99734B (fr)
TW (1)	TW212749B (fr)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5430046A (en) *	1994-03-11	1995-07-04	Rohm And Haas Company	Solid 3-isothiazolone biocidal concentrates
JP2587582B2 (ja) *	1994-03-22	1997-03-05	株式会社日本アルミ	ヒートシンク及びその製造方法
GB9504630D0 (en) *	1995-03-08	1995-04-26	Kodak Ltd	A material and method for inhibiting bacterial growth in an aqueous medium
US6093387A (en) *	1997-04-29	2000-07-25	United Technologies Corporation	Extended-release chemical formulation in tablet form for urine pretreatment
US5910503A (en) *	1997-10-28	1999-06-08	Rohm And Haas Company	Stable microbicide formulation
US6270786B1 (en) *	1998-07-09	2001-08-07	Eastman Kodak Company	Method of preparing a biocidal material
US6069142A (en) *	1998-12-23	2000-05-30	Calgon Corporation	Synergistic antimicrobial combination of 4,5-dichloro-2-N-octyl-4-isothiazolin-3-one and a mixture of a chlorinated isocyanurate and a bromide compound and methods of using same
FR2801767B1 (fr) *	1999-12-01	2002-09-13	Eastman Kodak Co	Materiau biocide ayant une activite amelioree
US6437020B1 (en) *	1999-12-21	2002-08-20	Amick David Richard	Polymer stabilization
KR100615571B1 (ko) *	1999-12-31	2006-08-25	에스케이케미칼주식회사	스케일 및 미생물 억제 수처리제 조성물
KR100383098B1 (ko) *	2000-05-10	2003-05-12	에스케이케미칼주식회사	이소티아졸론 용액의 침전형성 방지방법 및 그 조성물
GB0019296D0 (en) *	2000-08-07	2000-09-27	Nipa Lab Limited	Treatment for part processed leather
AUPR040600A0 (en) *	2000-09-27	2000-10-19	Chemeq Ltd	Polymeric formulation
KR100817136B1 (ko) *	2001-03-07	2008-03-27	롬 앤드 하스 캄파니	수지 고정된 살균제
DE102004026274A1 (de) *	2004-05-05	2006-02-16	Ecs Environment Care Systems Gmbh	Wasserlösliche Folie zur Freisetzung von Wirkstoffen
US20100239679A1 (en) *	2007-10-02	2010-09-23	World Minerals, Inc.	Enhanced retention capabilities through methods comprising surface treatment of functional particulate carrier materials, and functional particulate carrier materials made therefrom
DE112008002943T5 (de)	2007-10-30	2010-09-09	World Minerals Inc., Santa Barbara	Modifizierte mineral-basierte Füllstoffe
CA2844791C (fr) *	2011-08-15	2016-12-06	John J. Matta	Composition antimicrobienne soluble dans l'eau
CN121263488A (zh) *	2023-05-30	2026-01-02	罗门哈斯公司	使胶乳中的1,2-苯并异噻唑啉-3-酮失活的方法

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BR8304987A (pt) *	1982-09-23	1984-09-04	Rohm & Haas	Composicao microbiocida,metodo para controlar microorganismos vivos em um sistema aquosos e metodo de proteger isotiazolonas microbiocidas
CA1223172A (fr) *	1982-09-23	1987-06-23	Sidney Melamed	Microbicide solide encapsule
US4542169A (en) *	1983-12-12	1985-09-17	Rohm And Haas Company	Biomedical devices containing isothiazolones to control bacteria growth
US4552591A (en) *	1984-05-15	1985-11-12	Petrolite Corporation	Oil field biocide composition
CA1334824C (fr) *	1987-02-11	1995-03-21	Stewart Nelson Paul	Protecteurs de biocides
CA1328175C (fr) *	1988-05-16	1994-04-05	John Robert Mattox	Stabilisants a epoxyde pour compositions biocides
GB8913513D0 (en) *	1989-06-13	1989-08-02	Ici Plc	Composition

1991
- 1991-10-11 TW TW080108003A patent/TW212749B/zh active
- 1991-10-30 US US07/784,852 patent/US5703105A/en not_active Expired - Lifetime
- 1991-11-13 CA CA002055380A patent/CA2055380A1/fr not_active Abandoned
- 1991-11-26 BR BR919105131A patent/BR9105131A/pt not_active IP Right Cessation
- 1991-12-04 NO NO914754A patent/NO179962C/no unknown
- 1991-12-04 DK DK91311279.3T patent/DK0492843T3/da active
- 1991-12-04 AT AT91311279T patent/ATE126419T1/de not_active IP Right Cessation
- 1991-12-04 ES ES91311279T patent/ES2077185T3/es not_active Expired - Lifetime
- 1991-12-04 EP EP91311279A patent/EP0492843B1/fr not_active Expired - Lifetime
- 1991-12-04 DE DE69112193T patent/DE69112193T2/de not_active Expired - Lifetime
- 1991-12-06 NZ NZ240893A patent/NZ240893A/en unknown
- 1991-12-06 AU AU88891/91A patent/AU656746B2/en not_active Ceased
- 1991-12-09 PT PT99734A patent/PT99734B/pt not_active IP Right Cessation
- 1991-12-09 IL IL10029191A patent/IL100291A/en not_active IP Right Cessation
- 1991-12-09 FI FI915784A patent/FI97268C/fi not_active IP Right Cessation
- 1991-12-09 IE IE427091A patent/IE68952B1/en not_active IP Right Cessation
- 1991-12-10 MX MX9102485A patent/MX9102485A/es unknown
- 1991-12-10 HU HU913879A patent/HU207786B/hu not_active IP Right Cessation
- 1991-12-10 KR KR1019910022537A patent/KR100225270B1/ko not_active Expired - Lifetime
- 1991-12-10 CN CN91111562A patent/CN1038979C/zh not_active Expired - Lifetime
- 1991-12-10 JP JP35004391A patent/JP3248589B2/ja not_active Expired - Lifetime
1995
- 1995-06-06 US US08/471,888 patent/US5648086A/en not_active Expired - Lifetime
- 1995-08-17 GR GR950402080T patent/GR3017149T3/el unknown

Also Published As

Publication number	Publication date
EP0492843B1 (fr)	1995-08-16
PT99734A (pt)	1992-11-30
HU207786B (en)	1993-06-28
ES2077185T3 (es)	1995-11-16
NO179962C (no)	1997-01-22
CN1064985A (zh)	1992-10-07
DK0492843T3 (da)	1995-09-18
US5703105A (en)	1997-12-30
NO914754L (no)	1992-06-11
FI97268B (fi)	1996-08-15
MX9102485A (es)	1992-06-01
CA2055380A1 (fr)	1992-06-11
KR920011360A (ko)	1992-07-24
IL100291A0 (en)	1992-09-06
FI915784L (fi)	1992-06-11
EP0492843A3 (fr)	1992-07-08
DE69112193T2 (de)	1996-03-07
HUT60100A (en)	1992-08-28
DE69112193D1 (de)	1995-09-21
AU8889191A (en)	1992-06-11
HU913879D0 (en)	1992-02-28
EP0492843A2 (fr)	1992-07-01
KR100225270B1 (ko)	1999-10-15
JP3248589B2 (ja)	2002-01-21
IE914270A1 (en)	1992-06-17
ATE126419T1 (de)	1995-09-15
BR9105131A (pt)	1992-08-18
FI97268C (fi)	1996-11-25
AU656746B2 (en)	1995-02-16
NO914754D0 (no)	1991-12-04
GR3017149T3 (en)	1995-11-30
CN1038979C (zh)	1998-07-08
NO179962B (no)	1996-10-14
JPH0558814A (ja)	1993-03-09
TW212749B (fr)	1993-09-11
US5648086A (en)	1997-07-15
IE68952B1 (en)	1996-07-24
FI915784A0 (fi)	1991-12-09
NZ240893A (en)	1994-04-27
PT99734B (pt)	1999-05-31

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
IL100291A (en)	1995-08-31	Compositions comprising 3-isothiazolones and a solid carrier and a method for their preparation
RU2153257C2 (ru)	2000-07-27	Фунгицидная композиция, содержащая 2-имидазолин-5-он, и способ борьбы с фитопатогенными грибками-паразитами культурных растений с помощью этой композиции.
US5304376A (en)	1994-04-19	Fungicidal composition
DK175268B1 (da)	2004-08-02	Pesticidpræparat og fremgangsmåde til fremstilling heraf
SK287365B6 (sk)	2010-08-09	Vodná suspenzia pesticídu
MXPA01010326A (es)	2002-03-27	Formulaciones agroquimicas.
CA1328599C (fr)	1994-04-19	Compositions de dithiocarbamate a resistance accrue a la pluie
HU229840B1 (en)	2014-09-29	Sulfamoyl compounds and agricultural and horticultural fungicide compositions
JP2012520259A (ja)	2012-09-06	殺有害生物剤及びベンゾトリアゾールｕｖ吸収剤を含む組成物
NZ516228A (en)	2004-05-28	Herbicidal emulsifiable concentrates
EP1225804B1 (fr)	2003-11-12	Conservants stables a basses temperatures
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