UA65545C2 - Concentrated liquid fungicidal composition and a method of inhibiting fungal growth - Google Patents

Concentrated liquid fungicidal composition and a method of inhibiting fungal growth Download PDF

Info

Publication number: UA65545C2
Authority: UA; Ukraine
Prior art keywords: water; composition according; formula; agent; active ingredient
Prior art date: 1998-04-20

Application number

UA99042157A

Other languages

English (en)

Ukrainian (uk)

Original Assignee

American Cyanamid Co

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.)

1998-04-20

Filing date

1999-04-16

Publication date

2004-04-15

1999-04-16 Application filed by American Cyanamid Co filed Critical American Cyanamid Co

2004-04-15 Publication of UA65545C2 publication Critical patent/UA65545C2/uk

Links

239000000203 mixture Substances 0.000 title claims abstract description 122
230000000855 fungicidal effect Effects 0.000 title claims abstract description 39
239000007788 liquid Substances 0.000 title claims abstract description 16
238000000034 method Methods 0.000 title claims abstract description 11
230000002538 fungal effect Effects 0.000 title description 2
230000002401 inhibitory effect Effects 0.000 title 1
239000004480 active ingredient Substances 0.000 claims abstract description 43
CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical compound ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 0.000 claims abstract description 34
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 34
150000001875 compounds Chemical class 0.000 claims abstract description 28
239000002904 solvent Substances 0.000 claims abstract description 22
239000002245 particle Substances 0.000 claims abstract description 19
239000002270 dispersing agent Substances 0.000 claims abstract description 12
241000233866 Fungi Species 0.000 claims abstract description 9
239000003495 polar organic solvent Substances 0.000 claims abstract description 9
150000003839 salts Chemical class 0.000 claims abstract description 9
230000002209 hydrophobic effect Effects 0.000 claims abstract description 8
239000000725 suspension Substances 0.000 claims abstract description 6
239000005868 Metconazole Substances 0.000 claims description 30
XWPZUHJBOLQNMN-UHFFFAOYSA-N metconazole Chemical compound C1=NC=NN1CC1(O)C(C)(C)CCC1CC1=CC=C(Cl)C=C1 XWPZUHJBOLQNMN-UHFFFAOYSA-N 0.000 claims description 30
239000003795 chemical substances by application Substances 0.000 claims description 21
-1 alkadienyl Chemical group 0.000 claims description 15
239000002253 acid Substances 0.000 claims description 10
239000003960 organic solvent Substances 0.000 claims description 8
150000007513 acids Chemical class 0.000 claims description 7
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125000000217 alkyl group Chemical group 0.000 claims description 6
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125000003118 aryl group Chemical group 0.000 claims description 4
239000003755 preservative agent Substances 0.000 claims description 4
125000000547 substituted alkyl group Chemical group 0.000 claims description 4
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 3
229920000578 graft copolymer Polymers 0.000 claims description 3
229910052757 nitrogen Inorganic materials 0.000 claims description 3
125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
238000007865 diluting Methods 0.000 claims description 2
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239000005800 Kresoxim-methyl Substances 0.000 abstract description 13
ZOTBXTZVPHCKPN-HTXNQAPBSA-N kresoxim-methyl Chemical group CO\N=C(\C(=O)OC)C1=CC=CC=C1COC1=CC=CC=C1C ZOTBXTZVPHCKPN-HTXNQAPBSA-N 0.000 abstract description 13
239000004094 surface-active agent Substances 0.000 abstract description 13
241000209140 Triticum Species 0.000 abstract description 10
235000021307 Triticum Nutrition 0.000 abstract description 10
239000005747 Chlorothalonil Substances 0.000 abstract description 5
235000013339 cereals Nutrition 0.000 abstract description 5
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239000010949 copper Substances 0.000 description 2
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JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
YPHMISFOHDHNIV-FSZOTQKASA-N cycloheximide Chemical compound C1[C@@H](C)C[C@H](C)C(=O)[C@@H]1[C@H](O)CC1CC(=O)NC(=O)C1 YPHMISFOHDHNIV-FSZOTQKASA-N 0.000 description 2
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FQKUGOMFVDPBIZ-UHFFFAOYSA-N flusilazole Chemical compound C=1C=C(F)C=CC=1[Si](C=1C=CC(F)=CC=1)(C)CN1C=NC=N1 FQKUGOMFVDPBIZ-UHFFFAOYSA-N 0.000 description 2
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TVLSRXXIMLFWEO-UHFFFAOYSA-N prochloraz Chemical compound C1=CN=CN1C(=O)N(CCC)CCOC1=C(Cl)C=C(Cl)C=C1Cl TVLSRXXIMLFWEO-UHFFFAOYSA-N 0.000 description 1
WZZLDXDUQPOXNW-UHFFFAOYSA-N propamocarb Chemical compound CCCOC(=O)NCCCN(C)C WZZLDXDUQPOXNW-UHFFFAOYSA-N 0.000 description 1
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 description 1
KKMLIVYBGSAJPM-UHFFFAOYSA-L propineb Chemical compound [Zn+2].[S-]C(=S)NC(C)CNC([S-])=S KKMLIVYBGSAJPM-UHFFFAOYSA-L 0.000 description 1
235000019260 propionic acid Nutrition 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
ZLIBICFPKPWGIZ-UHFFFAOYSA-N pyrimethanil Chemical compound CC1=CC(C)=NC(NC=2C=CC=CC=2)=N1 ZLIBICFPKPWGIZ-UHFFFAOYSA-N 0.000 description 1
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
FBQQHUGEACOBDN-UHFFFAOYSA-N quinomethionate Chemical compound N1=C2SC(=O)SC2=NC2=CC(C)=CC=C21 FBQQHUGEACOBDN-UHFFFAOYSA-N 0.000 description 1
229960004889 salicylic acid Drugs 0.000 description 1
239000013049 sediment Substances 0.000 description 1
238000004062 sedimentation Methods 0.000 description 1
238000000926 separation method Methods 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
241000894007 species Species 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
229960005322 streptomycin Drugs 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
230000009885 systemic effect Effects 0.000 description 1
ROZUQUDEWZIBHV-UHFFFAOYSA-N tecloftalam Chemical compound OC(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C(=O)NC1=CC=CC(Cl)=C1Cl ROZUQUDEWZIBHV-UHFFFAOYSA-N 0.000 description 1
XQTLDIFVVHJORV-UHFFFAOYSA-N tecnazene Chemical compound [O-][N+](=O)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl XQTLDIFVVHJORV-UHFFFAOYSA-N 0.000 description 1
239000004308 thiabendazole Substances 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
235000010296 thiabendazole Nutrition 0.000 description 1
229960004546 thiabendazole Drugs 0.000 description 1
QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical group COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 1
KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
229960002447 thiram Drugs 0.000 description 1
229910052718 tin Inorganic materials 0.000 description 1
OBZIQQJJIKNWNO-UHFFFAOYSA-N tolclofos-methyl Chemical group COP(=S)(OC)OC1=C(Cl)C=C(C)C=C1Cl OBZIQQJJIKNWNO-UHFFFAOYSA-N 0.000 description 1
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
HYVWIQDYBVKITD-UHFFFAOYSA-N tolylfluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=C(C)C=C1 HYVWIQDYBVKITD-UHFFFAOYSA-N 0.000 description 1
BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 description 1
IQGKIPDJXCAMSM-UHFFFAOYSA-N triazoxide Chemical compound N=1C2=CC=C(Cl)C=C2[N+]([O-])=NC=1N1C=CN=C1 IQGKIPDJXCAMSM-UHFFFAOYSA-N 0.000 description 1
YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 0.000 description 1
HSMVPDGQOIQYSR-KGENOOAVSA-N triflumizole Chemical compound C1=CN=CN1C(/COCCC)=N/C1=CC=C(Cl)C=C1C(F)(F)F HSMVPDGQOIQYSR-KGENOOAVSA-N 0.000 description 1
RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 description 1
JARYYMUOCXVXNK-CSLFJTBJSA-N validamycin A Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-CSLFJTBJSA-N 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc Substances 0.000 description 1
DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 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
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles

Landscapes

Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

UA99042157A 1998-04-20 1999-04-16 Concentrated liquid fungicidal composition and a method of inhibiting fungal growth UA65545C2 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US09/063,199 US6096769A (en)	1998-04-20	1998-04-20	Fungicidal co-formulation

Publications (1)

Publication Number	Publication Date
UA65545C2 true UA65545C2 (en)	2004-04-15

Family

ID=22047628

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
UA99042157A UA65545C2 (en)	1998-04-20	1999-04-16	Concentrated liquid fungicidal composition and a method of inhibiting fungal growth

Country Status (13)

Country	Link
US (1)	US6096769A (de)
EP (1)	EP0951831B1 (de)
JP (1)	JP2000001407A (de)
AR (1)	AR019082A1 (de)
AT (1)	ATE242599T1 (de)
BR (1)	BR9901100B1 (de)
CA (3)	CA2691601C (de)
DE (1)	DE69908701T2 (de)
DK (1)	DK0951831T3 (de)
ES (1)	ES2201635T3 (de)
PT (1)	PT951831E (de)
RU (1)	RU2242124C2 (de)
UA (1)	UA65545C2 (de)

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JP4743831B2 (ja) *	2004-11-17	2011-08-10	北興化学工業株式会社	液状農薬製剤
EP3036994B1 (de) *	2005-09-29	2018-11-14	Janssen Pharmaceutica NV	Synergistische imazalil-kombinationen
WO2007045455A1 (en) *	2005-10-20	2007-04-26	Syngenta Participations Ag	Fungicidal compositions
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CL2008002420A1 (es)	2007-08-16	2009-10-23	Basf Se	Uso de una composicion que comprende a) un ingrediente activo seleccionado de piraclostrobina; b) un sulfato de eter poliarilfenol polialcoxi; y c) un co-polimero basado en esteres metaacrilicos para el tratamiento de semillas y composicion para el tratamiento de semillas.
CA2716548A1 (en) *	2008-02-28	2009-09-03	Syngenta Participations Ag	Pesticidal combinations
TWI524844B (zh)	2008-05-12	2016-03-11	先正達合夥公司	除害組成物
US8871679B2 (en)	2008-07-04	2014-10-28	Basf Se	Fungicidal mixtures comprising substituted 1-methylpyrazol-4-ylcarboxanilides
RU2373711C1 (ru) *	2008-08-20	2009-11-27	Закрытое Акионерное Общество Фирма "Август"	Фунгицидная композиция и способ борьбы с фитопатогенными грибами
JPWO2012165499A1 (ja)	2011-05-31	2015-02-23	株式会社クレハ	トリアゾール化合物、およびその利用
BR112013030438A2 (pt) *	2011-06-07	2016-08-16	Kureha Corp	agente químico agrícola ou hortícola, composição para controlar doenças de plantas, método para controlar doenças de plantas, e produto para controlar doenças de plantas
WO2013026470A1 (en) *	2011-08-22	2013-02-28	Agriphar S.A.	Aqueous suspension concentrate comprising dodecylguanidine
WO2015083436A1 (ja)	2013-12-05	2015-06-11	株式会社クレハ	農園芸用薬剤、植物病害防除方法および植物病害防除用製品
EP3078265B1 (de) *	2013-12-05	2017-06-07	Kureha Corporation	Landwirtschaftliche und gärtnerische präparate, verfahren zur bekämpfung von pflanzenkrankheiten und produkt zur bekämpfung von pflanzenkrankheiten
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1998
- 1998-04-20 US US09/063,199 patent/US6096769A/en not_active Expired - Lifetime
1999
- 1999-04-12 CA CA2691601A patent/CA2691601C/en not_active Expired - Fee Related
- 1999-04-12 CA CA2691758A patent/CA2691758C/en not_active Expired - Fee Related
- 1999-04-12 BR BRPI9901100-0B1A patent/BR9901100B1/pt not_active IP Right Cessation
- 1999-04-12 CA CA2268619A patent/CA2268619C/en not_active Expired - Fee Related
- 1999-04-12 JP JP11104264A patent/JP2000001407A/ja active Pending
- 1999-04-16 EP EP99302964A patent/EP0951831B1/de not_active Expired - Lifetime
- 1999-04-16 DE DE69908701T patent/DE69908701T2/de not_active Expired - Lifetime
- 1999-04-16 PT PT99302964T patent/PT951831E/pt unknown
- 1999-04-16 UA UA99042157A patent/UA65545C2/uk unknown
- 1999-04-16 ES ES99302964T patent/ES2201635T3/es not_active Expired - Lifetime
- 1999-04-16 DK DK99302964T patent/DK0951831T3/da active
- 1999-04-16 AT AT99302964T patent/ATE242599T1/de active
- 1999-04-19 AR ARP990101805A patent/AR019082A1/es active IP Right Grant
- 1999-04-19 RU RU99108250/04A patent/RU2242124C2/ru not_active IP Right Cessation

Also Published As

Publication number	Publication date
CA2268619A1 (en)	1999-10-20
BR9901100B1 (pt)	2013-06-18
ATE242599T1 (de)	2003-06-15
DK0951831T3 (da)	2003-07-14
RU2242124C2 (ru)	2004-12-20
DE69908701D1 (de)	2003-07-17
EP0951831A1 (de)	1999-10-27
BR9901100A (pt)	2000-03-21
DE69908701T2 (de)	2004-04-29
JP2000001407A (ja)	2000-01-07
US6096769A (en)	2000-08-01
CA2691601A1 (en)	1999-10-20
PT951831E (pt)	2003-10-31
CA2268619C (en)	2010-09-14
CA2691758A1 (en)	1999-10-20
AR019082A1 (es)	2001-12-26
CA2691758C (en)	2012-06-05
ES2201635T3 (es)	2004-03-16
CA2691601C (en)	2012-10-02
EP0951831B1 (de)	2003-06-11

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US6268371B1 (en)	2001-07-31	Fungicidal mixtures
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