CA1072443A - Hydrazide de l'acide 2,6-dichloropyridine-4-carboxylique utilise pour la lutte contre les micro-organismes - Google Patents

Hydrazide de l'acide 2,6-dichloropyridine-4-carboxylique utilise pour la lutte contre les micro-organismes

Info

Publication number: CA1072443A
Authority: CA; Canada
Prior art keywords: phytopathogenic; microorganisms; parts; carboxylic acid; dichloropyridine
Prior art date: 1975-05-14
Legal status (The legal status 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 status listed.): Expired

Application number

CA252,367A

Other languages

English (en)

Inventor

Karl Gatzi

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Novartis AG

Original Assignee

Ciba Geigy AG

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.)

1975-05-14

Filing date

1976-05-12

Publication date

1980-02-26

1976-05-12 Application filed by Ciba Geigy AG filed Critical Ciba Geigy AG

1980-02-26 Application granted granted Critical

1980-02-26 Publication of CA1072443A publication Critical patent/CA1072443A/fr

Status Expired legal-status Critical Current

Links

244000005700 microbiome Species 0.000 title claims abstract description 16
QZTMHCLQBRFNOF-UHFFFAOYSA-N 2,6-dichloropyridine-4-carbohydrazide Chemical compound NNC(=O)C1=CC(Cl)=NC(Cl)=C1 QZTMHCLQBRFNOF-UHFFFAOYSA-N 0.000 title claims abstract description 11
239000000203 mixture Substances 0.000 claims abstract description 19
230000003032 phytopathogenic effect Effects 0.000 claims abstract description 18
150000001875 compounds Chemical class 0.000 claims description 13
238000000034 method Methods 0.000 claims description 8
241000894006 Bacteria Species 0.000 claims description 7
239000003085 diluting agent Substances 0.000 claims description 7
239000008187 granular material Substances 0.000 claims description 7
241000233866 Fungi Species 0.000 claims description 6
239000000969 carrier Substances 0.000 claims description 5
208000015181 infectious disease Diseases 0.000 claims description 4
239000007788 liquid Substances 0.000 claims description 4
239000002689 soil Substances 0.000 claims description 4
239000007787 solid Substances 0.000 claims description 4
241000589516 Pseudomonas Species 0.000 claims description 3
239000003795 chemical substances by application Substances 0.000 claims description 3
239000000428 dust Substances 0.000 claims description 3
239000003380 propellant Substances 0.000 claims description 3
241000588698 Erwinia Species 0.000 claims description 2
241000233614 Phytophthora Species 0.000 claims description 2
241000317942 Venturia <ichneumonid wasp> Species 0.000 claims description 2
241000589634 Xanthomonas Species 0.000 claims description 2
231100000252 nontoxic Toxicity 0.000 claims description 2
230000003000 nontoxic effect Effects 0.000 claims description 2
239000008188 pellet Substances 0.000 claims description 2
239000004094 surface-active agent Substances 0.000 claims description 2
244000000010 microbial pathogen Species 0.000 claims 2
241000186216 Corynebacterium Species 0.000 claims 1
241000221787 Erysiphe Species 0.000 claims 1
239000004491 dispersible concentrate Substances 0.000 claims 1
239000013543 active substance Substances 0.000 abstract description 13
239000004480 active ingredient Substances 0.000 abstract description 2
241000196324 Embryophyta Species 0.000 description 9
239000000725 suspension Substances 0.000 description 7
239000005995 Aluminium silicate Substances 0.000 description 6
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
235000012211 aluminium silicate Nutrition 0.000 description 6
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 6
239000000126 substance Substances 0.000 description 6
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
206010061217 Infestation Diseases 0.000 description 4
235000019993 champagne Nutrition 0.000 description 4
TWBYWOBDOCUKOW-UHFFFAOYSA-N isonicotinic acid Chemical compound OC(=O)C1=CC=NC=C1 TWBYWOBDOCUKOW-UHFFFAOYSA-N 0.000 description 4
239000000843 powder Substances 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
240000004160 Capsicum annuum Species 0.000 description 3
240000008067 Cucumis sativus Species 0.000 description 3
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 3
239000000654 additive Substances 0.000 description 3
JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 3
239000012141 concentrate Substances 0.000 description 3
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 3
229920000151 polyglycol Polymers 0.000 description 3
239000010695 polyglycol Substances 0.000 description 3
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 3
235000012239 silicon dioxide Nutrition 0.000 description 3
239000011734 sodium Substances 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
239000000243 solution Substances 0.000 description 3
235000010799 Cucumis sativus var sativus Nutrition 0.000 description 2
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 2
ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
239000002202 Polyethylene glycol Substances 0.000 description 2
241000521936 Pseudomonas amygdali pv. lachrymans Species 0.000 description 2
241000589655 Xanthomonas citri Species 0.000 description 2
241000567019 Xanthomonas vesicatoria Species 0.000 description 2
201000010099 disease Diseases 0.000 description 2
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
238000011156 evaluation Methods 0.000 description 2
235000019447 hydroxyethyl cellulose Nutrition 0.000 description 2
238000011534 incubation Methods 0.000 description 2
229920005610 lignin Polymers 0.000 description 2
125000000913 palmityl 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])[H] 0.000 description 2
229920001223 polyethylene glycol Polymers 0.000 description 2
239000007921 spray Substances 0.000 description 2
238000005507 spraying Methods 0.000 description 2
230000009885 systemic effect Effects 0.000 description 2
239000000454 talc Substances 0.000 description 2
235000012222 talc Nutrition 0.000 description 2
229910052623 talc Inorganic materials 0.000 description 2
239000004563 wettable powder Substances 0.000 description 2
NWZSZGALRFJKBT-KNIFDHDWSA-N (2s)-2,6-diaminohexanoic acid;(2s)-2-hydroxybutanedioic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O.NCCCC[C@H](N)C(O)=O NWZSZGALRFJKBT-KNIFDHDWSA-N 0.000 description 1
SQSYNRCXIZHKAI-UHFFFAOYSA-N 2,6-dichloroisonicotinic acid Chemical compound OC(=O)C1=CC(Cl)=NC(Cl)=C1 SQSYNRCXIZHKAI-UHFFFAOYSA-N 0.000 description 1
FILKGCRCWDMBKA-UHFFFAOYSA-N 2,6-dichloropyridine Chemical compound ClC1=CC=CC(Cl)=N1 FILKGCRCWDMBKA-UHFFFAOYSA-N 0.000 description 1
IULJSGIJJZZUMF-UHFFFAOYSA-N 2-hydroxybenzenesulfonic acid Chemical compound OC1=CC=CC=C1S(O)(=O)=O IULJSGIJJZZUMF-UHFFFAOYSA-N 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
235000008534 Capsicum annuum var annuum Nutrition 0.000 description 1
241000595586 Coryne Species 0.000 description 1
235000009849 Cucumis sativus Nutrition 0.000 description 1
239000004606 Fillers/Extenders Substances 0.000 description 1
244000141359 Malus pumila Species 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
240000007594 Oryza sativa Species 0.000 description 1
235000007164 Oryza sativa Nutrition 0.000 description 1
241000589613 Pseudomonas savastanoi pv. phaseolicola Species 0.000 description 1
241000589615 Pseudomonas syringae Species 0.000 description 1
206010039509 Scab Diseases 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
244000061456 Solanum tuberosum Species 0.000 description 1
235000002595 Solanum tuberosum Nutrition 0.000 description 1
241000228452 Venturia inaequalis Species 0.000 description 1
240000006365 Vitis vinifera Species 0.000 description 1
235000014787 Vitis vinifera Nutrition 0.000 description 1
241000589652 Xanthomonas oryzae Species 0.000 description 1
241000194062 Xanthomonas phaseoli Species 0.000 description 1
240000008042 Zea mays Species 0.000 description 1
235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
235000002017 Zea mays subsp mays Nutrition 0.000 description 1
230000000895 acaricidal effect Effects 0.000 description 1
239000000642 acaricide Substances 0.000 description 1
239000002253 acid Substances 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
239000000443 aerosol Substances 0.000 description 1
229940115440 aluminum sodium silicate Drugs 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
244000309464 bull Species 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
239000001511 capsicum annuum Substances 0.000 description 1
235000013339 cereals Nutrition 0.000 description 1
239000000470 constituent Substances 0.000 description 1
239000013078 crystal Substances 0.000 description 1
238000005520 cutting process Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000003814 drug Substances 0.000 description 1
238000010410 dusting Methods 0.000 description 1
235000013399 edible fruits Nutrition 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000004495 emulsifiable concentrate Substances 0.000 description 1
-1 fatty alcohol sulphates Chemical class 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
238000009472 formulation Methods 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
238000000227 grinding Methods 0.000 description 1
IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine monohydrate Substances O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
235000009973 maize Nutrition 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
XSKGHSUHOYEBTK-UHFFFAOYSA-N methyl 2,6-dichloropyridine-4-carboxylate Chemical compound COC(=O)C1=CC(Cl)=NC(Cl)=C1 XSKGHSUHOYEBTK-UHFFFAOYSA-N 0.000 description 1
239000011707 mineral Substances 0.000 description 1
238000002156 mixing Methods 0.000 description 1
239000002245 particle Substances 0.000 description 1
239000006072 paste Substances 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
230000008635 plant growth Effects 0.000 description 1
235000012015 potatoes Nutrition 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
235000012217 sodium aluminium silicate Nutrition 0.000 description 1
239000000429 sodium aluminium silicate Substances 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
KZOJQMWTKJDSQJ-UHFFFAOYSA-M sodium;2,3-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S([O-])(=O)=O)=C(CCCC)C(CCCC)=CC2=C1 KZOJQMWTKJDSQJ-UHFFFAOYSA-M 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
244000045561 useful plants Species 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
238000009736 wetting Methods 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000008096 xylene 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings

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)

CA252,367A 1975-05-14 1976-05-12 Hydrazide de l'acide 2,6-dichloropyridine-4-carboxylique utilise pour la lutte contre les micro-organismes Expired CA1072443A (fr)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH619175A CH608341A5 (en)	1975-05-14	1975-05-14	Method of controlling phytopathogenic bacteria

Publications (1)

Publication Number	Publication Date
CA1072443A true CA1072443A (fr)	1980-02-26

Family

ID=4305691

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA252,367A Expired CA1072443A (fr)	1975-05-14	1976-05-12	Hydrazide de l'acide 2,6-dichloropyridine-4-carboxylique utilise pour la lutte contre les micro-organismes

Country Status (3)

Country	Link
JP (1)	JPS51142539A (fr)
CA (1)	CA1072443A (fr)
CH (1)	CH608341A5 (fr)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4959096A (en) *	1988-03-25	1990-09-25	Ciba-Geigy Corporation	Compositions for protecting plants against disease
US4966908A (en) *	1988-03-21	1990-10-30	Ciba-Geigy Corporation	Isonicotinic acid amides for protecting plants against disease
US4980355A (en) *	1988-03-09	1990-12-25	Ciba-Geigy Corporation	Compositions for protecting plants against disease

1975
- 1975-05-14 CH CH619175A patent/CH608341A5/de not_active IP Right Cessation
1976
- 1976-05-12 CA CA252,367A patent/CA1072443A/fr not_active Expired
- 1976-05-14 JP JP5519976A patent/JPS51142539A/ja active Pending

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4980355A (en) *	1988-03-09	1990-12-25	Ciba-Geigy Corporation	Compositions for protecting plants against disease
US5112840A (en) *	1988-03-09	1992-05-12	Ciba-Geigy Corporation	Compositions for protecting plants against disease
US4966908A (en) *	1988-03-21	1990-10-30	Ciba-Geigy Corporation	Isonicotinic acid amides for protecting plants against disease
US4959096A (en) *	1988-03-25	1990-09-25	Ciba-Geigy Corporation	Compositions for protecting plants against disease

Also Published As

Publication number	Publication date
CH608341A5 (en)	1979-01-15
JPS51142539A (en)	1976-12-08

Legal Events

Date	Code	Title	Description
1997-02-26	MKEX	Expiry

Publication	Publication Date	Title
US4279639A (en)	1981-07-21	N-(2-Substituted-4-pyridyl)ureas and thioureas as well as plant growth regulators containing same, and method for using compounds as plant growth regulators
JPS6254096B2 (fr)	1987-11-13
EP0248086B1 (fr)	1993-03-17	Derives d'imidazole, bactericides les contenant et procede permettant leur preparation
US4264604A (en)	1981-04-28	Quinolonecarboxylic acid derivatives as bactericides
JPS6215548B2 (fr)	1987-04-08
US3291683A (en)	1966-12-13	Controlling fungi and bacteria with alkoxy or alkylthio alkylamine ethers
JPS5910321B2 (ja)	1984-03-08	有害微生物防除剤及びその製法
GB1583007A (en)	1981-01-21	Substituted n-alkanoyl-anilines their preparation and use as pesticides
US4100290A (en)	1978-07-11	Pyridine-4-carboxylic acid hydrazones for combatting phytopathogenic microorganisms
CA1072443A (fr)	1980-02-26	Hydrazide de l'acide 2,6-dichloropyridine-4-carboxylique utilise pour la lutte contre les micro-organismes
KR910009416B1 (ko)	1991-11-15	살균성 아닐린 유도체의 제조방법
DE2637886C2 (fr)	1988-10-13
US4746678A (en)	1988-05-24	Phenanthrene derivatives
IE43631L (en)	1977-03-30	Anilides
US4029785A (en)	1977-06-14	Amino containing isonicotinic acid derivatives
JPH02279670A (ja)	1990-11-15	殺微生物組成物
EP0751120A2 (fr)	1997-01-02	Dérivés d'hydroxylamine et fongicides les contenant
JPS63284162A (ja)	1988-11-21	ヒドラジン誘導体、その組成物及び微生物に対する植物保護方法
US3826846A (en)	1974-07-30	Antifungal composition and method of alkylenebisdithiocarbamate complex compounds
US3536742A (en)	1970-10-27	Alkylenebisdithiocarbamate complex compounds
US4000311A (en)	1976-12-28	Substituted 1,3-benzodioxane agents for the control of plant bacteria
US4007278A (en)	1977-02-08	1-(1-Carbamoyloxy-2,2,2-trichloroethyl)-1,2,4-triazole derivatives as pesticides
US4285959A (en)	1981-08-25	3-(N-1,3,4-Thiadiazolyl-2)-aminoalkyl-alkyl-acrylates and use thereof as bactericides
US3323986A (en)	1967-06-06	Method for control of powdery mildew
US4477459A (en)	1984-10-16	Fungicidal 4-substituted-5-trifluoromethyl-3-(1,2-dichloro-2-cyanovinyl thio)-1,2,4-triazoles