DD263685A1 - Fungizide mittel mit zusaetzlicher pflanzenwachstumsregulierender wirkung - Google Patents

Fungizide mittel mit zusaetzlicher pflanzenwachstumsregulierender wirkung Download PDF

Info

Publication number: DD263685A1
Authority: DD; German Democratic Republic
Prior art keywords: atoms; tridecyl; iso; alkyl; chain
Prior art date: 1985-07-05

Application number

DD27832385A

Other languages

German (de)

English (en)

Inventor

Lothar Banasiak

Brita Leuner

Horst Lyr

Eva Nega

Original Assignee

Inst Pflanzenschutzforschung

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.)

1985-07-05

Filing date

1985-07-05

Publication date

1989-01-11

1985-07-05 Application filed by Inst Pflanzenschutzforschung filed Critical Inst Pflanzenschutzforschung

1985-07-05 Priority to DD27832385A priority Critical patent/DD263685A1/de

1986-06-30 Priority to AU59401/86A priority patent/AU5940186A/en

1986-07-01 Priority to EP86108916A priority patent/EP0209763A1/de

1986-07-02 Priority to DK315186A priority patent/DK315186A/da

1986-07-04 Priority to PL1986260474A priority patent/PL146362B1/pl

1986-07-04 Priority to PT82915A priority patent/PT82915B/pt

1986-07-04 Priority to HU282686A priority patent/HUT42288A/hu

1986-07-04 Priority to ES8600125A priority patent/ES2001853A6/es

1986-07-04 Priority to FI862851A priority patent/FI862851A7/fi

1986-07-04 Priority to ZA865002A priority patent/ZA865002B/xx

1986-07-04 Priority to IL79334A priority patent/IL79334A0/xx

1986-07-04 Priority to JP15634986A priority patent/JPS6284065A/ja

1986-07-07 Priority to CS865135A priority patent/CS264279B2/cs

1989-01-11 Publication of DD263685A1 publication Critical patent/DD263685A1/de

Links

239000000417 fungicide Substances 0.000 title claims abstract description 19
230000008635 plant growth Effects 0.000 title claims description 4
230000001105 regulatory effect Effects 0.000 title description 2
239000003795 chemical substances by application Substances 0.000 claims abstract description 8
238000000034 method Methods 0.000 claims abstract description 8
125000004432 carbon atom Chemical group C* 0.000 claims description 37
239000000203 mixture Substances 0.000 claims description 18
241000233866 Fungi Species 0.000 claims description 14
125000000217 alkyl group Chemical group 0.000 claims description 12
238000009472 formulation Methods 0.000 claims description 10
239000002904 solvent Substances 0.000 claims description 10
239000002253 acid Substances 0.000 claims description 8
229910052736 halogen Inorganic materials 0.000 claims description 8
150000002367 halogens Chemical group 0.000 claims description 8
125000003545 alkoxy group Chemical group 0.000 claims description 6
125000003118 aryl group Chemical group 0.000 claims description 6
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125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 6
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
150000001450 anions Chemical class 0.000 claims description 3
229910052717 sulfur Inorganic materials 0.000 claims description 3
239000011593 sulfur Substances 0.000 claims description 3
125000002252 acyl group Chemical group 0.000 claims description 2
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239000001301 oxygen Substances 0.000 claims description 2
239000000546 pharmaceutical excipient Substances 0.000 claims 1
238000002360 preparation method Methods 0.000 abstract description 12
244000053095 fungal pathogen Species 0.000 abstract description 5
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238000012360 testing method Methods 0.000 description 12
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208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 4
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238000002329 infrared spectrum Methods 0.000 description 4
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125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 description 3
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239000011707 mineral Substances 0.000 description 3
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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 3
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QABLOFMHHSOFRJ-UHFFFAOYSA-N methyl 2-chloroacetate Chemical compound COC(=O)CCl QABLOFMHHSOFRJ-UHFFFAOYSA-N 0.000 description 1
ZQEIXNIJLIKNTD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(methoxyacetyl)alaninate Chemical compound COCC(=O)N(C(C)C(=O)OC)C1=C(C)C=CC=C1C ZQEIXNIJLIKNTD-UHFFFAOYSA-N 0.000 description 1
CIEXPHRYOLIQQD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-2-furoylalaninate Chemical compound CC=1C=CC=C(C)C=1N(C(C)C(=O)OC)C(=O)C1=CC=CO1 CIEXPHRYOLIQQD-UHFFFAOYSA-N 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
MTDQTHOKIZBFQQ-UHFFFAOYSA-N methyl sulfate;morpholin-4-ium Chemical compound COS([O-])(=O)=O.C1COCC[NH2+]1 MTDQTHOKIZBFQQ-UHFFFAOYSA-N 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
244000005700 microbiome Species 0.000 description 1
238000002156 mixing Methods 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
STUHQDIOZQUPGP-UHFFFAOYSA-N morpholin-4-ium-4-carboxylate Chemical class OC(=O)N1CCOCC1 STUHQDIOZQUPGP-UHFFFAOYSA-N 0.000 description 1
DADSZOFTIIETSV-UHFFFAOYSA-N n,n-dichloroaniline Chemical compound ClN(Cl)C1=CC=CC=C1 DADSZOFTIIETSV-UHFFFAOYSA-N 0.000 description 1
YGZFQTWYPGGBTE-UHFFFAOYSA-N n-(2,2,2-trichloro-1-piperazin-1-ylethyl)formamide Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCNCC1 YGZFQTWYPGGBTE-UHFFFAOYSA-N 0.000 description 1
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
BLGKZHYJQGUCRZ-UHFFFAOYSA-N naphthalen-1-yl 2-bromopropanoate Chemical compound C1=CC=C2C(OC(=O)C(Br)C)=CC=CC2=C1 BLGKZHYJQGUCRZ-UHFFFAOYSA-N 0.000 description 1
239000005645 nematicide Substances 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
230000000050 nutritive effect Effects 0.000 description 1
CBFCDTFDPHXCNY-UHFFFAOYSA-N octyldodecane Natural products CCCCCCCCCCCCCCCCCCCC CBFCDTFDPHXCNY-UHFFFAOYSA-N 0.000 description 1
239000011368 organic material Substances 0.000 description 1
125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
125000006505 p-cyanobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C#N)C([H])([H])* 0.000 description 1
125000006503 p-nitrobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1[N+]([O-])=O)C([H])([H])* 0.000 description 1
125000000636 p-nitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)[N+]([O-])=O 0.000 description 1
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 1
235000020232 peanut Nutrition 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
229940044654 phenolsulfonic acid Drugs 0.000 description 1
AGUWUIVKDXDKBT-UHFFFAOYSA-N phenyl 2-chloroacetate Chemical compound ClCC(=O)OC1=CC=CC=C1 AGUWUIVKDXDKBT-UHFFFAOYSA-N 0.000 description 1
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
150000003014 phosphoric acid esters Chemical class 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
235000012015 potatoes Nutrition 0.000 description 1
238000004321 preservation Methods 0.000 description 1
238000012545 processing Methods 0.000 description 1
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical class CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
AHIHJODVQGBOND-UHFFFAOYSA-M propan-2-yl carbonate Chemical compound CC(C)OC([O-])=O AHIHJODVQGBOND-UHFFFAOYSA-M 0.000 description 1
239000001294 propane Substances 0.000 description 1
239000003380 propellant Substances 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
235000019423 pullulan Nutrition 0.000 description 1
235000021251 pulses Nutrition 0.000 description 1
239000008262 pumice Substances 0.000 description 1
238000011403 purification operation Methods 0.000 description 1
FGVVTMRZYROCTH-UHFFFAOYSA-N pyridine-2-thiol N-oxide Chemical compound [O-][N+]1=CC=CC=C1S FGVVTMRZYROCTH-UHFFFAOYSA-N 0.000 description 1
239000010453 quartz Substances 0.000 description 1
150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
238000011160 research Methods 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
239000004576 sand Substances 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
239000000741 silica gel Substances 0.000 description 1
229910002027 silica gel Inorganic materials 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000007921 spray Substances 0.000 description 1
235000021012 strawberries Nutrition 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
208000024891 symptom Diseases 0.000 description 1
230000002195 synergetic effect Effects 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 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
QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
238000005406 washing Methods 0.000 description 1
239000008096 xylene Substances 0.000 description 1

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Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

DD27832385A 1985-07-05 1985-07-05 Fungizide mittel mit zusaetzlicher pflanzenwachstumsregulierender wirkung DD263685A1 (de)

Priority Applications (13)

Application Number	Priority Date	Filing Date	Title
DD27832385A DD263685A1 (de)	1985-07-05	1985-07-05	Fungizide mittel mit zusaetzlicher pflanzenwachstumsregulierender wirkung
AU59401/86A AU5940186A (en)	1985-07-05	1986-06-30	2, 6 - dimethyl - morpholine quartenary compounds
EP86108916A EP0209763A1 (de)	1985-07-05	1986-07-01	Morpholinio-carbonsäureester- und Morpholinio-alkylphenylethersalze, Verfahren zu ihrer Herstellung und ihre Verwendung als Fungizide
DK315186A DK315186A (da)	1985-07-05	1986-07-02	Morpholinio-carbonsyreester- og morpholinio-alkylphenylethersalte, fremgangsmaade til deres fremstilling og deres anvendelse som fungicider
PL1986260474A PL146362B1 (en)	1985-07-05	1986-07-04	Fungicide with a plant growth controlling additive
PT82915A PT82915B (pt)	1985-07-05	1986-07-04	Processo para a preparacao de sais de morfolinio-carboxilatos e de eteres morfolinio-alquilfenilicos uteis como fungicidas
HU282686A HUT42288A (en)	1985-07-05	1986-07-04	Fungicides containing as active substance morfolinioalcane carbonic acid amid salts and process for production of the active substance
ES8600125A ES2001853A6 (es)	1985-07-05	1986-07-04	Procedimiento para la preparacion de sales de n-alquil-2,6-dimetilmorfolinio-esteres de acidos carboxilicos y sales de n-alquil-2,6-dimetilmorfolinio-alquilfenileteres
FI862851A FI862851A7 (fi)	1985-07-05	1986-07-04	Morfoliniokarboxylsyraester- och morfolinioalkylfenyletersalter, deras framstaellningsfoerfarande och deras anvaendning saosom fungicider.
ZA865002A ZA865002B (en)	1985-07-05	1986-07-04	N-alkyl-2,6-dimethyl-morpholinocarboxylic acid esters and n-alkyl-2,6-dimethyl-morpholinoalkyl phenyl ether salts,their preparation and their use as fungicides
IL79334A IL79334A0 (en)	1985-07-05	1986-07-04	N-alkyl-2,6-dimethyl-morpholinocarboxylic acid esters and n-alkyl-2,6-dimethyl-morpholinoalkyl phenyl ether salts,processes for their preparation and fungicidal compositions containing the same
JP15634986A JPS6284065A (ja)	1985-07-05	1986-07-04	Ｎ−アルキル−２，６−ジメチルモルホリニオ−カルボン酸エステル−及びｎ−アルキル−２，６−ジメチルモルホリニオ−アルキルフエニルエ−テル塩、その製法及び該化合物を含有する、付加的な植物成長調節作用を有する駆カビ剤
CS865135A CS264279B2 (en)	1985-07-05	1986-07-07	Fungicide with plants growth regulation activity

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DD27832385A DD263685A1 (de)	1985-07-05	1985-07-05	Fungizide mittel mit zusaetzlicher pflanzenwachstumsregulierender wirkung

Publications (1)

Publication Number	Publication Date
DD263685A1 true DD263685A1 (de)	1989-01-11

Family

ID=5569407

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD27832385A DD263685A1 (de)	1985-07-05	1985-07-05	Fungizide mittel mit zusaetzlicher pflanzenwachstumsregulierender wirkung

Country Status (4)

Country	Link
JP (1)	JPS6284065A (ja)
DD (1)	DD263685A1 (ja)
HU (1)	HUT42288A (ja)
ZA (1)	ZA865002B (ja)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN114766546A (zh) *	2021-12-29	2022-07-22	淮阴工学院	地衣芽孢杆菌hg03在防治葡枝根霉所致水蜜桃采后软腐病中的应用及应用方法

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2005316443A (ja)	2004-03-30	2005-11-10	Canon Inc	像加熱装置及びこの装置に用いられる搬送ローラ

1985
- 1985-07-05 DD DD27832385A patent/DD263685A1/de not_active IP Right Cessation
1986
- 1986-07-04 JP JP15634986A patent/JPS6284065A/ja active Pending
- 1986-07-04 HU HU282686A patent/HUT42288A/hu unknown
- 1986-07-04 ZA ZA865002A patent/ZA865002B/xx unknown

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN114766546A (zh) *	2021-12-29	2022-07-22	淮阴工学院	地衣芽孢杆菌hg03在防治葡枝根霉所致水蜜桃采后软腐病中的应用及应用方法

Also Published As

Publication number	Publication date
ZA865002B (en)	1987-03-25
JPS6284065A (ja)	1987-04-17
HUT42288A (en)	1987-07-28

Legal Events

Date	Code	Title	Description
1998-11-05	ENJ	Ceased due to non-payment of renewal fee

Publication	Publication Date	Title
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EP0984686A1 (de)	2000-03-15	Verfahren zur bekämpfung von schadpilzen
EP0193131B1 (de)	1989-12-06	5-Isoxazolcarbonsäureamide, ihre Herstellung und Verwendung als Fungizide
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DD263690A1 (de)	1989-01-11	Fungizide mittel mit zusaetzlicher pflanzenwachstumsregulierender wirkung
EP0156255A2 (de)	1985-10-02	N-((2,3-Dihydrobenzofuran)-2yl)-azolylharnstoffe und diese enthaltende Fungizide
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DD263685A1 - Fungizide mittel mit zusaetzlicher pflanzenwachstumsregulierender wirkung - Google Patents

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Priority Applications (13)

Applications Claiming Priority (1)

Publications (1)

Family

ID=5569407

Family Applications (1)

Country Status (4)

Cited By (1)

Families Citing this family (1)

Cited By (1)

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