LU82726A1 - Compositions antidotes d'herbicides contenant des n-(acetyle substitue)-n-(4-methyl-2-pentanon-4-yl)-amides - Google Patents

Compositions antidotes d'herbicides contenant des n-(acetyle substitue)-n-(4-methyl-2-pentanon-4-yl)-amides Download PDF

Info

Publication number: LU82726A1
Authority: LU; Luxembourg
Prior art keywords: thiolcarbamate; herbicide; carbon atoms; methyl; antidote
Prior art date: 1980-08-25

Application number

LU82726A

Other languages

English (en)

French (fr)

Inventor

Goeroeg Katalin

Kocsis Maria

Gardi Ivan

Gaal Sandor

Dudar Erzsebet

Kovacs Gabor

Original Assignee

Nitrokemia Ipartelepek

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.)

1980-08-25

Filing date

1980-08-25

Publication date

1980-12-15

1980-08-25 Application filed by Nitrokemia Ipartelepek filed Critical Nitrokemia Ipartelepek

1980-12-15 Publication of LU82726A1 publication Critical patent/LU82726A1/fr

Links

239000004009 herbicide Substances 0.000 title claims description 37
239000000203 mixture Substances 0.000 title claims description 29
-1 4-METHYL-2-PENTANON-4-YL Chemical class 0.000 title description 17
125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 title 1
230000002605 anti-dotal effect Effects 0.000 title 1
230000002363 herbicidal effect Effects 0.000 claims description 34
239000000729 antidote Substances 0.000 claims description 27
150000001875 compounds Chemical class 0.000 claims description 23
125000004432 carbon atom Chemical group C* 0.000 claims description 15
239000000460 chlorine Substances 0.000 claims description 14
229910052801 chlorine Inorganic materials 0.000 claims description 14
125000000217 alkyl group Chemical group 0.000 claims description 7
238000000034 method Methods 0.000 claims description 7
229910052739 hydrogen Inorganic materials 0.000 claims description 6
239000001257 hydrogen Substances 0.000 claims description 6
125000003342 alkenyl group Chemical group 0.000 claims description 5
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 4
125000004965 chloroalkyl group Chemical group 0.000 claims description 4
231100001184 nonphytotoxic Toxicity 0.000 claims description 3
JKEUSFLBLHRRPZ-UHFFFAOYSA-N 2,2-dichloro-n-(2-methyl-4-oxopentan-2-yl)acetamide Chemical compound CC(=O)CC(C)(C)NC(=O)C(Cl)Cl JKEUSFLBLHRRPZ-UHFFFAOYSA-N 0.000 claims description 2
DEFNFNVSSXJTBX-UHFFFAOYSA-N 3-chloro-N-(2-methyl-4-oxopentan-2-yl)propanamide Chemical compound CC(=O)CC(C)(C)NC(=O)CCCl DEFNFNVSSXJTBX-UHFFFAOYSA-N 0.000 claims description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
125000002947 alkylene group Chemical group 0.000 claims description 2
125000001309 chloro group Chemical group Cl* 0.000 claims description 2
150000002431 hydrogen Chemical class 0.000 claims 2
241000607479 Yersinia pestis Species 0.000 claims 1
239000003085 diluting agent Substances 0.000 claims 1
RRMXNBZSHDZAJJ-UHFFFAOYSA-N ethyl n-thiophen-2-ylcarbamate Chemical compound CCOC(=O)NC1=CC=CS1 RRMXNBZSHDZAJJ-UHFFFAOYSA-N 0.000 claims 1
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 27
241000196324 Embryophyta Species 0.000 description 13
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
239000004495 emulsifiable concentrate Substances 0.000 description 7
239000002689 soil Substances 0.000 description 7
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 6
231100000674 Phytotoxicity Toxicity 0.000 description 5
240000008042 Zea mays Species 0.000 description 5
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 5
235000002017 Zea mays subsp mays Nutrition 0.000 description 5
229940075522 antidotes Drugs 0.000 description 5
235000005822 corn Nutrition 0.000 description 5
238000009472 formulation Methods 0.000 description 5
PABISXFQAHDPMS-UHFFFAOYSA-N 2-hydroxy-2-oxoacetate;(2-methyl-4-oxopentan-2-yl)azanium Chemical compound OC(=O)C(O)=O.CC(=O)CC(C)(C)N PABISXFQAHDPMS-UHFFFAOYSA-N 0.000 description 4
238000004458 analytical method Methods 0.000 description 4
GUVLYNGULCJVDO-UHFFFAOYSA-N EPTC Chemical compound CCCN(CCC)C(=O)SCC GUVLYNGULCJVDO-UHFFFAOYSA-N 0.000 description 3
239000002253 acid Substances 0.000 description 3
150000001408 amides Chemical class 0.000 description 3
239000007864 aqueous solution Substances 0.000 description 3
239000011230 binding agent Substances 0.000 description 3
FBCCMZVIWNDFMO-UHFFFAOYSA-N dichloroacetyl chloride Chemical compound ClC(Cl)C(Cl)=O FBCCMZVIWNDFMO-UHFFFAOYSA-N 0.000 description 3
230000000694 effects Effects 0.000 description 3
238000002474 experimental method Methods 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
239000000725 suspension Substances 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
VVJKKWFAADXIJK-UHFFFAOYSA-N Allylamine Chemical compound NCC=C VVJKKWFAADXIJK-UHFFFAOYSA-N 0.000 description 2
QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
239000005557 antagonist Substances 0.000 description 2
239000008346 aqueous phase Substances 0.000 description 2
WCGGWVOVFQNRRS-UHFFFAOYSA-N dichloroacetamide Chemical class NC(=O)C(Cl)Cl WCGGWVOVFQNRRS-UHFFFAOYSA-N 0.000 description 2
238000001914 filtration Methods 0.000 description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
230000007935 neutral effect Effects 0.000 description 2
235000006408 oxalic acid Nutrition 0.000 description 2
239000012071 phase Substances 0.000 description 2
230000000885 phytotoxic effect Effects 0.000 description 2
239000000843 powder Substances 0.000 description 2
239000002244 precipitate Substances 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
239000000047 product Substances 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
238000003756 stirring Methods 0.000 description 2
239000008096 xylene Substances 0.000 description 2
OZXIZRZFGJZWBF-UHFFFAOYSA-N 1,3,5-trimethyl-2-(2,4,6-trimethylphenoxy)benzene Chemical compound CC1=CC(C)=CC(C)=C1OC1=C(C)C=C(C)C=C1C OZXIZRZFGJZWBF-UHFFFAOYSA-N 0.000 description 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
INUNLMUAPJVRME-UHFFFAOYSA-N 3-chloropropanoyl chloride Chemical compound ClCCC(Cl)=O INUNLMUAPJVRME-UHFFFAOYSA-N 0.000 description 1
206010067484 Adverse reaction Diseases 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
244000237956 Amaranthus retroflexus Species 0.000 description 1
235000013479 Amaranthus retroflexus Nutrition 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
YRMLFORXOOIJDR-UHFFFAOYSA-N Dichlormid Chemical compound ClC(Cl)C(=O)N(CC=C)CC=C YRMLFORXOOIJDR-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
125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 1
230000006838 adverse reaction Effects 0.000 description 1
BHELZAPQIKSEDF-UHFFFAOYSA-N allyl bromide Chemical compound BrCC=C BHELZAPQIKSEDF-UHFFFAOYSA-N 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
230000003042 antagnostic effect Effects 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
239000000969 carrier Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
238000005352 clarification Methods 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
238000004821 distillation Methods 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
238000004817 gas chromatography Methods 0.000 description 1
239000008187 granular material Substances 0.000 description 1
208000037824 growth disorder Diseases 0.000 description 1
230000009931 harmful effect Effects 0.000 description 1
239000003815 herbicide antidote Substances 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
HVTICUPFWKNHNG-UHFFFAOYSA-N iodoethane Chemical compound CCI HVTICUPFWKNHNG-UHFFFAOYSA-N 0.000 description 1
125000000555 isopropenyl group Chemical group [H]\C([H])=C(\*)C([H])([H])[H] 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
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 1
230000002147 killing effect Effects 0.000 description 1
239000007788 liquid Substances 0.000 description 1
210000001699 lower leg Anatomy 0.000 description 1
230000036244 malformation Effects 0.000 description 1
239000000463 material Substances 0.000 description 1
239000000155 melt Substances 0.000 description 1
SHOJXDKTYKFBRD-UHFFFAOYSA-N mesityl oxide Natural products CC(C)=CC(C)=O SHOJXDKTYKFBRD-UHFFFAOYSA-N 0.000 description 1
125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
HRRDCWDFRIJIQZ-UHFFFAOYSA-N naphthalene-1,8-dicarboxylic acid Chemical compound C1=CC(C(O)=O)=C2C(C(=O)O)=CC=CC2=C1 HRRDCWDFRIJIQZ-UHFFFAOYSA-N 0.000 description 1
231100000208 phytotoxic Toxicity 0.000 description 1
238000000746 purification Methods 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
239000007787 solid Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
238000004659 sterilization and disinfection Methods 0.000 description 1
230000029305 taxis Effects 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
239000004563 wettable powder 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/32—Ingredients for reducing the noxious effect of the active substances to organisms other than pests, e.g. toxicity reducing compositions, self-destructing compositions

Landscapes

Life Sciences & Earth Sciences (AREA)
General Health & Medical Sciences (AREA)
Health & Medical Sciences (AREA)
Toxicology (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Agronomy & Crop Science (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

LU82726A 1980-08-25 1980-08-25 Compositions antidotes d'herbicides contenant des n-(acetyle substitue)-n-(4-methyl-2-pentanon-4-yl)-amides LU82726A1 (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
FR8018436		1980-08-25
FR8018436A FR2488782B1 (fr)	1980-08-25	1980-08-25	Compositions antidotes d'herbicides contenant des n-(acetyle substitue)-n-(4-methyl-2-pentanon-4-yl)-amides

Publications (1)

Publication Number	Publication Date
LU82726A1 true LU82726A1 (fr)	1980-12-15

Family

ID=9245377

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
LU82726A LU82726A1 (fr)	1980-08-25	1980-08-25	Compositions antidotes d'herbicides contenant des n-(acetyle substitue)-n-(4-methyl-2-pentanon-4-yl)-amides

Country Status (9)

Country	Link
AT (1)	AT368679B (de)
AU (1)	AU534607B2 (de)
BE (1)	BE884911A (de)
CH (1)	CH647390A5 (de)
DE (1)	DE3031996A1 (de)
FR (1)	FR2488782B1 (de)
GB (1)	GB2082458B (de)
LU (1)	LU82726A1 (de)
NL (1)	NL8004788A (de)

1980
- 1980-08-25 LU LU82726A patent/LU82726A1/fr unknown
- 1980-08-25 BE BE0/201854A patent/BE884911A/fr not_active IP Right Cessation
- 1980-08-25 DE DE19803031996 patent/DE3031996A1/de not_active Withdrawn
- 1980-08-25 FR FR8018436A patent/FR2488782B1/fr not_active Expired
- 1980-08-25 AT AT0428880A patent/AT368679B/de not_active IP Right Cessation
- 1980-08-25 AU AU61709/80A patent/AU534607B2/en not_active Ceased
- 1980-08-25 CH CH6391/80A patent/CH647390A5/de not_active IP Right Cessation
- 1980-08-25 NL NL8004788A patent/NL8004788A/nl not_active Application Discontinuation
- 1980-08-26 GB GB8027576A patent/GB2082458B/en not_active Expired

Also Published As

Publication number	Publication date
DE3031996A1 (de)	1982-04-08
FR2488782A1 (fr)	1982-02-26
GB2082458B (en)	1983-06-02
AT368679B (de)	1982-10-25
CH647390A5 (de)	1985-01-31
ATA428880A (de)	1982-03-15
AU6170980A (en)	1982-03-04
BE884911A (fr)	1980-12-16
FR2488782B1 (fr)	1986-03-28
GB2082458A (en)	1982-03-10
NL8004788A (nl)	1982-04-01
AU534607B2 (en)	1984-02-09

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EP0044262A1 (de)	1982-01-20	Anilinderivate, Verfahren zu ihrer Herstellung und ihre Verwendung als selektive Unkrautvertilgungsmittel
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FR2533416A1 (fr)	1984-03-30	Nouvelles compositions pesticides renfermant un photostabilisant
EP0112262A1 (de)	1984-06-27	Benzylcarbamoylpyridin-Derivate
LU82726A1 (fr)	1980-12-15	Compositions antidotes d'herbicides contenant des n-(acetyle substitue)-n-(4-methyl-2-pentanon-4-yl)-amides
CH660179A5 (fr)	1987-03-31	Derives de 1-phenoxy(phenylthio)-4-arylalkynyloxy-benzene pourvus d'une activite acaricide et d'une activite hormonale juvenile.
EP0189358B1 (de)	1988-09-28	N-(Phosphonomethylglycyl)-Sulfonylamine-ähnliche Herbizide
EP0034556B1 (de)	1984-02-01	Das Pflanzenwachstum regulierende Zusammensetzungen, die als aktive Substanz Derivate von 2-Methylen-succinamidsäure enthalten, und Derivate dieser Säure, die in diesen Zusammensetzungen verwendbar sind
EP0017602B1 (de)	1982-10-20	2-Phenyl-4-pyron-Derivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Fungizide
SU1209017A3 (ru)	1986-01-30	Гербицидна композици
EP0253291B1 (de)	1991-10-02	5-Iminomethyl-haloacyloxazolidine mit einer hemmenden Wirkung auf die Phytotoxizität von Herbiziden
BE862325A (fr)	1978-06-27	Nouveaux derives d'acide pyridyloxy-phenoxypropionique ayant une action herbicide et phytoregulatrice
BE886127A (fr)	1981-05-13	Nouveaux derives de l'imidazole, leur preparation et leur application comme agents fongicides
FR2645404A1 (fr)	1990-10-12	Compositions herbicides contenant un antidote et compositions antidotes ainsi obtenues
LU86116A1 (fr)	1986-03-24	Compositions herbicides selectives ayant une action prolongee et contenant,a titre d'ingredient actif,des derives d'alpha-chloracetamide
BE633594A (de)
CH637950A5 (fr)	1983-08-31	Derive de phenyl-2 dihydro-5,6 pyrone-4.
BE828596A (fr)	1975-10-30	Nouveaux composes d'oxiranne
FR2507184A1 (fr)	1982-12-10	Derives du type pyrrolo (3,4-e) (1,4) diazepin-2 (1h)-one utilisables comme agents anxiolytiques et anticonvulsivants, et procede pour leur preparation
EP0030514A1 (de)	1981-06-17	Anilin-Derivate, Verfahren zu ihrer Herstellung und diese enthaltende Zusammensetzungen zur Regulierung des Pflanzenwachstums
FR2509580A1 (fr)	1983-01-21	1-phenyl-1,2,3-triazoles utilisables comme anti-appetants et leur preparation
BE851616A (fr)	1977-08-18	Traitement des semences pour les proteger