CA1168056A - Substance herbicide contenant des amides comme antidote contre les alpha-halo-acetanilides - Google Patents

Substance herbicide contenant des amides comme antidote contre les alpha-halo-acetanilides

Info

Publication number: CA1168056A
Authority: CA; Canada
Prior art keywords: formula; composition; compound; weed; alkyl
Prior art date: 1981-10-20
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

CA000413740A

Other languages

English (en)

Inventor

Attilio Formigoni

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.)

Sipcam SpA

Original Assignee

Sipcam SpA

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.)

1981-10-20

Filing date

1982-10-19

Publication date

1984-05-29

1981-10-20 Priority claimed from IT24566/81A external-priority patent/IT1168041B/it

1982-04-30 Priority claimed from IT21022/82A external-priority patent/IT1190795B/it

1982-10-19 Application filed by Sipcam SpA filed Critical Sipcam SpA

1984-05-29 Application granted granted Critical

1984-05-29 Publication of CA1168056A publication Critical patent/CA1168056A/fr

Status Expired legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 29
239000000729 antidote Substances 0.000 title claims abstract description 17
239000004009 herbicide Substances 0.000 title claims abstract description 11
YZHUMGUJCQRKBT-UHFFFAOYSA-M sodium chlorate Chemical compound [Na+].[O-]Cl(=O)=O YZHUMGUJCQRKBT-UHFFFAOYSA-M 0.000 title claims abstract description 11
229940075522 antidotes Drugs 0.000 title description 12
150000001408 amides Chemical class 0.000 title description 4
239000000460 chlorine Substances 0.000 claims abstract description 86
125000000217 alkyl group Chemical group 0.000 claims abstract description 10
125000001188 haloalkyl group Chemical group 0.000 claims abstract description 9
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims abstract description 8
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 8
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims abstract description 8
229910052794 bromium Inorganic materials 0.000 claims abstract description 8
229910052799 carbon Inorganic materials 0.000 claims abstract description 8
125000006193 alkinyl group Chemical group 0.000 claims abstract description 6
229910052801 chlorine Inorganic materials 0.000 claims abstract description 6
125000000262 haloalkenyl group Chemical group 0.000 claims abstract description 6
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 5
125000003342 alkenyl group Chemical group 0.000 claims abstract description 4
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 3
239000001257 hydrogen Substances 0.000 claims abstract description 3
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 3
125000004429 atom Chemical group 0.000 claims abstract 4
WYNCHZVNFNFDNH-UHFFFAOYSA-N Oxazolidine Chemical compound C1COCN1 WYNCHZVNFNFDNH-UHFFFAOYSA-N 0.000 claims abstract 2
229910052736 halogen Inorganic materials 0.000 claims abstract 2
150000002367 halogens Chemical class 0.000 claims abstract 2
125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract 2
125000005936 piperidyl group Chemical group 0.000 claims abstract 2
150000001875 compounds Chemical class 0.000 claims description 26
240000008042 Zea mays Species 0.000 claims description 11
235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 claims description 11
235000002017 Zea mays subsp mays Nutrition 0.000 claims description 11
235000009973 maize Nutrition 0.000 claims description 11
240000006394 Sorghum bicolor Species 0.000 claims description 7
235000011684 Sorghum saccharatum Nutrition 0.000 claims description 7
238000010899 nucleation Methods 0.000 claims description 4
-1 weed-killer compound Chemical class 0.000 claims description 3
239000013543 active substance Substances 0.000 claims description 2
238000000034 method Methods 0.000 claims description 2
235000013350 formula milk Nutrition 0.000 claims 13
125000004432 carbon atom Chemical group C* 0.000 claims 2
FOMHMPJALXOZGZ-UHFFFAOYSA-N 2,2-dichloro-1-(2,2-dimethyl-1,3-oxazolidin-3-yl)ethanone Chemical compound CC1(C)OCCN1C(=O)C(Cl)Cl FOMHMPJALXOZGZ-UHFFFAOYSA-N 0.000 claims 1
AICFIUAJBIDQQB-UHFFFAOYSA-N 2,2-dichloro-1-[5-(methoxymethyl)-2,2-dimethyl-1,3-oxazolidin-3-yl]ethanone Chemical compound COCC1CN(C(=O)C(Cl)Cl)C(C)(C)O1 AICFIUAJBIDQQB-UHFFFAOYSA-N 0.000 claims 1
VSHIRTNKIXRXMI-UHFFFAOYSA-N 2,2-dimethyl-1,3-oxazolidine Chemical compound CC1(C)NCCO1 VSHIRTNKIXRXMI-UHFFFAOYSA-N 0.000 claims 1
LUZLJVVCYVXQTC-UHFFFAOYSA-N 2-bromo-n-(2-tert-butyl-6-methylphenyl)-n-(methoxymethyl)acetamide Chemical compound COCN(C(=O)CBr)C1=C(C)C=CC=C1C(C)(C)C LUZLJVVCYVXQTC-UHFFFAOYSA-N 0.000 claims 1
IYLMCARCSCXVNP-UHFFFAOYSA-N 2-chloro-n-(2,6-dimethylphenyl)-n-(propan-2-yloxymethyl)acetamide Chemical compound CC(C)OCN(C(=O)CCl)C1=C(C)C=CC=C1C IYLMCARCSCXVNP-UHFFFAOYSA-N 0.000 claims 1
VTNQPKFIQCLBDU-UHFFFAOYSA-N Acetochlor Chemical compound CCOCN(C(=O)CCl)C1=C(C)C=CC=C1CC VTNQPKFIQCLBDU-UHFFFAOYSA-N 0.000 claims 1
DPLCXQMLVOSUGV-UHFFFAOYSA-N N1(CCCCC1)NC(C(Cl)Cl)=O Chemical compound N1(CCCCC1)NC(C(Cl)Cl)=O DPLCXQMLVOSUGV-UHFFFAOYSA-N 0.000 claims 1
ZSIQJIWKELUFRJ-UHFFFAOYSA-N azepane Chemical compound C1CCCNCC1 ZSIQJIWKELUFRJ-UHFFFAOYSA-N 0.000 claims 1
125000001309 chloro group Chemical group Cl* 0.000 claims 1
230000000694 effects Effects 0.000 description 7
231100000208 phytotoxic Toxicity 0.000 description 7
230000000885 phytotoxic effect Effects 0.000 description 7
231100000674 Phytotoxicity Toxicity 0.000 description 6
244000058871 Echinochloa crus-galli Species 0.000 description 5
241000196324 Embryophyta Species 0.000 description 5
239000002689 soil Substances 0.000 description 5
244000025254 Cannabis sativa Species 0.000 description 4
150000002500 ions Chemical class 0.000 description 4
241000257303 Hymenoptera Species 0.000 description 3
239000003995 emulsifying agent Substances 0.000 description 3
239000007788 liquid Substances 0.000 description 3
210000001699 lower leg Anatomy 0.000 description 3
230000003442 weekly effect Effects 0.000 description 3
241000192043 Echinochloa Species 0.000 description 2
235000011999 Panicum crusgalli Nutrition 0.000 description 2
239000004113 Sepiolite Substances 0.000 description 2
229960001413 acetanilide Drugs 0.000 description 2
239000002671 adjuvant Substances 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
229940125904 compound 1 Drugs 0.000 description 2
MZZBPDKVEFVLFF-UHFFFAOYSA-N cyanazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C#N)=N1 MZZBPDKVEFVLFF-UHFFFAOYSA-N 0.000 description 2
238000009472 formulation Methods 0.000 description 2
AHLBNYSZXLDEJQ-FWEHEUNISA-N orlistat Chemical compound CCCCCCCCCCC[C@H](OC(=O)[C@H](CC(C)C)NC=O)C[C@@H]1OC(=O)[C@H]1CCCCCC AHLBNYSZXLDEJQ-FWEHEUNISA-N 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
229910052624 sepiolite Inorganic materials 0.000 description 2
235000019355 sepiolite Nutrition 0.000 description 2
239000000126 substance Substances 0.000 description 2
ONBQEOIKXPHGMB-VBSBHUPXSA-N 1-[2-[(2s,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-4,6-dihydroxyphenyl]-3-(4-hydroxyphenyl)propan-1-one Chemical compound O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1OC1=CC(O)=CC(O)=C1C(=O)CCC1=CC=C(O)C=C1 ONBQEOIKXPHGMB-VBSBHUPXSA-N 0.000 description 1
TVTJUIAKQFIXCE-HUKYDQBMSA-N 2-amino-9-[(2R,3S,4S,5R)-4-fluoro-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-7-prop-2-ynyl-1H-purine-6,8-dione Chemical compound NC=1NC(C=2N(C(N(C=2N=1)[C@@H]1O[C@@H]([C@H]([C@H]1O)F)CO)=O)CC#C)=O TVTJUIAKQFIXCE-HUKYDQBMSA-N 0.000 description 1
XKJMBINCVNINCA-UHFFFAOYSA-N Alfalone Chemical compound CON(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XKJMBINCVNINCA-UHFFFAOYSA-N 0.000 description 1
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
101000654316 Centruroides limpidus Beta-toxin Cll2 Proteins 0.000 description 1
GUVLYNGULCJVDO-UHFFFAOYSA-N EPTC Chemical compound CCCN(CCC)C(=O)SCC GUVLYNGULCJVDO-UHFFFAOYSA-N 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
241000864933 Lampedusa Species 0.000 description 1
239000005573 Linuron Substances 0.000 description 1
OKUGPJPKMAEJOE-UHFFFAOYSA-N S-propyl dipropylcarbamothioate Chemical compound CCCSC(=O)N(CCC)CCC OKUGPJPKMAEJOE-UHFFFAOYSA-N 0.000 description 1
MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
230000000295 complement effect Effects 0.000 description 1
229940126142 compound 16 Drugs 0.000 description 1
229940125851 compound 27 Drugs 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
125000001475 halogen functional group Chemical group 0.000 description 1
239000006193 liquid solution Substances 0.000 description 1
238000010297 mechanical methods and process Methods 0.000 description 1
230000005226 mechanical processes and functions Effects 0.000 description 1
LMAZKPOSWVOFGY-FBAUPLQOSA-N orine Natural products CO[C@H]1C[C@H](O[C@H]2CC[C@]3(C)[C@H]4C[C@@H](OC(=O)C=Cc5ccccc5)[C@]6(C)[C@@](O)(CC[C@]6(O)[C@]4(O)CC=C3C2)[C@H](C)OC(=O)C=Cc7ccccc7)O[C@H](C)[C@H]1O LMAZKPOSWVOFGY-FBAUPLQOSA-N 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
229940055764 triaz Drugs 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/22—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides
- 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
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/26—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof containing the group; Thio analogues thereof

Landscapes

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

CA000413740A 1981-10-20 1982-10-19 Substance herbicide contenant des amides comme antidote contre les alpha-halo-acetanilides Expired CA1168056A (fr)

Applications Claiming Priority (4)

Application Number	Priority Date	Filing Date	Title
IT24566/81A IT1168041B (it)	1981-10-20	1981-10-20	Composizione erbicida selettiva per mais contenente di-aloacetamidi antidoti di alfa-alo-acetanilidi
IT24566A/81		1981-10-20
IT21022/82A IT1190795B (it)	1982-04-30	1982-04-30	Composizione erbicida selettiva per mais contenente ammidi antidoti di alfa-alo-acetanilidi
IT21022A/82		1982-04-30

Publications (1)

Publication Number	Publication Date
CA1168056A true CA1168056A (fr)	1984-05-29

Family

ID=26327733

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000413740A Expired CA1168056A (fr)	1981-10-20	1982-10-19	Substance herbicide contenant des amides comme antidote contre les alpha-halo-acetanilides

Country Status (3)

Country	Link
BR (1)	BR8206082A (fr)
CA (1)	CA1168056A (fr)
FR (1)	FR2514611A1 (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4762548A (en) *	1985-08-12	1988-08-09	Stauffer Chemical Co.	Herbicide compositions of extended soil life
CN117185951A (zh) *	2023-09-11	2023-12-08	山东中石药业有限公司	一种含2-氯-n-(2,6-二甲基苯基)的乙酰苯胺化合物、制备方法及应用

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
NZ222993A (en) *	1986-12-22	1989-09-27	Stauffer Agricultural Chemical	Herbicidal compositions containing an acyl substituted oxazolidone antidote and two active herbicides
EE9500018A (et) *	1994-06-03	1995-12-15	Ciba-Geigy Ag	Selektiivne herbitsiid ja meetod selle kasutamiseks
FR2762475B1 (fr) *	1997-04-25	1999-07-16	Nitrokemia Rt	Compositions herbicides a base de chloroacetamide et de 1,3,5-triazine et leur utilisation

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4033756A (en) *	1971-09-17	1977-07-05	Gulf Research & Development Company	Dichloroacetamide treated rice seeds
US4021224A (en) *	1971-12-09	1977-05-03	Stauffer Chemical Company	Herbicide compositions
US4243811A (en) *	1972-10-13	1981-01-06	Stauffer Chemical Company	2,2,4-Trimethyl-4-hydroxymethyl-3-dichloroacetyl oxazolidine
CH574207A5 (fr) *	1973-01-25	1976-04-15	Ciba Geigy Ag
IT1079199B (it) *	1976-10-29	1985-05-08	Montedison Spa	Antidoti,della classe delle dicloroacetamidi particolarmente attivi a proteggere il mais dalla azione tossica esercitata da esteri delle glicine n,n sostituite ebricide e associazione erbicida per culture di mais
IT1114195B (it) *	1977-12-23	1986-01-27	Montedison Spa	Due antidotti dicloroacetamidici per erbicidi non selettivi particolarmente attivi a proteggere il mais dall'azione tossica esercitata da esteri della glicina n,n disostituita erbicidi
BE874361A (fr) *	1978-02-06	1979-06-18	Nitrokemia Ipartelepek	Composition herbicide selective

1982
- 1982-10-19 CA CA000413740A patent/CA1168056A/fr not_active Expired
- 1982-10-19 BR BR8206082A patent/BR8206082A/pt unknown
- 1982-10-20 FR FR8217559A patent/FR2514611A1/fr active Pending

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4762548A (en) *	1985-08-12	1988-08-09	Stauffer Chemical Co.	Herbicide compositions of extended soil life
CN117185951A (zh) *	2023-09-11	2023-12-08	山东中石药业有限公司	一种含2-氯-n-(2,6-二甲基苯基)的乙酰苯胺化合物、制备方法及应用

Also Published As

Publication number	Publication date
BR8206082A (pt)	1983-09-13
FR2514611A1 (fr)	1983-04-22

Legal Events

Date	Code	Title	Description
2001-05-29	MKEX	Expiry

Publication	Publication Date	Title
RU2221787C2 (ru)	2004-01-20	Производные 3-гидрокси-4-арил-5-оксопиразолина, обладающие гербицидным действием, композиция и способ борьбы с нежелательной растительностью
RU2113120C1 (ru)	1998-06-20	Акарицидное средство, применение и способ борьбы с клещами
US4692181A (en)	1987-09-08	Herbicidal compositions
FR2407671A1 (fr)	1979-06-01	Compositions herbicides, leur preparation et leur application au controle des plantes non desirees
CA1168056A (fr)	1984-05-29	Substance herbicide contenant des amides comme antidote contre les alpha-halo-acetanilides
US4064268A (en)	1977-12-20	Halobenzoylpropionate and N,N-diethyl-m-toluamide as insect repellents
JPH08291004A (ja)	1996-11-05	害虫防除剤組成物
US4900350A (en)	1990-02-13	5-Iminomethyl-halo-acyloxazolidines having an inhibiting action on the phytotoxicity of herbicides
JP2920446B2 (ja)	1999-07-19	除草剤組成物及び除草方法
US3681406A (en)	1972-08-01	N-alkoxyalkylidenesulfonamide compounds
DE2823355A1 (de)	1978-12-21	Sulfonamide, verwendung derselben bei der bekaempfung von zu den gliederfuessern gehoerigen schaedlingen und diese enthaltende pestizide mittel
JPS5948403A (ja)	1984-03-19	水田用除草剤
SU1069599A3 (ru)	1984-01-23	Способ борьбы с вредными насекомыми
US4390549A (en)	1983-06-28	N-Tetrachloroethylthio benzoyl anilides useful as acaricides and to control mosquitoes
AU595010B2 (en)	1990-03-22	Synergistic herbicidal compositions and method of use
KR950013369A (ko)	1995-06-15	쌀 농작물의 잡초를 방제하기 위한 제초제 조성물
US4720508A (en)	1988-01-19	Halogenated saturated hydrocarbons and saturated hydrocarbon in combination as acaricidal compounds
SU849977A3 (ru)	1981-07-23	Инсекто-акарицидное средство
JPH0572881B2 (fr)	1993-10-13
JPH0665669B2 (ja)	1994-08-24	テトラヒドロフタルイミド誘導体およびそれを有効成分とする除草剤
JPH0764812B2 (ja)	1995-07-12	テトラヒドロフタルイミド誘導体およびそれを有効成分とする除草剤
JPH0330562B2 (fr)	1991-04-30
JPS61194003A (ja)	1986-08-28	除草組成物
JPS6317810A (ja)	1988-01-25	除草剤組成物
JPH0446921B2 (fr)	1992-07-31

CA1168056A - Substance herbicide contenant des amides comme antidote contre les alpha-halo-acetanilides - Google Patents

Info

Links

Classifications

Landscapes

Applications Claiming Priority (4)

Publications (1)

Family

ID=26327733

Family Applications (1)

Country Status (3)

Cited By (2)

Families Citing this family (3)

Family Cites Families (7)

Cited By (2)

Also Published As

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Legal Events