DD209099A5 - Herbizide zusammensetzung - Google Patents

Herbizide zusammensetzung Download PDF

Info

Publication number: DD209099A5
Authority: DD; German Democratic Republic
Prior art keywords: carbon atoms; inclusive; ppi; alkyl; antidote
Prior art date: 1981-09-08

Application number

DD82243069A

Other languages

German (de)

English (en)

Inventor

Edmund J Gaughan

Original Assignee

Stauffer Chemical 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.)

1981-09-08

Filing date

1982-09-07

Publication date

1984-04-25

1982-09-07 Application filed by Stauffer Chemical Co filed Critical Stauffer Chemical Co

1984-04-25 Publication of DD209099A5 publication Critical patent/DD209099A5/de

Links

230000002363 herbicidal effect Effects 0.000 title claims abstract description 55
239000000203 mixture Substances 0.000 title claims abstract description 33
239000000729 antidote Substances 0.000 claims abstract description 42
GNVMUORYQLCPJZ-UHFFFAOYSA-M Thiocarbamate Chemical compound NC([S-])=O GNVMUORYQLCPJZ-UHFFFAOYSA-M 0.000 claims abstract description 6
150000001875 compounds Chemical class 0.000 claims description 27
125000004432 carbon atom Chemical group C* 0.000 claims description 19
-1 dichloroacetyl Chemical group 0.000 claims description 17
238000000034 method Methods 0.000 claims description 15
125000000217 alkyl group Chemical group 0.000 claims description 12
239000000460 chlorine Substances 0.000 claims description 12
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 8
229910052801 chlorine Inorganic materials 0.000 claims description 8
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 6
125000003342 alkenyl group Chemical group 0.000 claims description 6
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 6
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 6
229910052794 bromium Inorganic materials 0.000 claims description 6
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 5
229910052736 halogen Inorganic materials 0.000 claims description 4
150000002367 halogens Chemical class 0.000 claims description 4
239000003085 diluting agent Substances 0.000 claims description 3
125000001188 haloalkyl group Chemical group 0.000 claims description 3
231100001184 nonphytotoxic Toxicity 0.000 claims description 3
125000000262 haloalkenyl group Chemical group 0.000 claims description 2
125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 claims description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 4
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 4
125000002947 alkylene group Chemical group 0.000 claims 1
125000001246 bromo group Chemical group Br* 0.000 claims 1
125000001309 chloro group Chemical group Cl* 0.000 claims 1
239000004009 herbicide Substances 0.000 abstract description 40
230000000694 effects Effects 0.000 abstract description 5
241000196324 Embryophyta Species 0.000 description 26
239000000243 solution Substances 0.000 description 17
230000006378 damage Effects 0.000 description 15
239000002689 soil Substances 0.000 description 15
GUVLYNGULCJVDO-UHFFFAOYSA-N EPTC Chemical compound CCCN(CCC)C(=O)SCC GUVLYNGULCJVDO-UHFFFAOYSA-N 0.000 description 13
OKUGPJPKMAEJOE-UHFFFAOYSA-N S-propyl dipropylcarbamothioate Chemical compound CCCSC(=O)N(CCC)CCC OKUGPJPKMAEJOE-UHFFFAOYSA-N 0.000 description 9
239000000126 substance Substances 0.000 description 8
238000009472 formulation Methods 0.000 description 7
238000010348 incorporation Methods 0.000 description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
238000009331 sowing Methods 0.000 description 6
241000894007 species Species 0.000 description 6
239000008187 granular material Substances 0.000 description 5
239000004094 surface-active agent Substances 0.000 description 5
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
239000000969 carrier Substances 0.000 description 4
230000008635 plant growth Effects 0.000 description 4
239000002904 solvent Substances 0.000 description 4
239000000725 suspension Substances 0.000 description 4
YTPMCWYIRHLEGM-BQYQJAHWSA-N 1-[(e)-2-propylsulfonylethenyl]sulfonylpropane Chemical compound CCCS(=O)(=O)\C=C\S(=O)(=O)CCC YTPMCWYIRHLEGM-BQYQJAHWSA-N 0.000 description 3
229920000742 Cotton Polymers 0.000 description 3
244000068988 Glycine max Species 0.000 description 3
235000010469 Glycine max Nutrition 0.000 description 3
244000299507 Gossypium hirsutum Species 0.000 description 3
240000005979 Hordeum vulgare Species 0.000 description 3
235000007340 Hordeum vulgare Nutrition 0.000 description 3
240000008042 Zea mays Species 0.000 description 3
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 3
235000002017 Zea mays subsp mays Nutrition 0.000 description 3
239000013543 active substance Substances 0.000 description 3
230000002303 anti-venom Effects 0.000 description 3
235000005822 corn Nutrition 0.000 description 3
239000004495 emulsifiable concentrate Substances 0.000 description 3
239000003337 fertilizer Substances 0.000 description 3
239000003815 herbicide antidote Substances 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
240000007594 Oryza sativa Species 0.000 description 2
235000007164 Oryza sativa Nutrition 0.000 description 2
231100000674 Phytotoxicity Toxicity 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
239000000654 additive Substances 0.000 description 2
230000004888 barrier function Effects 0.000 description 2
230000001276 controlling effect Effects 0.000 description 2
238000007865 diluting Methods 0.000 description 2
239000000428 dust Substances 0.000 description 2
239000003995 emulsifying agent Substances 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
238000002474 experimental method Methods 0.000 description 2
150000002191 fatty alcohols Chemical class 0.000 description 2
239000000706 filtrate Substances 0.000 description 2
230000009931 harmful effect Effects 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
239000003921 oil Substances 0.000 description 2
239000002245 particle Substances 0.000 description 2
239000003208 petroleum Substances 0.000 description 2
231100000208 phytotoxic Toxicity 0.000 description 2
230000000885 phytotoxic effect Effects 0.000 description 2
239000000843 powder Substances 0.000 description 2
235000009566 rice Nutrition 0.000 description 2
238000012360 testing method Methods 0.000 description 2
239000008096 xylene Substances 0.000 description 2
SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
QETZVGMMDJFMLI-UHFFFAOYSA-N 2,2-dichloro-1-[5-(ethylsulfanylmethyl)-2,2-dimethyl-1,3-oxazolidin-3-yl]ethanone Chemical compound CCSCC1CN(C(=O)C(Cl)Cl)C(C)(C)O1 QETZVGMMDJFMLI-UHFFFAOYSA-N 0.000 description 1
NHQDETIJWKXCTC-UHFFFAOYSA-N 3-chloroperbenzoic acid Chemical compound OOC(=O)C1=CC=CC(Cl)=C1 NHQDETIJWKXCTC-UHFFFAOYSA-N 0.000 description 1
125000006283 4-chlorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1Cl)C([H])([H])* 0.000 description 1
244000105624 Arachis hypogaea Species 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical class OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
BMTAFVWTTFSTOG-UHFFFAOYSA-N Butylate Chemical compound CCSC(=O)N(CC(C)C)CC(C)C BMTAFVWTTFSTOG-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
239000001692 EU approved anti-caking agent Substances 0.000 description 1
244000058871 Echinochloa crus-galli Species 0.000 description 1
101150055539 HADH gene Proteins 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
240000004322 Lens culinaris Species 0.000 description 1
235000014647 Lens culinaris subsp culinaris Nutrition 0.000 description 1
235000007688 Lycopersicon esculentum Nutrition 0.000 description 1
229910002651 NO3 Inorganic materials 0.000 description 1
244000061176 Nicotiana tabacum Species 0.000 description 1
235000002637 Nicotiana tabacum Nutrition 0.000 description 1
NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
235000011999 Panicum crusgalli Nutrition 0.000 description 1
240000004713 Pisum sativum Species 0.000 description 1
235000010582 Pisum sativum Nutrition 0.000 description 1
235000005775 Setaria Nutrition 0.000 description 1
241000232088 Setaria <nematode> Species 0.000 description 1
240000003461 Setaria viridis Species 0.000 description 1
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
240000003768 Solanum lycopersicum Species 0.000 description 1
244000061456 Solanum tuberosum Species 0.000 description 1
235000002595 Solanum tuberosum Nutrition 0.000 description 1
235000011684 Sorghum saccharatum Nutrition 0.000 description 1
244000062793 Sorghum vulgare Species 0.000 description 1
244000300264 Spinacia oleracea Species 0.000 description 1
235000009337 Spinacia oleracea Nutrition 0.000 description 1
208000003028 Stuttering Diseases 0.000 description 1
PHSUVQBHRAWOQD-UHFFFAOYSA-N Tiocarbazil Chemical compound CCC(C)N(C(C)CC)C(=O)SCC1=CC=CC=C1 PHSUVQBHRAWOQD-UHFFFAOYSA-N 0.000 description 1
235000021307 Triticum Nutrition 0.000 description 1
244000098338 Triticum aestivum Species 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
208000027418 Wounds and injury Diseases 0.000 description 1
241001148683 Zostera marina Species 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
239000002253 acid Substances 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
125000003158 alcohol group Chemical group 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
239000003945 anionic surfactant Substances 0.000 description 1
239000005557 antagonist Substances 0.000 description 1
229940075522 antidotes Drugs 0.000 description 1
239000002216 antistatic agent Substances 0.000 description 1
239000012736 aqueous medium Substances 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
238000009835 boiling Methods 0.000 description 1
YYRMJZQKEFZXMX-UHFFFAOYSA-N calcium;phosphoric acid Chemical compound [Ca+2].OP(O)(O)=O.OP(O)(O)=O YYRMJZQKEFZXMX-UHFFFAOYSA-N 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
238000005266 casting Methods 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000004927 clay Substances 0.000 description 1
239000002361 compost Substances 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
239000002837 defoliant Substances 0.000 description 1
238000011161 development Methods 0.000 description 1
230000018109 developmental process Effects 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
239000003814 drug Substances 0.000 description 1
229940079593 drug Drugs 0.000 description 1
238000010410 dusting Methods 0.000 description 1
235000013399 edible fruits Nutrition 0.000 description 1
239000003974 emollient agent Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
238000000605 extraction Methods 0.000 description 1
210000003608 fece Anatomy 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
239000000295 fuel oil Substances 0.000 description 1
230000000855 fungicidal effect Effects 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
230000012010 growth Effects 0.000 description 1
125000001475 halogen functional group Chemical group 0.000 description 1
239000003864 humus Substances 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
208000014674 injury Diseases 0.000 description 1
230000003993 interaction Effects 0.000 description 1
239000003621 irrigation water Substances 0.000 description 1
239000003350 kerosene Substances 0.000 description 1
230000002147 killing effect Effects 0.000 description 1
239000006193 liquid solution Substances 0.000 description 1
239000010871 livestock manure Substances 0.000 description 1
150000004668 long chain fatty acids Chemical class 0.000 description 1
230000007246 mechanism Effects 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
239000011259 mixed solution Substances 0.000 description 1
238000002156 mixing Methods 0.000 description 1
238000012544 monitoring process Methods 0.000 description 1
150000002790 naphthalenes Chemical class 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
238000010899 nucleation Methods 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
230000036961 partial effect Effects 0.000 description 1
235000020232 peanut Nutrition 0.000 description 1
230000035515 penetration Effects 0.000 description 1
239000003090 pesticide formulation Substances 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
235000012015 potatoes Nutrition 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
230000001737 promoting effect Effects 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
229910052903 pyrophyllite Inorganic materials 0.000 description 1
230000002829 reductive effect Effects 0.000 description 1
238000010992 reflux Methods 0.000 description 1
230000001105 regulatory effect Effects 0.000 description 1
230000004044 response Effects 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000004576 sand Substances 0.000 description 1
230000007226 seed germination Effects 0.000 description 1
230000035945 sensitivity Effects 0.000 description 1
235000017557 sodium bicarbonate Nutrition 0.000 description 1
229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
239000007787 solid Substances 0.000 description 1
238000010183 spectrum analysis Methods 0.000 description 1
239000007921 spray Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
230000007480 spreading Effects 0.000 description 1
238000003892 spreading Methods 0.000 description 1
230000004936 stimulating effect Effects 0.000 description 1
239000011550 stock solution Substances 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
239000002426 superphosphate Substances 0.000 description 1
238000004381 surface treatment Methods 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
150000003558 thiocarbamic acid derivatives Chemical class 0.000 description 1
239000013638 trimer Substances 0.000 description 1
230000000007 visual effect Effects 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/04—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- 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
- A01N35/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
- 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)
Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Zoology (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Engineering & Computer Science (AREA)
Environmental Sciences (AREA)
Plant Pathology (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Toxicology (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

DD82243069A 1981-09-08 1982-09-07 Herbizide zusammensetzung DD209099A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US30015781A	1981-09-08	1981-09-08

Publications (1)

Publication Number	Publication Date
DD209099A5 true DD209099A5 (de)	1984-04-25

Family

ID=23157951

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD82243069A DD209099A5 (de)	1981-09-08	1982-09-07	Herbizide zusammensetzung

Country Status (14)

Country	Link
EP (1)	EP0074255A1 (fr)
JP (1)	JPS5859976A (fr)
KR (1)	KR840001244A (fr)
AU (1)	AU8808582A (fr)
BR (1)	BR8205085A (fr)
DD (1)	DD209099A5 (fr)
DK (1)	DK394982A (fr)
ES (1)	ES515528A0 (fr)
IL (1)	IL66744A0 (fr)
PL (1)	PL130877B1 (fr)
PT (1)	PT75509B (fr)
RO (1)	RO84633B (fr)
TR (1)	TR21560A (fr)
ZA (1)	ZA826523B (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5225570A (en) *	1987-08-13	1993-07-06	Monsanto Company	5-heterocyclic-substituted oxazolidine dihaloacetamides

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
AR228034A1 (es) *	1979-06-18	1983-01-14	Stauffer Chemical Co	Compuestos de 3-alcanoil-5-metil substituido-oxazolidina y composicion herbicida que lo comprende como antidoto

1982
- 1982-08-30 BR BR8205085A patent/BR8205085A/pt unknown
- 1982-09-02 TR TR21560A patent/TR21560A/xx unknown
- 1982-09-03 EP EP82304641A patent/EP0074255A1/fr not_active Withdrawn
- 1982-09-03 DK DK394982A patent/DK394982A/da not_active Application Discontinuation
- 1982-09-06 KR KR1019820004029A patent/KR840001244A/ko not_active Abandoned
- 1982-09-06 PT PT75509A patent/PT75509B/pt unknown
- 1982-09-07 ES ES515528A patent/ES515528A0/es active Granted
- 1982-09-07 DD DD82243069A patent/DD209099A5/de unknown
- 1982-09-07 IL IL66744A patent/IL66744A0/xx unknown
- 1982-09-07 AU AU88085/82A patent/AU8808582A/en not_active Abandoned
- 1982-09-07 RO RO108577A patent/RO84633B/ro unknown
- 1982-09-07 ZA ZA826523A patent/ZA826523B/xx unknown
- 1982-09-07 PL PL1982238165A patent/PL130877B1/pl unknown
- 1982-09-08 JP JP57156476A patent/JPS5859976A/ja active Pending

Also Published As

Publication number	Publication date
PL238165A1 (en)	1983-03-28
RO84633A (fr)	1984-07-17
JPS5859976A (ja)	1983-04-09
BR8205085A (pt)	1983-08-09
KR840001244A (ko)	1984-04-30
PL130877B1 (en)	1984-09-29
PT75509B (en)	1984-12-04
ZA826523B (en)	1983-10-26
RO84633B (ro)	1984-09-30
DK394982A (da)	1983-03-09
ES8401046A1 (es)	1983-12-01
ES515528A0 (es)	1983-12-01
EP0074255A1 (fr)	1983-03-16
PT75509A (en)	1982-10-01
IL66744A0 (en)	1982-12-31
AU8808582A (en)	1983-03-17
TR21560A (tr)	1986-07-25

Publication	Publication Date	Title
DE2350800C2 (fr)	1992-06-11
DE2218097C2 (fr)	1987-07-30
DE3884076T2 (de)	1994-02-10	Herbizide Zusammensetzungen von acylierten 1,3-Dicarbonyl-Herbiziden und Antidots dafür.
DE1567212C3 (de)	1974-05-02	Fungicides Mittel nut bactericider Nebenwirkung
DE2350547C2 (de)	1986-10-23	N-Dichloracetyl-2,2,5-trimethyl-oxazolidin
DE1567075B1 (de)	1970-07-23	Verfahren zum Unterdruecken der Schaedigung junger Getreidepflanzen durch herbizide Carbamate
DE1567027B1 (de)	1971-03-04	Unkrautvernichtungsmittel
DE2141586C2 (de)	1983-07-21	Herbizides Saatschutzmittel auf Sulfonatbasis
EP0031938A2 (fr)	1981-07-15	Utilisation de nitriles et d'amidoximes d'acides aryloxy(thio)carboxyliques comme antidotes contre des herbicides
CH636600A5 (de)	1983-06-15	2-hydroxybenzamidderivate und verwendung derselben als fungizide.
DE1667982A1 (de)	1971-07-29	Netzmittelzusammensetzung
DE2421195C2 (de)	1982-12-23	Thiazolidinverbindungen sowie dieselben enthaltendes Herbizid-Antidot
DD209099A5 (de)	1984-04-25	Herbizide zusammensetzung
DE2605586C2 (fr)	1988-01-14
DD231978A5 (de)	1986-01-15	Herbizide zusammensetzung
DE1618968C2 (fr)	1973-11-08
DE1032971B (de)	1958-06-26	Verfahren zum Bekaempfen von Unkraut auf bestellten Flaechen
DE2266035C2 (fr)	1987-10-29
DE2362333C3 (de)	1978-07-13	Thionophosphorsäureesteramide, Verfahren zu deren Herstellung und Verwendung derselben
DE4011781A1 (de)	1990-10-31	Herbizides mittel
DE1542959C2 (fr)	1973-01-04
CH628210A5 (en)	1982-02-26	Herbicidal preparation
DE2826531C2 (fr)	1988-04-14
DD236868A5 (de)	1986-06-25	Mittel zum protahieren der wirkungsdauer und zur erhoehung der selektivitaet von herbiziden zusammensetzungen
DE2441741C2 (de)	1984-10-04	Saatschützende herbizide Zubereitung und ihre Verwendung