DD204197A5 - Dinitrophenolherbizidantidote - Google Patents

Dinitrophenolherbizidantidote Download PDF

Info

Publication number: DD204197A5
Authority: DD; German Democratic Republic
Prior art keywords: carbon atoms; vernam; inclusive; group; ppi
Prior art date: 1981-02-27

Application number

DD82237737A

Other languages

German (de)

English (en)

Inventor

Reed A Gray

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.)

1981-02-27

Filing date

1982-02-26

Publication date

1983-11-23

1982-02-26 Application filed by Stauffer Chemical Co filed Critical Stauffer Chemical Co

1983-11-23 Publication of DD204197A5 publication Critical patent/DD204197A5/de

Links

230000002363 herbicidal effect Effects 0.000 claims abstract description 50
150000001875 compounds Chemical class 0.000 claims abstract description 32
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 28
125000000217 alkyl group Chemical group 0.000 claims abstract description 20
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 11
239000001257 hydrogen Substances 0.000 claims abstract description 11
239000000203 mixture Substances 0.000 claims description 25
238000000034 method Methods 0.000 claims description 19
239000000460 chlorine Substances 0.000 claims description 10
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 10
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 9
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 9
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 9
229910052794 bromium Inorganic materials 0.000 claims description 9
229910052801 chlorine Inorganic materials 0.000 claims description 9
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 8
229910052736 halogen Inorganic materials 0.000 claims description 7
150000002367 halogens Chemical class 0.000 claims description 7
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
-1 oxyl Chemical group 0.000 claims description 6
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 3
125000002947 alkylene group Chemical group 0.000 claims description 3
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 3
125000000262 haloalkenyl group Chemical group 0.000 claims description 3
125000001188 haloalkyl group Chemical group 0.000 claims description 3
229910052740 iodine Inorganic materials 0.000 claims description 3
239000011630 iodine Substances 0.000 claims description 3
231100001184 nonphytotoxic Toxicity 0.000 claims description 3
125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 claims description 3
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 7
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 4
125000001475 halogen functional group Chemical group 0.000 claims 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims 1
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
239000000729 antidote Substances 0.000 abstract description 54
239000004009 herbicide Substances 0.000 abstract description 49
230000000694 effects Effects 0.000 abstract description 5
MHKBMNACOMRIAW-UHFFFAOYSA-N 2,3-dinitrophenol Chemical class OC1=CC=CC([N+]([O-])=O)=C1[N+]([O-])=O MHKBMNACOMRIAW-UHFFFAOYSA-N 0.000 abstract description 4
GNVMUORYQLCPJZ-UHFFFAOYSA-M Thiocarbamate Chemical compound NC([S-])=O GNVMUORYQLCPJZ-UHFFFAOYSA-M 0.000 abstract description 4
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
OKUGPJPKMAEJOE-UHFFFAOYSA-N S-propyl dipropylcarbamothioate Chemical compound CCCSC(=O)N(CCC)CCC OKUGPJPKMAEJOE-UHFFFAOYSA-N 0.000 description 79
241000196324 Embryophyta Species 0.000 description 25
GUVLYNGULCJVDO-UHFFFAOYSA-N EPTC Chemical compound CCCN(CCC)C(=O)SCC GUVLYNGULCJVDO-UHFFFAOYSA-N 0.000 description 21
230000006378 damage Effects 0.000 description 20
BMTAFVWTTFSTOG-UHFFFAOYSA-N Butylate Chemical compound CCSC(=O)N(CC(C)C)CC(C)C BMTAFVWTTFSTOG-UHFFFAOYSA-N 0.000 description 17
239000002689 soil Substances 0.000 description 13
239000000243 solution Substances 0.000 description 11
238000009472 formulation Methods 0.000 description 8
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
244000068988 Glycine max Species 0.000 description 6
239000004094 surface-active agent Substances 0.000 description 6
235000010469 Glycine max Nutrition 0.000 description 5
239000008187 granular material Substances 0.000 description 5
238000010348 incorporation Methods 0.000 description 5
230000008635 plant growth Effects 0.000 description 5
239000000843 powder Substances 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
229940075522 antidotes Drugs 0.000 description 4
239000003921 oil Substances 0.000 description 4
244000025254 Cannabis sativa Species 0.000 description 3
SGEJQUSYQTVSIU-UHFFFAOYSA-N Pebulate Chemical compound CCCCN(CC)C(=O)SCCC SGEJQUSYQTVSIU-UHFFFAOYSA-N 0.000 description 3
239000004495 emulsifiable concentrate Substances 0.000 description 3
239000003995 emulsifying agent Substances 0.000 description 3
239000002904 solvent Substances 0.000 description 3
239000007921 spray Substances 0.000 description 3
239000011550 stock solution Substances 0.000 description 3
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
235000007688 Lycopersicon esculentum Nutrition 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 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
240000003768 Solanum lycopersicum Species 0.000 description 2
239000000654 additive Substances 0.000 description 2
230000009286 beneficial effect Effects 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
239000000969 carrier Substances 0.000 description 2
238000007865 diluting Methods 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
150000002191 fatty alcohols Chemical class 0.000 description 2
239000003337 fertilizer Substances 0.000 description 2
239000003815 herbicide antidote 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
238000005507 spraying Methods 0.000 description 2
239000000126 substance Substances 0.000 description 2
239000008096 xylene Substances 0.000 description 2
LDVVMCZRFWMZSG-OLQVQODUSA-N (3ar,7as)-2-(trichloromethylsulfanyl)-3a,4,7,7a-tetrahydroisoindole-1,3-dione Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)Cl)C(=O)[C@H]21 LDVVMCZRFWMZSG-OLQVQODUSA-N 0.000 description 1
PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-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
241000219144 Abutilon Species 0.000 description 1
244000105624 Arachis hypogaea Species 0.000 description 1
241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 1
235000005637 Brassica campestris Nutrition 0.000 description 1
235000014750 Brassica kaber Nutrition 0.000 description 1
240000008100 Brassica rapa Species 0.000 description 1
235000010149 Brassica rapa subsp chinensis Nutrition 0.000 description 1
235000010570 Brassica rapa var. rapa Nutrition 0.000 description 1
239000005745 Captan Substances 0.000 description 1
244000285774 Cyperus esculentus Species 0.000 description 1
235000005853 Cyperus esculentus Nutrition 0.000 description 1
102100035619 DNA-(apurinic or apyrimidinic site) lyase Human genes 0.000 description 1
241000052043 Dasyochloa Species 0.000 description 1
206010013883 Dwarfism Diseases 0.000 description 1
239000001692 EU approved anti-caking agent Substances 0.000 description 1
241000100623 Festuca arvernensis Species 0.000 description 1
241000287828 Gallus gallus Species 0.000 description 1
108010093488 His-His-His-His-His-His Proteins 0.000 description 1
101001137256 Homo sapiens DNA-(apurinic or apyrimidinic site) lyase Proteins 0.000 description 1
240000005979 Hordeum vulgare Species 0.000 description 1
235000007340 Hordeum vulgare Nutrition 0.000 description 1
206010061217 Infestation Diseases 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
240000004658 Medicago sativa Species 0.000 description 1
235000017587 Medicago sativa ssp. sativa Nutrition 0.000 description 1
XNPOFXIBHOVFFH-UHFFFAOYSA-N N-cyclohexyl-N'-(2-(4-morpholinyl)ethyl)carbodiimide Chemical compound C1CCCCC1N=C=NCCN1CCOCC1 XNPOFXIBHOVFFH-UHFFFAOYSA-N 0.000 description 1
244000061176 Nicotiana tabacum Species 0.000 description 1
235000002637 Nicotiana tabacum Nutrition 0.000 description 1
244000088461 Panicum crus-galli Species 0.000 description 1
235000011999 Panicum crusgalli Nutrition 0.000 description 1
244000046052 Phaseolus vulgaris Species 0.000 description 1
235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
240000004713 Pisum sativum Species 0.000 description 1
235000010582 Pisum sativum Nutrition 0.000 description 1
240000003461 Setaria viridis Species 0.000 description 1
235000002248 Setaria viridis Nutrition 0.000 description 1
244000061456 Solanum tuberosum Species 0.000 description 1
235000002595 Solanum tuberosum 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
235000021536 Sugar beet Nutrition 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
235000002096 Vicia faba var. equina Nutrition 0.000 description 1
208000027418 Wounds and injury Diseases 0.000 description 1
241000607479 Yersinia pestis Species 0.000 description 1
240000008042 Zea mays Species 0.000 description 1
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
235000002017 Zea mays subsp mays Nutrition 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
230000000890 antigenic effect Effects 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
239000000440 bentonite Substances 0.000 description 1
229910000278 bentonite Inorganic materials 0.000 description 1
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
230000033228 biological regulation 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
229940117949 captan Drugs 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000004927 clay Substances 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
239000002361 compost Substances 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
235000005822 corn Nutrition 0.000 description 1
244000038559 crop plants Species 0.000 description 1
230000035613 defoliation Effects 0.000 description 1
230000018044 dehydration Effects 0.000 description 1
238000006297 dehydration reaction Methods 0.000 description 1
238000012217 deletion Methods 0.000 description 1
230000037430 deletion Effects 0.000 description 1
230000001066 destructive effect Effects 0.000 description 1
238000011161 development Methods 0.000 description 1
230000018109 developmental process Effects 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
235000021186 dishes Nutrition 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
244000013123 dwarf bean Species 0.000 description 1
235000005489 dwarf bean Nutrition 0.000 description 1
235000013399 edible fruits Nutrition 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
244000230030 foxtail bristlegrass Species 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
230000035784 germination Effects 0.000 description 1
230000012010 growth Effects 0.000 description 1
230000009036 growth inhibition Effects 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
239000003864 humus Substances 0.000 description 1
229940060367 inert ingredients Drugs 0.000 description 1
208000014674 injury Diseases 0.000 description 1
230000002452 interceptive effect Effects 0.000 description 1
239000003350 kerosene Substances 0.000 description 1
239000006193 liquid solution Substances 0.000 description 1
150000004668 long chain fatty acids Chemical class 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000000463 material Substances 0.000 description 1
235000012054 meals Nutrition 0.000 description 1
238000005259 measurement Methods 0.000 description 1
230000007246 mechanism Effects 0.000 description 1
235000019713 millet Nutrition 0.000 description 1
150000002790 naphthalenes Chemical class 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
FKMRTVWOZYGANU-UHFFFAOYSA-N o-propyl n,n-dipropylcarbamothioate Chemical compound CCCOC(=S)N(CCC)CCC FKMRTVWOZYGANU-UHFFFAOYSA-N 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
235000020232 peanut Nutrition 0.000 description 1
239000003090 pesticide formulation Substances 0.000 description 1
230000008654 plant damage Effects 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
239000003223 protective agent Substances 0.000 description 1
229910052903 pyrophyllite Inorganic materials 0.000 description 1
230000009467 reduction 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
241000894007 species Species 0.000 description 1
230000000638 stimulation Effects 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
150000003460 sulfonic acids Chemical class 0.000 description 1
239000002426 superphosphate Substances 0.000 description 1
238000004381 surface treatment Methods 0.000 description 1
239000000375 suspending agent Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
238000012360 testing method Methods 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
150000003558 thiocarbamic acid derivatives Chemical class 0.000 description 1
238000012549 training Methods 0.000 description 1
239000010455 vermiculite Substances 0.000 description 1
229910052902 vermiculite Inorganic materials 0.000 description 1
235000019354 vermiculite Nutrition 0.000 description 1
230000000007 visual effect Effects 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
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring

Landscapes

Life Sciences & Earth Sciences (AREA)
General Health & Medical Sciences (AREA)
Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Agronomy & Crop Science (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Toxicology (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

DD82237737A 1981-02-27 1982-02-26 Dinitrophenolherbizidantidote DD204197A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US23891581A	1981-02-27	1981-02-27

Publications (1)

Publication Number	Publication Date
DD204197A5 true DD204197A5 (de)	1983-11-23

Family

ID=22899856

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD82237737A DD204197A5 (de)	1981-02-27	1982-02-26	Dinitrophenolherbizidantidote

Country Status (19)

Country	Link
EP (1)	EP0060056B1 (fr)
JP (1)	JPS57150606A (fr)
KR (1)	KR830008480A (fr)
AR (1)	AR229049A1 (fr)
AT (1)	ATE7196T1 (fr)
AU (1)	AU546501B2 (fr)
BR (1)	BR8201013A (fr)
CA (1)	CA1182658A (fr)
DD (1)	DD204197A5 (fr)
DE (1)	DE3260115D1 (fr)
DK (1)	DK85582A (fr)
FI (1)	FI67290C (fr)
GR (1)	GR75866B (fr)
IL (1)	IL65120A (fr)
PH (1)	PH18251A (fr)
PL (1)	PL129634B1 (fr)
PT (1)	PT74492B (fr)
RO (1)	RO90094A (fr)
ZA (1)	ZA821288B (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO2019166404A1 (fr) *	2018-02-28	2019-09-06	Bayer Aktiengesellschaft	Procédé de réduction des dommages causés aux cultures

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1073796B (de) *		1960-01-21	Farbwerke Hoechst Aktiengesellschaft vormals Meister Lucius S- Brüning, Frankfurt/M	Verfahren zur Regulierung der Selektivität und der Phytotoxizität von Schädlingsund Unkrautbekämpfungsmitteln auf Basis von dinitrierten Phenolen und Naphtolen
FR751855A (fr) *	1932-06-04	1933-09-11		Destruction sélective des plantes adventices et amélioration des récoltes
BE561449A (fr) *	1956-10-09
US3822357A (en) *	1969-09-23	1974-07-02	Rohm & Haas	Safening agents for dinitrophenols and their derivatives

1982
- 1982-02-03 GR GR67201A patent/GR75866B/el unknown
- 1982-02-17 JP JP57022897A patent/JPS57150606A/ja active Pending
- 1982-02-24 EP EP82300943A patent/EP0060056B1/fr not_active Expired
- 1982-02-24 AT AT82300943T patent/ATE7196T1/de active
- 1982-02-24 CA CA000396937A patent/CA1182658A/fr not_active Expired
- 1982-02-24 DE DE8282300943T patent/DE3260115D1/de not_active Expired
- 1982-02-24 PH PH26907A patent/PH18251A/en unknown
- 1982-02-24 KR KR1019820000817A patent/KR830008480A/ko not_active Abandoned
- 1982-02-26 PT PT74492A patent/PT74492B/pt unknown
- 1982-02-26 AR AR288590A patent/AR229049A1/es active
- 1982-02-26 RO RO82106748A patent/RO90094A/fr unknown
- 1982-02-26 DD DD82237737A patent/DD204197A5/de unknown
- 1982-02-26 ZA ZA821288A patent/ZA821288B/xx unknown
- 1982-02-26 BR BR8201013A patent/BR8201013A/pt unknown
- 1982-02-26 FI FI820687A patent/FI67290C/fi not_active IP Right Cessation
- 1982-02-26 DK DK85582A patent/DK85582A/da not_active Application Discontinuation
- 1982-02-26 IL IL65120A patent/IL65120A/xx unknown
- 1982-02-26 PL PL1982235247A patent/PL129634B1/pl unknown
- 1982-02-26 AU AU80931/82A patent/AU546501B2/en not_active Ceased

Also Published As

Publication number	Publication date
DE3260115D1 (en)	1984-05-30
FI67290C (fi)	1985-03-11
PT74492A (en)	1982-03-01
AR229049A1 (es)	1983-05-31
PT74492B (en)	1983-07-08
IL65120A (en)	1985-11-29
PL129634B1 (en)	1984-05-31
EP0060056B1 (fr)	1984-04-25
FI67290B (fi)	1984-11-30
FI820687L (fi)	1982-08-28
CA1182658A (fr)	1985-02-19
AU546501B2 (en)	1985-09-05
PL235247A1 (fr)	1982-09-27
AU8093182A (en)	1982-09-02
RO90094A (fr)	1986-09-30
JPS57150606A (en)	1982-09-17
EP0060056A1 (fr)	1982-09-15
IL65120A0 (en)	1982-04-30
KR830008480A (ko)	1983-12-10
GR75866B (fr)	1984-08-02
ZA821288B (en)	1983-03-30
DK85582A (da)	1982-08-28
BR8201013A (pt)	1983-01-04
ATE7196T1 (de)	1984-05-15
PH18251A (en)	1985-05-13

Publication	Publication Date	Title
DE3884076T2 (de)	1994-02-10	Herbizide Zusammensetzungen von acylierten 1,3-Dicarbonyl-Herbiziden und Antidots dafür.
CH368015A (de)	1963-03-15	Unkrautvertilgungsmittel
DE2135768B2 (de)	1973-06-07	Synergistisches herbizides mittel
DE3520760A1 (de)	1986-03-20	Mittel zur verzoegerung der wirkung herbizider praeparate und herbizide praeparate mit verzoegerter wirkung und verfahren zu deren herstellung
DE2440787A1 (de)	1975-03-06	Verfahren zur selektiven bekaempfung von unkraut in kentucky-blaugras
DD204197A5 (de)	1983-11-23	Dinitrophenolherbizidantidote
DE1618968C2 (fr)	1973-11-08
EP0005516B1 (fr)	1981-01-14	Pyridazinones substituées, leur procédé de préparation et leur utilisation comme herbicides
DE2539396C3 (de)	1979-10-25	Pestizide
DE2941658A1 (de)	1980-04-24	Praeparat mit wachstumsregulierender wirkung und anwendung dieses praeparats im acker- und gartenbau, sowie neue hexahydropyrimidine und imidazolidine
DE3300056C2 (de)	1985-06-27	3-Nitrobenzolsulfonanilid-Derivate und diese enthaltende fungizide Mittel
DD202233A5 (de)	1983-09-07	Verfahren und zusammensetzung zur verminderung der herbiziden schaedigung von kulturpflanzen
DE1166547B (de)	1964-03-26	Herbicide Mittel mit einem Gehalt an Aniliden
DE4011781A1 (de)	1990-10-31	Herbizides mittel
DE2144700A1 (de)	1972-03-16	Benzyl-N,N-di-sek.~butylthiolcarbamat und seine Verwendung
DE2266035C2 (fr)	1987-10-29
DE2348022A1 (de)	1975-04-03	Sulfonamid-zubereitungen fuer herbicide
CH628210A5 (en)	1982-02-26	Herbicidal preparation
DE1668081A1 (de)	1971-05-13	Verfahren zur Herstellung von neuen Mucononitrilen und diese enthaltende pesticide Zusammensetzungen sowie neue Muconitrile
DD209099A5 (de)	1984-04-25	Herbizide zusammensetzung
DE1249582B (fr)	1967-09-07
AT254609B (de)	1967-05-26	Herbizide Zubereitungen
DD153314A5 (de)	1982-01-06	Herbizide zusammensetzung
DE2438598A1 (de)	1975-03-06	Herbizide mittel
DD202490A5 (de)	1983-09-21	Herbizide zusammensetzung