DD208535A5 - Herbizide zusammensetzung - Google Patents

Herbizide zusammensetzung Download PDF

Info

Publication number: DD208535A5
Authority: DD; German Democratic Republic
Prior art keywords: salt; amine; item; thiocarbamate; alkyl
Prior art date: 1981-10-23

Application number

DD82244247A

Other languages

German (de)

English (en)

Inventor

Raymond A Felix

Joanna K Hsu

Daniel L Hyzak

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.)

1981-10-23

Filing date

1982-10-25

Publication date

1984-04-04

1982-10-25 Application filed by Stauffer Chemical Co filed Critical Stauffer Chemical Co

1984-04-04 Publication of DD208535A5 publication Critical patent/DD208535A5/de

Links

230000002363 herbicidal effect Effects 0.000 title claims abstract description 50
239000000203 mixture Substances 0.000 title claims description 64
239000002689 soil Substances 0.000 claims abstract description 68
150000003839 salts Chemical class 0.000 claims abstract description 40
GNVMUORYQLCPJZ-UHFFFAOYSA-M Thiocarbamate Chemical compound NC([S-])=O GNVMUORYQLCPJZ-UHFFFAOYSA-M 0.000 claims abstract description 32
150000001412 amines Chemical class 0.000 claims abstract description 25
-1 amine salt Chemical class 0.000 claims abstract description 22
125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 16
239000001257 hydrogen Substances 0.000 claims abstract description 14
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 14
229910052736 halogen Inorganic materials 0.000 claims abstract description 10
150000002367 halogens Chemical class 0.000 claims abstract description 10
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims abstract description 6
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 5
125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 4
230000002035 prolonged effect Effects 0.000 claims abstract description 4
150000002431 hydrogen Chemical class 0.000 claims abstract 3
238000000034 method Methods 0.000 claims description 27
150000001875 compounds Chemical class 0.000 claims description 25
GUVLYNGULCJVDO-UHFFFAOYSA-N EPTC Chemical compound CCCN(CCC)C(=O)SCC GUVLYNGULCJVDO-UHFFFAOYSA-N 0.000 claims description 15
239000000729 antidote Substances 0.000 claims description 15
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 14
125000000217 alkyl group Chemical group 0.000 claims description 14
125000003342 alkenyl group Chemical group 0.000 claims description 13
230000000694 effects Effects 0.000 claims description 11
229910000039 hydrogen halide Inorganic materials 0.000 claims description 11
239000012433 hydrogen halide Substances 0.000 claims description 11
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 9
239000002253 acid Substances 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
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
231100001184 nonphytotoxic Toxicity 0.000 claims description 6
229910052757 nitrogen Inorganic materials 0.000 claims description 5
125000002768 hydroxyalkyl group Chemical group 0.000 claims description 4
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
229910052760 oxygen Inorganic materials 0.000 claims description 3
239000001301 oxygen Substances 0.000 claims description 3
229910052717 sulfur Chemical group 0.000 claims description 3
239000011593 sulfur Chemical group 0.000 claims description 3
125000000753 cycloalkyl group Chemical group 0.000 claims description 2
125000001188 haloalkyl group Chemical group 0.000 claims description 2
125000000008 (C1-C10) alkyl group Chemical group 0.000 claims 2
DYUWTXWIYMHBQS-UHFFFAOYSA-N n-prop-2-enylprop-2-en-1-amine Chemical group C=CCNCC=C DYUWTXWIYMHBQS-UHFFFAOYSA-N 0.000 claims 2
125000004982 dihaloalkyl group Chemical group 0.000 claims 1
IXCSERBJSXMMFS-UHFFFAOYSA-N hcl hcl Chemical group Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 claims 1
PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical group C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 claims 1
239000004009 herbicide Substances 0.000 abstract description 26
150000003558 thiocarbamic acid derivatives Chemical class 0.000 abstract description 8
230000015556 catabolic process Effects 0.000 abstract description 3
238000006731 degradation reaction Methods 0.000 abstract description 2
239000004606 Fillers/Extenders Substances 0.000 description 34
239000008187 granular material Substances 0.000 description 19
241000196324 Embryophyta Species 0.000 description 16
238000012360 testing method Methods 0.000 description 13
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 10
239000004480 active ingredient Substances 0.000 description 10
239000007788 liquid Substances 0.000 description 9
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
239000000080 wetting agent Substances 0.000 description 8
244000062793 Sorghum vulgare Species 0.000 description 7
238000009472 formulation Methods 0.000 description 7
239000000243 solution Substances 0.000 description 7
240000008042 Zea mays Species 0.000 description 6
239000003995 emulsifying agent Substances 0.000 description 6
239000000463 material Substances 0.000 description 6
239000002904 solvent Substances 0.000 description 6
235000002017 Zea mays subsp mays Nutrition 0.000 description 5
239000004495 emulsifiable concentrate Substances 0.000 description 5
230000006872 improvement Effects 0.000 description 5
235000019713 millet Nutrition 0.000 description 5
238000002360 preparation method Methods 0.000 description 5
244000075850 Avena orientalis Species 0.000 description 4
241000287828 Gallus gallus Species 0.000 description 4
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 4
150000001408 amides Chemical class 0.000 description 4
125000000129 anionic group Chemical group 0.000 description 4
229960000892 attapulgite Drugs 0.000 description 4
239000000969 carrier Substances 0.000 description 4
235000013330 chicken meat Nutrition 0.000 description 4
239000000460 chlorine Substances 0.000 description 4
239000004927 clay Substances 0.000 description 4
230000001276 controlling effect Effects 0.000 description 4
235000005822 corn Nutrition 0.000 description 4
239000000428 dust Substances 0.000 description 4
239000003094 microcapsule Substances 0.000 description 4
229910052625 palygorskite Inorganic materials 0.000 description 4
239000002245 particle Substances 0.000 description 4
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
235000007319 Avena orientalis Nutrition 0.000 description 3
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 3
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
239000013543 active substance Substances 0.000 description 3
239000011575 calcium Substances 0.000 description 3
229910052791 calcium Inorganic materials 0.000 description 3
229910052799 carbon Inorganic materials 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
229910052801 chlorine Inorganic materials 0.000 description 3
230000007423 decrease Effects 0.000 description 3
235000014113 dietary fatty acids Nutrition 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
239000000194 fatty acid Substances 0.000 description 3
229930195729 fatty acid Natural products 0.000 description 3
230000012010 growth Effects 0.000 description 3
239000004615 ingredient Substances 0.000 description 3
150000002576 ketones Chemical class 0.000 description 3
230000000051 modifying effect Effects 0.000 description 3
239000003208 petroleum Chemical class 0.000 description 3
230000008635 plant growth Effects 0.000 description 3
239000000843 powder Substances 0.000 description 3
150000003141 primary amines Chemical class 0.000 description 3
239000011734 sodium Substances 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
239000007787 solid Substances 0.000 description 3
238000003892 spreading Methods 0.000 description 3
239000000126 substance Substances 0.000 description 3
239000004094 surface-active agent Substances 0.000 description 3
239000005995 Aluminium silicate Substances 0.000 description 2
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
244000061176 Nicotiana tabacum Species 0.000 description 2
235000002637 Nicotiana tabacum Nutrition 0.000 description 2
241001579678 Panthea coenobita Species 0.000 description 2
235000011684 Sorghum saccharatum Nutrition 0.000 description 2
239000011149 active material Substances 0.000 description 2
239000000654 additive Substances 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
150000001299 aldehydes Chemical class 0.000 description 2
235000012211 aluminium silicate Nutrition 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
229910052794 bromium Inorganic materials 0.000 description 2
239000012141 concentrate Substances 0.000 description 2
235000008504 concentrate Nutrition 0.000 description 2
239000003085 diluting agent Substances 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
238000009826 distribution Methods 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
238000011156 evaluation Methods 0.000 description 2
239000011521 glass Substances 0.000 description 2
238000000227 grinding Methods 0.000 description 2
150000002466 imines Chemical class 0.000 description 2
229910052500 inorganic mineral Inorganic materials 0.000 description 2
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 2
238000005259 measurement Methods 0.000 description 2
239000011707 mineral Substances 0.000 description 2
235000010755 mineral Nutrition 0.000 description 2
238000002156 mixing Methods 0.000 description 2
239000003921 oil Substances 0.000 description 2
230000002688 persistence Effects 0.000 description 2
238000012545 processing Methods 0.000 description 2
150000003335 secondary amines Chemical class 0.000 description 2
230000007480 spreading Effects 0.000 description 2
239000007858 starting material Substances 0.000 description 2
150000003871 sulfonates Chemical class 0.000 description 2
239000010455 vermiculite Substances 0.000 description 2
229910052902 vermiculite Inorganic materials 0.000 description 2
235000019354 vermiculite Nutrition 0.000 description 2
COAABSMONFNYQH-TTWCUHKNSA-N (2r,3s,4s,5r,6s)-2-(hydroxymethyl)-6-(oxiran-2-ylmethylsulfanyl)oxane-3,4,5-triol Chemical group O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1SCC1OC1 COAABSMONFNYQH-TTWCUHKNSA-N 0.000 description 1
NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
240000001592 Amaranthus caudatus Species 0.000 description 1
235000009328 Amaranthus caudatus Nutrition 0.000 description 1
235000007320 Avena fatua Nutrition 0.000 description 1
235000016068 Berberis vulgaris Nutrition 0.000 description 1
241000335053 Beta vulgaris Species 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
229920000298 Cellophane Polymers 0.000 description 1
206010012559 Developmental delay Diseases 0.000 description 1
239000001692 EU approved anti-caking agent Substances 0.000 description 1
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
229920001732 Lignosulfonate Polymers 0.000 description 1
235000007688 Lycopersicon esculentum Nutrition 0.000 description 1
240000004658 Medicago sativa Species 0.000 description 1
235000017587 Medicago sativa ssp. sativa Nutrition 0.000 description 1
244000070788 Milium effusum Species 0.000 description 1
GRSMWKLPSNHDHA-UHFFFAOYSA-N Naphthalic anhydride Chemical group C1=CC(C(=O)OC2=O)=C3C2=CC=CC3=C1 GRSMWKLPSNHDHA-UHFFFAOYSA-N 0.000 description 1
240000007594 Oryza sativa Species 0.000 description 1
235000007164 Oryza sativa Nutrition 0.000 description 1
235000007199 Panicum miliaceum Nutrition 0.000 description 1
244000046052 Phaseolus vulgaris Species 0.000 description 1
235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
239000004721 Polyphenylene oxide Substances 0.000 description 1
229920001214 Polysorbate 60 Polymers 0.000 description 1
239000004372 Polyvinyl alcohol Substances 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
235000008515 Setaria glauca Nutrition 0.000 description 1
235000001155 Setaria leucopila Nutrition 0.000 description 1
244000010062 Setaria pumila Species 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
240000006394 Sorghum bicolor Species 0.000 description 1
244000300264 Spinacia oleracea Species 0.000 description 1
235000009337 Spinacia oleracea Nutrition 0.000 description 1
229920002472 Starch Polymers 0.000 description 1
235000009430 Thespesia populnea Nutrition 0.000 description 1
235000005373 Uvularia sessilifolia Nutrition 0.000 description 1
241000282485 Vulpes vulpes Species 0.000 description 1
241000209149 Zea Species 0.000 description 1
235000007244 Zea mays Nutrition 0.000 description 1
235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
CWVZGJORVTZXFW-UHFFFAOYSA-N [benzyl(dimethyl)silyl]methyl carbamate Chemical compound NC(=O)OC[Si](C)(C)CC1=CC=CC=C1 CWVZGJORVTZXFW-UHFFFAOYSA-N 0.000 description 1
150000003869 acetamides Chemical class 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000008186 active pharmaceutical agent Substances 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
238000005054 agglomeration Methods 0.000 description 1
230000002776 aggregation Effects 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
150000004996 alkyl benzenes Chemical class 0.000 description 1
150000001347 alkyl bromides Chemical class 0.000 description 1
150000001350 alkyl halides Chemical class 0.000 description 1
230000029936 alkylation Effects 0.000 description 1
238000005804 alkylation reaction Methods 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
239000002216 antistatic agent Substances 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
KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 1
229940073608 benzyl chloride Drugs 0.000 description 1
VMEOFRRFNIVESX-UHFFFAOYSA-N bis(2-methylpropyl)carbamothioic s-acid Chemical compound CC(C)CN(C(S)=O)CC(C)C VMEOFRRFNIVESX-UHFFFAOYSA-N 0.000 description 1
239000012267 brine Substances 0.000 description 1
239000002775 capsule Substances 0.000 description 1
150000001721 carbon Chemical group 0.000 description 1
230000034303 cell budding Effects 0.000 description 1
239000003638 chemical reducing agent Substances 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
230000001427 coherent effect Effects 0.000 description 1
238000007906 compression Methods 0.000 description 1
230000006835 compression Effects 0.000 description 1
239000000470 constituent Substances 0.000 description 1
238000013270 controlled release Methods 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
244000038559 crop plants Species 0.000 description 1
FFNKZSVHHUBFHT-UHFFFAOYSA-N cyanamide;sodium Chemical compound [Na].[Na].NC#N FFNKZSVHHUBFHT-UHFFFAOYSA-N 0.000 description 1
150000001912 cyanamides Chemical class 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
230000035613 defoliation Effects 0.000 description 1
239000008367 deionised water Substances 0.000 description 1
229910021641 deionized water Inorganic materials 0.000 description 1
238000011161 development Methods 0.000 description 1
WCGGWVOVFQNRRS-UHFFFAOYSA-N dichloro-acetic acid amide Natural products NC(=O)C(Cl)Cl WCGGWVOVFQNRRS-UHFFFAOYSA-N 0.000 description 1
238000007865 diluting Methods 0.000 description 1
SPCNPOWOBZQWJK-UHFFFAOYSA-N dimethoxy-(2-propan-2-ylsulfanylethylsulfanyl)-sulfanylidene-$l^{5}-phosphane Chemical compound COP(=S)(OC)SCCSC(C)C SPCNPOWOBZQWJK-UHFFFAOYSA-N 0.000 description 1
JMGZBMRVDHKMKB-UHFFFAOYSA-L disodium;2-sulfobutanedioate Chemical compound [Na+].[Na+].OS(=O)(=O)C(C([O-])=O)CC([O-])=O JMGZBMRVDHKMKB-UHFFFAOYSA-L 0.000 description 1
238000001035 drying Methods 0.000 description 1
238000010410 dusting Methods 0.000 description 1
239000000975 dye Substances 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
238000001125 extrusion Methods 0.000 description 1
239000004744 fabric Substances 0.000 description 1
238000009313 farming Methods 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
238000004817 gas chromatography Methods 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
230000009931 harmful effect Effects 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
239000011630 iodine Substances 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
238000003973 irrigation Methods 0.000 description 1
230000002262 irrigation Effects 0.000 description 1
239000003621 irrigation water Substances 0.000 description 1
235000014666 liquid concentrate Nutrition 0.000 description 1
239000012280 lithium aluminium hydride Substances 0.000 description 1
230000007774 longterm Effects 0.000 description 1
239000000391 magnesium silicate Substances 0.000 description 1
235000012243 magnesium silicates Nutrition 0.000 description 1
235000009973 maize Nutrition 0.000 description 1
239000003550 marker Substances 0.000 description 1
239000011159 matrix material Substances 0.000 description 1
239000012528 membrane Substances 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
239000010445 mica Substances 0.000 description 1
229910052618 mica group Inorganic materials 0.000 description 1
229920003052 natural elastomer Polymers 0.000 description 1
229920001194 natural rubber Polymers 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
235000019198 oils Nutrition 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
150000002917 oxazolidines Chemical class 0.000 description 1
238000011056 performance test Methods 0.000 description 1
230000000737 periodic effect Effects 0.000 description 1
230000002085 persistent effect Effects 0.000 description 1
239000000546 pharmaceutical excipient Substances 0.000 description 1
238000005191 phase separation Methods 0.000 description 1
239000002367 phosphate rock Substances 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
229920002239 polyacrylonitrile Polymers 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920000056 polyoxyethylene ether Polymers 0.000 description 1
229920002635 polyurethane Polymers 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
239000011148 porous material Substances 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
235000012015 potatoes Nutrition 0.000 description 1
230000008569 process Effects 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229910052903 pyrophyllite Inorganic materials 0.000 description 1
230000009467 reduction Effects 0.000 description 1
230000026267 regulation of growth Effects 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
239000012279 sodium borohydride Substances 0.000 description 1
229910000033 sodium borohydride Inorganic materials 0.000 description 1
BEOOHQFXGBMRKU-UHFFFAOYSA-N sodium cyanoborohydride Chemical compound [Na+].[B-]C#N BEOOHQFXGBMRKU-UHFFFAOYSA-N 0.000 description 1
235000011121 sodium hydroxide Nutrition 0.000 description 1
HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
HIEHAIZHJZLEPQ-UHFFFAOYSA-M sodium;naphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 HIEHAIZHJZLEPQ-UHFFFAOYSA-M 0.000 description 1
238000004856 soil analysis Methods 0.000 description 1
238000009331 sowing Methods 0.000 description 1
241000894007 species Species 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
239000007921 spray Substances 0.000 description 1
239000008107 starch Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
230000000638 stimulation Effects 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
229920003051 synthetic elastomer Polymers 0.000 description 1
239000005061 synthetic rubber Substances 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
150000003548 thiazolidines Chemical class 0.000 description 1
239000012485 toluene extract Substances 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
239000012991 xanthate 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
- A01N25/22—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 containing ingredients stabilising the active ingredients
- 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)

DD82244247A 1981-10-23 1982-10-25 Herbizide zusammensetzung DD208535A5 (de)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US31398481A	1981-10-23	1981-10-23
US38058682A	1982-05-21	1982-05-21

Publications (1)

Publication Number	Publication Date
DD208535A5 true DD208535A5 (de)	1984-04-04

Family

ID=26979158

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD82244247A DD208535A5 (de)	1981-10-23	1982-10-25	Herbizide zusammensetzung

Country Status (12)

Country	Link
EP (1)	EP0078146B1 (fr)
AU (1)	AU553346B2 (fr)
BG (1)	BG38782A3 (fr)
DD (1)	DD208535A5 (fr)
DE (1)	DE3270284D1 (fr)
DK (1)	DK465782A (fr)
ES (1)	ES8308472A1 (fr)
IL (1)	IL67043A (fr)
PL (1)	PL238709A1 (fr)
PT (1)	PT75723B (fr)
RO (1)	RO85261B (fr)
TR (1)	TR21525A (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
HU193577B (en) *	1984-06-14	1987-10-28	Noevenyvedelmi Kutato Intezet	Preparatives prolonging the effect of herbicides containing derivatives of diamin-methan and herbicides with prolonged effect
US5395816A (en) *	1990-12-12	1995-03-07	Imperial Chemical Industries Plc	Antidoting herbicidal 3-ixoxazolidinone compounds
ATE117169T1 (de) *	1990-12-12	1995-02-15	Zeneca Inc	Pflanzenschützende herbizide 3-isoxazolidinone zusammensetzungen.
US5527762A (en) *	1990-12-12	1996-06-18	Zeneca Limited	Antidoting herbicidal 3-isoxazolidinone compounds

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3564768A (en) *	1968-10-25	1971-02-23	Gulf Research Development Co	Coated corn seed
US3959304A (en) *	1974-07-01	1976-05-25	Stauffer Chemical Company	Certain 3-haloacyl-2,2,5-trimethyl-oxazolidines
PH16010A (en) *	1978-09-20	1983-05-20	Stauffer Chemical Co	Herbicides compositions of extended soil life
US4299616A (en) *	1980-03-31	1981-11-10	Stauffer Chemical Company	Herbicide compositions of extended soil life

1982
- 1982-10-20 EP EP82305574A patent/EP0078146B1/fr not_active Expired
- 1982-10-20 DE DE8282305574T patent/DE3270284D1/de not_active Expired
- 1982-10-20 DK DK465782A patent/DK465782A/da not_active Application Discontinuation
- 1982-10-21 IL IL67043A patent/IL67043A/xx unknown
- 1982-10-22 AU AU89694/82A patent/AU553346B2/en not_active Ceased
- 1982-10-22 PL PL23870982A patent/PL238709A1/xx unknown
- 1982-10-22 ES ES516753A patent/ES8308472A1/es not_active Expired
- 1982-10-22 PT PT75723A patent/PT75723B/pt unknown
- 1982-10-22 RO RO108853A patent/RO85261B/ro unknown
- 1982-10-22 BG BG058374A patent/BG38782A3/xx unknown
- 1982-10-25 DD DD82244247A patent/DD208535A5/de not_active IP Right Cessation
1983
- 1983-01-01 TR TR21525A patent/TR21525A/xx unknown

Also Published As

Publication number	Publication date
PL238709A1 (en)	1983-07-18
IL67043A0 (en)	1983-02-23
BG38782A3 (en)	1986-02-28
RO85261A (fr)	1984-09-29
DE3270284D1 (en)	1986-05-07
RO85261B (ro)	1984-10-30
EP0078146B1 (fr)	1986-04-02
ES516753A0 (es)	1983-09-16
AU8969482A (en)	1983-04-28
AU553346B2 (en)	1986-07-10
TR21525A (tr)	1984-09-01
ES8308472A1 (es)	1983-09-16
DK465782A (da)	1983-04-24
PT75723B (en)	1985-06-28
PT75723A (en)	1982-11-01
IL67043A (en)	1985-11-29
EP0078146A1 (fr)	1983-05-04

Legal Events

Date	Code	Title	Description
1997-09-25	ENJ	Ceased due to non-payment of renewal fee

Publication	Publication Date	Title
DE2639405C2 (de)	1983-12-29	Phenylglyoxylnitril-2-oximcyanmethyläther, Verfahren zu dessen Herstellung und Mittel, welche diesen als Gegenmittel für Kulturpflanzen schädigende Herbizide enthalten
US4299616A (en)	1981-11-10	Herbicide compositions of extended soil life
DE2135768B2 (de)	1973-06-07	Synergistisches herbizides mittel
DE2118317A1 (fr)	1971-11-04
DD208535A5 (de)	1984-04-04	Herbizide zusammensetzung
US4381195A (en)	1983-04-26	N-Methylcarbamoyloxy anilides as herbicide extenders
DD215002A5 (de)	1984-10-31	Pestizide zusammensetzung
US4629499A (en)	1986-12-16	Herbicide compositions of extended soil life
DE2607785A1 (de)	1976-09-09	Aufbereitetes saatgut
CH506237A (de)	1971-04-30	Gegebenenfalls substituiertes N,N'-Bis-(carbamoyloxy)-dithiooxalimidat enthaltendes Schädlingsbekämpfungsmittel
US4433999A (en)	1984-02-28	Herbicide compositions containing soil life extenders and antidotes
US4648894A (en)	1987-03-10	Herbicide compositions of extended soil life
DD145993A5 (de)	1981-01-21	Herbizide zusammensetzung
DE1301819B (de)	1969-08-28	Substituierte 2, 4-Diamino-6-chlor-s-triazine
US4662930A (en)	1987-05-05	Herbicide compositions of extended soil life
DE2141227A1 (de)	1972-02-24	Carbamoyloximverbindungen sowie deren Verwendung
DE3110525C2 (de)	1986-10-30	2-Chloracetanilide und sie enthaltende Herbizide
DE1812762A1 (de)	1969-07-03	Carbamoyloximverbindungen und -mischungen,Verfahren zu deren Herstellung und deren Verwendung
US4490166A (en)	1984-12-25	Iminophenyl N-methylcarbamates as herbicide extenders
EP0100909B1 (fr)	1986-06-04	Compositions herbicides à durée de vie prolongée dans le sol
US4381936A (en)	1983-05-03	Herbicide compositions of extended soil life
AT358866B (de)	1980-10-10	Verfahren zur selektiven bekaempfung von unkraeutern in kulturpflanzen
DE1567218C3 (de)	1973-09-27	Verwendung von 4-Chlorphenoxyessigsäureamid-Derivaten als Herbizide
US4478636A (en)	1984-10-23	Herbicidal compositions of extended soil life
DD223905A5 (de)	1985-06-26	Herbizide mittel