DD206318A5 - Herbizidzusammensetzung - Google Patents

Herbizidzusammensetzung Download PDF

Info

Publication number: DD206318A5
Authority: DD; German Democratic Republic
Prior art keywords: phenyl; benzyl; substituted; alkyl; independently selected
Prior art date: 1981-08-24

Application number

DD82241872A

Other languages

German (de)

English (en)

Inventor

George B Large

Lawrence L Buren

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.)

1981-08-24

Filing date

1982-07-22

Publication date

1984-01-25

1981-08-24 Priority claimed from US06/295,345 external-priority patent/US4341549A/en

1982-07-22 Application filed by Stauffer Chemical Co filed Critical Stauffer Chemical Co

1984-01-25 Publication of DD206318A5 publication Critical patent/DD206318A5/de

Links

239000000203 mixture Substances 0.000 title claims abstract description 31
230000002363 herbicidal effect Effects 0.000 title claims abstract description 24
239000004009 herbicide Substances 0.000 title abstract description 11
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 25
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract description 22
229910052736 halogen Inorganic materials 0.000 claims abstract description 5
150000002367 halogens Chemical class 0.000 claims abstract description 5
150000001875 compounds Chemical class 0.000 claims description 32
238000000034 method Methods 0.000 claims description 16
125000000217 alkyl group Chemical group 0.000 claims description 14
125000003545 alkoxy group Chemical group 0.000 claims description 5
229910052799 carbon Inorganic materials 0.000 claims description 4
239000003085 diluting agent Substances 0.000 claims description 2
239000003701 inert diluent Substances 0.000 claims 4
XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical class [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 claims 2
150000001450 anions Chemical class 0.000 claims 1
239000012876 carrier material Substances 0.000 claims 1
239000004480 active ingredient Substances 0.000 abstract description 10
239000005648 plant growth regulator Substances 0.000 abstract description 4
239000004471 Glycine Substances 0.000 abstract description 2
SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical class [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-UHFFFAOYSA-N 0.000 abstract 2
125000000008 (C1-C10) alkyl group Chemical group 0.000 abstract 1
CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 1
150000003017 phosphorus Chemical class 0.000 abstract 1
150000003254 radicals Chemical class 0.000 abstract 1
241000196324 Embryophyta Species 0.000 description 47
-1 alkali metal salts Chemical class 0.000 description 30
150000003839 salts Chemical class 0.000 description 20
NDVLTYZPCACLMA-UHFFFAOYSA-N silver oxide Chemical compound [O-2].[Ag+].[Ag+] NDVLTYZPCACLMA-UHFFFAOYSA-N 0.000 description 20
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 18
238000012360 testing method Methods 0.000 description 17
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
239000000243 solution Substances 0.000 description 15
238000002360 preparation method Methods 0.000 description 13
XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical class OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 description 12
230000001105 regulatory effect Effects 0.000 description 11
230000012010 growth Effects 0.000 description 10
229910001923 silver oxide Inorganic materials 0.000 description 10
239000000126 substance Substances 0.000 description 10
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
239000000047 product Substances 0.000 description 9
239000007787 solid Substances 0.000 description 9
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
125000004432 carbon atom Chemical group C* 0.000 description 8
150000004714 phosphonium salts Chemical class 0.000 description 8
230000008018 melting Effects 0.000 description 7
238000002844 melting Methods 0.000 description 7
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 6
238000005481 NMR spectroscopy Methods 0.000 description 6
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 6
125000000129 anionic group Chemical group 0.000 description 6
239000000428 dust Substances 0.000 description 6
230000000694 effects Effects 0.000 description 6
239000011541 reaction mixture Substances 0.000 description 6
239000011734 sodium Substances 0.000 description 6
229910052708 sodium Inorganic materials 0.000 description 6
125000001424 substituent group Chemical group 0.000 description 6
230000009105 vegetative growth Effects 0.000 description 6
239000000080 wetting agent Substances 0.000 description 6
235000011684 Sorghum saccharatum Nutrition 0.000 description 5
239000002253 acid Substances 0.000 description 5
238000004458 analytical method Methods 0.000 description 5
238000011161 development Methods 0.000 description 5
230000018109 developmental process Effects 0.000 description 5
235000014113 dietary fatty acids Nutrition 0.000 description 5
235000013399 edible fruits Nutrition 0.000 description 5
150000002148 esters Chemical class 0.000 description 5
239000000194 fatty acid Substances 0.000 description 5
229930195729 fatty acid Natural products 0.000 description 5
239000000706 filtrate Substances 0.000 description 5
238000003306 harvesting Methods 0.000 description 5
239000002904 solvent Substances 0.000 description 5
239000004094 surface-active agent Substances 0.000 description 5
JKFYKCYQEWQPTM-UHFFFAOYSA-N 2-azaniumyl-2-(4-fluorophenyl)acetate Chemical compound OC(=O)C(N)C1=CC=C(F)C=C1 JKFYKCYQEWQPTM-UHFFFAOYSA-N 0.000 description 4
229910021612 Silver iodide Inorganic materials 0.000 description 4
240000006394 Sorghum bicolor Species 0.000 description 4
239000013543 active substance Substances 0.000 description 4
239000007864 aqueous solution Substances 0.000 description 4
230000033228 biological regulation Effects 0.000 description 4
239000003795 chemical substances by application Substances 0.000 description 4
230000035613 defoliation Effects 0.000 description 4
239000002270 dispersing agent Substances 0.000 description 4
239000006185 dispersion Substances 0.000 description 4
239000004495 emulsifiable concentrate Substances 0.000 description 4
239000003995 emulsifying agent Substances 0.000 description 4
239000003921 oil Substances 0.000 description 4
235000019198 oils Nutrition 0.000 description 4
230000008635 plant growth Effects 0.000 description 4
239000000843 powder Substances 0.000 description 4
229940045105 silver iodide Drugs 0.000 description 4
238000003756 stirring Methods 0.000 description 4
XNXADQRVRLZXAD-UHFFFAOYSA-N 2-(2-phosphonoethylamino)acetic acid Chemical class OC(=O)CNCCP(O)(O)=O XNXADQRVRLZXAD-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
241001148683 Zostera marina Species 0.000 description 3
150000004996 alkyl benzenes Chemical class 0.000 description 3
239000000460 chlorine Substances 0.000 description 3
235000021186 dishes Nutrition 0.000 description 3
150000002191 fatty alcohols Chemical class 0.000 description 3
238000001914 filtration Methods 0.000 description 3
235000011389 fruit/vegetable juice Nutrition 0.000 description 3
150000002334 glycols Chemical class 0.000 description 3
229910052500 inorganic mineral Inorganic materials 0.000 description 3
238000005259 measurement Methods 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
239000011707 mineral Substances 0.000 description 3
235000010755 mineral Nutrition 0.000 description 3
239000003208 petroleum Chemical class 0.000 description 3
239000002689 soil Substances 0.000 description 3
238000009331 sowing Methods 0.000 description 3
239000007921 spray Substances 0.000 description 3
238000005507 spraying Methods 0.000 description 3
150000003871 sulfonates Chemical class 0.000 description 3
238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 2
JTXKZMGARKMLQL-UHFFFAOYSA-N 2-[ethyl(phosphonomethyl)amino]acetic acid Chemical compound OC(=O)CN(CC)CP(O)(O)=O JTXKZMGARKMLQL-UHFFFAOYSA-N 0.000 description 2
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
244000025254 Cannabis sativa Species 0.000 description 2
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
229920001732 Lignosulfonate Polymers 0.000 description 2
241000209504 Poaceae Species 0.000 description 2
239000004372 Polyvinyl alcohol Substances 0.000 description 2
240000000111 Saccharum officinarum Species 0.000 description 2
235000007201 Saccharum officinarum Nutrition 0.000 description 2
108010077895 Sarcosine Proteins 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
235000007230 Sorghum bicolor Nutrition 0.000 description 2
244000138286 Sorghum saccharatum Species 0.000 description 2
CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 2
229930006000 Sucrose Natural products 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
239000000654 additive Substances 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
229910052783 alkali metal Inorganic materials 0.000 description 2
150000001408 amides Chemical class 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
229960000892 attapulgite Drugs 0.000 description 2
239000011575 calcium Substances 0.000 description 2
229910052791 calcium Inorganic materials 0.000 description 2
150000001720 carbohydrates Chemical class 0.000 description 2
235000014633 carbohydrates Nutrition 0.000 description 2
239000000969 carrier Substances 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
229910052801 chlorine Inorganic materials 0.000 description 2
125000001309 chloro group Chemical group Cl* 0.000 description 2
239000004927 clay Substances 0.000 description 2
239000012141 concentrate Substances 0.000 description 2
230000001276 controlling effect Effects 0.000 description 2
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 2
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 2
GELSOTNVVKOYAW-UHFFFAOYSA-N ethyl(triphenyl)phosphanium Chemical compound C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(CC)C1=CC=CC=C1 GELSOTNVVKOYAW-UHFFFAOYSA-N 0.000 description 2
238000002474 experimental method Methods 0.000 description 2
238000009472 formulation Methods 0.000 description 2
239000012456 homogeneous solution Substances 0.000 description 2
230000005764 inhibitory process Effects 0.000 description 2
JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical class CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 2
239000007788 liquid Substances 0.000 description 2
239000000463 material Substances 0.000 description 2
229920000609 methyl cellulose Polymers 0.000 description 2
239000001923 methylcellulose Substances 0.000 description 2
235000010981 methylcellulose Nutrition 0.000 description 2
230000004660 morphological change Effects 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
239000002736 nonionic surfactant Substances 0.000 description 2
229910052625 palygorskite Inorganic materials 0.000 description 2
239000002245 particle Substances 0.000 description 2
229920002451 polyvinyl alcohol Polymers 0.000 description 2
230000009467 reduction Effects 0.000 description 2
FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical compound C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 description 2
SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 2
159000000000 sodium salts Chemical class 0.000 description 2
239000012265 solid product Substances 0.000 description 2
241000894007 species Species 0.000 description 2
238000003892 spreading Methods 0.000 description 2
230000007480 spreading Effects 0.000 description 2
239000005720 sucrose Substances 0.000 description 2
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
239000000725 suspension Substances 0.000 description 2
235000015112 vegetable and seed oil Nutrition 0.000 description 2
239000008158 vegetable oil Substances 0.000 description 2
239000003039 volatile agent Substances 0.000 description 2
239000002888 zwitterionic surfactant Substances 0.000 description 2
RSSDWSPWORHGIE-UHFFFAOYSA-N $l^{1}-phosphanylbenzene Chemical compound [P]C1=CC=CC=C1 RSSDWSPWORHGIE-UHFFFAOYSA-N 0.000 description 1
PCTMTFRHKVHKIS-BMFZQQSSSA-N (1s,3r,4e,6e,8e,10e,12e,14e,16e,18s,19r,20r,21s,25r,27r,30r,31r,33s,35r,37s,38r)-3-[(2r,3s,4s,5s,6r)-4-amino-3,5-dihydroxy-6-methyloxan-2-yl]oxy-19,25,27,30,31,33,35,37-octahydroxy-18,20,21-trimethyl-23-oxo-22,39-dioxabicyclo[33.3.1]nonatriaconta-4,6,8,10 Chemical compound C1C=C2C[C@@H](OS(O)(=O)=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2.O[C@H]1[C@@H](N)[C@H](O)[C@@H](C)O[C@H]1O[C@H]1/C=C/C=C/C=C/C=C/C=C/C=C/C=C/[C@H](C)[C@@H](O)[C@@H](C)[C@H](C)OC(=O)C[C@H](O)C[C@H](O)CC[C@@H](O)[C@H](O)C[C@H](O)C[C@](O)(C[C@H](O)[C@H]2C(O)=O)O[C@H]2C1 PCTMTFRHKVHKIS-BMFZQQSSSA-N 0.000 description 1
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
SYSZENVIJHPFNL-UHFFFAOYSA-N (alpha-D-mannosyl)7-beta-D-mannosyl-diacetylchitobiosyl-L-asparagine, isoform B (protein) Chemical compound COC1=CC=C(I)C=C1 SYSZENVIJHPFNL-UHFFFAOYSA-N 0.000 description 1
IHBWFODPLKRAME-UHFFFAOYSA-N 2',3',4',5'-tetraphenyl-1,1'-spirobi[fluorene] Chemical compound C12=CC=CC=C2C=C2C1=CC=CC21C2=CC3=CC=CC(C=4C=CC=CC=4)=C3C2=C(C=2C=CC=CC=2)C(C=2C=CC=CC=2)=C1C1=CC=CC=C1 IHBWFODPLKRAME-UHFFFAOYSA-N 0.000 description 1
240000006995 Abutilon theophrasti Species 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
241000209761 Avena Species 0.000 description 1
235000007320 Avena fatua Nutrition 0.000 description 1
241000209764 Avena fatua Species 0.000 description 1
235000007319 Avena orientalis Nutrition 0.000 description 1
235000016068 Berberis vulgaris Nutrition 0.000 description 1
241000335053 Beta vulgaris Species 0.000 description 1
235000011331 Brassica Nutrition 0.000 description 1
241000220243 Brassica sp. Species 0.000 description 1
241001148727 Bromus tectorum Species 0.000 description 1
239000005745 Captan Substances 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
244000037364 Cinnamomum aromaticum Species 0.000 description 1
235000014489 Cinnamomum aromaticum Nutrition 0.000 description 1
241000207892 Convolvulus Species 0.000 description 1
206010010904 Convulsion Diseases 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
244000241257 Cucumis melo Species 0.000 description 1
235000015510 Cucumis melo subsp melo Nutrition 0.000 description 1
240000004230 Cyperus compressus Species 0.000 description 1
235000005853 Cyperus esculentus Nutrition 0.000 description 1
241000208296 Datura Species 0.000 description 1
239000001692 EU approved anti-caking agent Substances 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000004606 Fillers/Extenders Substances 0.000 description 1
238000004566 IR spectroscopy Methods 0.000 description 1
206010061217 Infestation Diseases 0.000 description 1
241000360065 Ligula Species 0.000 description 1
240000006240 Linum usitatissimum Species 0.000 description 1
235000004431 Linum usitatissimum Nutrition 0.000 description 1
241000209082 Lolium Species 0.000 description 1
LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 1
241001140649 Miscanthus ecklonii Species 0.000 description 1
244000061176 Nicotiana tabacum Species 0.000 description 1
235000002637 Nicotiana tabacum Nutrition 0.000 description 1
244000046052 Phaseolus vulgaris Species 0.000 description 1
229920001213 Polysorbate 20 Polymers 0.000 description 1
244000275012 Sesbania cannabina Species 0.000 description 1
235000005775 Setaria Nutrition 0.000 description 1
241000232088 Setaria <nematode> Species 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
229910021607 Silver chloride Inorganic materials 0.000 description 1
235000012480 Solanum sp Nutrition 0.000 description 1
244000061456 Solanum tuberosum Species 0.000 description 1
235000002595 Solanum tuberosum Nutrition 0.000 description 1
229920002472 Starch Polymers 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
241000219094 Vitaceae Species 0.000 description 1
241000607479 Yersinia pestis Species 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
229910052784 alkaline earth metal Inorganic materials 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
150000003863 ammonium salts Chemical class 0.000 description 1
239000003945 anionic surfactant Substances 0.000 description 1
239000002518 antifoaming agent Substances 0.000 description 1
239000008346 aqueous phase Substances 0.000 description 1
239000002585 base Substances 0.000 description 1
BNQRPLGZFADFGA-UHFFFAOYSA-N benzyl(triphenyl)phosphanium Chemical class C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(C=1C=CC=CC=1)CC1=CC=CC=C1 BNQRPLGZFADFGA-UHFFFAOYSA-N 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
239000001506 calcium phosphate Substances 0.000 description 1
229910000389 calcium phosphate Inorganic materials 0.000 description 1
235000011010 calcium phosphates Nutrition 0.000 description 1
PASHVRUKOFIRIK-UHFFFAOYSA-L calcium sulfate dihydrate Chemical compound O.O.[Ca+2].[O-]S([O-])(=O)=O PASHVRUKOFIRIK-UHFFFAOYSA-L 0.000 description 1
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239000003093 cationic surfactant Substances 0.000 description 1
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150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
239000000470 constituent Substances 0.000 description 1
230000007797 corrosion Effects 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
239000012043 crude product Substances 0.000 description 1
238000005520 cutting process Methods 0.000 description 1
125000004122 cyclic group Chemical group 0.000 description 1
125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
125000006286 dichlorobenzyl group Chemical group 0.000 description 1
LXCYSACZTOKNNS-UHFFFAOYSA-N diethoxy(oxo)phosphanium Chemical compound CCO[P+](=O)OCC LXCYSACZTOKNNS-UHFFFAOYSA-N 0.000 description 1
238000009826 distribution Methods 0.000 description 1
238000001035 drying Methods 0.000 description 1
230000008030 elimination Effects 0.000 description 1
238000003379 elimination reaction Methods 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
NTNZTEQNFHNYBC-UHFFFAOYSA-N ethyl 2-aminoacetate Chemical compound CCOC(=O)CN NTNZTEQNFHNYBC-UHFFFAOYSA-N 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000004744 fabric Substances 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
239000012065 filter cake Substances 0.000 description 1
238000005189 flocculation Methods 0.000 description 1
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229910052731 fluorine Inorganic materials 0.000 description 1
230000000855 fungicidal effect Effects 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
239000008187 granular material Substances 0.000 description 1
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238000000227 grinding Methods 0.000 description 1
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239000005556 hormone Substances 0.000 description 1
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238000001802 infusion Methods 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
239000003112 inhibitor Substances 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
230000002045 lasting effect Effects 0.000 description 1
239000012263 liquid product Substances 0.000 description 1
XCOBTUNSZUJCDH-UHFFFAOYSA-B lithium magnesium sodium silicate Chemical compound [Li+].[Li+].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Na+].[Na+].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3 XCOBTUNSZUJCDH-UHFFFAOYSA-B 0.000 description 1
239000000391 magnesium silicate Substances 0.000 description 1
235000012243 magnesium silicates Nutrition 0.000 description 1
239000010445 mica Substances 0.000 description 1
229910052618 mica group Inorganic materials 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
231100001160 nonlethal Toxicity 0.000 description 1
231100001184 nonphytotoxic Toxicity 0.000 description 1
238000010899 nucleation Methods 0.000 description 1
239000002674 ointment Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
239000008188 pellet Substances 0.000 description 1
238000003359 percent control normalization Methods 0.000 description 1
125000001476 phosphono group Chemical group [H]OP(*)(=O)O[H] 0.000 description 1
230000035790 physiological processes and functions Effects 0.000 description 1
230000008654 plant damage Effects 0.000 description 1
229940051841 polyoxyethylene ether Drugs 0.000 description 1
229920000056 polyoxyethylene ether Polymers 0.000 description 1
239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
235000012015 potatoes Nutrition 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
KCXFHTAICRTXLI-UHFFFAOYSA-N propane-1-sulfonic acid Chemical compound CCCS(O)(=O)=O KCXFHTAICRTXLI-UHFFFAOYSA-N 0.000 description 1
229910052903 pyrophyllite Inorganic materials 0.000 description 1
238000011084 recovery Methods 0.000 description 1
239000011347 resin Chemical class 0.000 description 1
229920005989 resin Chemical class 0.000 description 1
239000011435 rock Substances 0.000 description 1
230000021749 root development Effects 0.000 description 1
150000005619 secondary aliphatic amines Chemical class 0.000 description 1
238000004904 shortening Methods 0.000 description 1
239000004460 silage Substances 0.000 description 1
HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
229910001961 silver nitrate Inorganic materials 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
230000007928 solubilization Effects 0.000 description 1
238000005063 solubilization Methods 0.000 description 1
230000003381 solubilizing effect Effects 0.000 description 1
238000004611 spectroscopical analysis Methods 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
239000008107 starch Substances 0.000 description 1
238000003860 storage Methods 0.000 description 1
235000001508 sulfur Nutrition 0.000 description 1
239000006228 supernatant Substances 0.000 description 1
230000001629 suppression Effects 0.000 description 1
229940104261 taurate Drugs 0.000 description 1
XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 1
150000003510 tertiary aliphatic amines Chemical class 0.000 description 1
239000012085 test solution Substances 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
TVVPMLFGPYQGTG-UHFFFAOYSA-M tetramethylphosphanium;iodide Chemical compound [I-].C[P+](C)(C)C TVVPMLFGPYQGTG-UHFFFAOYSA-M 0.000 description 1
USFPINLPPFWTJW-UHFFFAOYSA-N tetraphenylphosphonium Chemical compound C1=CC=CC=C1[P+](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 USFPINLPPFWTJW-UHFFFAOYSA-N 0.000 description 1
QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
ITPUYOMXIFNXBE-UHFFFAOYSA-N tris(4-chlorophenyl)-methylphosphanium Chemical class C=1C=C(Cl)C=CC=1[P+](C=1C=CC(Cl)=CC=1)(C)C1=CC=C(Cl)C=C1 ITPUYOMXIFNXBE-UHFFFAOYSA-N 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
238000009736 wetting Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/50—Organo-phosphines
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P40/00—Technologies relating to the processing of minerals
- Y02P40/50—Glass production, e.g. reusing waste heat during processing or shaping
- Y02P40/57—Improving the yield, e-g- reduction of reject rates

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Biochemistry (AREA)
General Health & Medical Sciences (AREA)
Molecular Biology (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

DD82241872A 1981-08-24 1982-07-22 Herbizidzusammensetzung DD206318A5 (de)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US06/295,345 US4341549A (en)	1981-08-24	1981-08-24	Phosphonium salts of N-phosphonomethylglycine and their use as herbicides and plant growth regulants
US37433982A	1982-05-05	1982-05-05

Publications (1)

Publication Number	Publication Date
DD206318A5 true DD206318A5 (de)	1984-01-25

Family

ID=26969067

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD82241872A DD206318A5 (de)	1981-08-24	1982-07-22	Herbizidzusammensetzung

Country Status (11)

Country	Link
KR (1)	KR840000577A (fr)
AU (1)	AU556954B2 (fr)
BG (2)	BG38331A3 (fr)
BR (1)	BR8204264A (fr)
CA (1)	CA1212690A (fr)
DD (1)	DD206318A5 (fr)
ES (1)	ES8401090A1 (fr)
HU (1)	HU189602B (fr)
IN (1)	IN155646B (fr)
MA (1)	MA19544A1 (fr)
RO (2)	RO86278B (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BR8605102A (pt) *	1985-10-21	1987-07-21	Stauffer Chemical Co	Composicao fitoativa liquida e composicao herbicida liquida

1982
- 1982-07-05 AU AU85596/82A patent/AU556954B2/en not_active Ceased
- 1982-07-09 CA CA000407027A patent/CA1212690A/fr not_active Expired
- 1982-07-13 BG BG067417A patent/BG38331A3/xx unknown
- 1982-07-13 BG BG057393A patent/BG37833A3/xx unknown
- 1982-07-16 KR KR1019820003179A patent/KR840000577A/ko not_active Ceased
- 1982-07-20 MA MA19752A patent/MA19544A1/fr unknown
- 1982-07-22 DD DD82241872A patent/DD206318A5/de unknown
- 1982-07-22 IN IN851/CAL/82A patent/IN155646B/en unknown
- 1982-07-22 HU HU822372A patent/HU189602B/hu unknown
- 1982-07-22 BR BR8204264A patent/BR8204264A/pt unknown
- 1982-07-23 RO RO108239A patent/RO86278B/ro unknown
- 1982-07-23 RO RO82116436A patent/RO90601A/fr unknown
- 1982-08-23 ES ES515175A patent/ES8401090A1/es not_active Expired

Also Published As

Publication number	Publication date
RO90601A (fr)	1987-02-27
ES515175A0 (es)	1983-12-01
CA1212690A (fr)	1986-10-14
IN155646B (fr)	1985-02-16
HU189602B (en)	1986-07-28
BR8204264A (pt)	1983-07-19
KR840000577A (ko)	1984-02-25
RO86278A (fr)	1985-03-15
BG37833A3 (en)	1985-08-15
BG38331A3 (en)	1985-11-15
MA19544A1 (fr)	1983-04-01
AU556954B2 (en)	1986-11-27
ES8401090A1 (es)	1983-12-01
RO86278B (ro)	1985-03-31
AU8559682A (en)	1983-03-03

Publication	Publication Date	Title
US4315765A (en)	1982-02-16	Trialkylsulfonium salts of n-phosphonomethylglycine and their use as plant growth regulators and herbicides
DD219104A5 (de)	1985-02-27	Zusammensetzung fuer den einsatz als pflanzenwachstumsregulator
DE3415820A1 (de)	1984-10-31	1-carbalkoxyalkyl-3-aryloxy-4-(2'-carboxyphenyl)-azet-2-one, diese enthaltende pflanzenwachstumsregulierende mittel und verfahren zum regulieren des pflanzenwachstums
US4525202A (en)	1985-06-25	Phosphonium salts of N-phosphonomethylglycine and their use as herbicides and plant growth regulants
CA1170666A (fr)	1984-07-10	Sels de trialkylsulfonium de n-phosphonomethyl- glycine, et leur utilisation comme regulateurs de la croissance des plantes et comme herbicides
US4341549A (en)	1982-07-27	Phosphonium salts of N-phosphonomethylglycine and their use as herbicides and plant growth regulants
EP0155911A1 (fr)	1985-09-25	Dérivés de la purine pour la régulation de croissance des plantes
DE2615878C2 (de)	1985-09-19	Polycyclische stickstoffhaltige Verbindungen
DE2338010A1 (de)	1974-02-14	Verfahren zur regulierung des wachstums und der entwicklung von pflanzen
DE2657380B2 (de)	1980-05-29	Halogenäthyl-sulfone, Verfahren zu ihrer Herstellung sowie ihre Verwendung zur Regulierung des Pflanzenwachstums
DE2524578A1 (de)	1975-12-11	Barbitursaeurederivate, verfahren zu ihrer herstellung und ihre verwendung als herbizide
DD206318A5 (de)	1984-01-25	Herbizidzusammensetzung
DD229299A5 (de)	1985-11-06	Herbizide und wachstumsregulierende mittel
DD218268A5 (de)	1985-02-06	Herbizide zusammensetzung
DE2825474C2 (fr)	1990-04-26
DD251067A5 (de)	1987-11-04	Herbizide zusammensetzung
DE2362333C3 (de)	1978-07-13	Thionophosphorsäureesteramide, Verfahren zu deren Herstellung und Verwendung derselben
DE2420627C2 (de)	1982-10-21	N-iso-Propyl-2-chloräthan-(thiono)-phosphonsäureesteramide, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Pflanzenwachstumsregulatoren
CH677664A5 (fr)	1991-06-14
DE2824517A1 (de)	1979-12-06	Mittel zur regulierung des pflanzenwachstums
DE4011781A1 (de)	1990-10-31	Herbizides mittel
DE2040367C3 (de)	1980-04-30	Pflanzenwachstumsregler auf der Basis von Carbamoylphosphonaten und deren Verwendung
DE2361189A1 (de)	1974-06-12	Oximino-thiolphosphorsaeureester, verfahren zu deren herstellung und deren verwendung als pestizide
DE2149680C3 (de)	1977-01-13	2-Halogenäthyl-organooxy-sllane, deren Herstelung und Mittel zur Regulierung des Pflanzenwachstums CIBA-GEIGY AG, Basel (Schweiz)
DE2356892B2 (de)	1977-05-18	Alpha-pyron-derivate, ihre herstellung und ihre verwendung als selektivherbicide