UA74775C2 - High concentrated aqueous composition of the monoethanolammonium salt of n-phosphonomethylglycine and a method to control undesired plants - Google Patents

High concentrated aqueous composition of the monoethanolammonium salt of n-phosphonomethylglycine and a method to control undesired plants Download PDF

Info

Publication number: UA74775C2
Authority: UA; Ukraine
Prior art keywords: composition; glyphosate; salt; phosphonomethylglycine; group
Prior art date: 1998-11-23

Application number

UA2001064346A

Other languages

English (en)

Ukrainian (uk)

Original Assignee

Monsanto Ci

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.)

1998-11-23

Filing date

1999-11-19

Publication date

2006-02-15

1999-11-19 Application filed by Monsanto Ci filed Critical Monsanto Ci

2006-02-15 Publication of UA74775C2 publication Critical patent/UA74775C2/uk

Links

239000000203 mixture Substances 0.000 title claims abstract description 227
150000003839 salts Chemical class 0.000 title claims abstract description 163
238000000034 method Methods 0.000 title claims description 20
XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 title abstract description 196
239000004094 surface-active agent Substances 0.000 claims abstract description 138
230000002363 herbicidal effect Effects 0.000 claims abstract description 68
239000007864 aqueous solution Substances 0.000 claims abstract description 47
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 31
239000000243 solution Substances 0.000 claims abstract description 28
239000002253 acid Substances 0.000 claims abstract description 25
239000006185 dispersion Substances 0.000 claims abstract description 6
239000012141 concentrate Substances 0.000 claims description 48
-1 polyoxyethylene chains Polymers 0.000 claims description 45
239000004009 herbicide Substances 0.000 claims description 42
239000013543 active substance Substances 0.000 claims description 34
229910052739 hydrogen Inorganic materials 0.000 claims description 22
239000001257 hydrogen Substances 0.000 claims description 22
125000000217 alkyl group Chemical group 0.000 claims description 21
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 18
125000001183 hydrocarbyl group Chemical group 0.000 claims description 18
125000000129 anionic group Chemical group 0.000 claims description 17
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 15
125000006353 oxyethylene group Chemical group 0.000 claims description 15
125000001931 aliphatic group Chemical group 0.000 claims description 13
229920006395 saturated elastomer Polymers 0.000 claims description 13
238000003860 storage Methods 0.000 claims description 12
125000003277 amino group Chemical group 0.000 claims description 11
150000007970 thio esters Chemical class 0.000 claims description 9
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150000002148 esters Chemical class 0.000 claims description 6
125000002312 hydrocarbylidene group Chemical group 0.000 claims description 6
150000002431 hydrogen Chemical class 0.000 claims description 6
JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical class CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 claims description 6
150000003462 sulfoxides Chemical class 0.000 claims description 6
125000002091 cationic group Chemical group 0.000 claims description 5
125000004430 oxygen atom Chemical group O* 0.000 claims description 4
125000004432 carbon atom Chemical group C* 0.000 claims description 3
238000002425 crystallisation Methods 0.000 claims description 3
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125000002723 alicyclic group Chemical group 0.000 claims description 2
125000003118 aryl group Chemical group 0.000 claims description 2
229910052799 carbon Inorganic materials 0.000 claims description 2
150000003568 thioethers Chemical group 0.000 claims description 2
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125000004429 atom Chemical group 0.000 claims 1
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230000000052 comparative effect Effects 0.000 description 10
239000013078 crystal Substances 0.000 description 10
239000004480 active ingredient Substances 0.000 description 9
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230000007423 decrease Effects 0.000 description 7
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150000007513 acids Chemical class 0.000 description 6
150000001875 compounds Chemical class 0.000 description 6
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RORFESPGBUIBMY-UHFFFAOYSA-N Talcamine Natural products COC(=O)c1ccc(Oc2c(OC)ccc(CC3N(C)CCc4cc(OC)c(OC)c(Oc5cc6C(=O)N(C)CCc6cc5OC)c34)c2OC)cc1 RORFESPGBUIBMY-UHFFFAOYSA-N 0.000 description 2
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NQQVFXUMIDALNH-UHFFFAOYSA-N picloram Chemical compound NC1=C(Cl)C(Cl)=NC(C(O)=O)=C1Cl NQQVFXUMIDALNH-UHFFFAOYSA-N 0.000 description 2
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125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
125000001453 quaternary ammonium group Chemical group 0.000 description 2
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PMHURSZHKKJGBM-UHFFFAOYSA-N isoxaben Chemical compound O1N=C(C(C)(CC)CC)C=C1NC(=O)C1=C(OC)C=CC=C1OC PMHURSZHKKJGBM-UHFFFAOYSA-N 0.000 description 1
CONWAEURSVPLRM-UHFFFAOYSA-N lactofen Chemical compound C1=C([N+]([O-])=O)C(C(=O)OC(C)C(=O)OCC)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 CONWAEURSVPLRM-UHFFFAOYSA-N 0.000 description 1
ZTMKADLOSYKWCA-UHFFFAOYSA-N lenacil Chemical compound O=C1NC=2CCCC=2C(=O)N1C1CCCCC1 ZTMKADLOSYKWCA-UHFFFAOYSA-N 0.000 description 1
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238000004519 manufacturing process Methods 0.000 description 1
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VHCNQEUWZYOAEV-UHFFFAOYSA-N metamitron Chemical compound O=C1N(N)C(C)=NN=C1C1=CC=CC=C1 VHCNQEUWZYOAEV-UHFFFAOYSA-N 0.000 description 1
STEPQTYSZVCJPV-UHFFFAOYSA-N metazachlor Chemical compound CC1=CC=CC(C)=C1N(C(=O)CCl)CN1N=CC=C1 STEPQTYSZVCJPV-UHFFFAOYSA-N 0.000 description 1
MFSWTRQUCLNFOM-UHFFFAOYSA-N methyl 2-(4-{[3-chloro-5-(trifluoromethyl)pyridin-2-yl]oxy}phenoxy)propanoate Chemical group C1=CC(OC(C)C(=O)OC)=CC=C1OC1=NC=C(C(F)(F)F)C=C1Cl MFSWTRQUCLNFOM-UHFFFAOYSA-N 0.000 description 1
RBNIGDFIUWJJEV-UHFFFAOYSA-N methyl 2-(n-benzoyl-3-chloro-4-fluoroanilino)propanoate Chemical group C=1C=C(F)C(Cl)=CC=1N(C(C)C(=O)OC)C(=O)C1=CC=CC=C1 RBNIGDFIUWJJEV-UHFFFAOYSA-N 0.000 description 1
NDNKHWUXXOFHTD-UHFFFAOYSA-N metizoline Chemical compound CC=1SC2=CC=CC=C2C=1CC1=NCCN1 NDNKHWUXXOFHTD-UHFFFAOYSA-N 0.000 description 1
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DSRNRYQBBJQVCW-UHFFFAOYSA-N metoxuron Chemical compound COC1=CC=C(NC(=O)N(C)C)C=C1Cl DSRNRYQBBJQVCW-UHFFFAOYSA-N 0.000 description 1
FOXFZRUHNHCZPX-UHFFFAOYSA-N metribuzin Chemical compound CSC1=NN=C(C(C)(C)C)C(=O)N1N FOXFZRUHNHCZPX-UHFFFAOYSA-N 0.000 description 1
239000004530 micro-emulsion Substances 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
DEDOPGXGGQYYMW-UHFFFAOYSA-N molinate Chemical compound CCSC(=O)N1CCCCCC1 DEDOPGXGGQYYMW-UHFFFAOYSA-N 0.000 description 1
238000012544 monitoring process Methods 0.000 description 1
231100000286 mucous membrane, eye irritation or corrosion testing Toxicity 0.000 description 1
LNOPIUAQISRISI-UHFFFAOYSA-N n'-hydroxy-2-propan-2-ylsulfonylethanimidamide Chemical compound CC(C)S(=O)(=O)CC(N)=NO LNOPIUAQISRISI-UHFFFAOYSA-N 0.000 description 1
YWFWDNVOPHGWMX-UHFFFAOYSA-N n,n-dimethyldodecan-1-amine Chemical compound CCCCCCCCCCCCN(C)C YWFWDNVOPHGWMX-UHFFFAOYSA-N 0.000 description 1
RTCOGUMHFFWOJV-UHFFFAOYSA-N nicosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CN=2)C(=O)N(C)C)=N1 RTCOGUMHFFWOJV-UHFFFAOYSA-N 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
NVGOPFQZYCNLDU-UHFFFAOYSA-N norflurazon Chemical compound O=C1C(Cl)=C(NC)C=NN1C1=CC=CC(C(F)(F)F)=C1 NVGOPFQZYCNLDU-UHFFFAOYSA-N 0.000 description 1
239000003921 oil Substances 0.000 description 1
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
LLLFASISUZUJEQ-UHFFFAOYSA-N orbencarb Chemical compound CCN(CC)C(=O)SCC1=CC=CC=C1Cl LLLFASISUZUJEQ-UHFFFAOYSA-N 0.000 description 1
UNAHYJYOSSSJHH-UHFFFAOYSA-N oryzalin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(S(N)(=O)=O)C=C1[N+]([O-])=O UNAHYJYOSSSJHH-UHFFFAOYSA-N 0.000 description 1
IOXAXYHXMLCCJJ-UHFFFAOYSA-N oxetan-3-yl 2-[(4,6-dimethylpyrimidin-2-yl)carbamoylsulfamoyl]benzoate Chemical compound CC1=CC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(=O)OC2COC2)=N1 IOXAXYHXMLCCJJ-UHFFFAOYSA-N 0.000 description 1
AHKZTVQIVOEVFO-UHFFFAOYSA-N oxide(2-) Chemical compound [O-2] AHKZTVQIVOEVFO-UHFFFAOYSA-N 0.000 description 1
238000004806 packaging method and process Methods 0.000 description 1
FIKAKWIAUPDISJ-UHFFFAOYSA-L paraquat dichloride Chemical compound [Cl-].[Cl-].C1=C[N+](C)=CC=C1C1=CC=[N+](C)C=C1 FIKAKWIAUPDISJ-UHFFFAOYSA-L 0.000 description 1
CHIFOSRWCNZCFN-UHFFFAOYSA-N pendimethalin Chemical compound CCC(CC)NC1=C([N+]([O-])=O)C=C(C)C(C)=C1[N+]([O-])=O CHIFOSRWCNZCFN-UHFFFAOYSA-N 0.000 description 1
JZPKLLLUDLHCEL-UHFFFAOYSA-N pentoxazone Chemical compound O=C1C(=C(C)C)OC(=O)N1C1=CC(OC2CCCC2)=C(Cl)C=C1F JZPKLLLUDLHCEL-UHFFFAOYSA-N 0.000 description 1
238000005191 phase separation Methods 0.000 description 1
IDOWTHOLJBTAFI-UHFFFAOYSA-N phenmedipham Chemical compound COC(=O)NC1=CC=CC(OC(=O)NC=2C=C(C)C=CC=2)=C1 IDOWTHOLJBTAFI-UHFFFAOYSA-N 0.000 description 1
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
230000000885 phytotoxic effect Effects 0.000 description 1
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229920001223 polyethylene glycol Polymers 0.000 description 1
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BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
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MFOUDYKPLGXPGO-UHFFFAOYSA-N propachlor Chemical compound ClCC(=O)N(C(C)C)C1=CC=CC=C1 MFOUDYKPLGXPGO-UHFFFAOYSA-N 0.000 description 1
LFULEKSKNZEWOE-UHFFFAOYSA-N propanil Chemical compound CCC(=O)NC1=CC=C(Cl)C(Cl)=C1 LFULEKSKNZEWOE-UHFFFAOYSA-N 0.000 description 1
FROBCXTULYFHEJ-OAHLLOKOSA-N propaquizafop Chemical compound C1=CC(O[C@H](C)C(=O)OCCON=C(C)C)=CC=C1OC1=CN=C(C=C(Cl)C=C2)C2=N1 FROBCXTULYFHEJ-OAHLLOKOSA-N 0.000 description 1
WJNRPILHGGKWCK-UHFFFAOYSA-N propazine Chemical compound CC(C)NC1=NC(Cl)=NC(NC(C)C)=N1 WJNRPILHGGKWCK-UHFFFAOYSA-N 0.000 description 1
VXPLXMJHHKHSOA-UHFFFAOYSA-N propham Chemical compound CC(C)OC(=O)NC1=CC=CC=C1 VXPLXMJHHKHSOA-UHFFFAOYSA-N 0.000 description 1
NQLVQOSNDJXLKG-UHFFFAOYSA-N prosulfocarb Chemical compound CCCN(CCC)C(=O)SCC1=CC=CC=C1 NQLVQOSNDJXLKG-UHFFFAOYSA-N 0.000 description 1
239000008213 purified water Substances 0.000 description 1
150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
238000011160 research Methods 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical compound C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 description 1
229930195734 saturated hydrocarbon Natural products 0.000 description 1
239000002689 soil Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
230000001629 suppression Effects 0.000 description 1
239000000725 suspension Substances 0.000 description 1
229940095064 tartrate Drugs 0.000 description 1
RJKCKKDSSSRYCB-UHFFFAOYSA-N tebutam Chemical compound CC(C)(C)C(=O)N(C(C)C)CC1=CC=CC=C1 RJKCKKDSSSRYCB-UHFFFAOYSA-N 0.000 description 1
BCQMBFHBDZVHKU-UHFFFAOYSA-N terbumeton Chemical compound CCNC1=NC(NC(C)(C)C)=NC(OC)=N1 BCQMBFHBDZVHKU-UHFFFAOYSA-N 0.000 description 1
IROINLKCQGIITA-UHFFFAOYSA-N terbutryn Chemical compound CCNC1=NC(NC(C)(C)C)=NC(SC)=N1 IROINLKCQGIITA-UHFFFAOYSA-N 0.000 description 1
FZXISNSWEXTPMF-UHFFFAOYSA-N terbutylazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C)=N1 FZXISNSWEXTPMF-UHFFFAOYSA-N 0.000 description 1
238000012360 testing method Methods 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
SRVJKTDHMYAMHA-WUXMJOGZSA-N thioacetazone Chemical group CC(=O)NC1=CC=C(\C=N\NC(N)=S)C=C1 SRVJKTDHMYAMHA-WUXMJOGZSA-N 0.000 description 1
229960003231 thioacetazone Drugs 0.000 description 1
XOPFESVZMSQIKC-UHFFFAOYSA-N triasulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)OCCCl)=N1 XOPFESVZMSQIKC-UHFFFAOYSA-N 0.000 description 1
BQZXUHDXIARLEO-UHFFFAOYSA-N tribenuron Chemical compound COC1=NC(C)=NC(N(C)C(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 BQZXUHDXIARLEO-UHFFFAOYSA-N 0.000 description 1
ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 1
AKTQJCBOGPBERP-UHFFFAOYSA-N triflusulfuron Chemical compound FC(F)(F)COC1=NC(N(C)C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2C)C(O)=O)=N1 AKTQJCBOGPBERP-UHFFFAOYSA-N 0.000 description 1
NRZWQKGABZFFKE-UHFFFAOYSA-N trimethylsulfonium Chemical class C[S+](C)C NRZWQKGABZFFKE-UHFFFAOYSA-N 0.000 description 1
229930195735 unsaturated hydrocarbon Natural products 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals
- 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
- A01N25/30—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 characterised by the surfactants

Landscapes

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

UA2001064346A 1998-11-23 1999-11-19 High concentrated aqueous composition of the monoethanolammonium salt of n-phosphonomethylglycine and a method to control undesired plants UA74775C2 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US10953298P	1998-11-23	1998-11-23
PCT/US1999/027602 WO2000030452A1 (fr)	1998-11-23	1999-11-19	Compositions aqueuses a base de glyphosate en forte concentration

Publications (1)

Publication Number	Publication Date
UA74775C2 true UA74775C2 (en)	2006-02-15

Family

ID=22328176

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
UA2001064346A UA74775C2 (en)	1998-11-23	1999-11-19	High concentrated aqueous composition of the monoethanolammonium salt of n-phosphonomethylglycine and a method to control undesired plants

Country Status (26)

Country	Link
US (2)	US6277788B1 (fr)
EP (1)	EP1133233B1 (fr)
JP (1)	JP4652573B2 (fr)
KR (1)	KR20010104684A (fr)
CN (1)	CN1277473C (fr)
AR (1)	AR018211A1 (fr)
AT (1)	ATE275342T1 (fr)
AU (1)	AU775094B2 (fr)
BR (1)	BR9915566B1 (fr)
CA (1)	CA2351386C (fr)
CO (1)	CO5210930A1 (fr)
CZ (1)	CZ304306B6 (fr)
DE (1)	DE69920035T2 (fr)
EA (1)	EA200100578A1 (fr)
ES (1)	ES2228161T3 (fr)
GT (1)	GT199900199A (fr)
HU (1)	HU229572B1 (fr)
IL (1)	IL143272A0 (fr)
MY (1)	MY122060A (fr)
NO (1)	NO20012502L (fr)
NZ (1)	NZ511850A (fr)
PL (1)	PL348907A1 (fr)
SK (1)	SK7072001A3 (fr)
TR (1)	TR200101524T2 (fr)
UA (1)	UA74775C2 (fr)
WO (1)	WO2000030452A1 (fr)

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CA2727924C (fr) *	2008-06-18	2016-05-24	Stepan Company	Concentres de glyphosate a concentration tres elevee
AU2009296340B2 (en)	2008-09-29	2015-02-12	Monsanto Technology Llc	Glyphosate formulations containing amidoalkylamine surfactants
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MX2011011203A (es) *	2009-04-24	2011-11-18	Huntsman Petrochemical Llc	Sal de acido isetionico que contiene nitrogeno en formulaciones agricolas, estables, que pueden registrarse.
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BR112013007819B1 (pt) *	2010-10-01	2018-05-08	Nufarm Australia Ltd	método de preparação de uma mistura aquosa de sais de glifosato para melhorar a manipulação da mistura
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JPH072608B2 (ja)	1986-12-04	1995-01-18	モンサントコンパニ−	水性濃厚除草剤配合物
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GB9002495D0 (en)	1990-02-05	1990-04-04	Monsanto Europe Sa	Glyphosate compositions
CA2047968C (fr)	1990-08-09	2000-05-23	Paul D. Berger	Compositions a proprietes tensio-actives, methode de preparation et compositions de pesticides qui en contiennent
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GB9412722D0 (en) *	1994-06-24	1994-08-17	Zeneca Ltd	Herbicidal composition
NZ305278A (en) *	1995-04-10	1999-02-25	Monsanto Co	Herbicidal compositions comprising glyphosate and an etheramine surfactant
US5750468A (en) *	1995-04-10	1998-05-12	Monsanto Company	Glyphosate formulations containing etheramine surfactants
AR004705A1 (es)	1995-11-07	1999-03-10	Sabba Da Silva Lima Michele	Composicion agroquimica liquida, metodo para convertirla en un liquido estable y composicion adyuvante para la preparacion de la misma.
MY129957A (en)	1996-03-06	2007-05-31	Kao Corp	Aqueous liquid agricultural composition
CZ299552B6 (cs)	1996-10-25	2008-09-03	Monsanto Technology Llc	Kompozice a zpusob pro ošetrení rostlin exogenními chemikáliemi
WO1998033385A1 (fr)	1997-01-31	1998-08-06	Monsanto Company	Procede et compositions permettant d'accroitre la fiabilite de substances chimiques exogenes que l'on applique sur les plantes
WO1998035561A1 (fr) *	1997-02-14	1998-08-20	Monsanto Company	Composition aqueuse d'herbicides et de tensio-actifs d'elimination des broussailles s'appliquant a la base et aux parties dormantes de la tige
GB9810861D0 (en)	1998-05-20	1998-07-22	Zeneca Ltd	Solid composition
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1999
- 1999-11-19 WO PCT/US1999/027602 patent/WO2000030452A1/fr not_active Ceased
- 1999-11-19 CZ CZ2001-1787A patent/CZ304306B6/cs not_active IP Right Cessation
- 1999-11-19 DE DE69920035T patent/DE69920035T2/de not_active Expired - Lifetime
- 1999-11-19 UA UA2001064346A patent/UA74775C2/uk unknown
- 1999-11-19 PL PL99348907A patent/PL348907A1/xx not_active Application Discontinuation
- 1999-11-19 CN CNB998151955A patent/CN1277473C/zh not_active Expired - Lifetime
- 1999-11-19 TR TR2001/01524T patent/TR200101524T2/xx unknown
- 1999-11-19 JP JP2000583350A patent/JP4652573B2/ja not_active Expired - Lifetime
- 1999-11-19 AT AT99965856T patent/ATE275342T1/de not_active IP Right Cessation
- 1999-11-19 NZ NZ511850A patent/NZ511850A/en not_active IP Right Cessation
- 1999-11-19 SK SK707-2001A patent/SK7072001A3/sk unknown
- 1999-11-19 ES ES99965856T patent/ES2228161T3/es not_active Expired - Lifetime
- 1999-11-19 IL IL14327299A patent/IL143272A0/xx unknown
- 1999-11-19 EP EP99965856A patent/EP1133233B1/fr not_active Expired - Lifetime
- 1999-11-19 HU HU0104355A patent/HU229572B1/hu unknown
- 1999-11-19 EA EA200100578A patent/EA200100578A1/ru unknown
- 1999-11-19 CA CA002351386A patent/CA2351386C/fr not_active Expired - Lifetime
- 1999-11-19 BR BRPI9915566-4A patent/BR9915566B1/pt not_active IP Right Cessation
- 1999-11-19 KR KR1020017006479A patent/KR20010104684A/ko not_active Withdrawn
- 1999-11-19 AU AU21541/00A patent/AU775094B2/en not_active Expired
- 1999-11-22 MY MYPI99005093A patent/MY122060A/en unknown
- 1999-11-22 AR ARP990105948A patent/AR018211A1/es not_active Application Discontinuation
- 1999-11-22 US US09/444,768 patent/US6277788B1/en not_active Expired - Lifetime
- 1999-11-23 CO CO99073751A patent/CO5210930A1/es not_active Application Discontinuation
- 1999-11-25 GT GT199900199A patent/GT199900199A/es unknown
2001
- 2001-04-03 US US09/825,480 patent/US6455473B2/en not_active Expired - Lifetime
- 2001-05-22 NO NO20012502A patent/NO20012502L/no not_active Application Discontinuation

Also Published As

Publication number	Publication date
CN1332605A (zh)	2002-01-23
ATE275342T1 (de)	2004-09-15
JP2002530305A (ja)	2002-09-17
HU229572B1 (en)	2014-02-28
EP1133233B1 (fr)	2004-09-08
IL143272A0 (en)	2002-04-21
PL348907A1 (en)	2002-06-17
SK7072001A3 (en)	2002-04-04
WO2000030452A1 (fr)	2000-06-02
US6277788B1 (en)	2001-08-21
KR20010104684A (ko)	2001-11-26
MY122060A (en)	2006-03-31
DE69920035T2 (de)	2005-09-15
NZ511850A (en)	2003-11-28
ES2228161T3 (es)	2005-04-01
NO20012502L (no)	2001-07-11
BR9915566B1 (pt)	2011-11-01
HUP0104355A2 (hu)	2002-04-29
BR9915566A (pt)	2002-01-15
CO5210930A1 (es)	2002-10-30
AR018211A1 (es)	2001-10-31
NO20012502D0 (no)	2001-05-22
EA200100578A1 (ru)	2001-12-24
AU775094B2 (en)	2004-07-15
CZ304306B6 (cs)	2014-02-26
CN1277473C (zh)	2006-10-04
CA2351386A1 (fr)	2000-06-02
CZ20011787A3 (cs)	2002-01-16
GT199900199A (es)	2001-05-18
DE69920035D1 (de)	2004-10-14
JP4652573B2 (ja)	2011-03-16
US20010019997A1 (en)	2001-09-06
AU2154100A (en)	2000-06-13
US6455473B2 (en)	2002-09-24
TR200101524T2 (tr)	2001-12-21
HUP0104355A3 (en)	2003-04-28
CA2351386C (fr)	2008-06-03
EP1133233A1 (fr)	2001-09-19

Publication	Publication Date	Title
UA74775C2 (en)	2006-02-15	High concentrated aqueous composition of the monoethanolammonium salt of n-phosphonomethylglycine and a method to control undesired plants
US11925179B2 (en)	2024-03-12	Glyphosate formulations containing amidoalkylamine surfactants
EP1389040B1 (fr)	2010-05-19	Concentres pesticides contenant des agents de surface d'etheramine
AU2002318146A1 (en)	2003-05-15	Pesticide concentrates containing etheramine surfactants
AU2002259275A1 (en)	2003-05-08	Stable liquid pesticide compositions
EP1395116A2 (fr)	2004-03-10	Compositions pesticides liquides stables
US20030096708A1 (en)	2003-05-22	Pesticide concentrates containing etheramine surfactants
CA3022682C (fr)	2025-11-18	Formulations de glyphosate contenant des tensioactifs d'amidoalkylamine
US20010019996A1 (en)	2001-09-06	Process and compositions promoting biological effectiveness of exogenous chemical substances in plants
ZA200104632B (en)	2002-09-06	Process and compositions promoting biological effectiveness of exogenous chemical substances in plants.
EP4620306A1 (fr)	2025-09-24	Composition herbicide
BR102025004352A2 (pt)	2025-09-30	Composição herbicida, método de formação da composição e composição herbicida aquosa
CN120660710A (zh)	2025-09-19	除草组合物
MXPA01005190A (en)	2002-06-05	Highly concentrated aqueous glyphosate compositions
UA76152C2 (en)	2006-07-17	Aqueous herbicidal composition containing etheramine surface-active agent and methods for weeds ravage or depression