DE2805251A1 - Herbizide zubereitung, verfahren zu ihrer herstellung und ihre verwendung - Google Patents

Herbizide zubereitung, verfahren zu ihrer herstellung und ihre verwendung

Info

Publication number: DE2805251A1
Authority: DE; Germany
Prior art keywords: weight; preparation; aqueous solution; emulsifier; solvent
Prior art date: 1977-02-09
Legal status (The legal status 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 Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Withdrawn

Application number

DE19782805251

Other languages

German (de)

English (en)

Inventor

Barry Arnold Hendriksen

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Lilly Industries Ltd

Original Assignee

Lilly Industries Ltd

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.)

1977-02-09

Filing date

1978-02-08

Publication date

1978-08-10

1978-02-08 Application filed by Lilly Industries Ltd filed Critical Lilly Industries Ltd

1978-08-10 Publication of DE2805251A1 publication Critical patent/DE2805251A1/de

Status Withdrawn legal-status Critical Current

Links

238000002360 preparation method Methods 0.000 title claims description 100
230000002363 herbicidal effect Effects 0.000 title claims description 52
238000000034 method Methods 0.000 title claims description 13
238000004519 manufacturing process Methods 0.000 title claims description 5
239000007864 aqueous solution Substances 0.000 claims description 56
239000003995 emulsifying agent Substances 0.000 claims description 51
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical group [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 40
239000002904 solvent Substances 0.000 claims description 39
239000000839 emulsion Substances 0.000 claims description 30
239000004009 herbicide Substances 0.000 claims description 29
239000000203 mixture Substances 0.000 claims description 26
239000011780 sodium chloride Substances 0.000 claims description 20
239000008096 xylene Substances 0.000 claims description 20
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 19
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 claims description 18
229910017053 inorganic salt Inorganic materials 0.000 claims description 17
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 16
239000000243 solution Substances 0.000 claims description 15
239000012074 organic phase Substances 0.000 claims description 14
QFUSCYRJMXLNRB-UHFFFAOYSA-N 2,6-dinitroaniline Chemical class NC1=C([N+]([O-])=O)C=CC=C1[N+]([O-])=O QFUSCYRJMXLNRB-UHFFFAOYSA-N 0.000 claims description 13
239000008346 aqueous phase Substances 0.000 claims description 11
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 10
239000002736 nonionic surfactant Substances 0.000 claims description 10
WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 claims description 8
-1 R 2 is C 2 ^ - alkyl Chemical group 0.000 claims description 8
239000012141 concentrate Substances 0.000 claims description 8
238000003756 stirring Methods 0.000 claims description 8
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 7
150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 7
239000004202 carbamide Substances 0.000 claims description 7
238000002844 melting Methods 0.000 claims description 7
230000008018 melting Effects 0.000 claims description 7
NEKOXWSIMFDGMA-UHFFFAOYSA-N Isopropalin Chemical group CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(C)C)C=C1[N+]([O-])=O NEKOXWSIMFDGMA-UHFFFAOYSA-N 0.000 claims description 6
125000002603 chloroethyl group Chemical group [H]C([*])([H])C([H])([H])Cl 0.000 claims description 6
229910052739 hydrogen Inorganic materials 0.000 claims description 6
239000001257 hydrogen Substances 0.000 claims description 6
238000009472 formulation Methods 0.000 claims description 5
UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 claims description 4
241000196324 Embryophyta Species 0.000 claims description 4
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
239000001110 calcium chloride Substances 0.000 claims description 4
229910001628 calcium chloride Inorganic materials 0.000 claims description 4
239000012071 phase Substances 0.000 claims description 4
239000001103 potassium chloride Substances 0.000 claims description 4
235000011164 potassium chloride Nutrition 0.000 claims description 4
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 3
239000004094 surface-active agent Substances 0.000 claims description 3
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
238000010790 dilution Methods 0.000 claims description 2
239000012895 dilution Substances 0.000 claims description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
239000003795 chemical substances by application Substances 0.000 description 8
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 6
239000003960 organic solvent Substances 0.000 description 6
150000003839 salts Chemical class 0.000 description 6
238000003860 storage Methods 0.000 description 6
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 4
BUADUHVXMFJVLH-UHFFFAOYSA-N 7-chloro-3-imidazol-1-yl-2H-1,2,4-benzotriazin-1-ium 1-oxide Chemical compound N1[N+](=O)C2=CC(Cl)=CC=C2N=C1N1C=CN=C1 BUADUHVXMFJVLH-UHFFFAOYSA-N 0.000 description 3
239000005471 Benfluralin Substances 0.000 description 3
239000003945 anionic surfactant Substances 0.000 description 3
SMDHCQAYESWHAE-UHFFFAOYSA-N benfluralin Chemical compound CCCCN(CC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O SMDHCQAYESWHAE-UHFFFAOYSA-N 0.000 description 3
230000000361 pesticidal effect Effects 0.000 description 3
239000000126 substance Substances 0.000 description 3
JKXYOQDLERSFPT-UHFFFAOYSA-N 2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-octadecoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol Chemical compound CCCCCCCCCCCCCCCCCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO JKXYOQDLERSFPT-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
125000000217 alkyl group Chemical group 0.000 description 2
235000019270 ammonium chloride Nutrition 0.000 description 2
125000000129 anionic group Chemical group 0.000 description 2
MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
239000003093 cationic surfactant Substances 0.000 description 2
238000004581 coalescence Methods 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
238000004821 distillation Methods 0.000 description 2
235000019441 ethanol Nutrition 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
150000002431 hydrogen Chemical class 0.000 description 2
239000007788 liquid Substances 0.000 description 2
239000000463 material Substances 0.000 description 2
229910000402 monopotassium phosphate Inorganic materials 0.000 description 2
235000019796 monopotassium phosphate Nutrition 0.000 description 2
PJNZPQUBCPKICU-UHFFFAOYSA-N phosphoric acid;potassium Chemical compound [K].OP(O)(O)=O PJNZPQUBCPKICU-UHFFFAOYSA-N 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
239000007921 spray Substances 0.000 description 2
150000005199 trimethylbenzenes Chemical class 0.000 description 2
238000010792 warming Methods 0.000 description 2
DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 1
XFRVVPUIAFSTFO-UHFFFAOYSA-N 1-Tridecanol Chemical class CCCCCCCCCCCCCO XFRVVPUIAFSTFO-UHFFFAOYSA-N 0.000 description 1
IBSQPLPBRSHTTG-UHFFFAOYSA-N 1-chloro-2-methylbenzene Chemical compound CC1=CC=CC=C1Cl IBSQPLPBRSHTTG-UHFFFAOYSA-N 0.000 description 1
PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 1
SPNQRCTZKIBOAX-UHFFFAOYSA-N Butralin Chemical compound CCC(C)NC1=C([N+]([O-])=O)C=C(C(C)(C)C)C=C1[N+]([O-])=O SPNQRCTZKIBOAX-UHFFFAOYSA-N 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
241000723346 Cinnamomum camphora Species 0.000 description 1
PTFJIKYUEPWBMS-UHFFFAOYSA-N Ethalfluralin Chemical compound CC(=C)CN(CC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O PTFJIKYUEPWBMS-UHFFFAOYSA-N 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
MNFMIVVPXOGUMX-UHFFFAOYSA-N Fluchloralin Chemical compound CCCN(CCCl)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O MNFMIVVPXOGUMX-UHFFFAOYSA-N 0.000 description 1
UMKANAFDOQQUKE-UHFFFAOYSA-N Nitralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(S(C)(=O)=O)C=C1[N+]([O-])=O UMKANAFDOQQUKE-UHFFFAOYSA-N 0.000 description 1
IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
239000005587 Oryzalin Substances 0.000 description 1
ITVQAKZNYJEWKS-UHFFFAOYSA-N Profluralin Chemical compound [O-][N+](=O)C=1C=C(C(F)(F)F)C=C([N+]([O-])=O)C=1N(CCC)CC1CC1 ITVQAKZNYJEWKS-UHFFFAOYSA-N 0.000 description 1
VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
150000001346 alkyl aryl ethers Chemical class 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
235000010210 aluminium Nutrition 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
239000001099 ammonium carbonate Substances 0.000 description 1
235000012501 ammonium carbonate Nutrition 0.000 description 1
XGGLLRJQCZROSE-UHFFFAOYSA-K ammonium iron(iii) sulfate Chemical compound [NH4+].[Fe+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O XGGLLRJQCZROSE-UHFFFAOYSA-K 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 1
229960000846 camphor Drugs 0.000 description 1
229930008380 camphor Natural products 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
229910000365 copper sulfate Inorganic materials 0.000 description 1
ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
238000002425 crystallisation Methods 0.000 description 1
230000008025 crystallization Effects 0.000 description 1
125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
230000006866 deterioration Effects 0.000 description 1
ZPWVASYFFYYZEW-UHFFFAOYSA-L dipotassium hydrogen phosphate Chemical compound [K+].[K+].OP([O-])([O-])=O ZPWVASYFFYYZEW-UHFFFAOYSA-L 0.000 description 1
229910000396 dipotassium phosphate Inorganic materials 0.000 description 1
235000019797 dipotassium phosphate Nutrition 0.000 description 1
230000000694 effects Effects 0.000 description 1
230000005484 gravity Effects 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
229910000360 iron(III) sulfate Inorganic materials 0.000 description 1
229910001629 magnesium chloride Inorganic materials 0.000 description 1
229910052943 magnesium sulfate Inorganic materials 0.000 description 1
235000019341 magnesium sulphate Nutrition 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
229920000847 nonoxynol Polymers 0.000 description 1
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-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
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
239000000575 pesticide Substances 0.000 description 1
229920005547 polycyclic aromatic hydrocarbon Polymers 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
239000002243 precursor Substances 0.000 description 1
239000001632 sodium acetate Substances 0.000 description 1
235000017281 sodium acetate Nutrition 0.000 description 1
235000011127 sodium aluminium sulphate Nutrition 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
238000005507 spraying Methods 0.000 description 1
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
150000003738 xylenes Chemical class 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
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds containing nitrogen-to-oxygen bonds
- A01N33/18—Nitro compounds
- 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
- A01N25/02—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 liquids as carriers, diluents or solvents
- A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
- 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
- A01N41/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom
- A01N41/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom containing a sulfur-to-oxygen double bond
- A01N41/04—Sulfonic acids; Derivatives thereof
- A01N41/06—Sulfonic acid amides
- 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
- A01N41/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom
- A01N41/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom containing a sulfur-to-oxygen double bond
- A01N41/10—Sulfones; Sulfoxides

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)
Chemical & Material Sciences (AREA)
Dispersion Chemistry (AREA)
Toxicology (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

DE19782805251 1977-02-09 1978-02-08 Herbizide zubereitung, verfahren zu ihrer herstellung und ihre verwendung Withdrawn DE2805251A1 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB5319/77A GB1594991A (en)	1977-02-09	1977-02-09	Pesticidal formulation

Publications (1)

Publication Number	Publication Date
DE2805251A1 true DE2805251A1 (de)	1978-08-10

Family

ID=9793862

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DE19782805251 Withdrawn DE2805251A1 (de)	1977-02-09	1978-02-08	Herbizide zubereitung, verfahren zu ihrer herstellung und ihre verwendung

Country Status (30)

Country	Link
JP (1)	JPS53101529A (cs)
AT (1)	AT360266B (cs)
AU (1)	AU520655B2 (cs)
BE (1)	BE863790A (cs)
BG (1)	BG30911A3 (cs)
BR (1)	BR7800768A (cs)
CA (1)	CA1111671A (cs)
CH (1)	CH629074A5 (cs)
CS (1)	CS195654B2 (cs)
DD (1)	DD133890A5 (cs)
DE (1)	DE2805251A1 (cs)
DK (1)	DK58278A (cs)
EG (1)	EG13275A (cs)
ES (1)	ES466798A1 (cs)
FR (1)	FR2379981A1 (cs)
GB (1)	GB1594991A (cs)
GR (1)	GR66186B (cs)
HU (1)	HU184155B (cs)
IE (1)	IE46401B1 (cs)
IL (1)	IL53989A (cs)
MX (1)	MX5720E (cs)
NL (1)	NL7801391A (cs)
NZ (1)	NZ186408A (cs)
PH (1)	PH14580A (cs)
PL (1)	PL109495B1 (cs)
PT (1)	PT67624B (cs)
RO (1)	RO72568A (cs)
SE (1)	SE7801423L (cs)
TR (1)	TR19841A (cs)
ZA (1)	ZA78767B (cs)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0196463A1 (de) *	1985-03-12	1986-10-08	Bayer Ag	Makroemulsionen
EP0197293A1 (de) *	1985-03-12	1986-10-15	Bayer Ag	Makroemulsionen

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
HU191184B (en) *	1982-07-09	1987-01-28	Chinoin Gyogyszer Es Vegyeszeti Termekek Gyara Rt,Hu	Stabilized herbicide suspension
BR8403829A (pt) *	1984-08-01	1984-12-18	Defensa Ind De Defensivos Agri	Aperfeicoamentos em ou referentes a composicao herbicida,defensivo agricola e formas de aplicacao
US4810279A (en) *	1987-01-27	1989-03-07	American Cyanamid Company	Herbicidal oil in water combination compositions of pendimethalin
WO1989011220A1 (en) *	1988-05-25	1989-11-30	Daratech Pty Ltd	Controlled release agrochemical composition
FR2673509A1 (fr) *	1991-03-06	1992-09-11	Rhone Poulenc Chimie	Emulsions phytosanitaires.
WO2010034808A1 (de) *	2008-09-26	2010-04-01	Basf Se	Flüssige, in wasser emulgierbare wirkstoffkonzentrate

1977
- 1977-02-09 GB GB5319/77A patent/GB1594991A/en not_active Expired
1978
- 1978-02-06 PT PT67624A patent/PT67624B/pt unknown
- 1978-02-07 NL NL7801391A patent/NL7801391A/xx not_active Application Discontinuation
- 1978-02-07 FR FR7803350A patent/FR2379981A1/fr active Granted
- 1978-02-07 AT AT84278A patent/AT360266B/de not_active IP Right Cessation
- 1978-02-07 AU AU33059/78A patent/AU520655B2/en not_active Expired
- 1978-02-07 SE SE7801423A patent/SE7801423L/xx unknown
- 1978-02-07 GR GR55373A patent/GR66186B/el unknown
- 1978-02-07 HU HU78LI321A patent/HU184155B/hu unknown
- 1978-02-07 IL IL53989A patent/IL53989A/xx unknown
- 1978-02-07 PH PH20758A patent/PH14580A/en unknown
- 1978-02-08 ZA ZA00780767A patent/ZA78767B/xx unknown
- 1978-02-08 BG BG038618A patent/BG30911A3/xx unknown
- 1978-02-08 ES ES466798A patent/ES466798A1/es not_active Expired
- 1978-02-08 BE BE6046350A patent/BE863790A/xx not_active IP Right Cessation
- 1978-02-08 CA CA296,643A patent/CA1111671A/en not_active Expired
- 1978-02-08 DE DE19782805251 patent/DE2805251A1/de not_active Withdrawn
- 1978-02-08 CS CS78821A patent/CS195654B2/cs unknown
- 1978-02-08 RO RO7893144A patent/RO72568A/ro unknown
- 1978-02-08 TR TR19841A patent/TR19841A/xx unknown
- 1978-02-08 JP JP1335378A patent/JPS53101529A/ja active Pending
- 1978-02-08 MX MX786831U patent/MX5720E/es unknown
- 1978-02-08 DD DD78203618A patent/DD133890A5/xx unknown
- 1978-02-08 IE IE271/78A patent/IE46401B1/en unknown
- 1978-02-08 DK DK58278A patent/DK58278A/da not_active Application Discontinuation
- 1978-02-08 CH CH139278A patent/CH629074A5/fr not_active IP Right Cessation
- 1978-02-08 NZ NZ186408A patent/NZ186408A/xx unknown
- 1978-02-08 EG EG80/78A patent/EG13275A/xx active
- 1978-02-09 PL PL1978204533A patent/PL109495B1/pl unknown
- 1978-02-09 BR BR7800768A patent/BR7800768A/pt unknown

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* Cited by examiner, † Cited by third party
Title
NICHTS-ERMITTELT *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0196463A1 (de) *	1985-03-12	1986-10-08	Bayer Ag	Makroemulsionen
EP0197293A1 (de) *	1985-03-12	1986-10-15	Bayer Ag	Makroemulsionen
US4814167A (en) *	1985-03-12	1989-03-21	Bayer Aktiengesellschaft	Pyrettroid macroemulsions containing polyvinyl alcohol
US4824663A (en) *	1985-03-12	1989-04-25	Bayer Aktiengesellschaft	Biocidal macroemulsions containing polyvinyl alcohol

Also Published As

Publication number	Publication date
MX5720E (es)	1983-12-26
JPS53101529A (en)	1978-09-05
BE863790A (fr)	1978-08-08
ZA78767B (en)	1979-09-26
ATA84278A (de)	1980-05-15
SE7801423L (sv)	1978-08-10
BG30911A3 (en)	1981-09-15
CA1111671A (en)	1981-11-03
AU3305978A (en)	1979-08-16
IL53989A0 (en)	1978-04-30
CS195654B2 (en)	1980-02-29
PH14580A (en)	1981-09-24
DD133890A5 (de)	1979-01-31
PL109495B1 (en)	1980-06-30
ES466798A1 (es)	1979-01-16
HU184155B (en)	1984-07-30
GR66186B (cs)	1981-01-21
PT67624B (en)	1980-08-18
AT360266B (de)	1980-12-29
NL7801391A (nl)	1978-08-11
AU520655B2 (en)	1982-02-18
IL53989A (en)	1980-09-16
DK58278A (da)	1978-08-10
PL204533A1 (pl)	1978-11-06
EG13275A (en)	1980-12-31
NZ186408A (en)	1980-11-14
FR2379981A1 (fr)	1978-09-08
CH629074A5 (en)	1982-04-15
PT67624A (en)	1978-03-01
GB1594991A (en)	1981-08-05
IE46401B1 (en)	1983-06-01
FR2379981B1 (cs)	1981-07-31
BR7800768A (pt)	1979-01-02
RO72568A (ro)	1981-07-30
TR19841A (tr)	1980-01-28
IE780271L (en)	1978-08-09

Legal Events

Date	Code	Title	Description
1985-04-18	8110	Request for examination paragraph 44
1985-11-14	8128	New person/name/address of the agent	Representative=s name: TUERK, D., DIPL.-CHEM. DR.RER.NAT. GILLE, C., DIPL
1987-02-19	8139	Disposal/non-payment of the annual fee

Publication	Publication Date	Title
DE2840273C2 (cs)	1992-06-11
EP0149051B1 (de)	1988-10-26	Wasserlösliche pestizide Formulierung
DE19752552A1 (de)	1999-06-02	Tensidsysteme für flüssige wässrige Zubereitungen
US4174960A (en)	1979-11-20	Pesticidal formulation
DE2808628C2 (cs)	1989-01-19
DE2805251A1 (de)	1978-08-10	Herbizide zubereitung, verfahren zu ihrer herstellung und ihre verwendung
DE3009944C2 (de)	1994-01-20	Insektizide Öl-in-Wasser-Emulsion
DE3700881A1 (de)	1987-07-23	Zur schaedlingsbekaempfung geeignete oel-in-wasser-emulsion, verfahren zu ihrer herstellung und verwendung derselben
DE3872356T2 (de)	1993-02-11	Pflanzenschutzzubereitung.
DE4108871A1 (de)	1992-09-24	Waessrige formulierung von prochloraz, ihre herstellung und ihre verwendung
DE3486285T2 (de)	1994-08-04	Stabilisierte, flüssige, herbizide Zusammensetzung und Verfahren zu deren Herstellung.
DE69307502T2 (de)	1997-07-24	Flüssige pestizide formulierungen
EP0044955B1 (de)	1983-04-13	Flüssige Herbizidmischung
EP0017001B1 (de)	1982-04-28	Herbizide in Form einer wässrigen Suspension, die Mischungen aus einem Pyridazon und einem Thiolcarbamat, einem Chloracetanilid oder einem Dinitroanilin enthalten, sowie ein Verfahren zu ihrer Herstellung und ihre Verwendung zur Bekämpfung unerwünschten Pflanzenwuchses
DE1542797A1 (de)	1970-06-04	Stabiles und erneut emulgierbares Praeparat fuer die Landwirtschaft
EP0074329A2 (de)	1983-03-16	Wässrige Pestizidkonzentrate
EP0017879B1 (de)	1982-06-02	Flüssige Formulierungen enthaltend 3-(3,4-Dichlorphenyl)-1-methyl-1-methoxy-harnstoff und ihre Verwendung zur Unkrautbekämpfung
EP0080226A1 (de)	1983-06-01	Fungizides Mittel
DE2902199A1 (de)	1979-08-02	Herbizide mittel
EP0085922B1 (de)	1986-03-05	Herbizide Mittel
DE2526455A1 (de)	1976-01-22	Herbizid
DE2035158C3 (de)	1980-01-10	Pestizide Zubereitung
DE2353432A1 (de)	1974-05-30	Insektizide stoffgemische
DE945664C (de)	1956-07-12	Verfahren zur Herstellung von Chlorat enthaltenden Unkrautvertilgungsmitteln mit verringerter Feuergefaehrlichkeit
DE1812965B1 (de)	1970-07-09	Fluessiges Stickstoffduengemittel in Form einer kaeltebestaendigen Loesung