IE46401B1 - Pesticidal formulation - Google Patents

Pesticidal formulation

Info

Publication number: IE46401B1
Authority: IE; Ireland
Prior art keywords: weight; formulation; aqueous solution; emulsifying agent; formulation according
Prior art date: 1977-02-09

Application number

IE271/78A

Other languages

English (en)

Other versions

IE780271L (en

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

1983-06-01

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

1978-08-09 Publication of IE780271L publication Critical patent/IE780271L/xx

1983-06-01 Publication of IE46401B1 publication Critical patent/IE46401B1/en

Links

239000000203 mixture Substances 0.000 title claims abstract description 129
238000009472 formulation Methods 0.000 title claims description 106
230000000361 pesticidal effect Effects 0.000 title description 4
239000007864 aqueous solution Substances 0.000 claims abstract description 64
230000002363 herbicidal effect Effects 0.000 claims abstract description 56
239000003995 emulsifying agent Substances 0.000 claims abstract description 53
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims abstract description 44
239000002904 solvent Substances 0.000 claims abstract description 42
239000004009 herbicide Substances 0.000 claims abstract description 31
239000011780 sodium chloride Substances 0.000 claims abstract description 22
229910017053 inorganic salt Inorganic materials 0.000 claims abstract description 20
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 abstract description 19
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 abstract description 17
150000003839 salts Chemical class 0.000 claims abstract description 9
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims abstract description 8
239000004202 carbamide Substances 0.000 claims abstract description 8
239000000839 emulsion Substances 0.000 claims description 29
235000002639 sodium chloride Nutrition 0.000 claims description 27
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
238000000034 method Methods 0.000 claims description 18
239000012074 organic phase Substances 0.000 claims description 14
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 12
239000002736 nonionic surfactant Substances 0.000 claims description 12
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
238000013019 agitation Methods 0.000 claims description 10
239000008346 aqueous phase Substances 0.000 claims description 10
239000000243 solution Substances 0.000 claims description 10
WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 claims description 8
150000004945 aromatic hydrocarbons Chemical class 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
239000012141 concentrate Substances 0.000 claims description 6
239000001257 hydrogen Substances 0.000 claims description 6
229910052739 hydrogen Inorganic materials 0.000 claims description 6
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
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
239000001110 calcium chloride Substances 0.000 claims description 4
229910001628 calcium chloride Inorganic materials 0.000 claims description 4
238000004519 manufacturing process Methods 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
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
239000006185 dispersion Substances 0.000 claims description 3
125000002924 primary amino group Chemical group [H]N([H])* 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
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
230000002401 inhibitory effect Effects 0.000 claims description 2
239000004094 surface-active agent Substances 0.000 claims description 2
238000001914 filtration Methods 0.000 claims 1
-1 trifluralin Chemical class 0.000 abstract description 14
238000003860 storage Methods 0.000 abstract description 7
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 6
239000003795 chemical substances by application Substances 0.000 description 6
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
125000000217 alkyl group Chemical group 0.000 description 5
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 4
239000003945 anionic surfactant Substances 0.000 description 4
125000002603 chloroethyl group Chemical group [H]C([*])([H])C([H])([H])Cl 0.000 description 4
239000003093 cationic surfactant Substances 0.000 description 3
238000005507 spraying Methods 0.000 description 3
239000000126 substance Substances 0.000 description 3
238000010792 warming Methods 0.000 description 3
239000005471 Benfluralin Substances 0.000 description 2
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 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
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
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 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
238000004821 distillation Methods 0.000 description 2
230000005484 gravity Effects 0.000 description 2
229930195733 hydrocarbon Natural products 0.000 description 2
150000002430 hydrocarbons 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
229920000847 nonoxynol Polymers 0.000 description 2
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 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
238000002360 preparation method Methods 0.000 description 2
150000005199 trimethylbenzenes Chemical class 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
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
DUIOKRXOKLLURE-UHFFFAOYSA-N 2-octylphenol Chemical class CCCCCCCCC1=CC=CC=C1O DUIOKRXOKLLURE-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
239000004215 Carbon black (E152) Substances 0.000 description 1
241000723346 Cinnamomum camphora Species 0.000 description 1
OFDYMSKSGFSLLM-UHFFFAOYSA-N Dinitramine Chemical compound CCN(CC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C(N)=C1[N+]([O-])=O OFDYMSKSGFSLLM-UHFFFAOYSA-N 0.000 description 1
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 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
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
229940037003 alum Drugs 0.000 description 1
239000001164 aluminium sulphate Substances 0.000 description 1
235000011128 aluminium sulphate 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
229960000541 cetyl alcohol Drugs 0.000 description 1
239000007859 condensation product Substances 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
125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 description 1
230000006866 deterioration Effects 0.000 description 1
BUACSMWVFUNQET-UHFFFAOYSA-H dialuminum;trisulfate;hydrate Chemical compound O.[Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O BUACSMWVFUNQET-UHFFFAOYSA-H 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
239000004495 emulsifiable concentrate Substances 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
125000005394 methallyl group Chemical group 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
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
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
235000015424 sodium Nutrition 0.000 description 1
239000001632 sodium acetate Substances 0.000 description 1
235000017281 sodium acetate 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
229910021653 sulphate ion Inorganic materials 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)
General Health & Medical Sciences (AREA)
Health & Medical Sciences (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Plant Pathology (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Dispersion Chemistry (AREA)
Chemical & Material Sciences (AREA)
Toxicology (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

IE271/78A 1977-02-09 1978-02-08 Pesticidal formulation IE46401B1 (en)

Applications Claiming Priority (1)

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

Publications (2)

Publication Number	Publication Date
IE780271L IE780271L (en)	1978-08-09
IE46401B1 true IE46401B1 (en)	1983-06-01

Family

ID=9793862

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IE271/78A IE46401B1 (en)	1977-02-09	1978-02-08	Pesticidal formulation

Country Status (30)

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

Families Citing this family (8)

* 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
ZW3486A1 (en) *	1985-03-12	1986-10-01	Bayer Ag	Macroemulsions
ZW3586A1 (en) *	1985-03-12	1986-06-11	Bayer Ag	Macroemulsions
US4810279A (en) *	1987-01-27	1989-03-07	American Cyanamid Company	Herbicidal oil in water combination compositions of pendimethalin
CA1336863C (en) *	1988-05-25	1995-09-05	Gottfried Lichti	Controlled release composition
FR2673509A1 (fr) *	1991-03-06	1992-09-11	Rhone Poulenc Chimie	Emulsions phytosanitaires.
JP5606442B2 (ja) *	2008-09-26	2014-10-15	ビーエーエスエフソシエタス・ヨーロピア	水に乳化可能な液体活性成分濃縮液

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

Also Published As

Publication number	Publication date
PT67624B (en)	1980-08-18
IL53989A (en)	1980-09-16
PL204533A1 (pl)	1978-11-06
NL7801391A (nl)	1978-08-11
RO72568A (ro)	1981-07-30
BG30911A3 (en)	1981-09-15
CA1111671A (en)	1981-11-03
ZA78767B (en)	1979-09-26
ATA84278A (de)	1980-05-15
GR66186B (de)	1981-01-21
TR19841A (tr)	1980-01-28
FR2379981A1 (fr)	1978-09-08
GB1594991A (en)	1981-08-05
NZ186408A (en)	1980-11-14
AU520655B2 (en)	1982-02-18
SE7801423L (sv)	1978-08-10
FR2379981B1 (de)	1981-07-31
MX5720E (es)	1983-12-26
AT360266B (de)	1980-12-29
AU3305978A (en)	1979-08-16
DD133890A5 (de)	1979-01-31
JPS53101529A (en)	1978-09-05
BR7800768A (pt)	1979-01-02
IE780271L (en)	1978-08-09
PL109495B1 (en)	1980-06-30
DK58278A (da)	1978-08-10
ES466798A1 (es)	1979-01-16
CS195654B2 (en)	1980-02-29
IL53989A0 (en)	1978-04-30
DE2805251A1 (de)	1978-08-10
PH14580A (en)	1981-09-24
CH629074A5 (en)	1982-04-15
EG13275A (en)	1980-12-31
PT67624A (en)	1978-03-01
BE863790A (fr)	1978-08-08
HU184155B (en)	1984-07-30

Publication	Publication Date	Title
US4174960A (en)	1979-11-20	Pesticidal formulation
CA1163191A (en)	1984-03-06	Flowable pesticides
US5547918A (en)	1996-08-20	Biocidal and agrochemical suspensions comprising a structured surfactant with an oil component
CZ125590A3 (cs)	1999-08-11	Biocidní a agrochemické suspenze
DE60111195T2 (de)	2006-03-23	Wässerige formulierungen und verfahren zu ihrer herstellung
CA2863813C (en)	2020-06-30	Agrochemical emulsifiable concentrate formulations using solvent system having benzyl acetate
JPH04504417A (ja)	1992-08-06	即時性および遅延性の放出性を兼ね備えたシングルパッケージの農薬処方物
IE63343B1 (en)	1995-04-19	Aqueous suspension concentrate compositions of pendimethalin
CA1106202A (en)	1981-08-04	Herbicidal concentrate containing ketone and amide solvent
IE46401B1 (en)	1983-06-01	Pesticidal formulation
JPH0676281B2 (ja)	1994-09-28	安定化された水中油型懸濁状農薬組成物
CA1201602A (en)	1986-03-11	Herbicidal concentrated emulsions
JP6765436B2 (ja)	2020-10-07	乳化性濃縮物
CA1138216A (en)	1982-12-28	Herbicides based on pyridazones
JP3083194B2 (ja)	2000-09-04	除草剤プロパニルの安定な溶液型組成物及び乳剤型組成物
EA015417B1 (ru)	2011-08-30	Пестицидные композиции с риском кристаллизации и способ их получения
EP0124253B1 (de)	1990-08-16	Landwirtschaftliche Zusammensetzungen, Verfahren zur Herstellung von landwirtschaftlichen Zusammensetzungen und Verfahren zur Verwendung von landwirtschaftlichen Zusammensetzungen
US6251415B1 (en)	2001-06-26	Solvent system for pesticide products
US5405825A (en)	1995-04-11	Emulsifiable suspension concentrate compositions of imidazolinyl benzoic acids, esters and salts thereof, and dinitroaniline herbicides
JPH0733605A (ja)	1995-02-03	改良された農薬乳剤組成物
AU675319B2 (en)	1997-01-30	Fluid concentrated formulations containing phosphated polyalkoxylated tristyrylphenol derivatives which are useful in particular in agrochemistry
TW587918B (en)	2004-05-21	Liquid formulation
CA2250262C (en)	2004-01-20	Mixtures and methods for suppressing precipitation of chloroacetamides
JPH01197403A (ja)	1989-08-09	農薬用マイクロエマルジョン
CA1195923A (en)	1985-10-29	Cold stabilization of aqueous herbicidal compositions with urea