LU85259A1 - Ester de l'hydroxyde de tricyclohexyletain acaricide - Google Patents

Ester de l'hydroxyde de tricyclohexyletain acaricide Download PDF

Info

Publication number: LU85259A1
Authority: LU; Luxembourg
Prior art keywords: active material; compositions; tricyclohexyltin; composition; water
Prior art date: 1983-03-22

Application number

LU85259A

Other languages

English (en)

French (fr)

Inventor

Gerard Graber

Bernard Marcoux

Original Assignee

Rhone Poulenc Agrochimie

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.)

1983-03-22

Filing date

1984-03-21

Publication date

1985-10-14

1984-03-21 Application filed by Rhone Poulenc Agrochimie filed Critical Rhone Poulenc Agrochimie

1985-10-14 Publication of LU85259A1 publication Critical patent/LU85259A1/fr

Links

230000000895 acaricidal effect Effects 0.000 title description 5
239000000642 acaricide Substances 0.000 title description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 title description 2
239000000203 mixture Substances 0.000 claims description 41
239000011149 active material Substances 0.000 claims description 17
150000001875 compounds Chemical class 0.000 claims description 15
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 14
239000004495 emulsifiable concentrate Substances 0.000 claims description 12
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 9
241000238876 Acari Species 0.000 claims description 7
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 5
RNVJQUPAEIQUTC-UHFFFAOYSA-N tricyclohexyltin Chemical compound C1CCCCC1[Sn](C1CCCCC1)C1CCCCC1 RNVJQUPAEIQUTC-UHFFFAOYSA-N 0.000 claims description 5
239000005711 Benzoic acid Substances 0.000 claims description 4
235000010233 benzoic acid Nutrition 0.000 claims description 4
238000000034 method Methods 0.000 claims description 4
239000003960 organic solvent Substances 0.000 claims description 4
241000238631 Hexapoda Species 0.000 claims description 3
238000002360 preparation method Methods 0.000 claims description 3
230000000749 insecticidal effect Effects 0.000 claims 2
230000008030 elimination Effects 0.000 claims 1
238000003379 elimination reaction Methods 0.000 claims 1
241000196324 Embryophyta Species 0.000 description 13
239000004480 active ingredient Substances 0.000 description 13
239000000843 powder Substances 0.000 description 11
239000000047 product Substances 0.000 description 9
239000000243 solution Substances 0.000 description 9
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
239000007788 liquid Substances 0.000 description 7
239000007787 solid Substances 0.000 description 7
239000004094 surface-active agent Substances 0.000 description 7
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 6
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
239000000654 additive Substances 0.000 description 5
239000003795 chemical substances by application Substances 0.000 description 5
239000000839 emulsion Substances 0.000 description 5
238000009472 formulation Methods 0.000 description 5
239000000377 silicon dioxide Substances 0.000 description 5
239000007921 spray Substances 0.000 description 5
239000003381 stabilizer Substances 0.000 description 5
239000004563 wettable powder Substances 0.000 description 5
239000005995 Aluminium silicate Substances 0.000 description 4
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
235000012211 aluminium silicate Nutrition 0.000 description 4
235000019993 champagne Nutrition 0.000 description 4
239000012141 concentrate Substances 0.000 description 4
239000008187 granular material Substances 0.000 description 4
239000002904 solvent Substances 0.000 description 4
239000000725 suspension Substances 0.000 description 4
239000008096 xylene Substances 0.000 description 4
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 3
WCMMILVIRZAPLE-UHFFFAOYSA-M cyhexatin Chemical compound C1CCCCC1[Sn](C1CCCCC1)(O)C1CCCCC1 WCMMILVIRZAPLE-UHFFFAOYSA-M 0.000 description 3
238000010410 dusting Methods 0.000 description 3
239000003995 emulsifying agent Substances 0.000 description 3
239000002917 insecticide Substances 0.000 description 3
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 3
230000000149 penetrating effect Effects 0.000 description 3
150000003839 salts Chemical class 0.000 description 3
238000003756 stirring Methods 0.000 description 3
YLTNMVLVPUHWLQ-UHFFFAOYSA-M tricyclohexylstannyl benzoate Chemical compound C=1C=CC=CC=1C(=O)O[Sn](C1CCCCC1)(C1CCCCC1)C1CCCCC1 YLTNMVLVPUHWLQ-UHFFFAOYSA-M 0.000 description 3
235000013311 vegetables Nutrition 0.000 description 3
239000000080 wetting agent Substances 0.000 description 3
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
244000046052 Phaseolus vulgaris Species 0.000 description 2
WFDIJRYMOXRFFG-UHFFFAOYSA-N acetic acid anhydride Natural products CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 2
239000013543 active substance Substances 0.000 description 2
239000000853 adhesive Substances 0.000 description 2
230000001070 adhesive effect Effects 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
-1 amino acids fatty acids Chemical class 0.000 description 2
238000009362 arboriculture Methods 0.000 description 2
239000010692 aromatic oil Substances 0.000 description 2
239000003849 aromatic solvent Substances 0.000 description 2
SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 2
229920005551 calcium lignosulfonate Polymers 0.000 description 2
239000000969 carrier Substances 0.000 description 2
239000004359 castor oil Substances 0.000 description 2
235000019438 castor oil Nutrition 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
238000005260 corrosion Methods 0.000 description 2
230000007797 corrosion Effects 0.000 description 2
235000014113 dietary fatty acids Nutrition 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
238000001035 drying Methods 0.000 description 2
239000000975 dye Substances 0.000 description 2
230000001804 emulsifying effect Effects 0.000 description 2
239000000194 fatty acid Substances 0.000 description 2
229930195729 fatty acid Natural products 0.000 description 2
150000002191 fatty alcohols Chemical class 0.000 description 2
239000003337 fertilizer Substances 0.000 description 2
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 2
235000019447 hydroxyethyl cellulose Nutrition 0.000 description 2
238000005470 impregnation Methods 0.000 description 2
239000003112 inhibitor Substances 0.000 description 2
229910052500 inorganic mineral Inorganic materials 0.000 description 2
238000002844 melting Methods 0.000 description 2
230000008018 melting Effects 0.000 description 2
239000011707 mineral Substances 0.000 description 2
239000010690 paraffinic oil Substances 0.000 description 2
150000002989 phenols Chemical class 0.000 description 2
230000008635 plant growth Effects 0.000 description 2
239000002244 precipitate Substances 0.000 description 2
238000005507 spraying Methods 0.000 description 2
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
239000000454 talc Substances 0.000 description 2
229910052623 talc Inorganic materials 0.000 description 2
XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 2
239000013008 thixotropic agent Substances 0.000 description 2
WTARULDDTDQWMU-IUCAKERBSA-N (-)-Nopinene Natural products C1[C@@H]2C(C)(C)[C@H]1CCC2=C WTARULDDTDQWMU-IUCAKERBSA-N 0.000 description 1
FOGYNLXERPKEGN-UHFFFAOYSA-N 3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfopropyl)phenoxy]propane-1-sulfonic acid Chemical class COC1=CC=CC(CC(CS(O)(=O)=O)OC=2C(=CC(CCCS(O)(=O)=O)=CC=2)OC)=C1O FOGYNLXERPKEGN-UHFFFAOYSA-N 0.000 description 1
KWXICGTUELOLSQ-UHFFFAOYSA-M 4-dodecylbenzenesulfonate Chemical compound CCCCCCCCCCCCC1=CC=C(S([O-])(=O)=O)C=C1 KWXICGTUELOLSQ-UHFFFAOYSA-M 0.000 description 1
KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Natural products CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 1
229920001817 Agar Polymers 0.000 description 1
235000011293 Brassica napus Nutrition 0.000 description 1
240000008100 Brassica rapa Species 0.000 description 1
235000000540 Brassica rapa subsp rapa Nutrition 0.000 description 1
239000005946 Cypermethrin Substances 0.000 description 1
239000001692 EU approved anti-caking agent Substances 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N EtOH Substances CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
208000031888 Mycoses Diseases 0.000 description 1
229910000503 Na-aluminosilicate Inorganic materials 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
231100000674 Phytotoxicity Toxicity 0.000 description 1
241000500439 Plutella Species 0.000 description 1
WTARULDDTDQWMU-UHFFFAOYSA-N Pseudopinene Natural products C1C2C(C)(C)C1CCC2=C WTARULDDTDQWMU-UHFFFAOYSA-N 0.000 description 1
229920002125 Sokalan® Polymers 0.000 description 1
ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
241001454293 Tetranychus urticae Species 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
239000012868 active agrochemical ingredient Substances 0.000 description 1
239000000443 aerosol Substances 0.000 description 1
239000008272 agar Substances 0.000 description 1
238000005054 agglomeration Methods 0.000 description 1
230000002776 aggregation Effects 0.000 description 1
238000013019 agitation Methods 0.000 description 1
239000003905 agrochemical Substances 0.000 description 1
239000003513 alkali Substances 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
XCPQUQHBVVXMRQ-UHFFFAOYSA-N alpha-Fenchene Natural products C1CC2C(=C)CC1C2(C)C XCPQUQHBVVXMRQ-UHFFFAOYSA-N 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
230000002528 anti-freeze Effects 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
239000007900 aqueous suspension Substances 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
239000002585 base Substances 0.000 description 1
150000001558 benzoic acid derivatives Chemical class 0.000 description 1
229930006722 beta-pinene Natural products 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
239000011575 calcium Substances 0.000 description 1
150000001669 calcium Chemical class 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
238000001816 cooling Methods 0.000 description 1
229960005424 cypermethrin Drugs 0.000 description 1
238000007865 diluting Methods 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
238000001125 extrusion Methods 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000012530 fluid Substances 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
LCWMKIHBLJLORW-UHFFFAOYSA-N gamma-carene Natural products C1CC(=C)CC2C(C)(C)C21 LCWMKIHBLJLORW-UHFFFAOYSA-N 0.000 description 1
239000007789 gas Substances 0.000 description 1
238000005469 granulation Methods 0.000 description 1
230000003179 granulation Effects 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
238000005286 illumination Methods 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
238000002386 leaching Methods 0.000 description 1
231100000518 lethal Toxicity 0.000 description 1
230000001665 lethal effect Effects 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
150000002680 magnesium Chemical class 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
239000008268 mayonnaise Substances 0.000 description 1
235000010746 mayonnaise Nutrition 0.000 description 1
239000003607 modifier Substances 0.000 description 1
239000003921 oil Substances 0.000 description 1
235000015927 pasta Nutrition 0.000 description 1
230000035515 penetration Effects 0.000 description 1
230000000361 pesticidal effect Effects 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
239000004584 polyacrylic acid Substances 0.000 description 1
229920000151 polyglycol Polymers 0.000 description 1
239000010695 polyglycol Substances 0.000 description 1
239000011148 porous material Substances 0.000 description 1
OVARTBFNCCXQKS-UHFFFAOYSA-N propan-2-one;hydrate Chemical compound O.CC(C)=O OVARTBFNCCXQKS-UHFFFAOYSA-N 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
150000004671 saturated fatty acids Chemical class 0.000 description 1
235000003441 saturated fatty acids Nutrition 0.000 description 1
238000004062 sedimentation Methods 0.000 description 1
239000003352 sequestering agent Substances 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000000429 sodium aluminium silicate Substances 0.000 description 1
235000012217 sodium aluminium silicate Nutrition 0.000 description 1
229920005552 sodium lignosulfonate Polymers 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
239000002689 soil Substances 0.000 description 1
239000008247 solid mixture Substances 0.000 description 1
241000894007 species Species 0.000 description 1
238000003860 storage Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
229920002994 synthetic fiber Polymers 0.000 description 1
229960003080 taurine Drugs 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
239000001993 wax Substances 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- 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
- A01N55/00—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur
- A01N55/02—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur containing metal atoms
- A01N55/04—Tin
- 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
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/22—Tin compounds
- C07F7/2224—Compounds having one or more tin-oxygen linkages

Landscapes

Life Sciences & Earth Sciences (AREA)
Organic Chemistry (AREA)
General Health & Medical Sciences (AREA)
Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Pest Control & Pesticides (AREA)
Zoology (AREA)
Wood Science & Technology (AREA)
Environmental Sciences (AREA)
Plant Pathology (AREA)
Agronomy & Crop Science (AREA)
Toxicology (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

LU85259A 1983-03-22 1984-03-21 Ester de l'hydroxyde de tricyclohexyletain acaricide LU85259A1 (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
FR8304884A FR2543142B1 (fr)	1983-03-22	1983-03-22	Ester de l'hydroxyde de tricyclohexyletain acaricide
FR8304884		1983-03-22

Publications (1)

Publication Number	Publication Date
LU85259A1 true LU85259A1 (fr)	1985-10-14

Family

ID=9287208

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
LU85259A LU85259A1 (fr)	1983-03-22	1984-03-21	Ester de l'hydroxyde de tricyclohexyletain acaricide

Country Status (24)

Country	Link
US (1)	US4602945A (xx)
JP (1)	JPS59176296A (xx)
KR (1)	KR840007808A (xx)
AU (1)	AU2591984A (xx)
BE (1)	BE899225A (xx)
BR (1)	BR8401318A (xx)
CA (1)	CA1231716A (xx)
CH (1)	CH660365A5 (xx)
DE (1)	DE3410064A1 (xx)
DK (1)	DK136284D0 (xx)
ES (1)	ES530812A0 (xx)
FR (1)	FR2543142B1 (xx)
GB (1)	GB2136811B (xx)
GR (1)	GR81825B (xx)
HU (1)	HUT33961A (xx)
IL (1)	IL71165A0 (xx)
IT (1)	IT1177597B (xx)
LU (1)	LU85259A1 (xx)
NL (1)	NL8400893A (xx)
NZ (1)	NZ207559A (xx)
OA (1)	OA07683A (xx)
PH (1)	PH20025A (xx)
PT (1)	PT78291B (xx)
ZA (1)	ZA842064B (xx)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4732456A (en) *	1984-08-28	1988-03-22	Taliq Corporation	Scattering display for contrast enhancement including target
US4832458A (en) *	1984-08-28	1989-05-23	Talig Corporation	Display for contrast enhancement
US8110608B2 (en)	2008-06-05	2012-02-07	Ecolab Usa Inc.	Solid form sodium lauryl sulfate (SLS) pesticide composition
US8968757B2 (en)	2010-10-12	2015-03-03	Ecolab Usa Inc.	Highly wettable, water dispersible, granules including two pesticides
CN103396437B (zh) *	2013-07-22	2015-09-09	衡阳师范学院	双(三环己基锡)二元羧酸酯及制备方法与应用

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BE573087A (xx) *	1957-11-18	1900-01-01
NL269911A (xx) *	1960-10-04	1900-01-01
US3129236A (en) *	1960-12-31	1964-04-14	Monsanto Chemicals	Bis(trihydrocarbyl tin oxy) aromatic compounds
NL299805A (xx) *	1962-10-29	1900-01-01
US3264177A (en) *	1964-02-17	1966-08-02	Dow Chemical Co	Methods for the control of arachnids
US3542824A (en) *	1968-07-31	1970-11-24	Dow Chemical Co	Perfluorocarboxylic acid ester of tricyclohexyltin hydroxide
US3598849A (en) *	1968-09-20	1971-08-10	Dow Chemical Co	Tricyclohexyltin esters
US3703588A (en) *	1969-11-21	1972-11-21	Norio Saito Nara Ken And Uniti	Method for imparting antistatic properties to polymeric materials
US3861949A (en) *	1971-04-27	1975-01-21	Kureha Chemical Ind Co Ltd	Article having applied to the surface thereof, an anti-fouling composition comprising a polymer and an organo-tin compound
US3790611A (en) *	1972-10-05	1974-02-05	M & T Chemicals Inc	Tris(cyclohexylalkyl)tin or hexakis(cyclohexylalkyl)tin compounds
DE2419208A1 (de) *	1974-04-18	1975-11-06	Schering Ag	Mittel mit selektiver, herbizider und algizider wirkung
FR2335514A1 (fr) *	1975-12-17	1977-07-15	M & T Chemicals Inc	Procede de preparation d'un derive de triorganoetain
US4224338A (en) *	1976-08-17	1980-09-23	The Dow Chemical Company	Simultaneous fungicidal and miticidal protection of plants employing certain tin compounds

1983
- 1983-03-22 FR FR8304884A patent/FR2543142B1/fr not_active Expired
1984
- 1984-02-29 DK DK1362/84A patent/DK136284D0/da not_active Application Discontinuation
- 1984-03-06 IL IL71165A patent/IL71165A0/xx unknown
- 1984-03-14 GR GR74100A patent/GR81825B/el unknown
- 1984-03-19 PH PH30411A patent/PH20025A/en unknown
- 1984-03-19 DE DE19843410064 patent/DE3410064A1/de not_active Withdrawn
- 1984-03-19 KR KR1019840001392A patent/KR840007808A/ko not_active Application Discontinuation
- 1984-03-20 IT IT47894/84A patent/IT1177597B/it active
- 1984-03-20 CA CA000449971A patent/CA1231716A/en not_active Expired
- 1984-03-20 AU AU25919/84A patent/AU2591984A/en not_active Abandoned
- 1984-03-20 NZ NZ207559A patent/NZ207559A/en unknown
- 1984-03-20 ZA ZA842064A patent/ZA842064B/xx unknown
- 1984-03-20 GB GB08407153A patent/GB2136811B/en not_active Expired
- 1984-03-21 CH CH1438/84A patent/CH660365A5/fr not_active IP Right Cessation
- 1984-03-21 BR BR8401318A patent/BR8401318A/pt unknown
- 1984-03-21 HU HU841132A patent/HUT33961A/hu unknown
- 1984-03-21 PT PT78291A patent/PT78291B/pt unknown
- 1984-03-21 ES ES530812A patent/ES530812A0/es active Granted
- 1984-03-21 NL NL8400893A patent/NL8400893A/nl not_active Application Discontinuation
- 1984-03-21 JP JP59054120A patent/JPS59176296A/ja active Pending
- 1984-03-21 LU LU85259A patent/LU85259A1/fr unknown
- 1984-03-22 OA OA58257A patent/OA07683A/xx unknown
- 1984-03-22 US US06/592,353 patent/US4602945A/en not_active Expired - Fee Related
- 1984-03-22 BE BE0/212613A patent/BE899225A/fr not_active IP Right Cessation

Also Published As

Publication number	Publication date
PT78291B (fr)	1986-08-08
BR8401318A (pt)	1984-10-30
NZ207559A (en)	1985-12-13
IT8447894A0 (it)	1984-03-20
GB2136811A (en)	1984-09-26
CH660365A5 (fr)	1987-04-15
AU2591984A (en)	1984-09-27
IT8447894A1 (it)	1985-09-20
FR2543142A1 (fr)	1984-09-28
IL71165A0 (en)	1984-06-29
FR2543142B1 (fr)	1986-01-03
KR840007808A (ko)	1984-12-11
JPS59176296A (ja)	1984-10-05
ES8506034A1 (es)	1985-06-16
NL8400893A (nl)	1984-10-16
GR81825B (xx)	1984-12-12
HUT33961A (en)	1985-01-28
DK136284D0 (da)	1984-02-29
OA07683A (fr)	1985-05-23
PH20025A (en)	1986-09-04
BE899225A (fr)	1984-09-24
GB8407153D0 (en)	1984-04-26
ZA842064B (en)	1984-10-31
PT78291A (fr)	1984-04-01
ES530812A0 (es)	1985-06-16
CA1231716A (en)	1988-01-19
GB2136811B (en)	1986-07-09
DE3410064A1 (de)	1984-09-27
IT1177597B (it)	1987-08-26
US4602945A (en)	1986-07-29

Publication	Publication Date	Title
FR2684519A1 (fr)	1993-06-11	Association d'un fongicide de la famille des triazoles et d'imidacloprid.
HU213177B (en)	1997-03-28	Fungicidal composition containing phenylbenzamide derivative, process for preparation of the active ingredients and for protection against fungi
EP0249566B1 (fr)	1991-12-11	Compositions bactéricides à base de dérivés de l'acide phosphoreux
EP0599749A1 (fr)	1994-06-01	Dérivés de 2-alkoxy 2-imidazoline-5 ones fongicides
LU85259A1 (fr)	1985-10-14	Ester de l'hydroxyde de tricyclohexyletain acaricide
DE60018253T2 (de)	2005-07-21	Die Verwendung von 5-Carboxanilido-2,4-bis-trifluoromethylthiazole gegen Reisbräune
FR2594437A1 (fr)	1987-08-21	Nouveaux derives du cyano-2 benzimidazole, leur preparation, les compositions les contenant et leur utilisation comme fongicide
EP0290354A2 (fr)	1988-11-09	Association herbicide
BE818849A (fr)	1975-02-14	Derives de cyclohexane
US4942178A (en)	1990-07-17	Plant protection agents for control of fungi
FR2598708A1 (fr)	1987-11-20	Compositions fongicides a base de derives nicotiniques, nouveaux derives nicotiniques et leur preparation
FR2598408A1 (fr)	1987-11-13	Derives propargyloxybenzenes : leur preparation et compositions fongicides les contenant
FR2607811A1 (fr)	1988-06-10	Derives de sulfonyl benzimidazole, leur preparation ainsi que leur utilisation a titre de fongicides
JPS5844643B2 (ja)	1983-10-04	シンキナジヨソウザイ
JPS6310124B2 (xx)	1988-03-04
EP0316246A1 (fr)	1989-05-17	Nicotinates d'oximes fongicides
EP0316245A1 (fr)	1989-05-17	Dérivés nicotiniques fongicides
JPH0643288B2 (ja)	1994-06-08	殺菌組成物
FR2617844A1 (fr)	1989-01-13	Compositions fongicides a base de derives nicotiniques. nouveaux derives nicotiniques et leur preparation
DE2548450A1 (de)	1976-05-13	Schaedlingsbekaempfungsmittel
FR2501203A1 (fr)	1982-09-10	Complexes metalliques d'acide ethylene-1,2-bis-dithiocarbamique et de 8-hydroxyquinoline, compositions fongicides et bactericides contenant ceux-ci, et procede pour preparer ces complexes
FR2608898A1 (fr)	1988-07-01	Associations fongicides a base de cyanobenzimidazole et d'un fongicide systemique
FR2648459A1 (fr)	1990-12-21	Diphenylamides fongicides
FR2640967A1 (en)	1990-06-29	(S)-1'-Methoxycarbonylethyl 2-bromo-5-(2-chloro-4-trifluoromethylphenoxy)benzoate and (S)-1'-ethoxycarbonylethyl 2-bromo-5-(2-chloro-4-trifluoromethylphenoxy)benzoate, process for their preparation and their use in herbicidal compositions
JPH0651605B2 (ja)	1994-07-06	殺菌組成物