DD284580A5 - Waessrige akarizidzusammensetzungen - Google Patents

Waessrige akarizidzusammensetzungen Download PDF

Info

Publication number: DD284580A5
Authority: DD; German Democratic Republic
Prior art keywords: fenbutatin oxide; clofentezine; composition according; weight; compositions
Prior art date: 1987-06-13

Application number

DD88316658A

Other languages

German (de)

English (en)

Inventor

Michael A Webb

Malcolm A Faers

Original Assignee

��@��@��k��

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.)

1987-06-13

Filing date

1988-06-10

Publication date

1990-11-21

1988-06-10 Application filed by ��@��@��k�� filed Critical ��@��@��k��

1990-11-21 Publication of DD284580A5 publication Critical patent/DD284580A5/de

Links

239000000203 mixture Substances 0.000 title claims abstract description 39
BOTNFCTYKJBUMU-UHFFFAOYSA-N 2-[4-(2-methylpropyl)piperazin-4-ium-1-yl]-2-oxoacetate Chemical compound CC(C)C[NH+]1CCN(C(=O)C([O-])=O)CC1 BOTNFCTYKJBUMU-UHFFFAOYSA-N 0.000 claims abstract description 28
UXADOQPNKNTIHB-UHFFFAOYSA-N clofentezine Chemical compound ClC1=CC=CC=C1C1=NN=C(C=2C(=CC=CC=2)Cl)N=N1 UXADOQPNKNTIHB-UHFFFAOYSA-N 0.000 claims abstract description 22
239000005654 Clofentezine Substances 0.000 claims abstract description 21
239000002245 particle Substances 0.000 claims abstract description 17
239000013078 crystal Substances 0.000 claims abstract description 8
230000000895 acaricidal effect Effects 0.000 claims description 7
239000000642 acaricide Substances 0.000 claims description 3
-1 2-methyl-3-phenylpropyl Chemical group 0.000 description 9
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
238000002360 preparation method Methods 0.000 description 4
239000004094 surface-active agent Substances 0.000 description 4
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
239000007900 aqueous suspension Substances 0.000 description 3
230000003247 decreasing effect Effects 0.000 description 3
NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Chemical compound C=1C=C(Cl)C=CC=1C(C(C)C)C(=O)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-UHFFFAOYSA-N 0.000 description 3
KAATUXNTWXVJKI-NSHGMRRFSA-N (1R)-cis-(alphaS)-cypermethrin Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-NSHGMRRFSA-N 0.000 description 2
241000238876 Acari Species 0.000 description 2
241000220225 Malus Species 0.000 description 2
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
241001454295 Tetranychidae Species 0.000 description 2
230000002528 anti-freeze Effects 0.000 description 2
235000021016 apples Nutrition 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
239000012141 concentrate Substances 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
235000013399 edible fruits Nutrition 0.000 description 2
230000000694 effects Effects 0.000 description 2
239000003755 preservative agent Substances 0.000 description 2
239000000375 suspending agent Substances 0.000 description 2
239000000725 suspension Substances 0.000 description 2
239000004546 suspension concentrate Substances 0.000 description 2
ZCVAOQKBXKSDMS-PVAVHDDUSA-N (+)-trans-(S)-allethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)O[C@@H]1C(C)=C(CC=C)C(=O)C1 ZCVAOQKBXKSDMS-PVAVHDDUSA-N 0.000 description 1
ZCVAOQKBXKSDMS-AQYZNVCMSA-N (+)-trans-allethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC1C(C)=C(CC=C)C(=O)C1 ZCVAOQKBXKSDMS-AQYZNVCMSA-N 0.000 description 1
CXBMCYHAMVGWJQ-CABCVRRESA-N (1,3-dioxo-4,5,6,7-tetrahydroisoindol-2-yl)methyl (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCN1C(=O)C(CCCC2)=C2C1=O CXBMCYHAMVGWJQ-CABCVRRESA-N 0.000 description 1
SBNFWQZLDJGRLK-RTWAWAEBSA-N (1R)-trans-phenothrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 SBNFWQZLDJGRLK-RTWAWAEBSA-N 0.000 description 1
YATDSXRLIUJOQN-SVRRBLITSA-N (2,3,4,5,6-pentafluorophenyl)methyl (1r,3s)-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(Cl)Cl)[C@H]1C(=O)OCC1=C(F)C(F)=C(F)C(F)=C1F YATDSXRLIUJOQN-SVRRBLITSA-N 0.000 description 1
FHNKBSDJERHDHZ-UHFFFAOYSA-N (2,4-dimethylphenyl)methyl 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)C(C=C(C)C)C1C(=O)OCC1=CC=C(C)C=C1C FHNKBSDJERHDHZ-UHFFFAOYSA-N 0.000 description 1
HECKNJZFKDZGJT-UHFFFAOYSA-K (2-methyl-2-phenylpropyl)tin(3+);trihydroxide Chemical compound [OH-].[OH-].[OH-].[Sn+3]CC(C)(C)C1=CC=CC=C1 HECKNJZFKDZGJT-UHFFFAOYSA-K 0.000 description 1
KPMWGGRSOPMANK-UHFFFAOYSA-N (6-chloro-1,3-benzodioxol-5-yl)methyl 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)C(C=C(C)C)C1C(=O)OCC(C(=C1)Cl)=CC2=C1OCO2 KPMWGGRSOPMANK-UHFFFAOYSA-N 0.000 description 1
FMTFEIJHMMQUJI-NJAFHUGGSA-N 102130-98-3 Natural products CC=CCC1=C(C)[C@H](CC1=O)OC(=O)[C@@H]1[C@@H](C=C(C)C)C1(C)C FMTFEIJHMMQUJI-NJAFHUGGSA-N 0.000 description 1
239000005877 Alpha-Cypermethrin Substances 0.000 description 1
239000005874 Bifenthrin Substances 0.000 description 1
RAPBNVDSDCTNRC-UHFFFAOYSA-N Chlorobenzilate Chemical compound C=1C=C(Cl)C=CC=1C(O)(C(=O)OCC)C1=CC=C(Cl)C=C1 RAPBNVDSDCTNRC-UHFFFAOYSA-N 0.000 description 1
239000005946 Cypermethrin Substances 0.000 description 1
239000005892 Deltamethrin Substances 0.000 description 1
MUMQYXACQUZOFP-UHFFFAOYSA-N Dialifor Chemical compound C1=CC=C2C(=O)N(C(CCl)SP(=S)(OCC)OCC)C(=O)C2=C1 MUMQYXACQUZOFP-UHFFFAOYSA-N 0.000 description 1
VBKKVDGJXVOLNE-UHFFFAOYSA-N Dioxation Chemical compound CCOP(=S)(OCC)SC1OCCOC1SP(=S)(OCC)OCC VBKKVDGJXVOLNE-UHFFFAOYSA-N 0.000 description 1
239000005895 Esfenvalerate Substances 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
239000005948 Formetanate Substances 0.000 description 1
FSYXMFXBRJFYBS-UHFFFAOYSA-N Furamethrin Chemical compound CC1(C)C(C=C(C)C)C1C(=O)OCC1=CC=C(CC#C)O1 FSYXMFXBRJFYBS-UHFFFAOYSA-N 0.000 description 1
229930182984 Jasmolin Natural products 0.000 description 1
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
QTXHFDHVLBDJIO-UHFFFAOYSA-N Prothoate Chemical compound CCOP(=S)(OCC)SCC(=O)NC(C)C QTXHFDHVLBDJIO-UHFFFAOYSA-N 0.000 description 1
VQXSOUPNOZTNAI-UHFFFAOYSA-N Pyrethrin I Natural products CC(=CC1CC1C(=O)OC2CC(=O)C(=C2C)CC=C/C=C)C VQXSOUPNOZTNAI-UHFFFAOYSA-N 0.000 description 1
239000007983 Tris buffer Substances 0.000 description 1
BZMIHNKNQJJVRO-LVZFUZTISA-N [(e)-c-(3-chloro-2,6-dimethoxyphenyl)-n-ethoxycarbonimidoyl] benzoate Chemical compound COC=1C=CC(Cl)=C(OC)C=1C(=N/OCC)\OC(=O)C1=CC=CC=C1 BZMIHNKNQJJVRO-LVZFUZTISA-N 0.000 description 1
INISTDXBRIBGOC-CGAIIQECSA-N [cyano-(3-phenoxyphenyl)methyl] (2s)-2-[2-chloro-4-(trifluoromethyl)anilino]-3-methylbutanoate Chemical compound N([C@@H](C(C)C)C(=O)OC(C#N)C=1C=C(OC=2C=CC=CC=2)C=CC=1)C1=CC=C(C(F)(F)F)C=C1Cl INISTDXBRIBGOC-CGAIIQECSA-N 0.000 description 1
CGTWCAVZZBLHQH-UHFFFAOYSA-N [cyano-(3-phenoxyphenyl)methyl] 2,2-dichloro-1-(4-ethoxyphenyl)cyclopropane-1-carboxylate Chemical compound C1=CC(OCC)=CC=C1C1(C(=O)OC(C#N)C=2C=C(OC=3C=CC=CC=3)C=CC=2)C(Cl)(Cl)C1 CGTWCAVZZBLHQH-UHFFFAOYSA-N 0.000 description 1
YXWCBRDRVXHABN-JCMHNJIXSA-N [cyano-(4-fluoro-3-phenoxyphenyl)methyl] 3-[(z)-2-chloro-2-(4-chlorophenyl)ethenyl]-2,2-dimethylcyclopropane-1-carboxylate Chemical compound C=1C=C(F)C(OC=2C=CC=CC=2)=CC=1C(C#N)OC(=O)C1C(C)(C)C1\C=C(/Cl)C1=CC=C(Cl)C=C1 YXWCBRDRVXHABN-JCMHNJIXSA-N 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
239000002671 adjuvant Substances 0.000 description 1
229940024113 allethrin Drugs 0.000 description 1
229960002587 amitraz Drugs 0.000 description 1
QXAITBQSYVNQDR-ZIOPAAQOSA-N amitraz Chemical compound C=1C=C(C)C=C(C)C=1/N=C/N(C)\C=N\C1=CC=C(C)C=C1C QXAITBQSYVNQDR-ZIOPAAQOSA-N 0.000 description 1
239000007798 antifreeze agent Substances 0.000 description 1
239000012736 aqueous medium Substances 0.000 description 1
OMFRMAHOUUJSGP-IRHGGOMRSA-N bifenthrin Chemical compound C1=CC=C(C=2C=CC=CC=2)C(C)=C1COC(=O)[C@@H]1[C@H](\C=C(/Cl)C(F)(F)F)C1(C)C OMFRMAHOUUJSGP-IRHGGOMRSA-N 0.000 description 1
229960001901 bioallethrin Drugs 0.000 description 1
229950002373 bioresmethrin Drugs 0.000 description 1
VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UXHICEINSA-N 0.000 description 1
229920001400 block copolymer Polymers 0.000 description 1
FOANIXZHAMJWOI-UHFFFAOYSA-N bromopropylate Chemical compound C=1C=C(Br)C=CC=1C(O)(C(=O)OC(C)C)C1=CC=C(Br)C=C1 FOANIXZHAMJWOI-UHFFFAOYSA-N 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
KAATUXNTWXVJKI-UHFFFAOYSA-N cypermethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-UHFFFAOYSA-N 0.000 description 1
229960005424 cypermethrin Drugs 0.000 description 1
229960002483 decamethrin Drugs 0.000 description 1
OWZREIFADZCYQD-NSHGMRRFSA-N deltamethrin Chemical compound CC1(C)[C@@H](C=C(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 OWZREIFADZCYQD-NSHGMRRFSA-N 0.000 description 1
UOAMTSKGCBMZTC-UHFFFAOYSA-N dicofol Chemical compound C=1C=C(Cl)C=CC=1C(C(Cl)(Cl)Cl)(O)C1=CC=C(Cl)C=C1 UOAMTSKGCBMZTC-UHFFFAOYSA-N 0.000 description 1
239000004205 dimethyl polysiloxane Substances 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
NYPJDWWKZLNGGM-RPWUZVMVSA-N esfenvalerate Chemical compound C=1C([C@@H](C#N)OC(=O)[C@@H](C(C)C)C=2C=CC(Cl)=CC=2)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-RPWUZVMVSA-N 0.000 description 1
RIZMRRKBZQXFOY-UHFFFAOYSA-N ethion Chemical compound CCOP(=S)(OCC)SCSP(=S)(OCC)OCC RIZMRRKBZQXFOY-UHFFFAOYSA-N 0.000 description 1
229950006668 fenfluthrin Drugs 0.000 description 1
XQUXKZZNEFRCAW-UHFFFAOYSA-N fenpropathrin Chemical compound CC1(C)C(C)(C)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 XQUXKZZNEFRCAW-UHFFFAOYSA-N 0.000 description 1
239000010419 fine particle Substances 0.000 description 1
GBIHOLCMZGAKNG-UHFFFAOYSA-N flucythrinate Chemical compound C=1C=C(OC(F)F)C=CC=1C(C(C)C)C(=O)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 GBIHOLCMZGAKNG-UHFFFAOYSA-N 0.000 description 1
RMFNNCGOSPBBAD-MDWZMJQESA-N formetanate Chemical compound CNC(=O)OC1=CC=CC(\N=C\N(C)C)=C1 RMFNNCGOSPBBAD-MDWZMJQESA-N 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
238000000034 method Methods 0.000 description 1
PZXOQEXFMJCDPG-UHFFFAOYSA-N omethoate Chemical compound CNC(=O)CSP(=O)(OC)OC PZXOQEXFMJCDPG-UHFFFAOYSA-N 0.000 description 1
229960000490 permethrin Drugs 0.000 description 1
RLLPVAHGXHCWKJ-UHFFFAOYSA-N permethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-UHFFFAOYSA-N 0.000 description 1
229960003536 phenothrin Drugs 0.000 description 1
229920001983 poloxamer Polymers 0.000 description 1
229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
230000002335 preservative effect Effects 0.000 description 1
QYMMJNLHFKGANY-UHFFFAOYSA-N profenofos Chemical compound CCCSP(=O)(OCC)OC1=CC=C(Br)C=C1Cl QYMMJNLHFKGANY-UHFFFAOYSA-N 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
ZYHMJXZULPZUED-UHFFFAOYSA-N propargite Chemical compound C1=CC(C(C)(C)C)=CC=C1OC1C(OS(=O)OCC#C)CCCC1 ZYHMJXZULPZUED-UHFFFAOYSA-N 0.000 description 1
HYJYGLGUBUDSLJ-UHFFFAOYSA-N pyrethrin Natural products CCC(=O)OC1CC(=C)C2CC3OC3(C)C2C2OC(=O)C(=C)C12 HYJYGLGUBUDSLJ-UHFFFAOYSA-N 0.000 description 1
VJFUPGQZSXIULQ-XIGJTORUSA-N pyrethrin II Chemical compound CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 VJFUPGQZSXIULQ-XIGJTORUSA-N 0.000 description 1
239000002728 pyrethroid Substances 0.000 description 1
229940108410 resmethrin Drugs 0.000 description 1
VEMKTZHHVJILDY-FIWHBWSRSA-N resmethrin Chemical compound CC1(C)[C@H](C=C(C)C)C1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-FIWHBWSRSA-N 0.000 description 1
229920005552 sodium lignosulfonate Polymers 0.000 description 1
239000002594 sorbent Substances 0.000 description 1
230000000087 stabilizing effect Effects 0.000 description 1
239000002641 tar oil Substances 0.000 description 1
MLGCXEBRWGEOQX-UHFFFAOYSA-N tetradifon Chemical compound C1=CC(Cl)=CC=C1S(=O)(=O)C1=CC(Cl)=C(Cl)C=C1Cl MLGCXEBRWGEOQX-UHFFFAOYSA-N 0.000 description 1
229960005199 tetramethrin Drugs 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
YWSCPYYRJXKUDB-KAKFPZCNSA-N tralomethrin Chemical compound CC1(C)[C@@H](C(Br)C(Br)(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 YWSCPYYRJXKUDB-KAKFPZCNSA-N 0.000 description 1
AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 description 1
229920001285 xanthan gum Polymers 0.000 description 1
239000000230 xanthan gum Substances 0.000 description 1
229940082509 xanthan gum Drugs 0.000 description 1
235000010493 xanthan gum Nutrition 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/713—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with four or more nitrogen atoms as the only ring hetero atoms
- 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
- 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

Landscapes

Life Sciences & Earth Sciences (AREA)
General Health & Medical Sciences (AREA)
Health & Medical Sciences (AREA)
Zoology (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Environmental Sciences (AREA)
Agronomy & Crop Science (AREA)
Dispersion Chemistry (AREA)
Toxicology (AREA)
Chemical & Material Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Treatment Of Water By Ion Exchange (AREA)
Physical Water Treatments (AREA)
Preventing Corrosion Or Incrustation Of Metals (AREA)
Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Treatment And Processing Of Natural Fur Or Leather (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Manufacturing Of Micro-Capsules (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

DD88316658A 1987-06-13 1988-06-10 Waessrige akarizidzusammensetzungen DD284580A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB878713849A GB8713849D0 (en)	1987-06-13	1987-06-13	Acaricidal formulation

Publications (1)

Publication Number	Publication Date
DD284580A5 true DD284580A5 (de)	1990-11-21

Family

ID=10618861

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD88316658A DD284580A5 (de)	1987-06-13	1988-06-10	Waessrige akarizidzusammensetzungen

Country Status (24)

Country	Link
US (1)	US4912099A (pl)
EP (1)	EP0295790B1 (pl)
JP (1)	JPS63316701A (pl)
KR (1)	KR890000010A (pl)
CN (1)	CN88103536A (pl)
AT (1)	ATE83354T1 (pl)
AU (1)	AU590156B2 (pl)
BR (1)	BR8802864A (pl)
DD (1)	DD284580A5 (pl)
DE (1)	DE3876692D1 (pl)
DK (1)	DK316288A (pl)
GB (1)	GB8713849D0 (pl)
HU (1)	HU204169B (pl)
IL (1)	IL86669A0 (pl)
MY (1)	MY103580A (pl)
NZ (1)	NZ224983A (pl)
PH (1)	PH23297A (pl)
PL (1)	PL152194B1 (pl)
PT (1)	PT87690B (pl)
RU (1)	RU1795880C (pl)
TR (1)	TR24918A (pl)
ZA (1)	ZA884162B (pl)
ZM (1)	ZM3488A1 (pl)
ZW (1)	ZW7688A1 (pl)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP3804072B2 (ja) *	1991-08-07	2006-08-02	日産化学工業株式会社	水性懸濁状農薬製剤
US5352672A (en) *	1993-10-20	1994-10-04	Fmc Corporation	Acaricidal combinations of neem seed extract and bifenthrin
CN1056032C (zh) *	1995-08-02	2000-09-06	化工部农药剂型工程技术中心	一种杀螨杀虫油悬浮混剂
JP5339055B2 (ja) *	2006-06-13	2013-11-13	日産化学工業株式会社	水性懸濁状農薬組成物
US20080090780A1 (en) *	2006-10-13	2008-04-17	Pbi/Gordon Corporation	Storage stable azadirachtin pesticide formulation
KR101034728B1 (ko) *	2008-10-23	2011-05-17	강남훈	안내 궤도식 고무차륜 경전철의 주행로 시공용 슬립폼
KR101040419B1 (ko) *	2008-11-05	2011-06-09	강남훈	안내 궤도식 고무차륜 경전철의 주행로 표면처리장치 및 이에 적합한 표면처리방법
KR101044340B1 (ko) *	2008-12-23	2011-06-29	강남훈	보조 레일을 이용한 고무차륜 경전철의 주행로 시공 방법 및 이에 적합한 주행로 시공 장치

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1987
- 1987-06-13 GB GB878713849A patent/GB8713849D0/en active Pending
1988
- 1988-05-18 AT AT88304480T patent/ATE83354T1/de not_active IP Right Cessation
- 1988-05-18 DE DE8888304480T patent/DE3876692D1/de not_active Expired - Lifetime
- 1988-05-18 EP EP88304480A patent/EP0295790B1/en not_active Expired - Lifetime
- 1988-06-06 TR TR88/0389A patent/TR24918A/xx unknown
- 1988-06-09 IL IL86669A patent/IL86669A0/xx unknown
- 1988-06-09 CN CN198888103536A patent/CN88103536A/zh active Pending
- 1988-06-09 PT PT87690A patent/PT87690B/pt not_active IP Right Cessation
- 1988-06-10 PL PL1988273000A patent/PL152194B1/pl unknown
- 1988-06-10 JP JP63141864A patent/JPS63316701A/ja active Pending
- 1988-06-10 BR BR8802864A patent/BR8802864A/pt not_active Application Discontinuation
- 1988-06-10 DK DK316288A patent/DK316288A/da not_active Application Discontinuation
- 1988-06-10 ZA ZA884162A patent/ZA884162B/xx unknown
- 1988-06-10 AU AU17598/88A patent/AU590156B2/en not_active Ceased
- 1988-06-10 ZW ZW76/88A patent/ZW7688A1/xx unknown
- 1988-06-10 NZ NZ224983A patent/NZ224983A/xx unknown
- 1988-06-10 HU HU883003A patent/HU204169B/hu not_active IP Right Cessation
- 1988-06-10 DD DD88316658A patent/DD284580A5/de not_active IP Right Cessation
- 1988-06-11 MY MYPI88000651A patent/MY103580A/en unknown
- 1988-06-13 US US07/206,101 patent/US4912099A/en not_active Expired - Fee Related
- 1988-06-13 PH PH37058A patent/PH23297A/en unknown
- 1988-06-13 ZM ZM34/88A patent/ZM3488A1/xx unknown
- 1988-06-13 KR KR1019880007054A patent/KR890000010A/ko not_active Withdrawn
- 1988-06-13 RU SU884355897A patent/RU1795880C/ru active

Also Published As

Publication number	Publication date
JPS63316701A (ja)	1988-12-26
MY103580A (en)	1993-08-28
IL86669A0 (en)	1988-11-30
EP0295790B1 (en)	1992-12-16
ZW7688A1 (en)	1989-01-04
ZM3488A1 (en)	1989-03-27
PT87690A (pt)	1988-07-01
ZA884162B (en)	1989-03-29
HU204169B (en)	1991-12-30
CN88103536A (zh)	1988-12-28
RU1795880C (ru)	1993-02-15
AU1759888A (en)	1988-12-15
PH23297A (en)	1989-06-30
EP0295790A2 (en)	1988-12-21
DE3876692D1 (de)	1993-01-28
KR890000010A (ko)	1989-03-11
BR8802864A (pt)	1989-01-03
US4912099A (en)	1990-03-27
DK316288A (da)	1988-12-14
GB8713849D0 (en)	1987-07-15
HUT49274A (en)	1989-09-28
NZ224983A (en)	1990-09-26
ATE83354T1 (de)	1993-01-15
PL273000A1 (en)	1989-02-20
PT87690B (pt)	1992-09-30
TR24918A (tr)	1992-07-21
PL152194B1 (en)	1990-11-30
AU590156B2 (en)	1989-10-26
DK316288D0 (da)	1988-06-10
EP0295790A3 (en)	1990-03-21

Legal Events

Date	Code	Title	Description
1996-11-07	ENJ	Ceased due to non-payment of renewal fee

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