DD202380A5 - Schaedlingsbekaempfungsmittel - Google Patents

Schaedlingsbekaempfungsmittel Download PDF

Info

Publication number: DD202380A5
Authority: DD; German Democratic Republic
Prior art keywords: formula; deep; halogen; alkyl; items
Prior art date: 1981-05-02

Application number

DD82239382A

Other languages

German (de)

English (en)

Inventor

Werner Knauf

Gerhard Salbeck

Anna Waltersdorfer

Original Assignee

Hoechst Ag

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.)

1981-05-02

Filing date

1982-04-28

Publication date

1983-09-14

1982-04-28 Application filed by Hoechst Ag filed Critical Hoechst Ag

1983-09-14 Publication of DD202380A5 publication Critical patent/DD202380A5/de

Links

150000001875 compounds Chemical class 0.000 claims abstract description 43
239000000203 mixture Substances 0.000 claims abstract description 36
241000238631 Hexapoda Species 0.000 claims abstract description 9
229910052736 halogen Inorganic materials 0.000 claims abstract description 9
150000002367 halogens Chemical class 0.000 claims abstract description 9
241000238876 Acari Species 0.000 claims abstract description 7
241000607479 Yersinia pestis Species 0.000 claims abstract description 7
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 7
239000001257 hydrogen Substances 0.000 claims abstract description 7
125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 5
238000000034 method Methods 0.000 claims abstract description 4
238000002156 mixing Methods 0.000 claims abstract description 4
HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Chemical group C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims abstract description 3
125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 3
125000001769 aryl amino group Chemical group 0.000 claims abstract description 3
125000004104 aryloxy group Chemical group 0.000 claims abstract description 3
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims abstract description 3
125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims abstract description 3
150000002431 hydrogen Chemical group 0.000 claims abstract description 3
239000004480 active ingredient Substances 0.000 claims description 29
-1 dibromovinyl Chemical group 0.000 claims description 12
239000003795 chemical substances by application Substances 0.000 claims description 8
239000000575 pesticide Substances 0.000 claims description 7
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
239000000890 drug combination Substances 0.000 claims description 2
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
230000003287 optical effect Effects 0.000 claims description 2
125000000217 alkyl group Chemical group 0.000 abstract description 3
229910052760 oxygen Inorganic materials 0.000 abstract 1
229910052717 sulfur Inorganic materials 0.000 abstract 1
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 20
239000000243 solution Substances 0.000 description 14
239000013543 active substance Substances 0.000 description 8
239000008187 granular material Substances 0.000 description 8
239000002253 acid Substances 0.000 description 6
238000009472 formulation Methods 0.000 description 6
239000000843 powder Substances 0.000 description 6
239000007921 spray Substances 0.000 description 6
239000004495 emulsifiable concentrate Substances 0.000 description 5
239000003995 emulsifying agent Substances 0.000 description 5
238000002360 preparation method Methods 0.000 description 5
239000000126 substance Substances 0.000 description 5
241000239290 Araneae Species 0.000 description 4
241000254173 Coleoptera Species 0.000 description 4
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
239000012141 concentrate Substances 0.000 description 4
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
238000010790 dilution Methods 0.000 description 4
239000012895 dilution Substances 0.000 description 4
230000000694 effects Effects 0.000 description 4
241000238657 Blattella germanica Species 0.000 description 3
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 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
241001454295 Tetranychidae Species 0.000 description 3
239000000969 carrier Substances 0.000 description 3
239000007859 condensation product Substances 0.000 description 3
235000014113 dietary fatty acids Nutrition 0.000 description 3
239000002270 dispersing agent Substances 0.000 description 3
239000000194 fatty acid Substances 0.000 description 3
229930195729 fatty acid Natural products 0.000 description 3
150000002191 fatty alcohols Chemical class 0.000 description 3
239000003337 fertilizer Substances 0.000 description 3
230000002147 killing effect Effects 0.000 description 3
239000000463 material Substances 0.000 description 3
125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 3
230000000361 pesticidal effect Effects 0.000 description 3
150000003254 radicals Chemical class 0.000 description 3
238000013207 serial dilution Methods 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
239000011734 sodium Substances 0.000 description 3
241000894007 species Species 0.000 description 3
238000005507 spraying Methods 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
239000000080 wetting agent Substances 0.000 description 3
239000005995 Aluminium silicate Substances 0.000 description 2
241000254175 Anthonomus grandis Species 0.000 description 2
241001124076 Aphididae Species 0.000 description 2
241001425390 Aphis fabae Species 0.000 description 2
241000238662 Blatta orientalis Species 0.000 description 2
241000255579 Ceratitis capitata Species 0.000 description 2
241000462639 Epilachna varivestis Species 0.000 description 2
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
235000016623 Fragaria vesca Nutrition 0.000 description 2
235000011363 Fragaria x ananassa Nutrition 0.000 description 2
241000257226 Muscidae Species 0.000 description 2
241000721621 Myzus persicae Species 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
241001454293 Tetranychus urticae Species 0.000 description 2
239000000853 adhesive Substances 0.000 description 2
230000001070 adhesive effect Effects 0.000 description 2
235000012211 aluminium silicate Nutrition 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
239000003814 drug Substances 0.000 description 2
229940079593 drug Drugs 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
VUNPVDGCKKSVOD-UHFFFAOYSA-N ethylsulfanyl-hydroxy-methyl-sulfanylidene-lambda5-phosphane Chemical compound CCSP(C)(O)=S VUNPVDGCKKSVOD-UHFFFAOYSA-N 0.000 description 2
239000000945 filler Substances 0.000 description 2
230000000749 insecticidal effect Effects 0.000 description 2
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 2
239000007788 liquid Substances 0.000 description 2
229920000570 polyether Polymers 0.000 description 2
239000007787 solid Substances 0.000 description 2
239000002904 solvent Substances 0.000 description 2
230000002195 synergetic effect Effects 0.000 description 2
239000000454 talc Substances 0.000 description 2
229910052623 talc Inorganic materials 0.000 description 2
125000006273 (C1-C3) alkyl group Chemical group 0.000 description 1
CMJUNAQINNWKAU-KTKRTIGZSA-N 2-[[(z)-2-oxononadec-10-enyl]amino]ethanesulfonic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)CNCCS(O)(=O)=O CMJUNAQINNWKAU-KTKRTIGZSA-N 0.000 description 1
ZMZNPVSNGBQGRW-UHFFFAOYSA-N 3-(2,2-dichloroethenyl)-2,2-dimethyl-1-[(3-phenoxyphenyl)methyl]cyclopropane-1-carboxylic acid Chemical compound CC1(C)C(C=C(Cl)Cl)C1(C(O)=O)CC1=CC=CC(OC=2C=CC=CC=2)=C1 ZMZNPVSNGBQGRW-UHFFFAOYSA-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 compound 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
125000000590 4-methylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
241001136265 Agriotes Species 0.000 description 1
241001136249 Agriotes lineatus Species 0.000 description 1
241001155998 Anthonomus rubi Species 0.000 description 1
241000952611 Aphis craccivora Species 0.000 description 1
235000016068 Berberis vulgaris Nutrition 0.000 description 1
241000335053 Beta vulgaris Species 0.000 description 1
241000238659 Blatta Species 0.000 description 1
241001674044 Blattodea Species 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
241001107116 Castanospermum australe Species 0.000 description 1
241000207199 Citrus Species 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
ZAKOWWREFLAJOT-CEFNRUSXSA-N D-alpha-tocopherylacetate Chemical compound CC(=O)OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C ZAKOWWREFLAJOT-CEFNRUSXSA-N 0.000 description 1
241000255925 Diptera Species 0.000 description 1
241001425477 Dysdercus Species 0.000 description 1
241000738498 Epitrix pubescens Species 0.000 description 1
244000307700 Fragaria vesca Species 0.000 description 1
240000009088 Fragaria x ananassa Species 0.000 description 1
241001670157 Gymnura Species 0.000 description 1
241000258937 Hemiptera Species 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
241000258916 Leptinotarsa decemlineata Species 0.000 description 1
241000257159 Musca domestica Species 0.000 description 1
SUZRRICLUFMAQD-UHFFFAOYSA-N N-Methyltaurine Chemical compound CNCCS(O)(=O)=O SUZRRICLUFMAQD-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
241000258913 Oncopeltus fasciatus Species 0.000 description 1
241000488581 Panonychus citri Species 0.000 description 1
241000488583 Panonychus ulmi Species 0.000 description 1
241000562493 Pegomya Species 0.000 description 1
244000046052 Phaseolus vulgaris Species 0.000 description 1
235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
241001674048 Phthiraptera Species 0.000 description 1
241000275067 Phyllotreta Species 0.000 description 1
239000004372 Polyvinyl alcohol Substances 0.000 description 1
235000005805 Prunus cerasus Nutrition 0.000 description 1
239000006004 Quartz sand Substances 0.000 description 1
241000254179 Sitophilus granarius Species 0.000 description 1
229920002125 Sokalan® Polymers 0.000 description 1
244000061456 Solanum tuberosum Species 0.000 description 1
235000002595 Solanum tuberosum Nutrition 0.000 description 1
241000254105 Tenebrio Species 0.000 description 1
244000098338 Triticum aestivum Species 0.000 description 1
240000006677 Vicia faba Species 0.000 description 1
235000010749 Vicia faba Nutrition 0.000 description 1
235000002096 Vicia faba var. equina Nutrition 0.000 description 1
230000000895 acaricidal effect Effects 0.000 description 1
239000000654 additive Substances 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
230000000274 adsorptive effect Effects 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
230000008485 antagonism Effects 0.000 description 1
239000007900 aqueous suspension Substances 0.000 description 1
229960000892 attapulgite Drugs 0.000 description 1
239000000440 bentonite Substances 0.000 description 1
229910000278 bentonite Inorganic materials 0.000 description 1
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
230000004071 biological effect Effects 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
235000021279 black bean Nutrition 0.000 description 1
238000009835 boiling Methods 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
229920005551 calcium lignosulfonate Polymers 0.000 description 1
159000000007 calcium salts Chemical class 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
RYAGRZNBULDMBW-UHFFFAOYSA-L calcium;3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Ca+2].COC1=CC=CC(CC(CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O RYAGRZNBULDMBW-UHFFFAOYSA-L 0.000 description 1
JNGZXGGOCLZBFB-IVCQMTBJSA-N compound E Chemical compound N([C@@H](C)C(=O)N[C@@H]1C(N(C)C2=CC=CC=C2C(C=2C=CC=CC=2)=N1)=O)C(=O)CC1=CC(F)=CC(F)=C1 JNGZXGGOCLZBFB-IVCQMTBJSA-N 0.000 description 1
238000010276 construction Methods 0.000 description 1
244000038559 crop plants Species 0.000 description 1
230000006378 damage Effects 0.000 description 1
238000010586 diagram Methods 0.000 description 1
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
231100000673 dose–response relationship Toxicity 0.000 description 1
238000001035 drying Methods 0.000 description 1
239000000428 dust Substances 0.000 description 1
235000005489 dwarf bean Nutrition 0.000 description 1
235000013399 edible fruits Nutrition 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
238000000227 grinding Methods 0.000 description 1
239000004009 herbicide Substances 0.000 description 1
244000080020 horsebean Species 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
DXVBUJOATHQUCY-UHFFFAOYSA-N hydroxy-methyl-sulfanyl-sulfanylidene-$l^{5}-phosphane Chemical compound CP(O)(S)=S DXVBUJOATHQUCY-UHFFFAOYSA-N 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
231100000636 lethal dose Toxicity 0.000 description 1
125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 description 1
238000003801 milling Methods 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 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
229920001522 polyglycol ester Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
239000008262 pumice Substances 0.000 description 1
229910052903 pyrophyllite Inorganic materials 0.000 description 1
239000010453 quartz Substances 0.000 description 1
239000004576 sand Substances 0.000 description 1
239000011343 solid material Substances 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 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
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
239000004563 wettable powder Substances 0.000 description 1
239000008096 xylene 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/22—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing aromatic radicals

Landscapes

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

DD82239382A 1981-05-02 1982-04-28 Schaedlingsbekaempfungsmittel DD202380A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19813117435 DE3117435A1 (de)	1981-05-02	1981-05-02	Schaedlingsbekaempfungsmittel

Publications (1)

Publication Number	Publication Date
DD202380A5 true DD202380A5 (de)	1983-09-14

Family

ID=6131325

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD82239382A DD202380A5 (de)	1981-05-02	1982-04-28	Schaedlingsbekaempfungsmittel

Country Status (16)

Country	Link
EP (1)	EP0064670A1 (cs)
JP (1)	JPS57209205A (cs)
AU (1)	AU8317382A (cs)
BR (1)	BR8202522A (cs)
CS (1)	CS227687B2 (cs)
DD (1)	DD202380A5 (cs)
DE (1)	DE3117435A1 (cs)
DK (1)	DK195282A (cs)
ES (1)	ES8405245A1 (cs)
GR (1)	GR75427B (cs)
IL (1)	IL65655A0 (cs)
MA (1)	MA19457A1 (cs)
OA (1)	OA07088A (cs)
PL (1)	PL236240A1 (cs)
ZA (1)	ZA822979B (cs)
ZW (1)	ZW8882A1 (cs)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
RU2087477C1 (ru) *	1995-06-30	1997-08-20	Институт элементоорганических соединений РАН	0,0-диалкил-s-[(n-алкокси(арокси)карбонил-n-алкоксикарбонилалкил)аминометил]ди(моно)тиофосфаты, проявляющие синергистическое действие к периметру в отношении комнатных мух и синатропных тараканов

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2617736C2 (de) *	1976-04-23	1982-12-09	Hoechst Ag, 6000 Frankfurt	Schädlingsbekämpfungsmittel

1981
- 1981-05-02 DE DE19813117435 patent/DE3117435A1/de not_active Withdrawn
1982
- 1982-04-21 MA MA19662A patent/MA19457A1/fr unknown
- 1982-04-26 ES ES511710A patent/ES8405245A1/es not_active Expired
- 1982-04-28 EP EP82103619A patent/EP0064670A1/de not_active Withdrawn
- 1982-04-28 DD DD82239382A patent/DD202380A5/de unknown
- 1982-04-30 OA OA57674A patent/OA07088A/xx unknown
- 1982-04-30 ZA ZA822979A patent/ZA822979B/xx unknown
- 1982-04-30 JP JP57071625A patent/JPS57209205A/ja active Pending
- 1982-04-30 GR GR68036A patent/GR75427B/el unknown
- 1982-04-30 PL PL23624082A patent/PL236240A1/xx unknown
- 1982-04-30 BR BR8202522A patent/BR8202522A/pt unknown
- 1982-04-30 AU AU83173/82A patent/AU8317382A/en not_active Abandoned
- 1982-04-30 DK DK195282A patent/DK195282A/da not_active Application Discontinuation
- 1982-04-30 ZW ZW88/82A patent/ZW8882A1/xx unknown
- 1982-04-30 IL IL65655A patent/IL65655A0/xx unknown
- 1982-04-30 CS CS823127A patent/CS227687B2/cs unknown

Also Published As

Publication number	Publication date
ZA822979B (en)	1983-03-30
CS227687B2 (en)	1984-05-14
GR75427B (cs)	1984-07-17
BR8202522A (pt)	1983-04-19
PL236240A1 (cs)	1982-12-06
MA19457A1 (fr)	1982-12-31
ES511710A0 (es)	1983-10-01
DE3117435A1 (de)	1982-11-18
OA07088A (fr)	1984-01-31
ES8405245A1 (es)	1983-10-01
EP0064670A1 (de)	1982-11-17
IL65655A0 (en)	1982-07-30
DK195282A (da)	1982-11-03
JPS57209205A (en)	1982-12-22
ZW8882A1 (en)	1982-11-24
AU8317382A (en)	1982-11-11

Publication	Publication Date	Title
DE2433680A1 (de)	1975-01-30	2,3-dihydro-2,2-dimethyl-7-benzofuranylmethylcarbamat-n-aminosulfenyl-derivate, verfahren zu deren herstellung und diese verbindungen enthaltende insektizide zusammensetzungen
IE47446B1 (en)	1984-03-21	Insecticidal and acaricidal compositions
DD212889A5 (de)	1984-08-29	Insektizide, akarizide und nematizide mittel
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EP0026829B1 (de)	1983-05-11	Ein Triazolderivat und ein Phosphorthioat enthaltende Schädlingsbekämpfungsmittel und deren Verwendung zur Bekämpfung von Schadinsekten und Akariden
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DE3120439A1 (de)	1982-12-09	Schaedlingsbekaempfungsmittel
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DE3208187A1 (de)	1983-10-06	Neue (di)thiophosphor- und phosphonsaeure-derivate, verfahren zu ihrer herstellung, sie enthaltende mittel und ihre verwendung im pflanzenschutz, sowie neue chlormethyl-1,2,4-thiadiazin-1,1-dioxide als vorprodukte und verfahren zu deren herstellung
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DE2818497A1 (de)	1979-11-08	Akarizide und insektizide mittel
DE3208193A1 (de)	1982-09-23	Neue organische pyrophosphorsaeureesterderivate