DD140414A1 - Insektizide,akarizide und ovizide - Google Patents

Insektizide,akarizide und ovizide Download PDF

Info

Publication number: DD140414A1
Authority: DD; German Democratic Republic
Prior art keywords: standard; days; soil; diethyl; insecticides
Prior art date: 1977-12-09

Application number

DD78209588A

Other languages

German (de)

English (en)

Inventor

Vaclav Konecny

Stefan Varkonda

Stefan Truchlik

Rudolf Steskal

Original Assignee

Vyzk Ustav Agrochem

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.)

1977-12-09

Filing date

1978-12-07

Publication date

1980-03-05

1978-12-07 Application filed by Vyzk Ustav Agrochem filed Critical Vyzk Ustav Agrochem

1980-03-05 Publication of DD140414A1 publication Critical patent/DD140414A1/de

Links

239000002917 insecticide Substances 0.000 title claims description 13
241000118205 Ovicides Species 0.000 title claims description 7
239000000642 acaricide Substances 0.000 title claims description 7
239000000203 mixture Substances 0.000 claims description 20
150000001875 compounds Chemical class 0.000 claims description 11
241000607479 Yersinia pestis Species 0.000 claims description 9
230000000895 acaricidal effect Effects 0.000 claims description 9
125000000217 alkyl group Chemical group 0.000 claims description 5
125000004432 carbon atom Chemical group C* 0.000 claims description 4
244000038559 crop plants Species 0.000 claims description 4
239000002689 soil Substances 0.000 description 17
QGTYWWGEWOBMAK-UHFFFAOYSA-N chlormephos Chemical compound CCOP(=S)(OCC)SCCl QGTYWWGEWOBMAK-UHFFFAOYSA-N 0.000 description 11
239000003795 chemical substances by application Substances 0.000 description 10
239000000126 substance Substances 0.000 description 10
230000000694 effects Effects 0.000 description 9
238000002360 preparation method Methods 0.000 description 9
-1 O-ethyl-O- Chemical class 0.000 description 8
229910052760 oxygen Inorganic materials 0.000 description 8
RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 8
241001136249 Agriotes lineatus Species 0.000 description 7
150000002903 organophosphorus compounds Chemical class 0.000 description 6
238000002474 experimental method Methods 0.000 description 5
238000000034 method Methods 0.000 description 5
239000013543 active substance Substances 0.000 description 4
230000004071 biological effect Effects 0.000 description 4
239000000460 chlorine Substances 0.000 description 4
SBPBAQFWLVIOKP-UHFFFAOYSA-N chlorpyrifos Chemical compound CCOP(=S)(OCC)OC1=NC(Cl)=C(Cl)C=C1Cl SBPBAQFWLVIOKP-UHFFFAOYSA-N 0.000 description 4
235000013601 eggs Nutrition 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
241000196324 Embryophyta Species 0.000 description 3
241000238631 Hexapoda Species 0.000 description 3
244000046052 Phaseolus vulgaris Species 0.000 description 3
241001674048 Phthiraptera Species 0.000 description 3
241001454293 Tetranychus urticae Species 0.000 description 3
240000008042 Zea mays Species 0.000 description 3
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 3
235000002017 Zea mays subsp mays Nutrition 0.000 description 3
DUEPRVBVGDRKAG-UHFFFAOYSA-N carbofuran Chemical compound CNC(=O)OC1=CC=CC2=C1OC(C)(C)C2 DUEPRVBVGDRKAG-UHFFFAOYSA-N 0.000 description 3
235000005822 corn Nutrition 0.000 description 3
235000021186 dishes Nutrition 0.000 description 3
230000000749 insecticidal effect Effects 0.000 description 3
KZAUOCCYDRDERY-UHFFFAOYSA-N oxamyl Chemical compound CNC(=O)ON=C(SC)C(=O)N(C)C KZAUOCCYDRDERY-UHFFFAOYSA-N 0.000 description 3
231100000419 toxicity Toxicity 0.000 description 3
230000001988 toxicity Effects 0.000 description 3
UWNADWZGEHDQAB-UHFFFAOYSA-N 2,5-dimethylhexane Chemical group CC(C)CCC(C)C UWNADWZGEHDQAB-UHFFFAOYSA-N 0.000 description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
239000005944 Chlorpyrifos Substances 0.000 description 2
241000254173 Coleoptera Species 0.000 description 2
241000255925 Diptera Species 0.000 description 2
241000255777 Lepidoptera Species 0.000 description 2
239000005950 Oxamyl Substances 0.000 description 2
235000010627 Phaseolus vulgaris Nutrition 0.000 description 2
241000251539 Vertebrata <Metazoa> Species 0.000 description 2
239000002253 acid Substances 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
229910052801 chlorine Inorganic materials 0.000 description 2
JXSJBGJIGXNWCI-UHFFFAOYSA-N diethyl 2-[(dimethoxyphosphorothioyl)thio]succinate Chemical compound CCOC(=O)CC(SP(=S)(OC)OC)C(=O)OCC JXSJBGJIGXNWCI-UHFFFAOYSA-N 0.000 description 2
YJVOECXUWYQORY-UHFFFAOYSA-N dihydroxy-methylsulfanyl-sulfanylidene-$l^{5}-phosphane Chemical compound CSP(O)(O)=S YJVOECXUWYQORY-UHFFFAOYSA-N 0.000 description 2
238000010410 dusting Methods 0.000 description 2
239000004744 fabric Substances 0.000 description 2
KVGLBTYUCJYMND-UHFFFAOYSA-N fonofos Chemical compound CCOP(=S)(CC)SC1=CC=CC=C1 KVGLBTYUCJYMND-UHFFFAOYSA-N 0.000 description 2
238000007654 immersion Methods 0.000 description 2
230000000977 initiatory effect Effects 0.000 description 2
CYQAYERJWZKYML-UHFFFAOYSA-N phosphorus pentasulfide Chemical compound S1P(S2)(=S)SP3(=S)SP1(=S)SP2(=S)S3 CYQAYERJWZKYML-UHFFFAOYSA-N 0.000 description 2
239000000758 substrate Substances 0.000 description 2
OVANCIHPSBMNEN-UHFFFAOYSA-N (2,2-dimethyl-3h-1-benzofuran-7-yl)methylcarbamic acid Chemical compound C1=CC(CNC(O)=O)=C2OC(C)(C)CC2=C1 OVANCIHPSBMNEN-UHFFFAOYSA-N 0.000 description 1
QMSVNDSDEZTYAS-UHFFFAOYSA-N 1-bromo-1-chloroethane Chemical compound CC(Cl)Br QMSVNDSDEZTYAS-UHFFFAOYSA-N 0.000 description 1
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
241001425390 Aphis fabae Species 0.000 description 1
101100025420 Arabidopsis thaliana XI-C gene Proteins 0.000 description 1
241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 1
UNMGRCLSYXRFPL-UHFFFAOYSA-N CC1C(OC2=C(C=CC=C12)CNC(=O)O)C Chemical compound CC1C(OC2=C(C=CC=C12)CNC(=O)O)C UNMGRCLSYXRFPL-UHFFFAOYSA-N 0.000 description 1
KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
YVGGHNCTFXOJCH-UHFFFAOYSA-N DDT Chemical compound C1=CC(Cl)=CC=C1C(C(Cl)(Cl)Cl)C1=CC=C(Cl)C=C1 YVGGHNCTFXOJCH-UHFFFAOYSA-N 0.000 description 1
239000004819 Drying adhesive Substances 0.000 description 1
241001427543 Elateridae Species 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
244000060234 Gmelina philippensis Species 0.000 description 1
241000257159 Musca domestica Species 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
244000061456 Solanum tuberosum Species 0.000 description 1
235000002595 Solanum tuberosum Nutrition 0.000 description 1
235000021536 Sugar beet Nutrition 0.000 description 1
241000254105 Tenebrio Species 0.000 description 1
241000254109 Tenebrio molitor Species 0.000 description 1
ANIAQSUBRGXWLS-UHFFFAOYSA-N Trichloronat Chemical compound CCOP(=S)(CC)OC1=CC(Cl)=C(Cl)C=C1Cl ANIAQSUBRGXWLS-UHFFFAOYSA-N 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
231100000460 acute oral toxicity Toxicity 0.000 description 1
239000002671 adjuvant Substances 0.000 description 1
238000012271 agricultural production Methods 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
DIZXBSHARPXAAZ-UHFFFAOYSA-N aminomethyl carbamate Chemical compound NCOC(N)=O DIZXBSHARPXAAZ-UHFFFAOYSA-N 0.000 description 1
230000003444 anaesthetic effect Effects 0.000 description 1
230000002824 aphicidal effect Effects 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
238000009395 breeding Methods 0.000 description 1
230000001488 breeding effect Effects 0.000 description 1
235000013339 cereals Nutrition 0.000 description 1
BIWJNBZANLAXMG-YQELWRJZSA-N chloordaan Chemical compound ClC1=C(Cl)[C@@]2(Cl)C3CC(Cl)C(Cl)C3[C@]1(Cl)C2(Cl)Cl BIWJNBZANLAXMG-YQELWRJZSA-N 0.000 description 1
125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 1
LOMUNVGWRGSERU-UHFFFAOYSA-N chloromethylsulfanyl-ethoxy-(2-methylpropoxy)-sulfanylidene-$l^{5}-phosphane Chemical compound CCOP(=S)(SCCl)OCC(C)C LOMUNVGWRGSERU-UHFFFAOYSA-N 0.000 description 1
230000001684 chronic effect Effects 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
230000001143 conditioned effect Effects 0.000 description 1
FHIVAFMUCKRCQO-UHFFFAOYSA-N diazinon Chemical compound CCOP(=S)(OCC)OC1=CC(C)=NC(C(C)C)=N1 FHIVAFMUCKRCQO-UHFFFAOYSA-N 0.000 description 1
DFBKLUNHFCTMDC-PICURKEMSA-N dieldrin Chemical compound C([C@H]1[C@H]2[C@@]3(Cl)C(Cl)=C([C@]([C@H]22)(Cl)C3(Cl)Cl)Cl)[C@H]2[C@@H]2[C@H]1O2 DFBKLUNHFCTMDC-PICURKEMSA-N 0.000 description 1
229950006824 dieldrin Drugs 0.000 description 1
NGPMUTDCEIKKFM-UHFFFAOYSA-N dieldrin Natural products CC1=C(Cl)C2(Cl)C3C4CC(C5OC45)C3C1(Cl)C2(Cl)Cl NGPMUTDCEIKKFM-UHFFFAOYSA-N 0.000 description 1
DOFZAZXDOSGAJZ-UHFFFAOYSA-N disulfoton Chemical compound CCOP(=S)(OCC)SCCSCC DOFZAZXDOSGAJZ-UHFFFAOYSA-N 0.000 description 1
229920001971 elastomer Polymers 0.000 description 1
239000004495 emulsifiable concentrate Substances 0.000 description 1
HGELWZQRZUOEOJ-UHFFFAOYSA-N ethyl-dihydroxy-sulfanylidene-$l^{5}-phosphane Chemical compound CCP(O)(O)=S HGELWZQRZUOEOJ-UHFFFAOYSA-N 0.000 description 1
AVGQPNBPXNPEPF-UHFFFAOYSA-N ethylsulfanyl-dihydroxy-sulfanylidene-$l^{5}-phosphane Chemical compound CCSP(O)(O)=S AVGQPNBPXNPEPF-UHFFFAOYSA-N 0.000 description 1
125000006351 ethylthiomethyl group Chemical group [H]C([H])([H])C([H])([H])SC([H])([H])* 0.000 description 1
239000011888 foil Substances 0.000 description 1
235000013305 food Nutrition 0.000 description 1
JLYXXMFPNIAWKQ-GNIYUCBRSA-N gamma-hexachlorocyclohexane Chemical compound Cl[C@H]1[C@H](Cl)[C@@H](Cl)[C@@H](Cl)[C@H](Cl)[C@H]1Cl JLYXXMFPNIAWKQ-GNIYUCBRSA-N 0.000 description 1
JLYXXMFPNIAWKQ-UHFFFAOYSA-N gamma-hexachlorocyclohexane Natural products ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 description 1
239000008187 granular material Substances 0.000 description 1
FRCCEHPWNOQAEU-UHFFFAOYSA-N heptachlor Chemical compound ClC1=C(Cl)C2(Cl)C3C=CC(Cl)C3C1(Cl)C2(Cl)Cl FRCCEHPWNOQAEU-UHFFFAOYSA-N 0.000 description 1
230000036039 immunity Effects 0.000 description 1
238000011534 incubation Methods 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
239000011630 iodine Substances 0.000 description 1
230000001418 larval effect Effects 0.000 description 1
229960002809 lindane Drugs 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000003094 microcapsule Substances 0.000 description 1
238000002156 mixing Methods 0.000 description 1
230000003151 ovacidal effect Effects 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
125000000636 p-nitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)[N+]([O-])=O 0.000 description 1
LCCNCVORNKJIRZ-UHFFFAOYSA-N parathion Chemical compound CCOP(=S)(OCC)OC1=CC=C([N+]([O-])=O)C=C1 LCCNCVORNKJIRZ-UHFFFAOYSA-N 0.000 description 1
230000000361 pesticidal effect Effects 0.000 description 1
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
235000012015 potatoes Nutrition 0.000 description 1
239000000843 powder Substances 0.000 description 1
150000003839 salts Chemical group 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
239000008399 tap water Substances 0.000 description 1
235000020679 tap water 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
- A01N57/12—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing acyclic or cycloaliphatic 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)

DD78209588A 1977-12-09 1978-12-07 Insektizide,akarizide und ovizide DD140414A1 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CS778233A CS197727B1 (en)	1977-12-09	1977-12-09	Insecticides,acaricides and ovicides

Publications (1)

Publication Number	Publication Date
DD140414A1 true DD140414A1 (de)	1980-03-05

Family

ID=5432638

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD78209588A DD140414A1 (de)	1977-12-09	1978-12-07	Insektizide,akarizide und ovizide

Country Status (10)

Country	Link
JP (1)	JPS5495731A (cs)
BE (1)	BE872626A (cs)
CH (1)	CH638951A5 (cs)
CS (1)	CS197727B1 (cs)
DD (1)	DD140414A1 (cs)
DE (1)	DE2853124A1 (cs)
FR (1)	FR2410958A1 (cs)
GB (1)	GB2012586B (cs)
HU (1)	HU184702B (cs)
IT (1)	IT1100790B (cs)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN113698430B (zh) *	2021-10-29	2022-01-25	潍坊新绿化工有限公司	一种除草剂莎稗磷的制备方法

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BE550399A (cs) *	1955-08-18
NL220830A (cs) *	1955-12-31
US3896219A (en) *	1968-05-27	1975-07-22	Murphy Chemical Ltd	S-chloromethyl diethyl phosphorothiolothionate as a soil insecticide
GB1258922A (cs) *	1968-05-27	1971-12-30
JPS5231414A (en) *	1975-09-03	1977-03-09	Hitachi Ltd	Safety device for electromobile

1977
- 1977-12-09 CS CS778233A patent/CS197727B1/cs unknown
1978
- 1978-12-06 CH CH1246378A patent/CH638951A5/de not_active IP Right Cessation
- 1978-12-07 FR FR7834505A patent/FR2410958A1/fr active Granted
- 1978-12-07 DD DD78209588A patent/DD140414A1/de not_active IP Right Cessation
- 1978-12-07 IT IT30677/78A patent/IT1100790B/it active
- 1978-12-08 DE DE19782853124 patent/DE2853124A1/de not_active Withdrawn
- 1978-12-08 JP JP15116478A patent/JPS5495731A/ja active Pending
- 1978-12-08 GB GB7847833A patent/GB2012586B/en not_active Expired
- 1978-12-08 BE BE192212A patent/BE872626A/xx unknown
- 1978-12-08 HU HU78VI1220A patent/HU184702B/hu unknown

Also Published As

Publication number	Publication date
HU184702B (en)	1984-10-29
DE2853124A1 (de)	1979-06-13
CS197727B1 (en)	1980-05-30
IT7830677A0 (it)	1978-12-07
IT1100790B (it)	1985-09-28
FR2410958B1 (cs)	1983-11-10
JPS5495731A (en)	1979-07-28
CH638951A5 (de)	1983-10-31
BE872626A (fr)	1979-03-30
GB2012586B (en)	1982-07-28
FR2410958A1 (fr)	1979-07-06
GB2012586A (en)	1979-08-01

Legal Events

Date	Code	Title	Description
1994-07-21	ENJ	Ceased due to non-payment of renewal fee

Publication	Publication Date	Title
DD202099A5 (de)	1983-08-31	Insektizid-zusammensetzung
PT734650E (pt)	2002-01-30	Preparacoes adesivas para tratamento de plantas
DE2250085C3 (de)	1979-08-09	Insektizides Mittel auf der Basis einer Mischung aus parasitären Mikroorganismen und Insektiziden
DE1060659B (de)	1959-07-02	Schaedlingsbekaempfungsmittel
US3896219A (en)	1975-07-22	S-chloromethyl diethyl phosphorothiolothionate as a soil insecticide
CH638951A5 (de)	1983-10-31	Insektizide, akarizide und ovizide auf der basis von 0,0-dialkyl-s-chlormethyldithiophosphaten.
CH616313A5 (en)	1980-03-31	Process for the preparation of novel phenoxybenzyl esters of spirocarboxylic acids and their optical and geometric isomers
DE2139046C3 (de)	1975-04-10	Formamidine und ihre Salze, Herstellung derselben und diese enthaltende Mittel zur Bekämpfung von Insekten und Vertretern der Ordnung Akarina
DE1966823C3 (de)	1981-04-30	Insecticide und acaricide Zubereitung auf Basis von Benzimidazolderivaten
DE1277624B (de)	1968-09-12	Insenkticides und acaricides Mittel
DE1935758C (de)	1973-03-08	(Thio) Phosphonsaureester und ihre Verwendung als Wirkstoffe in Schädlings bekampfungsmitteln
AT265743B (de)	1968-10-25	Schädlingsbekämpfungsmittel
AT325896B (de)	1975-11-10	Insektizide und akarizide zusammensetzungen
DE1642294C (de)	1971-12-30	Insektizide, mitizide und fungizide Mittel
DE1044503B (de)	1958-11-20	Schaedlingsbekaempfungsmittel
AT253861B (de)	1967-04-25	Insektizide Mischung
DE1542901A1 (de)	1970-05-27	Insektizide Mittel
DE861168C (de)	1952-12-29	Schaedlingsbekaempfungsmittel
DE2010053A1 (de)	1970-09-17	Schädlingsbekämpfungsmittel
DE2851025A1 (de)	1979-06-07	Insektizides mittel
DE1642294B1 (de)	1971-05-19	Insektizide,mitizide und fungizide Mittel
DD200709A1 (de)	1983-06-08	Insektizide und akarizide mittel
CH645381A5 (de)	1984-09-28	Xanthenon-yl-ester von phosphor- und phosphonsaeure.
Cohen	1980	THE PHYSICOCHEMICAL AND BIOLOGICAL CHARACTERIZATION OF INSECTICIDE DELIVERY SYSTEMS PREPARED BY ENTRAPMENT IN LATEX DISPERSIONS (POLYMETHYL METHACRYLATE, METHYL PARATHION)
DE1274399B (de)	1968-08-01	Insecticides Mittel