CS197727B1 - Insecticides,acaricides and ovicides - Google Patents

Insecticides,acaricides and ovicides Download PDF

Info

Publication number: CS197727B1
Authority: CS; Czechoslovakia
Prior art keywords: standard; days; diethyl; mixture; component
Prior art date: 1977-12-09

Application number

CS778233A

Other languages

Czech (cs)

English (en)

Slovak (sk)

Inventor

Vaclav Konecny

Stefan Varkonda

Stefan Truchlik

Rudolf Steskal

Original Assignee

Vaclav Konecny

Stefan Varkonda

Stefan Truchlik

Rudolf Steskal

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

1977-12-09

Publication date

1980-05-30

1977-12-09 Application filed by Vaclav Konecny, Stefan Varkonda, Stefan Truchlik, Rudolf Steskal filed Critical Vaclav Konecny

1977-12-09 Priority to CS778233A priority Critical patent/CS197727B1/cs

1978-12-06 Priority to CH1246378A priority patent/CH638951A5/de

1978-12-07 Priority to FR7834505A priority patent/FR2410958A1/fr

1978-12-07 Priority to DD78209588A priority patent/DD140414A1/de

1978-12-07 Priority to IT30677/78A priority patent/IT1100790B/it

1978-12-08 Priority to BE192212A priority patent/BE872626A/xx

1978-12-08 Priority to DE19782853124 priority patent/DE2853124A1/de

1978-12-08 Priority to JP15116478A priority patent/JPS5495731A/ja

1978-12-08 Priority to GB7847833A priority patent/GB2012586B/en

1978-12-08 Priority to HU78VI1220A priority patent/HU184702B/hu

1980-05-30 Publication of CS197727B1 publication Critical patent/CS197727B1/cs

Links

230000000895 acaricidal effect Effects 0.000 title claims abstract description 10
239000002917 insecticide Substances 0.000 title description 6
241000118205 Ovicides Species 0.000 title 1
239000000642 acaricide Substances 0.000 title 1
239000000203 mixture Substances 0.000 claims abstract description 33
150000001875 compounds Chemical class 0.000 claims abstract description 16
230000000749 insecticidal effect Effects 0.000 claims abstract description 8
239000004480 active ingredient Substances 0.000 claims abstract description 7
230000003151 ovacidal effect Effects 0.000 claims abstract description 7
231100000194 ovacidal Toxicity 0.000 claims abstract description 5
125000006273 (C1-C3) alkyl group Chemical group 0.000 claims abstract 2
229910052760 oxygen Inorganic materials 0.000 claims description 22
241000607479 Yersinia pestis Species 0.000 claims description 10
JPOXNPPZZKNXOV-UHFFFAOYSA-N bromochloromethane Chemical compound ClCBr JPOXNPPZZKNXOV-UHFFFAOYSA-N 0.000 abstract description 4
NAGJZTKCGNOGPW-UHFFFAOYSA-N dithiophosphoric acid Chemical class OP(O)(S)=S NAGJZTKCGNOGPW-UHFFFAOYSA-N 0.000 abstract 1
239000002689 soil Substances 0.000 description 16
241001136249 Agriotes lineatus Species 0.000 description 9
QGTYWWGEWOBMAK-UHFFFAOYSA-N chlormephos Chemical compound CCOP(=S)(OCC)SCCl QGTYWWGEWOBMAK-UHFFFAOYSA-N 0.000 description 9
239000013543 active substance Substances 0.000 description 7
230000000694 effects Effects 0.000 description 5
235000013601 eggs Nutrition 0.000 description 5
KVGLBTYUCJYMND-UHFFFAOYSA-N fonofos Chemical compound CCOP(=S)(CC)SC1=CC=CC=C1 KVGLBTYUCJYMND-UHFFFAOYSA-N 0.000 description 5
238000007689 inspection Methods 0.000 description 5
238000000034 method Methods 0.000 description 5
150000002903 organophosphorus compounds Chemical class 0.000 description 5
-1 2-isopropyl-6-methylpyrimidin-4-yl Chemical group 0.000 description 4
241000255925 Diptera Species 0.000 description 4
238000002360 preparation method Methods 0.000 description 4
239000000126 substance Substances 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
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 3
241000196324 Embryophyta Species 0.000 description 3
244000046052 Phaseolus vulgaris 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
239000002253 acid Substances 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
SBPBAQFWLVIOKP-UHFFFAOYSA-N chlorpyrifos Chemical compound CCOP(=S)(OCC)OC1=NC(Cl)=C(Cl)C=C1Cl SBPBAQFWLVIOKP-UHFFFAOYSA-N 0.000 description 3
235000005822 corn Nutrition 0.000 description 3
238000002474 experimental method Methods 0.000 description 3
230000000977 initiatory effect Effects 0.000 description 3
238000012360 testing method Methods 0.000 description 3
231100000419 toxicity Toxicity 0.000 description 3
230000001988 toxicity Effects 0.000 description 3
241001124076 Aphididae Species 0.000 description 2
241000254173 Coleoptera Species 0.000 description 2
241000238631 Hexapoda Species 0.000 description 2
241000905789 Lactobacillus larvae Species 0.000 description 2
241000255777 Lepidoptera Species 0.000 description 2
239000004677 Nylon Substances 0.000 description 2
235000010627 Phaseolus vulgaris Nutrition 0.000 description 2
241000254109 Tenebrio molitor Species 0.000 description 2
ANIAQSUBRGXWLS-UHFFFAOYSA-N Trichloronat Chemical compound CCOP(=S)(CC)OC1=CC(Cl)=C(Cl)C=C1Cl ANIAQSUBRGXWLS-UHFFFAOYSA-N 0.000 description 2
241000526174 Trioza urticae Species 0.000 description 2
125000000217 alkyl group Chemical group 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
235000021186 dishes Nutrition 0.000 description 2
239000004744 fabric Substances 0.000 description 2
239000011888 foil Substances 0.000 description 2
239000008187 granular material Substances 0.000 description 2
WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 description 2
239000000463 material Substances 0.000 description 2
229920001778 nylon Polymers 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
239000004033 plastic Substances 0.000 description 2
239000000843 powder Substances 0.000 description 2
239000001993 wax Substances 0.000 description 2
UAECOHJYXUJDOF-UHFFFAOYSA-N 2-methyl-1h-pyridazine-3,6-dione Chemical compound CN1N=C(O)C=CC1=O UAECOHJYXUJDOF-UHFFFAOYSA-N 0.000 description 1
241001425390 Aphis fabae Species 0.000 description 1
241000219310 Beta vulgaris subsp. vulgaris Species 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
BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
241001465754 Metazoa Species 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
244000018633 Prunus armeniaca Species 0.000 description 1
235000009827 Prunus armeniaca Nutrition 0.000 description 1
241000700157 Rattus norvegicus Species 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
PKHDYSQMVVKCSM-UHFFFAOYSA-N [2-(dimethylamino)-1-(methylsulfanylmethylideneamino)-2-oxoethyl]carbamic acid Chemical compound CN(C)C(=O)C(NC(=O)O)N=CSC PKHDYSQMVVKCSM-UHFFFAOYSA-N 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
231100000460 acute oral toxicity Toxicity 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
239000008280 blood Substances 0.000 description 1
235000013339 cereals Nutrition 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
238000012272 crop production Methods 0.000 description 1
230000034994 death Effects 0.000 description 1
231100000517 death Toxicity 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
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 1
238000007598 dipping method Methods 0.000 description 1
238000001035 drying Methods 0.000 description 1
239000000428 dust Substances 0.000 description 1
238000010410 dusting Methods 0.000 description 1
229920001971 elastomer Polymers 0.000 description 1
239000004495 emulsifiable concentrate Substances 0.000 description 1
150000002148 esters Chemical class 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
235000013305 food Nutrition 0.000 description 1
238000009472 formulation Methods 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
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
238000007654 immersion Methods 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
238000002156 mixing Methods 0.000 description 1
239000003992 organochlorine insecticide Substances 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
230000000361 pesticidal effect Effects 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
235000012015 potatoes Nutrition 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
238000002791 soaking Methods 0.000 description 1
239000002594 sorbent Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000008399 tap water Substances 0.000 description 1
235000020679 tap water Nutrition 0.000 description 1
RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 1
230000000699 topical effect Effects 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)

CS778233A 1977-12-09 1977-12-09 Insecticides,acaricides and ovicides CS197727B1 (en)

Priority Applications (10)

Application Number	Priority Date	Filing Date	Title
CS778233A CS197727B1 (en)	1977-12-09	1977-12-09	Insecticides,acaricides and ovicides
CH1246378A CH638951A5 (de)	1977-12-09	1978-12-06	Insektizide, akarizide und ovizide auf der basis von 0,0-dialkyl-s-chlormethyldithiophosphaten.
FR7834505A FR2410958A1 (fr)	1977-12-09	1978-12-07	Insecticides, acaricides et ovicides a base de dithiophosphates de o,o-dialcoyl-s-chloromethyle
DD78209588A DD140414A1 (de)	1977-12-09	1978-12-07	Insektizide,akarizide und ovizide
IT30677/78A IT1100790B (it)	1977-12-09	1978-12-07	Composizione insetticida,acaricida ed ovicida
BE192212A BE872626A (fr)	1977-12-09	1978-12-08	Insecticides, acaricides et ovicides
DE19782853124 DE2853124A1 (de)	1977-12-09	1978-12-08	Insektizide, akarizide und ovizide
JP15116478A JPS5495731A (en)	1977-12-09	1978-12-08	Pesticide * mitecide and egg killing agent
GB7847833A GB2012586B (en)	1977-12-09	1978-12-08	Insecticide acaricide and ovicide agents
HU78VI1220A HU184702B (en)	1977-12-09	1978-12-08	Insecticide, acaricide and ovicide composition

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
CS197727B1 true CS197727B1 (en)	1980-05-30

Family

ID=5432638

Family Applications (1)

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

Country Status (10)

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

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
NL105236C (de) *	1955-08-18
NL96707C (de) *	1955-12-31
GB1258922A (de) *	1968-05-27	1971-12-30
US3896219A (en) *	1968-05-27	1975-07-22	Murphy Chemical Ltd	S-chloromethyl diethyl phosphorothiolothionate as a soil insecticide
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 JP JP15116478A patent/JPS5495731A/ja active Pending
- 1978-12-08 DE DE19782853124 patent/DE2853124A1/de not_active Withdrawn
- 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
CH638951A5 (de)	1983-10-31
DE2853124A1 (de)	1979-06-13
FR2410958B1 (de)	1983-11-10
GB2012586A (en)	1979-08-01
BE872626A (fr)	1979-03-30
GB2012586B (en)	1982-07-28
IT1100790B (it)	1985-09-28
HU184702B (en)	1984-10-29
DD140414A1 (de)	1980-03-05
JPS5495731A (en)	1979-07-28
FR2410958A1 (fr)	1979-07-06
IT7830677A0 (it)	1978-12-07

Publication	Publication Date	Title
JPH0219840B2 (de)	1990-05-07
CS197727B1 (en)	1980-05-30	Insecticides,acaricides and ovicides
US3517089A (en)	1970-06-23	N-phenyl-n-alkyl ester phosphate acetamides
JPH01153671A (ja)	1989-06-15	新規チオイミデート及びアミジン殺虫剤
Kenaga et al.	1962	Laboratory insecticidal tests with 4-dimethylamino-3, 5-xylyl methylcarbamate
US3733406A (en)	1973-05-15	Use of n-alpha-dialkoxyphosphinothioacetyl-n-methylcarbamates of phenols as insecticides and acaricides
EP0229417B1 (de)	1989-09-20	Phosphonamidthioate-Insektizide
US4468389A (en)	1984-08-28	Pesticidal N-sulfonyl phosphorodiamido(di)thioates
US4588714A (en)	1986-05-13	S-dithiocarbamoylmethyl trithiophosphonate insecticides, compositions and use
US3600471A (en)	1971-08-17	N - alpha - dialkoxyphosphinothioacetyl-n-methylcarbamates of phenols and their use as pesticides
US3590074A (en)	1971-06-29	Chlor-methyl-isopropyl-phenyl-n-methyl carbamate
EP0068823B1 (de)	1988-05-04	Phosphoroamido(DI oder TRI)thioate-Derivate, sie enthaltende pestizide Zubereitungen und die Verwendung der neuen Derivaten als Schädlingsbekämpfungsmittel
US4657936A (en)	1987-04-14	Halogenated saturated hydrocarbons as acaricidal compounds
US3151022A (en)	1964-09-29	Omicron, omicron-dimethyl-omicron-(4-methylmercaptophenyl) phosphate and pesticidal use
US3886273A (en)	1975-05-27	Certain thiophosphate synergists
US4468387A (en)	1984-08-28	Pesticidal N-sulfonyl N'-oxalate phosphorodiamido(di)thioates
US3470229A (en)	1969-09-30	O,o-dialkyl-o-(dithiocarbonato) ethyl-phosphoric acid esters
US4083970A (en)	1978-04-11	Activated insecticide composition employing a certain phosphorodithioate and an activator
JPH0288590A (ja)	1990-03-28	光学活性有機リン系化合物、それらの製造方法及びそれらを含有する有害動物防除剤
US4737490A (en)	1988-04-12	S-(3-buten-1-yl) trithiophosphonate insecticides
US4071556A (en)	1978-01-31	Formamidine insecticidal compounds
US4720508A (en)	1988-01-19	Halogenated saturated hydrocarbons and saturated hydrocarbon in combination as acaricidal compounds
US4390549A (en)	1983-06-28	N-Tetrachloroethylthio benzoyl anilides useful as acaricides and to control mosquitoes
US3728451A (en)	1973-04-17	Cyclic urea amide phosphates useful as insecticides
SU247148A1 (ru)		Инсектофунгицидный состав