CH638951A5 - Insektizide, akarizide und ovizide auf der basis von 0,0-dialkyl-s-chlormethyldithiophosphaten. - Google Patents

Insektizide, akarizide und ovizide auf der basis von 0,0-dialkyl-s-chlormethyldithiophosphaten. Download PDF

Info

Publication number: CH638951A5
Authority: CH; Switzerland
Prior art keywords: insecticides; compounds; soil; diethyl; pests
Prior art date: 1977-12-09

Application number

CH1246378A

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

1978-12-06

Publication date

1983-10-31

1978-12-06 Application filed by Vyzk Ustav Agrochem filed Critical Vyzk Ustav Agrochem

1983-10-31 Publication of CH638951A5 publication Critical patent/CH638951A5/de

Links

239000002917 insecticide Substances 0.000 title claims description 11
241000118205 Ovicides Species 0.000 title claims description 5
239000000642 acaricide Substances 0.000 title claims description 5
239000003795 chemical substances by application Substances 0.000 claims description 25
239000000203 mixture Substances 0.000 claims description 22
239000002689 soil Substances 0.000 claims description 16
241000607479 Yersinia pestis Species 0.000 claims description 10
150000001875 compounds Chemical class 0.000 claims description 10
238000002360 preparation method Methods 0.000 claims description 8
230000000895 acaricidal effect Effects 0.000 claims description 7
238000000034 method Methods 0.000 claims description 6
125000000217 alkyl group Chemical group 0.000 claims description 5
239000000126 substance Substances 0.000 claims description 5
125000004432 carbon atom Chemical group C* 0.000 claims description 4
150000002903 organophosphorus compounds Chemical class 0.000 claims description 4
241000196324 Embryophyta Species 0.000 claims description 3
240000008042 Zea mays Species 0.000 claims description 3
235000002017 Zea mays subsp mays Nutrition 0.000 claims description 3
244000038559 crop plants Species 0.000 claims description 3
229910019142 PO4 Inorganic materials 0.000 claims description 2
235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 claims description 2
239000002253 acid Substances 0.000 claims description 2
235000009973 maize Nutrition 0.000 claims description 2
241000219310 Beta vulgaris subsp. vulgaris Species 0.000 claims 1
229920000742 Cotton Polymers 0.000 claims 1
244000061456 Solanum tuberosum Species 0.000 claims 1
235000002595 Solanum tuberosum Nutrition 0.000 claims 1
235000021536 Sugar beet Nutrition 0.000 claims 1
ANIAQSUBRGXWLS-UHFFFAOYSA-N Trichloronat Chemical compound CCOP(=S)(CC)OC1=CC(Cl)=C(Cl)C=C1Cl ANIAQSUBRGXWLS-UHFFFAOYSA-N 0.000 claims 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
235000013339 cereals Nutrition 0.000 claims 1
150000002148 esters Chemical class 0.000 claims 1
235000013305 food Nutrition 0.000 claims 1
230000005923 long-lasting effect Effects 0.000 claims 1
229910052760 oxygen Inorganic materials 0.000 claims 1
239000001301 oxygen Substances 0.000 claims 1
LCCNCVORNKJIRZ-UHFFFAOYSA-N parathion Chemical compound CCOP(=S)(OCC)OC1=CC=C([N+]([O-])=O)C=C1 LCCNCVORNKJIRZ-UHFFFAOYSA-N 0.000 claims 1
235000012015 potatoes Nutrition 0.000 claims 1
230000000694 effects Effects 0.000 description 11
230000000052 comparative effect Effects 0.000 description 7
238000002474 experimental method Methods 0.000 description 7
241001136249 Agriotes lineatus Species 0.000 description 6
239000013543 active substance Substances 0.000 description 6
RFONJRMUUALMBA-UHFFFAOYSA-N 2-methanidylpropane Chemical compound CC(C)[CH2-] RFONJRMUUALMBA-UHFFFAOYSA-N 0.000 description 5
235000013601 eggs Nutrition 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
239000005944 Chlorpyrifos Substances 0.000 description 3
241000255925 Diptera Species 0.000 description 3
241000238631 Hexapoda Species 0.000 description 3
239000005950 Oxamyl Substances 0.000 description 3
244000046052 Phaseolus vulgaris Species 0.000 description 3
241001674048 Phthiraptera Species 0.000 description 3
-1 aliphatic alcohols Chemical class 0.000 description 3
QGTYWWGEWOBMAK-UHFFFAOYSA-N chlormephos Chemical compound CCOP(=S)(OCC)SCCl QGTYWWGEWOBMAK-UHFFFAOYSA-N 0.000 description 3
230000000749 insecticidal effect Effects 0.000 description 3
231100000419 toxicity Toxicity 0.000 description 3
230000001988 toxicity Effects 0.000 description 3
241000254173 Coleoptera Species 0.000 description 2
235000010627 Phaseolus vulgaris Nutrition 0.000 description 2
241000254109 Tenebrio molitor Species 0.000 description 2
241001454293 Tetranychus urticae Species 0.000 description 2
241000251539 Vertebrata <Metazoa> Species 0.000 description 2
JPOXNPPZZKNXOV-UHFFFAOYSA-N bromochloromethane Chemical compound ClCBr JPOXNPPZZKNXOV-UHFFFAOYSA-N 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-$l^{5}-phosphane Chemical compound CSP(O)(O)=S YJVOECXUWYQORY-UHFFFAOYSA-N 0.000 description 2
AVGQPNBPXNPEPF-UHFFFAOYSA-N ethylsulfanyl-dihydroxy-sulfanylidene-$l^{5}-phosphane Chemical compound CCSP(O)(O)=S AVGQPNBPXNPEPF-UHFFFAOYSA-N 0.000 description 2
239000004744 fabric Substances 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
RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 2
MQTMIQSZMVPFQB-UHFFFAOYSA-N (2,2-dimethyl-3H-1-benzofuran-7-yl)-methylcarbamic acid Chemical compound OC(=O)N(C)C1=CC=CC2=C1OC(C)(C)C2 MQTMIQSZMVPFQB-UHFFFAOYSA-N 0.000 description 1
241000059559 Agriotes sordidus Species 0.000 description 1
241000393993 Aphia Species 0.000 description 1
NZYIXBQJBPJJST-UHFFFAOYSA-N CCSCC[SH2]P(O)(O)=S Chemical compound CCSCC[SH2]P(O)(O)=S NZYIXBQJBPJJST-UHFFFAOYSA-N 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
JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
244000060234 Gmelina philippensis Species 0.000 description 1
241000255777 Lepidoptera Species 0.000 description 1
241000257159 Musca domestica Species 0.000 description 1
LBTWDJVJZXYTSZ-UHFFFAOYSA-N OP(O)([SH2]CCl)=S Chemical compound OP(O)([SH2]CCl)=S LBTWDJVJZXYTSZ-UHFFFAOYSA-N 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
235000005824 Zea mays ssp. parviglumis 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
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
DIZXBSHARPXAAZ-UHFFFAOYSA-N aminomethyl carbamate Chemical compound NCOC(N)=O DIZXBSHARPXAAZ-UHFFFAOYSA-N 0.000 description 1
230000002824 aphicidal effect Effects 0.000 description 1
230000004071 biological effect Effects 0.000 description 1
GTCAXTIRRLKXRU-UHFFFAOYSA-N carbamic acid methyl ester Natural products COC(N)=O GTCAXTIRRLKXRU-UHFFFAOYSA-N 0.000 description 1
DUEPRVBVGDRKAG-UHFFFAOYSA-N carbofuran Chemical compound CNC(=O)OC1=CC=CC2=C1OC(C)(C)C2 DUEPRVBVGDRKAG-UHFFFAOYSA-N 0.000 description 1
BIWJNBZANLAXMG-UHFFFAOYSA-N chlordane Chemical compound ClC1=C(Cl)C2(Cl)C3CC(Cl)C(Cl)C3C1(Cl)C2(Cl)Cl BIWJNBZANLAXMG-UHFFFAOYSA-N 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
235000005822 corn Nutrition 0.000 description 1
230000003111 delayed effect Effects 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
230000009189 diving Effects 0.000 description 1
229920001971 elastomer Polymers 0.000 description 1
239000004495 emulsifiable concentrate Substances 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
239000011888 foil Substances 0.000 description 1
KVGLBTYUCJYMND-UHFFFAOYSA-N fonofos Chemical compound CCOP(=S)(CC)SC1=CC=CC=C1 KVGLBTYUCJYMND-UHFFFAOYSA-N 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
239000008187 granular material Substances 0.000 description 1
238000000227 grinding Methods 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
AWRSCPRMXMNBKN-UHFFFAOYSA-N hydroxy-(2-phenylethyl)-sulfanyl-sulfanylidene-lambda5-phosphane Chemical compound OP(S)(=S)CCC1=CC=CC=C1 AWRSCPRMXMNBKN-UHFFFAOYSA-N 0.000 description 1
238000007654 immersion Methods 0.000 description 1
238000011534 incubation Methods 0.000 description 1
230000001418 larval effect Effects 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
230000000361 pesticidal effect Effects 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
239000000843 powder Substances 0.000 description 1
150000003839 salts Chemical class 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)

CH1246378A 1977-12-09 1978-12-06 Insektizide, akarizide und ovizide auf der basis von 0,0-dialkyl-s-chlormethyldithiophosphaten. CH638951A5 (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
CH638951A5 true CH638951A5 (de)	1983-10-31

Family

ID=5432638

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH1246378A CH638951A5 (de)	1977-12-09	1978-12-06	Insektizide, akarizide und ovizide auf der basis von 0,0-dialkyl-s-chlormethyldithiophosphaten.

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
NL105236C (cs) *	1955-08-18
NL96707C (cs) *	1955-12-31
GB1258922A (cs) *	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
DE2853124A1 (de)	1979-06-13
FR2410958B1 (cs)	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
CS197727B1 (en)	1980-05-30
FR2410958A1 (fr)	1979-07-06
IT7830677A0 (it)	1978-12-07

Legal Events

Date	Code	Title	Description
1984-08-31	PL	Patent ceased
2024-10-31	PL	Patent ceased

Publication	Publication Date	Title
DE1046938B (de)	1958-12-18	Schaedlingsbekaempfungsmittel
CH638223A5 (de)	1983-09-15	N-((phosphinyl)amino)thio-methylcarbamate bzw. n-((phosphinothioyl)amino)thio-methylcarbamate, verfahren zu ihrer herstellung sowie ihre verwendung in pestiziden.
DE1208115B (de)	1965-12-30	Insektizide Mittel
DE2250085A1 (de)	1973-04-26	Pesticides gemisch und verwendung von aktiven mischungen dafuer
CH638951A5 (de)	1983-10-31	Insektizide, akarizide und ovizide auf der basis von 0,0-dialkyl-s-chlormethyldithiophosphaten.
CH662814A5 (de)	1987-10-30	N-alkyl bzw. alkenyl-n-(0,0-disubstituierte-thiophosphoryl)-n'n'-disubstituierte-glycinamide, deren herstellung und diese verbindungen enthaltende akarizide, insektizide und fungizide mittel.
DE1171200B (de)	1964-05-27	Insektizide synergistische Gemische
CH657750A5 (de)	1986-09-30	Schaedlingsbekaempfungsmittel.
DE1181200B (de)	1964-11-12	Verfahren zur Herstellung des N-Mono-methylamids der O, O-Di-(ª-fluoraethyl)-dithiophosphorylessigsaeure
DE2139046C3 (de)	1975-04-10	Formamidine und ihre Salze, Herstellung derselben und diese enthaltende Mittel zur Bekämpfung von Insekten und Vertretern der Ordnung Akarina
DE1277624B (de)	1968-09-12	Insenkticides und acaricides Mittel
AT253861B (de)	1967-04-25	Insektizide Mischung
AT246492B (de)	1966-04-25	Schädlingsbekämpfungsmittel
DE1668838C2 (de)	1973-01-04	O-Methyl- und O-Äthyl-O-(2,5-dichlor-4-bromphenyl)-phenylthiophosphonatund deren Verwendung als Wirkstoff in Insektiziden
EP0252983B1 (de)	1992-09-09	Salze der n-(vinyloxyäthyl)dithiokarbamidsäure, herstellungsverfahren und schädlingsbekämpfungsmittel
DE1542901A1 (de)	1970-05-27	Insektizide Mittel
DE1642294C (de)	1971-12-30	Insektizide, mitizide und fungizide Mittel
DE2718719A1 (de)	1978-11-09	Pestizides mittel
AT265743B (de)	1968-10-25	Schädlingsbekämpfungsmittel
DE3108182A1 (de)	1981-12-10	Xanthenonylester von phosphorsaeuren und phosphonsaeuren
DE1542993C3 (de)	1974-05-16	Verwendung von N-Cyanoalkylchloracetamiden als Pflanzenfungizide
DE1935758C (de)	1973-03-08	(Thio) Phosphonsaureester und ihre Verwendung als Wirkstoffe in Schädlings bekampfungsmitteln
CH664258A5 (de)	1988-02-29	Synergetische wirkstoffkombinationen enthaltende herbizide mittel.
Slife et al.	1979	Mechanisms of Selective and Nonselective Toxicities of Plant Protection Chemicals
DE2851025A1 (de)	1979-06-07	Insektizides mittel