SU695522A3 - Insecticide composition - Google Patents

Insecticide composition

Info

Publication number
SU695522A3
SU695522A3 SU741994403A SU1994403A SU695522A3 SU 695522 A3 SU695522 A3 SU 695522A3 SU 741994403 A SU741994403 A SU 741994403A SU 1994403 A SU1994403 A SU 1994403A SU 695522 A3 SU695522 A3 SU 695522A3
Authority
SU
USSR - Soviet Union
Prior art keywords
propyl
insecticidal
butyl
compound
insecticide composition
Prior art date
Application number
SU741994403A
Other languages
Russian (ru)
Inventor
Кристианзен Одд
Original Assignee
Циба-Гейги Аг (Фирма)
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.)
Filing date
Publication date
Priority claimed from CH175673A external-priority patent/CH574713A5/en
Application filed by Циба-Гейги Аг (Фирма) filed Critical Циба-Гейги Аг (Фирма)
Application granted granted Critical
Publication of SU695522A3 publication Critical patent/SU695522A3/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N57/00Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
    • A01N57/10Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
    • A01N57/16Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing heterocyclic radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/553Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
    • C07F9/576Six-membered rings
    • C07F9/58Pyridine rings

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Pest Control & Pesticides (AREA)
  • Molecular Biology (AREA)
  • Agronomy & Crop Science (AREA)
  • Biochemistry (AREA)
  • Plant Pathology (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Description

(54) ИНСЕКТИЦИДНЫЙ СОСТАВ каны атомами С, простые эфира наприйе э дисэкеан i те рагидрофуран ; сл ные эфиры;этиловый эфир уксусной-ки Лоты йетоны ацетон,мётилэтилкетон, диэтидкетон, нитрилы; ацетонитрил и др. П р и м ер 1. Получение О-этил-Н-пропил-S- 2 ,б-дихлорпиридил-(3) .-метил1-дитиофосфата. 14 г 2,б-дихлоргтиколил-3-хлорид раствор ют в 150 мл ацетонитрила. В раствор ввод т по порци м 16,9 г калий-0-этил-8-Н-пропилдитиофосфата . Реакционную смесь перемешивают 16 ч Яри кейна йой температуре. После отгонки растворител  в :вво д т простой эфир промывают его вод и сушат сульфатом натри , свободным от воды. - Послеупаривани  простогоэфира получают соединение формулы CHj-gJcr s л 5СзН7(н} , к С1 с рефракцией Кд : 1,57 40. АналогичШМ стгосрбом можно и следующйе соединени :(54) INSECTICIDE COMPOSITION of the cana by C atoms, ethers, for example, e diskean i te rahydrofuran; solid esters; ethyl acetate; Lots of ions acetone, methyl ethyl ketone, diethy ketone, nitriles; acetonitrile and others. Example 1. Preparation of O-ethyl-N-propyl-S-2, b-dichloropyridyl- (3).-methyl 1-dithiophosphate. 14 g of 2, b-dichlorgicolyl-3-chloride is dissolved in 150 ml of acetonitrile. 16.9 g of potassium-0-ethyl-8-H-propyl dithiophosphate are introduced into the solution in portions. The reaction mixture is stirred for 16 hours. After distilling off the solvent, the simple ether is washed with water and dried over sodium sulfate, which is free of water. - After the simple evaporation of the ether, a compound of the formula CHj-gJcr s l 5СзН7 is obtained (n}, c1 with refraction cd: 1.57 40. Similarly, the following compound can be used with the same method:

СоединениеCompound

Смертность после 3 дней,%Mortality after 3 days,%

LeptinotarsaLeptinotarsa

Spodoptera Spodoptera

decemlineafca littoralis , Х1 ОП . CHi-S-P 5-СН-СНз 2о N 1,5530. Формы применени  пртепаратов обычные. . . Инсектицидное кишечноедействие. Посаженные в гсршки картофельные растени  в стадии 4-5 .листьев погружают в полученную из 10%-ного эмульгируемого концентрата 0, водную эмульсйю испытуемого соединени . После присыхани  осадка на растени хсажают по 5 личинок Spodoptera littoralis или Leptinotarsa decemline.ata встадии .iSj, ; Обработанные растени  покрывают йласт ическйм цилиндром,; заделанным сверху проволочной сетью, чтобы предотвратить уход личинок. . После 3 дней Уценивают смертность./ Результаты испытани-  приведены в аблице. . . : .Т а б л и ц аdecemlineafca littoralis, X1 OP. CHi-S-P 5-CH-CH3 2 N 1.5530. The application forms of the products are conventional. . . Insecticidal enteric effects. Planted potato plants in stage 4-5 of the sheet are immersed in a water emulsion of the test compound obtained from a 10% emulsifiable concentrate 0. After the sediment has dried on the plants, 5 Spodoptera littoralis or Leptinotarsa decemline.ata larvae of .iSj,; Treated plants are covered with a cylinder and a cylinder; wire netted over the top to prevent larvae from leaving. . After 3 days Mortality is exaggerated. . . : .T a b l and c a

,/Л, / L

. C. К-СзН.З. C. K-SzN.Z

-.1 хГЛ  -.1 xGL

::р-5-сн,-( -С1 H-CjH S у/ :: p-5-sn, - (-C1 H-CjH S y /

С1C1

гН50 г;:gN50 g ;:

VciVci

uao-CjH S uao-cjh s

ClCl

, flm-CjHyS Y-Hflm-CjHyS Y-H

ClCl

100100

100100

100100

100100

CJIsO S/CJIsO S /

P-S-CH,4 / CjHs-CH-S V -ffP-S-CH, 4 / CjHs-CH-S V -ff

ИзвестноеKnown

С2Н50 и/C2H50 and /

Р-0-СНгЧч /)R-0-SNGHH /)

Claims (2)

CiHgO Vjj Таким образом, предложенный инсек тицидный состав обладает ус.иленным инсектицидным действием, : Формула изобретени  Инсектицидный состав, содержздий действующее начало на основе пиридиновых производных тиофосфорных кис лот и добавки, . выбранные из группы носитель, разбавитель и наполнитель, о т. л и чающийс  тем/ что, с целью усилени  инсектицидного действи , он содержит в качестве пи ридинового производного тиЬфосфорной кислоты соединение формулы О ; p-s-cH,jCiHgO Vjj Thus, the proposed insecticidal composition possesses a strong insecticidal action,: Invention Insecticidal composition containing the active principle based on pyridine derivatives of thiophosphoric acids and additives,. selected from the group of carrier, diluent and filler, that is, and because, in order to enhance the insecticidal effect, it contains, as a pyridine derivative of phosphoric acid, a compound of the formula O; ps-cH, j Продолжение таблицыTable continuation 100100 100 где - пропил или бутил П - О или 2, в количестве О,1-95 вес,%. Приоритет по признакам: 07.02.73 при R- пропил, П- О „ или 2 . 20.12.73 при Х- бутил. Источники информации, прин тые во внимание при экспертизе 1. Патент ФРГ 1445739, кл. С 07F 9/58, опублик. 1972. 100 where - propyl or butyl P - O or 2, in the amount of O, 1-95 weight,%. Priority signs: 07.02.73 with R-propyl, П-О „or 2. 12.20.73 at X-butyl. Sources of information taken into account in the examination 1. The patent of Germany 1445739, cl. From 07F 9/58, published 1972. 2. Патент США № 3371095, кл. 260-294.8, опублик. 1968 (прототип ) .2. US Patent No. 3371095, cl. 260-294.8, publ. 1968 (prototype).
SU741994403A 1973-02-07 1974-02-01 Insecticide composition SU695522A3 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH175673A CH574713A5 (en) 1973-02-07 1973-02-07 s-Picolyl phosphoridithioates - useful as insecticides, acaricides and plant-growth regulators
CH1777473 1973-12-20

Publications (1)

Publication Number Publication Date
SU695522A3 true SU695522A3 (en) 1979-10-30

Family

ID=25688571

Family Applications (1)

Application Number Title Priority Date Filing Date
SU741994403A SU695522A3 (en) 1973-02-07 1974-02-01 Insecticide composition

Country Status (9)

Country Link
JP (1) JPS49109542A (en)
CA (1) CA1053238A (en)
DD (1) DD110751A5 (en)
DE (1) DE2405189A1 (en)
FR (1) FR2221459B1 (en)
GB (1) GB1456896A (en)
IL (1) IL44085A (en)
NL (1) NL7401207A (en)
SU (1) SU695522A3 (en)

Also Published As

Publication number Publication date
IL44085A0 (en) 1974-05-16
FR2221459B1 (en) 1978-01-06
JPS49109542A (en) 1974-10-18
DD110751A5 (en) 1975-01-12
GB1456896A (en) 1976-12-01
IL44085A (en) 1976-11-30
CA1053238A (en) 1979-04-24
FR2221459A1 (en) 1974-10-11
NL7401207A (en) 1974-08-09
DE2405189A1 (en) 1974-08-08

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