SU713522A3 - Insecticidic composition - Google Patents

Insecticidic composition Download PDF

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Publication number
SU713522A3
SU713522A3 SU762415057A SU2415057A SU713522A3 SU 713522 A3 SU713522 A3 SU 713522A3 SU 762415057 A SU762415057 A SU 762415057A SU 2415057 A SU2415057 A SU 2415057A SU 713522 A3 SU713522 A3 SU 713522A3
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SU
USSR - Soviet Union
Prior art keywords
pesticide
active
active ingredient
derivative
compound
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Application number
SU762415057A
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Russian (ru)
Inventor
Шнайдер Руперт
Original Assignee
Сандос Аг (Фирма)
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Application filed by Сандос Аг (Фирма) filed Critical Сандос Аг (Фирма)
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Publication of SU713522A3 publication Critical patent/SU713522A3/en

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    • 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
    • A01N41/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom
    • A01N41/12Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom not containing sulfur-to-oxygen bonds, e.g. polysulfides

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  • 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)

Abstract

The pesticide contains as active component at least one compound of the formula I <IMAGE> in which R1 and R2 individually are methyl or ethyl or together, along with the nitrogen atom, are pyrrolidine, piperidine or morpholine. The active ingredient can be prepared by two process variants. The pesticide has a strong insecticidal, acaricidal and fungicidal action. As an insecticide, it acts on contact and ingestion as well as systemically. The pesticide is particularly suitable for controlling pests in which a certain duration of action of the applied active ingredients is required. The pesticide is applied as a liquid spray, as a dusting powder, as granules, as a paste or as an aerosol. The formulations can contain from 1 to 90% by weight of active ingredient.

Description

(54) ИНСЕКТИЦИДНОЕ СРЕДСТВО(54) INSECTICIDE MEANS

Изобрстенне относитс  к хнмическим средствам защиты растений, а нменно к ннсоктицидиому средству на основе производного N,N%uiMeTnnaMHHonponaHa. Изр.естсн ннсектицид, действующим началом которого  вл етс  1,3-бис-(карбамонлтио ) -2- (X,N-димeтнлaми o) -проиан, гидрохлорид (картап, иадан) 1. Однако нзвестный иисектицид недостаточно активен. Це.лыо изобретени   вл етс  изыскаН1 е нового инсектнцидиого средетва, обладаюHtero высокой инсектнцидиой активностью. Указанна  цель достигаетс  исиользованием писектшдидного средства, активным вещеетвом которого  вл етс  1,3-бис (грег-бутилдитио) - 2-днметнламннонроиан форму.1Ы S - -CfiH;); -$-CltH3)j в виде свооодного осиованн  или солей - гндрооксалата, гидро.хлорида. Содержание активного вещества в средетве от 0,02 до 90 вее. %. Соединение формулы I и его соли нолучают взаимодействием соединени  формулы ::: L - остаток S -Ri, нричем RI - алкил , арил, т 0,1, или L - остаток SOsMi, где - калий, натрий с соединением формулы ( СИз)зС5М2 М2-кали11, натрий, а в конкретном случае иутем иеревода в кислую со.ть. Таким образом получают следующие соединени : 1.1.3 - .быс-(грег-бути.тдптио) - 2-диметнламшю-иронан , т. пл. 45°С. 2.Гидрооксалат ,3-бис - (гр г-бутплдит11о )-2-диметилами1Юиронан. т. нл. 114- 115°С. 3.Гидрохлорид 1,3-бис-(грег-бутилтно)2-диметиламннопроиан , т. ил. 158°С. Формы ирнменени  средств обычные; гранулы, аэрозоли, смачивающиес  порощKii . Их получаю методами --oonuiMii iipa изготоилспип лрепиратпвпых фозхм пестицидов .The image refers to chemical plant protection products, and, in particular, to an nnsocticidioma based on the N, N% uiMeTnnaMHHonponaHa derivative. A known insecticide, the active principle of which is 1,3-bis- (carbamolthio) -2- (X, N-dimethyl) o) -proian, hydrochloride (cartap, iadan) 1. However, the well-known insecticide is not sufficiently active. The purpose of the invention is to find a new insecticide medium, having Htero high insecticidal activity. This goal is achieved through the use of a PCIT agent whose active substance is 1,3-bis (Greg-butyldithio) - 2-day methylamino-Neuro form 1x S - -CfiH;); - $ - CltH3) j in the form of free axis oiovann or salts - gdroksalata, hydro. Chloride. The content of the active substance in the medium is from 0.02 to 90 ve. % The compound of formula I and its salts are obtained by reacting a compound of the formula: ::: L - the residue is S -Ri, while RI is alkyl, aryl, m 0.1, or L is the residue SOsMi, where is potassium, sodium with the compound of the formula (SIS) sC5M2 M2-Kali11, sodium, and in the specific case and by the addition of irevod to acid so.t. Thus, the following compounds are obtained: 1.1.3 - .bys- (greg-buti.tdptio) - 2-dimethyl-ironan, m. Pl. 45 ° C. 2. Hydrooxalate, 3-bis - (g g-butpldith 11o) -2-dimethylamide 1 Yuronan. so nl 114-115 ° C. 3. Hydrochloride 1,3-bis- (greg-butyltno) 2-dimethylamine, t. Il. 158 ° C. Forms of conventional means; granules, aerosols, wettable powdersKii. I get them with the methods --oonuiMii iipa izgotilsippe lrepiratpvpyh pesticides.

Пример 1. 1 liiecKiiiiutUioe де 1ет1М1е.Example 1. 1 liiecKiiiiutUioe de 1Т1М1е.

Петри диаметром 7 мм обрыз 1Ь вают 0,4 мл )еии, в концентрации 10 часте; |/м:1Н. акт |вно1о еоединени , иод .тежаиюго neiibiraiHio. После сушки в течение 4 ч 30 аееком1 1Х иенытуем(,мх) вида по метают в и закрывают ме.чко сеткой . Пасекомым ие дают н;пци. Через 72 ч подсчитывают чис.то мер1вв1х паеекомых. Petri with a diameter of 7 mm bite the lip with a volume of 0.4 ml), at a concentration of 10 parts; | / m: 1H. Actu ally, iodine neiibiraiHio. After drying for 4 h 30 aecom1 1X, yenuten (, mx) of the species is thrown in and closed with a mesh. Patekami not give n; After 72 h, count the number of measures in 1 in 1 paecomas.

Дл  каждого исг1ытуемого активного еоедннеии  и дл  каждо1-о вида насекомых чис;10 чаетс на 1 млн. акти1 ного еосдииенн  измен ют до 95%-ного уннчтожеии  иасеко.мых.For each active species being consumed and for each insect species number, 10 times per 1 million of the active species is changed to 95% of the total number of insects.

В качестве cpaoiieHiui иснол1 зуют изопроиилгомо .тог третичного еоед 111енн  бутила (соединение Л) н торговьи нреиарат- иисектцццд картагт.As cpaoiieHiui, the isopropyltomy of the tertiary alcohol butyl (compound L) and the trade of narayarathiscountry cartes is considered one.

Результатв нснытанин приведеив вта6;1. 1, 2 н 3.Result in the introduction of vsnytanin vta6; 1. 1, 2 n 3.

Т а б л и ц а IT a b l and c a I

KajnaiiKajnaii

Sp ;djpteraSp; djptera

AnagastaAnagasta

TcncbrioTcncbrio

TriboliuiiiTriboliuiii

SitphilusSitphilus

AcantosCLlidesAcantosCLlides

Таким образом, нредложенные соединени  об-ладангт xopouieii иисектлцнднон акТИВИОСТ1ЛО .Thus, the proposed compounds of the olagant xopouieii and the electrolyte of aktiviotlo.

Фор м у л а II 3 о б р е т С) и  Form m lol II 3 about b r e C) and

Пнсектнцидиое средство, содержащее производное N,N-димeтилaминoIIpoнaиa какPssektsidiye tool containing a derivative of N, N-dimethylaminoIIponaia

активное вещество н добавку, выбранную из грунны, вк;почаюн1ен твердви носнте.тв, |)астворите.11), поверхностно-активный агент, о т;: и ч а ю И1 е с с   тем, что, с целвю усилени  инсектицндной активности, оно содержит в качестве производного Х.М-днметиламиионроиаиа 1,3-и/«:-(7рег-бутнлдитио ) - 2-димети;1ам11нонрона11 фо).му,1В1active substance n additive selected from soil, VK; every day it is hardened by nosnte.tv, |) a solution; 11), surface-active agent, o t; A: and with the aim of enhancing insecticidal activity , it contains as a derivative H.M-dnmethyamionioiaia 1,3-and / ":-( 7reg-butnldithio) - 2-dimeti; 1am11nonron11 pho) .mu, 1В1

-.-$-ClCH3)j -.- $ - ClCH3) j

CHj - -CCH}ljCHj - -CCH} lj

UHjUhj

ii.;:ii его соли - гидрооксалат, гидрохлорид, и)ичем содержанне активного венхсства в средстве от 0.02 до 90 вес. %.ii.;: ii its salts are hydroxalate, hydrochloride, and i) the content of active venhsstvo in the product from 0.02 to 90 wt. %

Псточникн iiiK|)OjiMaiuiH, прин тые во внимание iij) экснертизс 1. Me.iBHHKOB П. П. Хими  и техио.тоги  пестицидов, М., «.Хими , 1974. с. 342 (прототип ) .Pstuchny iiiK |) OjiMaiuiH, taken into consideration iij) exerties 1. Me.iBHHKOB P.P. Chemistry and technical pesticides, M., “. Chemie, 1974. p. 342 (prototype).

Claims (1)

Инсектицидное средство, содержащее производное Ν,Ν-диметиламинопроиапа как активное вещество и добавку, выбранную из группы, включающей твердый носитель, р а ст вор и тел ь, поверхностно-активный агент, отличающееся тем, что, с целью усиления инсектицидной активности, оно соΉ держит в качестве производного Ν,Ν-диметилампнопропана 1,3-бис- (трет-бутилдитио) - 2-диметиламиноиропап формулы An insecticidal agent containing a derivative of Ν, Ν-dimethylaminoproiap as an active substance and an additive selected from the group consisting of a solid carrier, a solution and a body, a surface-active agent, characterized in that, in order to enhance insecticidal activity, it contains holds as a derivative of Ν, Ν-dimethylampnopropane 1,3-bis- (tert-butyldithio) - 2-dimethylamino-pyrope formula CHj бн5 шт его соли — гидрооксалат, гидрохлорид, причем содержание активного вещества в средстве от 0.02 до 90 вес. °ό·CHj bn 5 pcs of its salt - hydroxylate, hydrochloride, and the active substance content in the agent is from 0.02 to 90 weight. ° ό
SU762415057A 1974-10-25 1976-10-28 Insecticidic composition SU713522A3 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH1431274A CH607741A5 (en) 1974-10-25 1974-10-25 Pesticide, and the use thereof for controlling insects

Publications (1)

Publication Number Publication Date
SU713522A3 true SU713522A3 (en) 1980-01-30

Family

ID=4399768

Family Applications (2)

Application Number Title Priority Date Filing Date
SU752183107A SU619103A3 (en) 1974-10-25 1975-10-23 Method of obtaining 1,3-bis-(tret.butyldithio)-2-dimethylaminopropane or its acid salts
SU762415057A SU713522A3 (en) 1974-10-25 1976-10-28 Insecticidic composition

Family Applications Before (1)

Application Number Title Priority Date Filing Date
SU752183107A SU619103A3 (en) 1974-10-25 1975-10-23 Method of obtaining 1,3-bis-(tret.butyldithio)-2-dimethylaminopropane or its acid salts

Country Status (27)

Country Link
JP (1) JPS5167724A (en)
AR (1) AR215424A1 (en)
AT (1) AT352091B (en)
AU (1) AU500951B2 (en)
BE (1) BE834812A (en)
BR (1) BR7506960A (en)
CA (1) CA1065345A (en)
CH (1) CH607741A5 (en)
DD (2) DD129146A5 (en)
DE (1) DE2546891A1 (en)
DK (1) DK139816B (en)
EG (1) EG12155A (en)
ES (1) ES442013A1 (en)
FR (1) FR2289496A1 (en)
GB (1) GB1513560A (en)
GR (1) GR58589B (en)
HU (1) HU172715B (en)
IE (1) IE41817B1 (en)
IL (1) IL48356A (en)
IT (1) IT1043648B (en)
NL (1) NL7512321A (en)
PL (2) PL97681B1 (en)
RO (1) RO68807A (en)
SE (1) SE7511705L (en)
SU (2) SU619103A3 (en)
TR (1) TR19032A (en)
ZA (1) ZA756704B (en)

Also Published As

Publication number Publication date
CH607741A5 (en) 1978-10-31
IE41817B1 (en) 1980-03-26
JPS5167724A (en) 1976-06-11
DD129146A5 (en) 1978-01-04
ZA756704B (en) 1977-05-25
RO68807A (en) 1980-08-15
DD123326A5 (en) 1976-12-12
FR2289496A1 (en) 1976-05-28
DE2546891A1 (en) 1976-04-29
SU619103A3 (en) 1978-08-05
ATA807575A (en) 1979-02-15
AU8598475A (en) 1977-04-28
CA1065345A (en) 1979-10-30
IL48356A (en) 1979-05-31
AT352091B (en) 1979-08-27
GB1513560A (en) 1978-06-07
AU500951B2 (en) 1979-06-07
IT1043648B (en) 1980-02-29
EG12155A (en) 1978-06-30
PL96642B1 (en) 1978-01-31
DK139816C (en) 1979-10-22
FR2289496B1 (en) 1979-07-13
GR58589B (en) 1977-11-10
SE7511705L (en) 1976-04-26
DK139816B (en) 1979-04-23
PL97681B1 (en) 1978-03-30
TR19032A (en) 1978-02-06
NL7512321A (en) 1976-04-27
HU172715B (en) 1978-11-28
ES442013A1 (en) 1977-06-16
AR215424A1 (en) 1979-10-15
BE834812A (en) 1976-04-23
DK466575A (en) 1976-04-26
IL48356A0 (en) 1975-12-31
BR7506960A (en) 1976-08-17
IE41817L (en) 1976-04-25

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