BE683901A - - Google Patents

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Publication number
BE683901A
BE683901A BE683901DA BE683901A BE 683901 A BE683901 A BE 683901A BE 683901D A BE683901D A BE 683901DA BE 683901 A BE683901 A BE 683901A
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BE
Belgium
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desc
weight
page number
clms page
parts
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French (fr)
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Publication of BE683901A publication Critical patent/BE683901A/fr

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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
    • A01N47/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/10Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
    • A01N47/22O-Aryl or S-Aryl esters thereof

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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)

Description

       

   <Desc/Clms Page number 1> 
 ayant pour   objet, :   Mélange insecticide , 

 <Desc/Clms Page number 2> 

 
 EMI2.1 
 I,a p':"30nt;J invention est relative à un mélange in80c- ' tic tso 'ju Z,:i 1.. i. quo l'on Pp.ut utiliser du néthyl-1-nphtyl ca:rb'1nt...', H)\1.,' combattre les .ri3ElCtLtN L'action de ce composé nt est '';:a.''.v;s?1"- pas 3Dtlsfoissnte. 



  On a constate qu'un mélamio contenant a} du i':"'f"'0';!1:,...1.-u8phtylcarbornatc, b) du 1:ali<x:,=;r:I; <1-i c.rrC,,.¯syle ou un solvant organique contenant m stj¯ :ât: '1"1 :x'ctz,.: -C0 %tl", c) un l ijr<1: ## .:i;:tk>#>.e arOITlDt Í4uO. et.' 
 EMI2.2 
 
 EMI2.3 
 d) un inï:1,c>i;tgc. d'un njunt tensio-nctif onionique et d'un agent tan .z.4rs:J. non. ionique, convient très bien pour combattre les ..m=j: j"3" ,:::S1n1C> solvant organique coix enant ou moins un groupe -CO-N"< ... I,..'.,t <:iw, par exompla,ie3 solvants solides ou li- 'j.. quiàùi c:a-..kF > parmi les cBrbonDrnidoe, la pyrrolidone ou les dé-'1 ;" t rivés ;.t:-..>, tels que la Ncnét?y'1-prrro¯idonQ-(2), le diméthyl- fornii;;I..1.3> " ,'1 Ü1.:>thyladtamido, la tétraméthylurÓe et les mes langes ''f .!:>' "..po.T3R :'un avec l'autre et/ou avec du sulfoxy.. j :? ,d(:.. .., f . 1 h ,'- ri: ".,.-. -" '.

   J ,,¯1 .; " .  w,:; .c;=: .arcs :ar rrr,a ir;u appropriés sont, par " , exemple 1", >;':;':-," '!'\'3 et. ses dérivez r!lky168, P;J):' exemple le talu8-r . ne, les divers 130<nbre- du xylèn0! 1*éthylbenzéne, lea di- et triéthy1benzèn')[1 .sc. i "H '1'; ro>,,alr,- :s et isomères, ainsi que les J " mélanges do ces <;J:1,¯ . 

 <Desc/Clms Page number 3> 

 



   Comme composée   tensio-actifs   anioniques, on peut citer, par exemple, les savons, les alkylbenzène   sulfonates   de métaux alcalino terreux, les alkylbenzène sulfonctes   d'ammonium '     1 alkyl- ! et les/benzène sulfonates d'ammonium substituée. Comme agents     tensio-actifs   non ioniques, on peut citer, par exemple, les produits d'oxéthylation d'huile de ricin, les amides d'acides gras, les alkylphénols et les alkylnaphtols. 



   Les quantités des divers composés (a) à (d) contenue dans les mélanges suivant la présente invention peuvent varier, 
Ainsi, mes mélanges peuvent renfermer 5 à 20,   e   préférence 10 à 15% en poids de l'ingrédient actif, N-méthyl-1-naphtylcarba-   mate, 5 à   70, de préférence 50 à 60% on poids du constituant (b), 5 à 60, da préférence 20 à 30% en poids du constituant (c) 
0,5 à 10, de préférence 3 à 6 % en poids du constituant (d). 



   Les proportions relatives des agents tensio-actifs anioniques et non ioniques dans le constituant (d) sont de 
0,1 à 2 :1, de préférence de   0,5 à   1 : 1, en poids. 



   Le   mélange   suivant la présente invention est   avanta-   geusement traité avec de l'eau et le liquide pulvérisable ainsi obtenu est utilisé de la manière usuelle en agriculture. Le rapport pondéral du mélange suivant   l'inventluu   à l'eau est. d'environ   1 :   100 à 2000, de préférence de 1:500, 
En plus des matières   indiquées   en (a)à (d), le mé- lange suivant la présente invention, peut encore renfermer des matières d'addition usuelles et connues, par exemple de   l'éther   octachlorodipropylique. 



   Les exemples suivants, dons lesquels les parties at les pourcentages sont en poids, indiquent la bonne activité du mélange suivant   l'i@@@tion.   Pour les   casais   nécessaires à cette fin, les préparations suivantes ont été   utilisées:     @   

 <Desc/Clms Page number 4> 

 
 EMI4.1 
 I. vr. N- méthyl i'-naphtylcarbamate connu du commerce / a été mêlant à \:ne m; l,ère solide inerte (argile), da manière ,<i à obtenir une xv:ro 'ilvériser contenant 10%. de matière le- '! tive, Cette 1.r,1,;;drf; r ensuite transformée, par addition d'eau, dans UM proportion de . 500, en une bouillie aqueuse de pulvé- . risutionj.

   A 1.!dA de quelle les essais ont été effectués. ,: II, On o pr'<pa'r'' jomme suit un thëlange suivant l'invention: J,1 10 parties ti t.ï...r,'HStI1Y' 11.-nDphtylcarbumote, 5 par t1ee d'agent 11 dmuloioon#," Ír,\ê ""C" l 'un agent tonsio-ectif anionique et d'un agent tt..l\:;;i(1...t:.;ti: noi:  .on.que dans un rapport pondéral de 1:1), 60 parties do ,'athf ;rolidanaw2, 20 parties d'un mélange dthydroQt1obux>O; Gl<Om9t hues (dérivés benzéniques)" 5 parties de 
 EMI4.2 
 xylône.. 
 EMI4.3 
 



  Cû cs> ¯,.skgc fa 4té transformé, par addition d'eau, dane une proportion de lis00, en une bouillie de pulvérisation aqueux- : se, à .L'a,d do laquelle les essais ont été effectués. III. Uns solution à lO de Nnéthyl-1-nophtylcorbamato donc' do z l'ac<Etnn#; ,; >Ft<à diluce avec de l'acétone pour obtenir la solu- tion d'ut.. . :û.a et j3 ét6 employée sous catte forme, 
 EMI4.4 
 " Q3931s suivants ont J16 effectués : Sxemple .,. :.;;a>3m commune (Muaca dcmestica) dans des boîtes de . ) : :1:;.1';;' d'un dianàtre da 10 cm, 2ximpi.# 2 - hfr:;:l.,O:1 du blé (Sitophilus groooris) dans des (.(',<1." '!) de ? tri de 10 cm de diamètre, ";xem;,;.: 7' . ',..'.'130,00 du bid (S1tophllu grenaria) sur plaquée . 
 EMI4.5 
 



  1 verre dépolies de 8 x 8 cm, Les j.',:wll totl5 sont indiq,u6t.\ aona fonte de LD 50 en ... m.,3,.,rmmcxda substunc1 t,a - .,alto ou plaque, 

 <Desc/Clms Page number 5> 

 
 EMI5.1 
 fil.,t"lPj,E 1 Mouches I;'(\i1''':1'i':;)':. ¯x.'s bettes do PC 4 : Substance ",,',1' l\";)! II III LD 50 j;ré:¯i z ¯;.=,ii.:=x 20 rriG (inactif' -;,9 ml!; 20 mg (inactif) LD 50 " 4 " 10 mg" < ,o mg 10 mg " LD 50 " 2J"t 11 30 ml]; 9r 1.,1 mg 14 mg " ±x81i>1Pi,± 2 Chorançc.;.i du bL>1 ;n boîtes de Pétri: Substance ;,c5.= ii, 11 II III LD 50 apr:5 1; h-iurca 5 , d rng 0,5$ nic 5.3 mag =.:xtP. J Charaiiço  #1>.> 01:5 sur pisques do verre : Substance -,r;ÂS,, 1 II III 
 EMI5.2 
 LD 50 aj,1 .#:" . ',:.h5 5 iogE i;actif> 4>iy mg 5 mg (inactif) 
 EMI5.3 
 a, ¯,1IC.s' i0N Sl',lat;;;, insecticide contenant 

**ATTENTION** fin du champ DESC peut contenir debut de CLMS **.



   <Desc / Clms Page number 1>
 having for object,: Insecticide mixture,

 <Desc / Clms Page number 2>

 
 EMI2.1
 I, a p ': "30nt; J invention relates to a mixture in80c-' tic tso 'ju Z,: i 1 .. i. Which one Pp.ut use of 1-methyl-nphtyl ca: rb' 1nt ... ', H) \ 1.,' Combat the .ri3ElCtLtN The action of this compound is '';: a. ''. V; s? 1 "- not 3Dtlsfoissnte.



  It was found that a melamine containing a} of i ': "' f" '0';! 1:, ... 1.-u8phtylcarbornatc, b) of 1: ali <x:, =; r: I; <1-i c.rrC ,,. ¯syl or an organic solvent containing m stj¯: ât: '1 "1: x'ctz,.: -C0% tl", c) un l ijr <1: ## .: i;: tk> #>. e arOITlDt Í4uO. and.'
 EMI2.2
 
 EMI2.3
 d) an ini: 1, c> i; tgc. of an onionic surfactant and a tan .z.4rs agent: J. no. ionic, very suitable for combating ..m = j: j "3", ::: S1n1C> organic solvent coix enant or less a group -CO-N "<... I, .. '., t < : iw, eg exompla, ie3 solid solvents or li- 'j .. quiàùi c: a - .. kF> among cBrbonDrnidoe, pyrrolidone or de-'1; " t riveted; .t: - ..>, such as Ncnét? y'1-prrrōidonQ- (2), dimethyl- fornii ;; I..1.3> ", '1 Ü1.:> thyladtamido, tetramethylurÓe and my diapers '' f.!:> '"..po.T3R:' one with the other and / or with sulfoxy .. j:? , d (: .. .., f. 1 h, '- ri: "., .-. -"'.

   J ,, ¯1.; Suitable ". w,:; .c; =:. arcs: ar rrr, a ir; u are, by", example 1 ",>; ':;': -," '!' \ '3 and. its derive r! lky168, P; J): 'example the talu8-r. ne, the various 130 <nbre- of xylen0! 1 * ethylbenzene, di- and triethylbenzen ') [1 .sc. i "H '1'; ro> ,, alr, -: s and isomers, as well as mixtures of these <; J: 1, ¯.

 <Desc / Clms Page number 3>

 



   As anionic surfactant compound, there may be mentioned, for example, soaps, alkaline earth metal alkylbenzenesulphonates, ammonium alkylbenzenesulphonates, 1 alkyl-! and substituted ammonium / benzene sulfonates. As nonionic surfactants, there may be mentioned, for example, the oxethylation products of castor oil, fatty acid amides, alkylphenols and alkylnaphthols.



   The amounts of the various compounds (a) to (d) contained in the mixtures according to the present invention can vary,
Thus, my mixtures may contain 5 to 20, preferably 10 to 15% by weight of the active ingredient, N-methyl-1-naphthylcarbamate, 5 to 70, preferably 50 to 60% by weight of component (b ), 5 to 60, preferably 20 to 30% by weight of component (c)
0.5 to 10, preferably 3 to 6% by weight of component (d).



   The relative proportions of anionic and nonionic surfactants in component (d) are
0.1 to 2: 1, preferably 0.5 to 1: 1, by weight.



   The mixture according to the present invention is advantageously treated with water and the sprayable liquid thus obtained is used in the usual manner in agriculture. The weight ratio of the mixture according to the invention to water is. from about 1: 100 to 2000, preferably from 1: 500,
In addition to the materials indicated in (a) to (d), the mixture according to the present invention may also contain customary and known additives, for example octachlorodipropyl ether.



   The following examples, in which parts and percentages are by weight, indicate the good activity of the mixture according to the invention. For the cases needed for this purpose, the following preparations were used: @

 <Desc / Clms Page number 4>

 
 EMI4.1
 I. vr. N-methyl i'-naphthylcarbamate known commercially / has been mixed with \: ne m; l, era inert solid (clay), so <i to obtain a xv: ro 'il spray containing 10%. of matter the- '! tive, This 1.r, 1, ;; drf; r then transformed, by addition of water, in UM proportion of. 500, to an aqueous pulverized slurry. risutionj.

   At 1.! DA from which the tests were carried out. ,: II, We o pr '<pa'r' 'jomme follows a thelange according to the invention: J, 1 10 parts ti t.ï ... r,' HStI1Y '11.-nDphtylcarbumote, 5 per t1ee d' agent 11 dmuloioon #, "Ír, \ ê" "C" l 'an anionic tonsio-ective agent and an agent tt..l \: ;; i (1 ... t:.; ti: noi:. that in a weight ratio of 1: 1), 60 parts of athf; rolidanaw2, 20 parts of a mixture of hydroQt1obux> O; Gl <Om9t hues (benzene derivatives) "5 parts of
 EMI4.2
 xylon ..
 EMI4.3
 



  Cû cs> ¯, .skgc fa 4té transformed, by addition of water, in a proportion of lis00, into an aqueous spray slurry-: se, to .L'a, d from which the tests were carried out. III. A lO solution of Nnethyl-1-nophthylcorbamato therefore 'do z the ac <Etnn #; ,; > Ft <diluted with acetone to obtain the solution of ut ... : û.a and j3 ét6 used in this form,
 EMI4.4
 "Q3931s have J16 carried out: Sxample.,.:. ;; a> 3m common (Muaca dcmestica) in boxes of.):: 1:;. 1 ';;' of a diameter of 10 cm, 2ximpi. # 2 - hfr:;: l., O: 1 of wheat (Sitophilus groooris) in (. (', <1. "'!) sorting of 10 cm of diameter, "; xem;,;.: 7 '.', .. '.' 130.00 of the bid (S1tophllu grenaria) on plated.
 EMI4.5
 



  1 frosted glass of 8 x 8 cm, The j. ',: wll totl5 are indicated, u6t. \ Aona cast of LD 50 in ... m., 3,., Rmmcxda substunc1 t, a -., Viola or plate ,

 <Desc / Clms Page number 5>

 
 EMI5.1
 fil., t "lPj, E 1 Flies I; '(\ i1' '': 1'i ':;)' :. ¯x.'s chard do PC 4: Substance" ,, ', 1' l \ ";)! II III LD 50 d; re: ¯iz ¯;. =, Ii.:=x 20 rriG (inactive '- ;, 9 ml !; 20 mg (inactive) LD 50" 4 "10 mg" < , o mg 10 mg "LD 50" 2J "t 11 30 ml]; 9r 1., 1 mg 14 mg" ± x81i> 1Pi, ± 2 Chorançc.;. i du bL> 1; n Petri dishes: Substance; , c5. = ii, 11 II III LD 50 apr: 5 1; h-iurca 5, d rng 0.5 $ nic 5.3 mag = .: xtP. J Charaiiço # 1>.> 01: 5 on glass pisks: Substance -, r; ÂS ,, 1 II III
 EMI5.2
 LD 50 aj, 1. #: ". ',:. H5 5 iogE i; active> 4> iy mg 5 mg (inactive)
 EMI5.3
 a, ¯, 1IC.s 'i0N Sl', lat ;;;, insecticide containing

** ATTENTION ** end of DESC field can contain start of CLMS **.


    

Claims (1)

EMI5.4 (0) du .',..m :.' ','ft--l...nl\;'!ltylc1'ri:)wT1Dte commnu ingrédient, actif, qaraet'j:)' -.':.' nfrme, su. ..i¯o;v>1,u8, (b) du sulfoxyde d d 1,n 1 1; hn-.i; > . , -; r: /: i G; u n i ù : jq ;> n ,i <, :,; ; r i: n 1. z r<n ,J n i=. > ià moins un :µi'oi.i... ,'".. ".,<" hy.'ro.'-jrbur n.ro;no#iquo et (d) un mé- langc ''-. i'-;i;-:.;; l t>?;x>1<-Jctif anµc>niqlàe et d'un aient ten- SiD*>5CÉllÎ : ,=l'i(1,..'ùlÔ **ATTENTION** fin du champ CLMS peut contenir debut de DESC **. EMI5.4 (0) from. ', .. m:.' ',' ft - l ... nl \; '! ltylc1'ri:) wT1Dte as ingredient, active, qaraet'j :)' -. ':.' nfrme, su. ..īo; v> 1, u8, (b) sulfoxide d d 1, n 1 1; hn-.i; >. , -; r: /: i G; u n i ù: jq;> n, i <,:,; ; r i: n 1. z r <n, J n i =. > i unless one: µi'oi.i ..., '".."., <"hy.'ro .'- jrbur n.ro; no # iquo and (d) a mixturec' '-. i '-; i; -:. ;; lt> ?; x> 1 <-Jctif anµc> niqlàe and one have ten- SiD *> 5CÉllÎ:, = i (1, ..' ùlÔ ** CAUTION ** end of field CLMS may contain start of DESC **.
BE683901D 1965-07-14 1966-07-08 BE683901A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEB0082826 1965-07-14

Publications (1)

Publication Number Publication Date
BE683901A true BE683901A (en) 1967-01-09

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3027767A1 (en) * 1979-07-27 1981-02-19 Montedison Spa SOLUTIONS AND FORMULATIONS OF CARBAMATE PESTICIDES

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3027767A1 (en) * 1979-07-27 1981-02-19 Montedison Spa SOLUTIONS AND FORMULATIONS OF CARBAMATE PESTICIDES

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