CS252895B1 - High Q, O-dimethyl-O- (3-methyl-4-nitrophenyl) thiophosphate emulsion concentrate - Google Patents

High Q, O-dimethyl-O- (3-methyl-4-nitrophenyl) thiophosphate emulsion concentrate Download PDF

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CS252895B1
CS252895B1 CS861092A CS109286A CS252895B1 CS 252895 B1 CS252895 B1 CS 252895B1 CS 861092 A CS861092 A CS 861092A CS 109286 A CS109286 A CS 109286A CS 252895 B1 CS252895 B1 CS 252895B1
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Czechoslovakia
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thiophosphate
dimethyl
methyl
emulsion concentrate
nitrophenyl
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CS861092A
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Czech (cs)
Slovak (sk)
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CS109286A1 (en
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Robert Poor
Lubomira Zakova
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Robert Poor
Lubomira Zakova
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Priority to CS861092A priority Critical patent/CS252895B1/en
Publication of CS109286A1 publication Critical patent/CS109286A1/en
Publication of CS252895B1 publication Critical patent/CS252895B1/en

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Abstract

Riešenie sa týká finalizácie insekticidu. Rieši emulzný koncentrát s vysokým obsa ­ hom O,O-dimetyi-O- ( 3-metyl-4-nitrofenyl )- -tiofiosfátu (fenitrotinu) v xyléne a v pří ­ tomnosti zmesi aniónaktívnych a katoaktív- ny-Cih povrchovoaiktívnycih látok obsahujú ­cich i butanol.The solution concerns the finalization of an insecticide. It concerns an emulsion concentrate with a high content of O,O-dimethyl-O-(3-methyl-4-nitrophenyl)-thiophosphate (fenitrotin) in xylene and in the presence of a mixture of anionic and cationic surfactants containing butanol.

Description

Vynález rieši finalizáciu 0,0-dimetyl-0-(3-metyl-4-nitro-fenylJ-tiofosfátu -do formy emulzného -koncentrátu obsahujúceho 65 až 85 % hmotnoetných fenitrotinu, 4 — 6 °/o xylenu a 11 — 15 % zmesi anionoaktívnych a kationových pov-rchovoaktívnych látolk obsa-hujúcich 10 až 20 % hmot, butanolu.The invention solves the finalization of O, O-dimethyl-O- (3-methyl-4-nitro-phenyl) -thiophosphate to form an emulsion-concentrate containing 65 to 85% by weight of phenitrotin, 4-6% xylene and 11-15% of the mixture % of anionic and cationic surfactants containing 10 to 20 wt.% butanol.

Post-rekový emulzný príp-ravoik -na báze 0,0-'dimethyl-0-(3-metyl-4-nitr-o-fenyl)-tiofosfátu (fenitrotinu) s přísadou emulgátorov a -organických rozpúšťadiel sa fln-allzuje do formy emulzného koncentrátu obsahujúceho 50 % hmot. účinnej látlky a je uvádzaný pod názvom Metation E 50.The post-emulsion preparation based on O, O-dimethyl-O- (3-methyl-4-nitr-o-phenyl) -thiophosphate (phenitrotin) with the addition of emulsifiers and -organic solvents is incorporated into the form % of an emulsion concentrate containing 50 wt. of the active substance and is referred to as Metation E 50.

Emulzný koncentrát Metation E 50 obsahujúci účinnú látku fenitrotion sa používá po na-riedení vodou -v 0,1 — 0,2-% koncemtrácii. Vyznačuje sa širokým spektro-m účinku, nízkou toxicitou -voči te-plofcrvným ži-v-očíchom a je určený na ničeinie molíc, vošiek, ciikád, mér, her-νον, -piliarok, mravcov, ploštíc, ihúseníc vo -veterinárnom sektore na ničenie múch, komárov, vší, š-váb-ov aj rezistentních voči chlórovaným inseikticídom.Metation E 50 emulsion concentrate containing the active substance fenitrotion is used after dilution with water at a concentration of 0.1-0.2%. It is characterized by a broad spectrum of action, low toxicity to warm-blooded eyes, and is intended for the destruction of whiteflies, aphids, cicadas, measures, herpes, ants, ants, bugs, mosquitoes in the veterinary sector on the control of flies, mosquitoes, lice, cockroaches and those resistant to chlorinated insecticides.

Emulzný koncentrát na báze fenitrotionu sa finalizuje za použitia organického rozpúšťadla emulgáto-rov typu Sl-ovanik M 640, Slovazol EL, Abeson CaX a za použitia tecihnickej účinnej látky 93 až 95-% čistoty. Výsledný produkt po finalizácii obsahuje 47,5 až 52,5 % fenitrotionu 10 %.The phenitrotion emulsion concentrate is finalized using an organic solvent of emulsifiers of the Slovanik M 640 type, Slovazol EL, Abeson CaX, and using the active ingredient 93-95% purity. The final product after finalization contained 47.5 to 52.5% phenitrotion 10%.

Zistili sme, že O,O-'dimetyl-O-(3-imetyl-4-nitrofenylj-tiofosfát možno finalizovať -do formy emulzného koncentrátu obsahujúceho 65 až 85 % hmot. fenitrotionu, 4 — 6 % xylenu a 11 — 15 °/o ih-m-ot. zmesi anio-no-a-ktívnych a kationových povrchovoaktí-vnych látoik obsahujúcich 10 — 20 % hmot. butanolu.We have found that O, O-dimethyl-O- (3-methyl-4-nitrophenyl) thiophosphate can be finalized to form an emulsion concentrate containing 65 to 85% by weight of phenitrotion, 4 - 6% of xylene and 11 - 15%. % of a mixture of anionic-a-active and cationic surfactants containing 10-20% by weight of butanol.

Zmes anionoaktívnych a kationových povrchových láto-k s vyme-dzeným obsahom 'butanolu má hustotu stano-venú pri 20 °C 995 kg/.m3 a vis-kozitu v rozme-dzí 580 až 680, prevažne 600 MPa . s.The mixture of anionic and cationic surfactants with a limited butanol content has a density determined at 20 ° C of 995 kg / m 3 and a viscosity in the range of 580 to 680, predominantly 600 MPa. with.

Finalizáciou uvedených láto-k pri teiplote miestnosti p-očas 30 až 60 minút sa získá emulzný koncentrát s .požadovaným obsahom účinných látoik pri splnění -podmienky nevylúčenia krému.Finalization of these substances at room temperature for a period of 30 to 60 minutes gives an emulsion concentrate having the desired content of active substances while satisfying the condition of non-exclusion of the cream.

Výhodou navrhovaného riešenia -podlá pre-dmetu vynálezu je inovácia výrobku s vyšším obsahom účinnej látky o 30 % h-motnostných oproti doposial' využívanému spósobu výroby. Ďalšou výhodou je úspora organického rozpúšťa-dla pri -výrobě emulzného- koncentrátu, a-ko aj pri jeho- aplikácii. Pri aplikácii rovnaké-ho množst-va účinnej látky dochádza -k úspoře obalo-v.An advantage of the proposed solution according to the invention is the innovation of a product with a higher active substance content by 30% by weight compared to the production method used hitherto. A further advantage is the saving of organic solvent in the manufacture of the emulsion concentrate, as in its application. Applying the same amount of active ingredient results in savings in packaging.

Výhodou navrhovaného riešenia je i to, že finalizáciu fenitrotionu s obsahom účinnej látky 65 — 85 % možno uskutočniť na výrobno-m zariadení, ktoré sa -používá na výrobu emulzného- -koncentrátu obsahujúceho 50 % fenitrotionu. Z-nížením množstva rozpúšťa-dla na finalizáciu fenitrotionu 65 až 85 % umožňuje zvýšiť výr-obnú kapacitu zariadenia. Výhody pre-dmetu vynálezu dokumentujú nasle-dujúce p-rlklady iprevedenia:An advantage of the proposed solution is that the finalization of phenitrotion with an active ingredient content of 65-85% can be carried out on a production plant which is used to produce an emulsion concentrate containing 50% phenitrotion. By reducing the amount of solvent to finalize phenitrotion by 65 to 85%, it makes it possible to increase the production capacity of the plant. The advantages of the subject matter of the invention are illustrated by the following examples and examples:

Příklad 1Example 1

Do 1 500 ml banky sa -nadávkovalo- 777,7 ml 94-% fenitrotionu [O,O-dimetyl-O-(3-metyl-á-nit-rofenylj-tiofosfá-t] a za miešania pri te-plote miestnosti sa -přidalo 72 ml xylénu. Ďalej sa za miešania pri-dalo 150 g Berolu 949, t. j. zmes anionoaktívnych a kationových povrchovoaktí-vnych látok, o-bsahujúca aj 10 — 20 % -butanolu, pričom jej vis-kozita pri 20- °C je okolo 600 mPa . s a hustota pri 20 GC je 995 kg/m3. Z-mes sa miešala pri teplotě miestnosti 1 hodinu. O-do-b-raná vzor-ka sa analyzovala metodou -plynovej cihromatografie, obsahovala 82,5 % fenitrotionu, pričom -bola stanovená nulová hodnota krému vo vzor-ke.777.7 ml of 94-% phenitrotione [O, O-dimethyl-O- (3-methyl-a-nitrophenyl) thiophosphate] was charged to a 1500 ml flask and stirred at room temperature with stirring. 72 ml of xylene were added and 150 g of Berol 949, i.e. a mixture of anionic and cationic surfactants, also containing 10-20% butanol, were added with stirring, and its viscosity at 20 ° C was about 600 mPa., the density at 20 G C is 995 kg / m 3. Off-months was stirred at room temperature for 1 hour. O-into-a-ka-early pattern was analyzed by -gas cihromatografie, containing 82.5% fenitrotion, wherein the cream value in the sample was zero.

P r í k 1 a -d 2Example 1 and -d 2

V poku-se sa postupovalo analogicky -aik-o v příklade 1, pričom -s-a zvýšila násada xylénu tak, aby výsledný produkt obsahoval 65 % účinnej látky fenitrotionu. D-o baníky sa nadávkoval naj-pr-v xylén, -potom fenitroti-on a na závěr Berol 949. O-dobraná vzorka obsahovala 65 % hmot. fenitrotionu 100 % a hodnota krému -bola nulová.The experiment was carried out analogously to -aik-o in Example 1, with -s-a increasing the xylene feed so that the resulting product contained 65% of the active ingredient fenitrotion. D-mines were dosed first-in-xylene, then fenitro-on, and finally Berol 949. The sample was 65% by weight. fenitrotion 100% and the cream value - zero.

Vynález sa dá využit -pri výrobě fenit-rotionu a jeho finalizácii na emulzný -koncentrát.The invention can be used in the production of fenitrotione and its finalization into an emulsion concentrate.

Claims (1)

PREDMET Emulzný koncentrát s vysokým obsahom O,O-dimetyl-O- (3-metyl-4-nitr of enyl j -tiofosfátu, vyznačený tým, že obsahuje 65 až 85 % hmot. O,O-dimetyl-O-(3-metyl-4-nitrofemylj-tiofosfátu, 4 — 6 % hmot. xyléinu a 11 — 15 % hmot. zmesi anionaktívnych a VYNALEZU toation-ak-tívnych povrchovoaktívnych látok obsahujúci 10 až 20 % hmot. butanolu, pričom hustota tejto zmesi pri 20 °C je 995 ikg/ /m3 a viskozita pri 20 °C je 580 až 680 mPa. . s.SUBSTANCE Emulsion concentrate high in O, O-dimethyl-O- (3-methyl-4-nitrophenyl) thiophosphate, characterized in that it contains 65 to 85% O, O-dimethyl-O- (3- methyl 4-nitrophemyl thiophosphate, 4 - 6 wt.% xylene and 11 - 15 wt.% anionic and DISCHARGE toation-active surfactants containing 10 to 20 wt.% butanol, the density of which at 20 ° C is 995 µg / m 3 and the viscosity at 20 ° C is 580 to 680 mPa · s.
CS861092A 1986-02-17 1986-02-17 High Q, O-dimethyl-O- (3-methyl-4-nitrophenyl) thiophosphate emulsion concentrate CS252895B1 (en)

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CS252895B1 true CS252895B1 (en) 1987-10-15

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