DE673138C - Insect repellants - Google Patents

Insect repellants

Info

Publication number
DE673138C
DE673138C DEI53569D DEI0053569D DE673138C DE 673138 C DE673138 C DE 673138C DE I53569 D DEI53569 D DE I53569D DE I0053569 D DEI0053569 D DE I0053569D DE 673138 C DE673138 C DE 673138C
Authority
DE
Germany
Prior art keywords
oxethylated
moles
insect repellants
effect
oxy
Prior art date
Legal status (The legal status 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 status listed.)
Expired
Application number
DEI53569D
Other languages
German (de)
Inventor
Dr Michael Erlenbach
Dr Kaspar Pfaff
Dr Wilhelm Staudermann
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie AG
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
Application filed by IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Priority to DEI53569D priority Critical patent/DE673138C/en
Application granted granted Critical
Publication of DE673138C publication Critical patent/DE673138C/en
Expired legal-status Critical Current

Links

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

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)

Description

Insektenbekämpfungsmittel Es ist bereits bekannt, organische, Oxy-, Carboxy- oder Aminogruppen enthaltende Verbindungen, in welche Polyglykoliätherreste mit vier oder mehr C@H,- Grüppen eingeführt sind, als Emulgiermittel für die Herstellung von Schädlingsbekämpfungsmitteln zu verwenden. Auch als Zusatz zu Schädlingsbekämpfungsmitteln, insbesondere solchen mit Polysulfidgehalt, z. B. der Schwefelkalkbrühe, sind derartige Verbindungen bereits benutzt worden. In allen Fällen wurde bisher lediglich die Emulgier- oder Netzwirkung der oxäthylierten Verbindungen ausgenutzt, um die Verwendung von insecticid oder fungicid wirkenden Stoffen zu ermöglichen oder deren Wirkung durch Erhöhung der Netzkraft zu verbessern.Insecticides It is already known to use organic, oxy, Compounds containing carboxy or amino groups, in which polyglycol ether residues with four or more C @ H, groups are introduced as emulsifiers for production of pesticides to use. Also as an additive to pesticides, especially those with polysulfide content, e.g. B. the sulphurous lime broth are such Connections have already been used. In all cases, only the Emulsifying or wetting effect of the oxyethylated compounds exploited to the use of insecticidal or fungicidal substances or their effect to improve by increasing the power of the network.

Es wurde nun gefunden, daß organische, Oxy-, Carboxy-, Amino- oder Amidogruppen enthaltende Verbindungen, auf welche t bis I2 Mol Alkylenoxyd je Molekül zur Einwirkung gelangt sind, und in denen gegebenenfalls die im Reaktionsprodukt etwa noch vorhandenen freien Hydroxylgruppen mit reaktionsfähigen Verbindungen umgesetzt sind, allein mit besonderem Vorteil als Kontaktgifte gegen Insekten Verwendung finden können. Sie eignen sich z. B. zur Vernichtung von saugenden Insekten, wie Blattläusen, und fressenden Raupen, wie Goldafter-, Frostspannerraupen und Heu- und Sauerwurm.It has now been found that organic, oxy, carboxy, amino or Compounds containing amido groups to which t to 12 moles of alkylene oxide per molecule have come into effect, and in which, where appropriate, those in the reaction product any remaining free hydroxyl groups reacted with reactive compounds are used alone with particular advantage as contact poisons against insects can. They are suitable e.g. B. to destroy sucking insects such as aphids, and eating caterpillars, such as golden oyster caterpillars, frost worm caterpillars, and hayworms and sourworms.

In Frage kommen beispielsweise oxäthylierter D,odecylalkohol, oxäthylierte Ölsäure, oxäthyliertes Anilin, oxäthyliertes Oleylamin, oxäthyliertes Stearylamid, oxäthyliertes Kokosfettsäureamid, oxäthyliertes Isooctylphenol, das Natriumsalz des Phosphorsäureesters dieser Verbindung, das Natriumsalz des sauren Schwefelsäureesters des oxäthylierten Isooctylphenols oder das Natriumsalz des Phosphorsäureesters des oxäthylierten Dodecylalkohols. Zur Bekämpfung von Blattläusen genügt z. B. D-odecylalkohol mit 8 Mol Äthylenoxyd in o,2oioiger Konzentration, ölsäure mit 6 Mol Äthylenoxyd in o,4oloiger Konzentration und Kokosfettsäureäthanolamid mit 3 Mol Äthylenoxyd in o, r %iger Konzentration.For example, oxethylated D, odecyl alcohol, oxethylated come into question Oleic acid, oxethylated aniline, oxethylated oleylamine, oxethylated stearylamide, oxethylated coconut fatty acid amide, oxethylated isooctylphenol, the sodium salt of the phosphoric acid ester of this compound, the sodium salt of the acid sulfuric acid ester of the oxyethylated isooctylphenol or the sodium salt of the phosphoric acid ester oxethylated dodecyl alcohol. To control aphids z. B. D-odecyl alcohol with 8 moles of ethylene oxide in o.2oioiger concentration, oleic acid with 6 moles of ethylene oxide in o, 4oloiger concentration and coconut fatty acid ethanolamide with 3 moles of ethylene oxide in o, r% concentration.

Claims (1)

PATENTANSPRUCH: Verwendung organischer, Oxy-, Carboxy-, Amino- oder Amidogruppen enthaltender Verbindungen, auf Welche i bis 12 Mol Alkylenoxyd je Molekül zur Ein-Wirkung gelangt sind, und in denen gegebenenfalls die im Reaktionsprodukt etwa noch vorhandenen freien Hydroxylgruppen mit reaktionsfähigen Verbindungen umgesetzt sind, als Insektenbekämpfungsmittel.PATENT CLAIM: Use of organic, oxy, carboxy, amino or Compounds containing amido groups, to which 1 to 12 moles of alkylene oxide per molecule have come into effect, and in which, if necessary, those in the reaction product any remaining free hydroxyl groups reacted with reactive compounds are used as insecticides.
DEI53569D 1935-11-05 1935-11-06 Insect repellants Expired DE673138C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DEI53569D DE673138C (en) 1935-11-05 1935-11-06 Insect repellants

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE222497X 1935-11-05
DEI53569D DE673138C (en) 1935-11-05 1935-11-06 Insect repellants

Publications (1)

Publication Number Publication Date
DE673138C true DE673138C (en) 1939-03-17

Family

ID=25763299

Family Applications (1)

Application Number Title Priority Date Filing Date
DEI53569D Expired DE673138C (en) 1935-11-05 1935-11-06 Insect repellants

Country Status (1)

Country Link
DE (1) DE673138C (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2710496A1 (en) * 1993-10-01 1995-04-07 James Lynn Sue Compositions of insecticides and insect repellents containing ethanolamine compounds.

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2710496A1 (en) * 1993-10-01 1995-04-07 James Lynn Sue Compositions of insecticides and insect repellents containing ethanolamine compounds.
NL9401569A (en) * 1993-10-01 1995-05-01 Lynn Sue James Insecticide and insect repellent compositions.
BE1009621A5 (en) * 1993-10-01 1997-06-03 Lynn Sue James COMPOSITIONS OF INSECTICIDES AND INSECT REPELLENTS.

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