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DE852176C - Insecticides - Google Patents

Insecticides

Info

Publication number
DE852176C
DE852176C DEB39A DEB0000039A DE852176C DE 852176 C DE852176 C DE 852176C DE B39 A DEB39 A DE B39A DE B0000039 A DEB0000039 A DE B0000039A DE 852176 C DE852176 C DE 852176C
Authority
DE
Germany
Prior art keywords
parts
insecticides
allyl radical
hexachlorocyclohexane
mixture
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
DEB39A
Other languages
German (de)
Inventor
Herbert Dr Stummeyer
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.)
BASF SE
Original Assignee
BASF SE
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 BASF SE filed Critical BASF SE
Priority to DEB39A priority Critical patent/DE852176C/en
Application granted granted Critical
Publication of DE852176C publication Critical patent/DE852176C/en
Expired legal-status Critical Current

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
    • A01N25/00Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/02Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Toxicology (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Agronomy & Crop Science (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Description

Pur eine erfolgreiche Anwendung der in neuerer Zeit l>ekanntgwordenen, als Berührungsgifte wirkenden Insektizide, wie Hexachlorcyclohexan, Dichlordiphenyltrichloräthan und ähnlich zusammengesetzter Verbindungen, ist es insbesondere bei ihrer Anwendung gegen saugende Insekten erforderlich, sie in sehr fein verteilter Form, am besten in einer zu verspritzenden Flüssigkeit, zur Einwirkung zu bringen. Da diese Stoffe in Wasser nicht oder schwer löslich sind, hat man vensucht, sie mit Hilfe von Dispergiermitteln in wäßrige Suspensionen ül>erzuführen.Purely a successful application of those that have recently become known to act as poisons to the touch Insecticides such as hexachlorocyclohexane, dichlorodiphenyltrichloroethane and compounds of a similar composition, it is particularly necessary when they are used against sucking insects, in a very finely divided form, ideally in a liquid to be sprayed, for action bring. Since these substances are insoluble or only sparingly soluble in water, one has tried to use them of dispersants in aqueous suspensions.

Es wurde nun gefunden, daß Lösungen der genannten Insektizide, insbesondere halogenierter Kohlenwasserstoffe, in nichtaromatischen Sekundaren oder tertiären Aminen oder Carbonsäureamiden, die am Stickstoffatom mindestens einen Allylrest oder einen substituierten Allylrest tragen, sich zur Herstellung wäßriger Emulsionen sehr gut eignen und daß solche Emulsionen Insektenvertilgungsmittel von ausgezeichneter Wirksamkeit und genereller Anwendbarkeit darstellen. Amine und Carbonsäureamide der genannten Art haben nicht nur ein gutes Lösungsvermögen gegenüber den genannten Kontaktinsektiziden, sondern sie sind auch selbst Insektizide.It has now been found that solutions of the insecticides mentioned, especially halogenated ones Hydrocarbons, in non-aromatic secondary or tertiary amines or carboxamides, which carry at least one allyl radical or a substituted allyl radical on the nitrogen atom to The preparation of aqueous emulsions is very suitable and that such emulsions are insecticides of excellent effectiveness and general applicability. Amines and carboxamides of the type mentioned not only have a good ability to solve the problems mentioned Contact insecticides, but they are also insecticides themselves.

Die Herstellung der Spritzftüssigikeiten erfolgt in ■ sehr einfacher Weise, indem man der Lösung einThe production of the Spritzftüssigikeiten takes place in ■ a very simple manner by adding the solution

Emulgiermittel, ζ. B. ein oxSthyliertes (Alkylnaphthol, zusetzt und dieses Gemisch mit der erforderlichen Menge Wasser versetzt. Die Haltbarkeit der Emulsion kann dadurch erhöht werden, daß man außer dem Emulgiermittel toben eine untergeordnete Menge Mineralöl zufügt.Emulsifier, ζ. B. an oxSthylated (alkylnaphthol, added and this mixture mixed with the required amount of water Emulsion can be increased by raging a subordinate one in addition to the emulsifier Add amount of mineral oil.

Beispiele:Examples:

i. 22,3 Teile /-Hexachlorcyclohexan werden in 33>7Teilen N-Formyl-N-methylällylcyclohexylamtn gelöst Der Lösung werden 31,3 Teile eines durch Umsetzung von Hexylheptylnaphthol mit Äthylenoxyd erhaltenen Emulgiermittels und 12,7 Teile Die^ selöl zugesetzt. Diese Mischung stellt in 0,075- bis »5 o,3%iger wäßriger Emulsion ein fsehr wirksames Insekten'bekämpfungsmittel dar. i. 22.3 parts of hexachlorocyclohexane are dissolved in 33> 7 parts of N-formyl-N-methylällylcyclohexylamtn. 31.3 parts of an emulsifying agent obtained by reacting hexylheptylnaphthol with ethylene oxide and 12.7 parts of diesel oil are added to the solution. This mixture is in 0.075 to "5 o, 3% aqueous emulsion, a very effective Insekten'bekämpfungsmittel f represents.

(Anstatt von /-Hexachlorcyclohexan kann man auch von Phenylchlorphenyltrichloräthan oder von Dichlordiphenyltrichloräthan ausgehen, ao 2. 18,8 Teile /^Hexachlorcyclohexan werden in einer Mischung von 8,5 Teilen N-iFormyl-N-dimethylallylamin und 25,6 Teilen N-iAcetyl-N-dimethylallylamin gelöst. Der Lösung werden 11,8 Teile eines Emulgiermittels und 35,3 Teile Dieselöl zugesetzt. Diese Mischung stellt in 0,1- bis o,3°/»iger wäßriger Emulsion ein sehr wirksames Insektenbekämpfungsmittel dar. (Instead of / -hexachlorocyclohexane one can also start from phenylchlorophenyltrichloroethane or from dichlorodiphenyltrichloroethane, ao 2. 18.8 parts / ^ hexachlorocyclohexane are mixed in a mixture of 8.5 parts N-iFormyl-N-dimethylallylamine and 25.6 parts N-acetyl 11.8 parts of an emulsifying agent and 35.3 parts of diesel oil are added to the solution . In 0.1 to 0.3% aqueous emulsion, this mixture is a very effective insect control agent.

3. 29,1 Teile /-Hexachlorcyclohexan werden in 23,9 Teilen NiAcetyl-N-methylällylcyclohexylamin gelöst. Der Lösung werden 30,6 Teile eines Emulgiermittels und 16,4 Teile Dieselöl zugesetzt. Diese Mischung stellt in 0,05- bis o,2°/oiger wäßriger Emulsion ein sehr wirksames Insektenbekämpfungsmittel dar. 3. 29.1 parts of hexachlorocyclohexane are dissolved in 23.9 parts of NiAcetyl-N-methylällylcyclohexylamine. To the solution are added 30.6 parts of an emulsifying agent and 16.4 parts of diesel oil. This mixture is a very effective insect control agent in 0.05 to 0.2% aqueous emulsion.

Claims (1)

PATENTANSPRUCH:PATENT CLAIM: Verwendung der Lösungen von als Benührungsgifte wirkenden Insektiziden, insbeson- « dere von halogenierten Kohlenwasserstoffen, in flüssigen, nichtaromatischen sekundären oder tertiären Aminen oder Carbonsäureamiden, die am Stickstoffatom mindestens einen Allylrest oder substituierten Allylrest tragen, als Wirkstoffe für die Bereitung von wäßrigen Emulsionen für die Insektenvertilgung. Use of the solutions of insecticides acting as toxins, in particular halogenated hydrocarbons, in liquid, non-aromatic secondary or tertiary amines or carboxamides, which carry at least one allyl radical or substituted allyl radical on the nitrogen atom, as active ingredients for the preparation of aqueous emulsions for the destruction of insects . Angezogene Druckschriften: Britische Patentschrift Nr. 615 137.Referred publications: British Patent No. 615 137. O 5395 10.O 5395 10.
DEB39A 1949-10-06 1949-10-06 Insecticides Expired DE852176C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DEB39A DE852176C (en) 1949-10-06 1949-10-06 Insecticides

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEB39A DE852176C (en) 1949-10-06 1949-10-06 Insecticides

Publications (1)

Publication Number Publication Date
DE852176C true DE852176C (en) 1952-10-13

Family

ID=6951663

Family Applications (1)

Application Number Title Priority Date Filing Date
DEB39A Expired DE852176C (en) 1949-10-06 1949-10-06 Insecticides

Country Status (1)

Country Link
DE (1) DE852176C (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1044501B (en) * 1955-06-22 1958-11-20 Glaxo Lab Ltd Process for the production of stable solutions of griseofulvin in organic solvents for fungicidal purposes

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB615137A (en) * 1946-07-27 1949-01-03 Geigy Ag J R Manufacture of amides of ª‡,ª‰-unsaturated carboxylic acids

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB615137A (en) * 1946-07-27 1949-01-03 Geigy Ag J R Manufacture of amides of ª‡,ª‰-unsaturated carboxylic acids

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1044501B (en) * 1955-06-22 1958-11-20 Glaxo Lab Ltd Process for the production of stable solutions of griseofulvin in organic solvents for fungicidal purposes

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