DE527267C - Insecticides - Google Patents
InsecticidesInfo
- Publication number
- DE527267C DE527267C DE1930527267D DE527267DD DE527267C DE 527267 C DE527267 C DE 527267C DE 1930527267 D DE1930527267 D DE 1930527267D DE 527267D D DE527267D D DE 527267DD DE 527267 C DE527267 C DE 527267C
- Authority
- DE
- Germany
- Prior art keywords
- phenyl
- alkyl
- insecticides
- aralkyl
- halogen
- 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
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
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/02—Amines; Quaternary ammonium compounds
- A01N33/06—Nitrogen directly attached to an aromatic ring system
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
AUSGEGEBEN AM 15. JUNI 1931ISSUED ON JUNE 15, 1931
M 527267 KLASSE 451 GRUPPE M 527267 CLASS 451 GROUP
451 Ig.451 Ig.
Zusatz zum Patent 512Addition to patent 512
Durch Patent 512 361 sind Insektenvertilgungsmittel geschützt, die sekundäre oder tertiäre Amine enthalten, deren Stickstoffatom mit mindestens zwei Phenylresten verbunden ist, Verbindungen der allgemeinen Formel:By patent 512,361 are insecticides protected, which contain secondary or tertiary amines, whose nitrogen atom with at least two phenyl radicals are connected, compounds of the general formula:
Phenyl — N — Phenyl
I
RPhenyl - N - phenyl
I.
R.
R = H, Alkyl, Aralkyl, Phenyl, wobei Phenylreste durch Alkyl oder Halogen substituiert sein können.R = H, alkyl, aralkyl, phenyl, with phenyl radicals being substituted by alkyl or halogen can.
Wie weiter gefunden wurde, wird die Wirkung vergrößert, wenn ein Phenylrest durch einen Cyclohexylrest ersetzt wird, so daß Verbindun-1^ gen der allgemeinen Formel:As has been further found the effect is increased as a phenyl radical is replaced by a cyclohexyl group, so that Verbindun- 1 ^ gen of the general formula:
Phenyl —-N — CyclohexylPhenyl - N - cyclohexyl
entstehen, R = H, Alkyl, Cycloalkyl, Aralkyl, Aryl, wobei die Phenylreste beispielsweise durch Alkyl oder Halogen substituiert sein können.arise, R = H, alkyl, cycloalkyl, aralkyl, aryl, the phenyl radicals, for example by Alkyl or halogen can be substituted.
So zeigt z. B. PhenylcyclohexylmethylaminSo shows z. B. Phenylcyclohexylmethylamine
eine vorzügliche insektizide Wirkung, die diejenige der in dem Hauptpatent genannten Verbindungen noch weit übertrifft. Die Verbindungen selbst besitzen angenehmen Geruch und sind für Mensch und Tier völlig unschädlich. Insekten, ja sogar die sehr widerstandsfähigen Fliegen, werden z. B. durch Zerstäuben einer 25 "/„igen Lösung von Phenylcyclohexylmethylamin in einem geeigneten Medium bei Anwendung von 0,6— 1 ecm auf den Kubikmeter Raum in kürzester Zeit vollkommen abgetötet.an excellent insecticidal effect, that of the one mentioned in the main patent Connections far exceeds. The compounds themselves have a pleasant odor and are completely harmless to humans and animals. Insects, even the very tough ones Flies, z. B. by atomizing a 25 "/" solution of phenylcyclohexylmethylamine in a suitable medium, applying 0.6-1 ecm to the cubic meter Room completely killed in a very short time.
Als weitere Verbindungen der genannten Art seien beispielsweise genannt: Cyclohexylbenzylanilin, Cyclohexylchloranilin und Methylcyclohexylmethylanilin. Further compounds of the type mentioned may be mentioned, for example: Cyclohexylbenzylaniline, Cyclohexylchloroaniline and methylcyclohexylmethylaniline.
Die Mittel können in unvermischtem Zustande sowie als Lösung, Suspension oder Emulsion und, soweit sie fest sind, als Pulver, gegebenenfalls in Mischung mit anderen Insektiziden, zur Vernichtung von Ungeziefer jeglicher Art, wie Mücken, Fliegen, Schwaben, Läusen, Flöhen, Milben, angewendet werden.The agents can be in the unmixed state and as a solution, suspension or emulsion and, if they are solid, as a powder, optionally mixed with other insecticides Destruction of vermin of any kind, such as mosquitoes, flies, Swabians, lice, fleas, Mites.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE527267T | 1930-01-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
DE527267C true DE527267C (en) | 1931-06-15 |
Family
ID=6553255
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE1930527267D Expired DE527267C (en) | 1930-01-30 | 1930-01-30 | Insecticides |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE527267C (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2535922A (en) * | 1946-12-19 | 1950-12-26 | Shell Dev | Isophorone imines |
-
1930
- 1930-01-30 DE DE1930527267D patent/DE527267C/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2535922A (en) * | 1946-12-19 | 1950-12-26 | Shell Dev | Isophorone imines |
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