DE693207C - Pest repellants - Google Patents
Pest repellantsInfo
- Publication number
- DE693207C DE693207C DE1936Z0023344 DEZ0023344D DE693207C DE 693207 C DE693207 C DE 693207C DE 1936Z0023344 DE1936Z0023344 DE 1936Z0023344 DE Z0023344 D DEZ0023344 D DE Z0023344D DE 693207 C DE693207 C DE 693207C
- Authority
- DE
- Germany
- Prior art keywords
- sulfur
- compounds
- parts
- reaction products
- isocyclic
- 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
- 241000607479 Yersinia pestis Species 0.000 title claims description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 8
- 229910052717 sulfur Inorganic materials 0.000 claims description 7
- 239000011593 sulfur Substances 0.000 claims description 7
- 239000007795 chemical reaction product Substances 0.000 claims description 6
- 150000001298 alcohols Chemical class 0.000 claims description 4
- 150000001636 bornane derivatives Chemical class 0.000 claims description 3
- 238000006243 chemical reaction Methods 0.000 claims description 3
- 150000002736 metal compounds Chemical class 0.000 claims description 3
- 239000000575 pesticide Substances 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 238000000034 method Methods 0.000 claims 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- 239000012084 conversion product Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 150000003464 sulfur compounds Chemical class 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 241000283690 Bos taurus Species 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- QGJOPFRUJISHPQ-NJFSPNSNSA-N carbon disulfide-14c Chemical compound S=[14C]=S QGJOPFRUJISHPQ-NJFSPNSNSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 229920001021 polysulfide Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 2
- 150000003568 thioethers Chemical class 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical compound C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 1
- SNICXCGAKADSCV-JTQLQIEISA-N (-)-Nicotine Chemical compound CN1CCC[C@H]1C1=CC=CN=C1 SNICXCGAKADSCV-JTQLQIEISA-N 0.000 description 1
- 229930006727 (-)-endo-fenchol Natural products 0.000 description 1
- REPVLJRCJUVQFA-UHFFFAOYSA-N (-)-isopinocampheol Natural products C1C(O)C(C)C2C(C)(C)C1C2 REPVLJRCJUVQFA-UHFFFAOYSA-N 0.000 description 1
- -1 B. mercury salts Chemical class 0.000 description 1
- IAIHUHQCLTYTSF-MRTMQBJTSA-N Fenchyl alcohol Chemical compound C1C[C@]2(C)[C@H](O)C(C)(C)[C@H]1C2 IAIHUHQCLTYTSF-MRTMQBJTSA-N 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001495 arsenic compounds Chemical class 0.000 description 1
- CKDOCTFBFTVPSN-UHFFFAOYSA-N borneol Natural products C1CC2(C)C(C)CC1C2(C)C CKDOCTFBFTVPSN-UHFFFAOYSA-N 0.000 description 1
- 229940116229 borneol Drugs 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- 150000002019 disulfides Chemical class 0.000 description 1
- DTGKSKDOIYIVQL-UHFFFAOYSA-N dl-isoborneol Natural products C1CC2(C)C(O)CC1C2(C)C DTGKSKDOIYIVQL-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- IAIHUHQCLTYTSF-UHFFFAOYSA-N fenchyl alcohol Natural products C1CC2(C)C(O)C(C)(C)C1C2 IAIHUHQCLTYTSF-UHFFFAOYSA-N 0.000 description 1
- 239000003502 gasoline Substances 0.000 description 1
- 229940093920 gynecological arsenic compound Drugs 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000002730 mercury Chemical class 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- APVPOHHVBBYQAV-UHFFFAOYSA-N n-(4-aminophenyl)sulfonyloctadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NS(=O)(=O)C1=CC=C(N)C=C1 APVPOHHVBBYQAV-UHFFFAOYSA-N 0.000 description 1
- 229960002715 nicotine Drugs 0.000 description 1
- SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Natural products CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 description 1
- 239000011022 opal Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000005077 polysulfide Substances 0.000 description 1
- 150000008117 polysulfides Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
Schädlingsbekämpfungsmittel Es ist bekannt, daß Schwefel in isocyclischen Alkoholen der Camphanreihe, wie in Fenchyl-und Isofenchylalkohol, löslich ist, ohne daß eine chemische Umsetzung stattfindet.Pesticides It is known that sulfur is present in isocyclic Alcohols of the camphane series, such as in fenchyl and isofenchyl alcohol, are soluble without that a chemical reaction takes place.
Setzt man aber derartige Lösungen längere Zeit höheren Temperaturen aus, indem man sie unter Rückfluß und bzw. oder unter Druck erwärmt, so tritt zwischen dem Schwefel und dem angewendeten isocyclischen Alkohol eine chemische Umsetzung ein. Zur Umsetzung kann man auch ein Gemisch. verschiedener isocyclischer Alkohole verwenden.However, if such solutions are used at higher temperatures for a longer period of time by heating them under reflux and / or under pressure, so occurs between a chemical reaction between the sulfur and the isocyclic alcohol used a. A mixture can also be used for implementation. various isocyclic alcohols use.
Die Umsetzungsprodukte stellen ein Gemisch verschiedenartiger chemischer Körper dar; hauptsächlich bestehen sie" aus Thioverbindungen verschiedenster Art, z. B. Thioalkoholen, Thioäthern, Di- und Polysulfiden.The reaction products represent a mixture of different chemical substances Body represent; they mainly consist of "various kinds of thio compounds, z. B. thioalcohols, thioethers, disulfides and polysulfides.
Die Umsetzungsprodukte sind unlöslich in Wasser, lassen sich aber in den verschiedensten organischen Lösungsmitteln, wie Benzol, Nitrobenzol, Toluol, Ligroinoder Schwefelkohlenstoff, lösen.The reaction products are insoluble in water, but can in various organic solvents such as benzene, nitrobenzene, toluene, Ligroin or carbon disulfide, dissolve.
Da organische Lösungsmittel, wie Benzin, Petroleum oder Schwefelkohlenstoff, selbst zur Schädlingsbekämpfung verwendet werden, kann man deren Wirkung durch Auflösen dieser Umsetzungsprodukte steigern. Man kann aber auch die Umsetzungsprodukte selbst zur Schädlingsbekämpfung verwenden, indem man beispielsweise diejenigen Umsiet'zungsprodukte, welche in öliger Form anfallen, von indifferenten Stoffen, wie Fullererde, 'aufsaugen läßt und das Gemisch verstäubt; man kann aber auch die Umsetzungsprodukte z. B. in Benzol lösen und diese Lösung mit Seifen oder seifenähnlich wirkenden Stoffen. (sulf. ölen, Tran, Harzen, Fettalkoholen, u. dg1. mehr) vermischen. Derartige Lösungen bzw. Emulsionen eignen sich zum Verspritzen, zuin Einreiben, Pinseln und zur Viehwäsche.Since organic solvents such as gasoline, petroleum or carbon disulfide, are even used for pest control, you can see their effect by dissolving of these conversion products. But you can also use the conversion products themselves use for pest control by, for example, those conversion products which occur in oily form, soak up inert substances such as fuller's earth leaves and dusts the mixture; but you can also use the reaction products z. B. Dissolve in benzene and this solution with soaps or soap-like substances. (sulf. oils, oil, resins, fatty alcohols, etc.) mix. Such solutions or emulsions are suitable for spraying, rubbing in, brushing and for washing cattle.
Die erhaltenen Umsetzungsprodukte lassen sich, wenigstens teilweise, weiterhin mit Metallsalzen, z. B. Quecksilbersalzen, zu Metallverbindungen umsetzen. Die auf diese Weise erhältlichen Verbindungen sind ebenfalls versprüh- oder verstäubbar.The reaction products obtained can be, at least in part, continue with metal salts, e.g. B. mercury salts, convert to metal compounds. The compounds obtainable in this way can also be sprayed or dusted.
Beispiele i. ioo Teile Fenchylalkohol werden mit 4o Teilen Schwefel 8 bis io Stunden unter Rückfluß auf Zoo bis 22o° erwärmt. Das Umsetzungsprodukt wird in 2 i o Teilen Benzol gelöst und mit 35o Teilen eines sulfonierten öles, z. B. Türkischrotöl 5o0%, gemischt. Das anfallende Produkt löst sich opal in Wasser.Examples i. 100 parts of fenchyl alcohol are mixed with 40 parts of sulfur Refluxed for 8 to 10 hours at zoo to 22o °. The conversion product is dissolved in 2 i o parts of benzene and 35o parts of a sulfonated oil, for. B. Turkish red oil 50%, mixed. The resulting product dissolves opal in water.
2. io Teile Borneol werden mit 5 Teilen Schwefel io Stunden unter Druck auf 22o° erwärmt; das anfallende Umsetzungsprodukt wird in 35 Teilen Steinkohlenteeröl gelöst und mit 5o Teilen Harzseife vermischt. Das Mittel eignet sich zum Verspritzen vorzugsweise auf Pflanzen und zur Viehwäsche.2. 10 parts of borneol are mixed with 5 parts of sulfur for 10 hours Pressure heated to 220 °; the resulting conversion product is in 35 parts of coal tar oil dissolved and mixed with 50 parts of resin soap. The middle is suitable for spraying preferably on plants and for washing cattle.
3: Einem trockenen Gemisch von Schwefel, Nicotin und bzw. oder Arsenverbindungen oder anderen trockenen Schädlingsbekämpfungsmitteln werden geringe bis überwiegende Anteile an Metallverbindungen der Umsetzungsprodukte von Schwefel mit isocyclischen Alkoholen der Camphanreihe zugesetzt. Die erhaltenen Mittel werden, besonders zum Pflanzenschutz, verstäubt.3: A dry mixture of sulfur, nicotine and / or arsenic compounds or other dry pesticides will be minor to predominant Fraction of metal compounds of the reaction products of sulfur with isocyclic Added to alcohols of the camphane series. The funds received are, especially for Plant protection, dusted.
Es sind zwar bereits die verschiedenartigsten Thioalkohole und Thioäther sowie andere organische Thio- und Polysulfidverbindungen zur Schädlingsbekämpfung vorgeschlagen wor= den. Diesen bekannten Schwefelverbhidungen gegenüber zeichnen sich die .erfindungsgemäß zu verwendenden Schwefelverbindungen dadurch aus, daß ihre Herstellung in überraschend einfacher Weise durchgeführt werden kann. Die erfindungsgemäß zu verwendenden Schwefelverbindungen sind, itn Gegensatt zu den ebenfalls verhältnismäßig leicht herzustellenden kolloidalen Lösungen von elementarem Schwefel, beständig gegen atmosphärische Einflüsse. Gegenüber anderen bekannten, gegen atmosphärische Einflüsse beständigen Schwefelverbindungen weisen sie den Vorteil auf, daß sie wasserunlöslich sind und infolgedessen ein verhältnismäßig hohes Haftvermögen besitzen. Die Wasserunlöslichkeit hindert dabei jedoch nicht, daß sie mit geeigneten Suspensionsmitteln in Form. wäßriger Suspensionen angewendet iverden könnerii.There are already the most varied of thioalcohols and thioethers as well as other organic thio and polysulphide compounds for pest control has been suggested. Draw against these well-known sulfur compounds the sulfur compounds to be used according to the invention are characterized in that their production can be carried out in a surprisingly simple manner. According to the invention Sulfur compounds to be used are, itn opposite to the likewise proportionate easy to prepare colloidal solutions of elemental sulfur, resistant against atmospheric influences. Against other well-known, against atmospheric Sulfur compounds resistant to influences have the advantage that they are insoluble in water are and consequently have a relatively high adhesive strength. The insolubility in water does not, however, prevent them from being in shape with suitable suspending agents. more watery Suspensions applied iverden kannnerii.
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE1936Z0023344 DE693207C (en) | 1936-08-05 | 1936-08-05 | Pest repellants |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE1936Z0023344 DE693207C (en) | 1936-08-05 | 1936-08-05 | Pest repellants |
Publications (1)
Publication Number | Publication Date |
---|---|
DE693207C true DE693207C (en) | 1940-08-20 |
Family
ID=7625876
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE1936Z0023344 Expired DE693207C (en) | 1936-08-05 | 1936-08-05 | Pest repellants |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE693207C (en) |
-
1936
- 1936-08-05 DE DE1936Z0023344 patent/DE693207C/en not_active Expired
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