DE1802375A1 - Fungicidal mixtures - Google Patents
Fungicidal mixturesInfo
- Publication number
- DE1802375A1 DE1802375A1 DE19681802375 DE1802375A DE1802375A1 DE 1802375 A1 DE1802375 A1 DE 1802375A1 DE 19681802375 DE19681802375 DE 19681802375 DE 1802375 A DE1802375 A DE 1802375A DE 1802375 A1 DE1802375 A1 DE 1802375A1
- Authority
- DE
- Germany
- Prior art keywords
- compound
- denotes
- formula
- compounds
- chlorine
- 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.)
- Pending
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
- A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
- A01N59/16—Heavy metals; Compounds thereof
-
- 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
- A01N55/00—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur
- A01N55/02—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur containing metal atoms
-
- 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
- A01N2300/00—Combinations or mixtures of active ingredients covered by classes A01N27/00 - A01N65/48 with other active or formulation relevant ingredients, e.g. specific carrier materials or surfactants, covered by classes A01N25/00 - A01N65/48
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Inorganic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
BOEHRIIiGER SOHN9 INGELHEIM AM RHEIITBOEHRIIiGER SON 9 INGELHEIM AM RHEIIT
Fungizide MischungenFungicidal mixtures
Es ist bekannt, daß Organozinnkomplexe mit pentakoordinigrten Zinn fungizide Wirkung besitzen« Pur die Bekämpfung phytopathogener Pilze sind diese Verbindungen häufig nicht geeignet, da sie, Tor allem bei empfindlicheren Pflanzen, zu stark phytotoxisch wirken,. Es let weiterhin bekannt, daß Metallsalze der Alkylenbisdithiocarbaminsäuren fungizid wirken und nur wenig phytotoxisch sind.It is known that organotin complexes with pentacoordinigten Tin has fungicidal effects «Purely the fight against phytopathogenic These compounds are often unsuitable for fungi, as they are particularly suitable for more sensitive plants have a strong phytotoxic effect. Let it continue to be known that Metal salts of alkylenebisdithiocarbamic acids have a fungicidal effect and are only slightly phytotoxic.
Wie nun gefunden wurde, 1st es überraschenderweise möglich, die Phytotoxizität von Zinnkouplexverbindungen der allgemeinen FormelAs has now been found, is it surprisingly possible the phytotoxicity of tin complex compounds of the general formula
SnII ^Jn- J^Kmt^J + (I) 009845/1882SnII ^ J n - J ^ Kmt ^ J + (I) 009845/1882
duroh Zusats τοη Alkylenbisdithioearbamaten der allgemeinen Formelduroh Zusats τοη Alkylenbisdithioearbamaten of the general formula
B-OH-HH-CSS ^B-OH-HH-CSS ^
\ (ID\ (ID
CH2-HH-OSS^CH 2 -HH-OSS ^
erheblich au verbessern. Zusätzlich ztigt eich bei der fungisiden Wirkung ein synergistiseher Effekt.improve significantly au. In addition, calibrates the fungicidal effect a synergistic effect.
[tat] * ein substituierte? Ammonium-, Phosphonium- oder Sulfoniumkation,[did] * a substituted? Ammonium, phosphonium or Sulfonium cation,
η 0 oder 1 und L Chlor* Broa oder Bhodanid» falla η gleich 1 iat» und einen Liganden ait einer Blektreaendonatorgruppe dea Typeη 0 or 1 and L chlorine * Broa or Bhodanid »falla η equal 1 iat »and a ligand with a Blektreaendonatorgruppe of the type
=P - 0 oder^TS » 0, fall· η gltioh 0 ist.= P - 0 or ^ TS »0, case η is equal to 0.
In den Verbindungen der Formel II bedeutet R ein Wasserstoff ate» oder eine Methylgruppe und He Zink» Mangan oder Eisen oder Mischungen davon·In the compounds of the formula II, R denotes a hydrogen or a methyl group and He denotes zinc or manganese Iron or mixtures thereof
Als Misohungskoaponenten eignen sieh besonders Verbindungen der Porael I, in denen η gleioh 1 ist und QtatJ + für •in Phoephoniumkation steht (insbesondere Verbindungen gemag der DAS 1 227 905). eowie al· Verbindungen der for« ■el II ZinkÄthyl*nbiSkhioeerba«at (Zineb), Maneb und Mangan-Zinkäthylenbiajthioearbaaat (Manooieb.)· Bewähr« hat eieh Tor all·« «in·Compounds of Porael I, in which η equals 1 and QtatJ + stands for • in Phoephoniumkation (in particular compounds according to DAS 1 227 905), are particularly suitable as misalignment components. eowie al · compounds of the for «■ el II zinc ethyl * nbiSkhioeerba« at (Zineb), Maneb and Mangan-Zinkäthylenbiajthioearbaaat (Manooieb.) · Proven has eieh Tor all · «« in ·
6 OfRiQtNAL6 OfRiQtNAL
009845/1882009845/1882
«= 3 —«= 3 -
Mischung aus Triphenyl-decyl-phosphonium-[triphenyl--bromchlor-stannatJ(Decafentin) und Manganäthylenbisdithiocarbamat (Maneb)o Mixture of triphenyl decyl phosphonium [triphenyl bromochlorostannate] (decafentine) and manganese ethylene bisdithiocarbamate (Maneb) or similar
Die Verbindungen der Formeln I und II sind bekannt, z«,B0 aus den deutschen AusiegeSchriften 1 215 709, 1216 30O9 1 219 028, 1 219 029, 1 222 950 und 1 22? 905, ferner aus der USA-Patentschrift 3 311 648 und der belgischen Patentschrift 686 314oThe compounds of formulas I and II are known, "eg, B 0 from the German AusiegeSchriften 1,215,709, 1216 30O 9 1,219,028, 1,219,029, 1,222,950 and 1 22? 905, furthermore from the USA patent specification 3 311 648 and the Belgian patent specification 686 314o
Die Mengenverhältnisse der Verbindungen I und II in den erfindungsgemäßen Mischungen betragen etwa 5 : 1 bis etwa 1 sThe proportions of the compounds I and II in the mixtures according to the invention are from about 5: 1 to about 1 s
Für die Anwendung werden d. a erfindungsgemäßen Wirketoffkombi-. nationen in üblicher Weise mit den gebräuchlichen Hilfe- und Trägerstoffen verarbeitete Als Anwendungeformen eignen sich beispielsweise Suspensionspulver, Granulate, Streupulver» Derartige Mittel können z„Bo wie folgt zusammengesetzt sein;For the application d. a active ingredient combination according to the invention. nations in the usual way with the usual help and Carrier materials processed as application forms are suitable for example suspension powder, granules, scattering powder »Such agents can be composed as follows;
Zu sammensetzung:Composition:
50 io Wirkstoffgemisch gemäß der Erfindung 40 i» Kaolin50 io active ingredient mixture according to the invention 40 i » kaolin
9 i> LigninsuIfonat (Dispergiermittel) 1 # Natriumtetrapropylenbenzolsulfonat (Netzmittel)9 i> LigninsuIfonat (dispersant) 1 # Natriumtetrapropylenbenzolsulfonat (wetting agent)
Die Bestandteile werden vermählen und die Mischung für die Anwendung in der ...gewünschten Menge WaeBer suspendiert.The ingredients are ground and the mixture for the Use in the ... desired amount of WaeBer suspended.
00Θ845/188200Θ845 / 1882
Zusammensetzung?Composition?
2 % Wirkstoff gemäß der Erfindung 97 i° TalkiäJED2 % active ingredient according to the invention 97 i ° TalkiäJED
1 $> Methylzellulose1 $> methyl cellulose
Die Bestandteile werden zur Herstellung des Stäubemittels homogen vermählen0 The components are ground homogeneously to produce the dusting agent 0
Die geringere Toxizität der erfindungsgemäßen Mischungen gegenüber den reinen Zinnverbindungen geht aus den folgender... Gegenüberstellungen hervor«, Die Benotung der Pflanzenschäden erfolgt gemäß dem System der Biologischen Bundes=- anstalt mit den Noten 1 bis 9? wobei 1 = keine Schaden9 9 = Pflanze vernichtet bedeuteteThe lower toxicity of the mixtures according to the invention compared to the pure tin compounds can be seen from the following ... where 1 = no damage 9 9 = plant meant destroyed
Die Dosis wird ausgedrückt in ppm der Zinnverbindung, Maneb wird zusätzlich gegebene Tomaten, feuchte Aufstellung,,The dose is expressed in ppm of the tin compound, Maneb is additionally given tomatoes, moist arrangement,
der Iv-rmulierung W wivicsTÖff in
the Iv-rmulation
der Zinnverbindung
1000 500 250 125 63Applied dose in ppm
the tin compound
1000 500 250 125 63
fentiiiDeca-
fentiii
2010
20th
3 2 2 2 22 2 2 2 2
3 2 2 2 2
5050
50
009845/ 1882009845/1882
Bei troclrener Aufstellung der Tomaten wurden auch, von 1000 ppm der Mittel keine Pflanzenachäden verursacht.When the tomatoes were placed in a dry place, from 1000 ppm of the agent does not cause any plant damage.
Teilweiser Ersatz von Decafentin durch Manebo Tomaten, feuchte Aufstellung.Partial replacement of decafentine with manebo tomatoes, damp installation.
der Formulierung
Decafentin Maneb 1> active ingredient in
the formulation
Decafentin Maneb
1520dose
1520
1015in ppm
1015
67£ 450of the preparation
67 pounds 450
20
3010
20th
30th
2,0
2,02.0
2.0
2.0
40
4040
40
40
2,0
2,0• 3 s 0
2.0
2.0
2,0
2903.0
2.0
2 9 0
2,0
2,02.0
2.0
2.0
2,0
2,02.0
2.0
2.0
2,0
2,02.0
2.0
2.0
Gemäß Tabelle 2 wird schon durch den Ersatz von 20 "fo des Decafentins in der Mischung durch die gleiche Menge Maneb eine deutliche Verbesserung der Verträglichkeit erzielt; diese kann durch Erhöhung des Manebgehalts noch weiter verbessert werdenβAccording to Table 2 is already by replacing 20 "fo the Decafentins in the mixture by the same amount maneb a significant improvement in the compatibility achieved, which may werdenβ by increasing the Manebgehalts further improved
Der Einfluß auf die fungizide Wirkung durch Zusatz von Verbindungen der Formel II zu den Verbindungen der Formel I wurde an Tomaten geprüft, die mit Phytophtora infestans infiziert waren» EDq0 bedeutet; 10 $> Befall, verglichen mit der Kontrolle, bzw ο 90 % Wirknr.goThe influence on the fungicidal action of adding compounds of the formula II to the compounds of the formula I was tested on tomatoes which were infected with Phytophthora infestans »EDq means 0; 10 $> infestation, compared to the control, or ο 90 % effect no
009845/1882009845/1882
in der Formulierung % of the active ingredients
in the formulation
Gesamtwirkstoffbased on
Total active ingredient
Zinnverbindung__based on
Tin compound__
2010
20th
1538
15th
5050
50
1132
11th
Wird Decafentin teilweise durch Maneb ersetzt, so ergeben sich die in der !Tabelle 4 aufgeführten Werte 0 If decafentine is partially replaced by maneb, the values listed in Table 4 result from 0
in der Formulierung% of the active ingredients
in the formulation
ppm PräparatED go ~ works,
ppm preparation
20
3010
20th
30th
17
29106
17th
29
Z40
-4040
Z 40
-40
Aus Tabelle 4 ist zu entnehmen, daß mit der Mischung Decafentin ein starker synergistischer Effekt zu erzielen ist, (Die ' fungizide Wirkung von Maneb gegen Phytophtora infestans an Tomaten ist geringer als die von Decafentin0)From Table 4 it can be seen that a strong synergistic effect can be achieved with the mixture of decafentine (the fungicidal effect of maneb against Phytophtora infestans on tomatoes is less than that of decafentine 0 )
009845/1882009845/1882
Claims (1)
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19681802375 DE1802375A1 (en) | 1968-10-10 | 1968-10-10 | Fungicidal mixtures |
CS6697A CS152465B2 (en) | 1968-10-10 | 1969-10-07 | |
FR6934708A FR2020338A1 (en) | 1968-10-10 | 1969-10-10 | Fungicide mixtures of tin cpds and cyclic bis - dithiocarbamates |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19681802375 DE1802375A1 (en) | 1968-10-10 | 1968-10-10 | Fungicidal mixtures |
Publications (1)
Publication Number | Publication Date |
---|---|
DE1802375A1 true DE1802375A1 (en) | 1970-11-05 |
Family
ID=5710225
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE19681802375 Pending DE1802375A1 (en) | 1968-10-10 | 1968-10-10 | Fungicidal mixtures |
Country Status (3)
Country | Link |
---|---|
CS (1) | CS152465B2 (en) |
DE (1) | DE1802375A1 (en) |
FR (1) | FR2020338A1 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0105843A2 (en) * | 1982-10-06 | 1984-04-18 | Ciba-Geigy Ag | Phosphonium organohalostannates (IV) |
EP0109354A1 (en) * | 1982-10-06 | 1984-05-23 | Ciba-Geigy Ag | Biocidally active mixture |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2504356A1 (en) * | 1981-04-27 | 1982-10-29 | Elf Aquitaine | BIOCIDAL COMPOSITION BASED ON SULFONIUM AND ORGANIC TIN COMPOUNDS |
-
1968
- 1968-10-10 DE DE19681802375 patent/DE1802375A1/en active Pending
-
1969
- 1969-10-07 CS CS6697A patent/CS152465B2/cs unknown
- 1969-10-10 FR FR6934708A patent/FR2020338A1/en active Granted
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0105843A2 (en) * | 1982-10-06 | 1984-04-18 | Ciba-Geigy Ag | Phosphonium organohalostannates (IV) |
EP0109354A1 (en) * | 1982-10-06 | 1984-05-23 | Ciba-Geigy Ag | Biocidally active mixture |
EP0105843A3 (en) * | 1982-10-06 | 1984-08-01 | Ciba-Geigy Ag | Phosphonium organohalostannates (iv) |
US4554367A (en) * | 1982-10-06 | 1985-11-19 | Ciga-Geigy Corporation | Phosphonium organohalogenostannates-IV |
Also Published As
Publication number | Publication date |
---|---|
FR2020338A1 (en) | 1970-07-10 |
CS152465B2 (en) | 1973-12-19 |
FR2020338B1 (en) | 1973-03-16 |
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