DE2265665C2 - herbicide - Google Patents

herbicide

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Publication number
DE2265665C2
DE2265665C2 DE19722265665 DE2265665A DE2265665C2 DE 2265665 C2 DE2265665 C2 DE 2265665C2 DE 19722265665 DE19722265665 DE 19722265665 DE 2265665 A DE2265665 A DE 2265665A DE 2265665 C2 DE2265665 C2 DE 2265665C2
Authority
DE
Germany
Prior art keywords
mixtures
active
active substance
halogen
methoxy
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
DE19722265665
Other languages
German (de)
Inventor
Adolf Dr. 6704 Mutterstadt Fischer
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 DE19722265665 priority Critical patent/DE2265665C2/en
Priority claimed from DE2217722A external-priority patent/DE2217722C2/en
Application granted granted Critical
Publication of DE2265665C2 publication Critical patent/DE2265665C2/en
Expired legal-status Critical Current

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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
    • A01N47/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/10Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
    • A01N47/24Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing the groups, or; Thio analogues thereof
    • 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
    • A01N35/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
    • A01N35/08Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical at least one of the bonds to hetero atoms is to nitrogen
    • A01N35/10Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical at least one of the bonds to hetero atoms is to nitrogen containing a carbon-to-nitrogen double bond
    • 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/88Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with three ring hetero atoms
    • 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
    • A01N45/00Biocides, pest repellants or attractants, or plant growth regulators, containing compounds having three or more carbocyclic rings condensed among themselves, at least one ring not being a six-membered ring
    • A01N45/02Biocides, pest repellants or attractants, or plant growth regulators, containing compounds having three or more carbocyclic rings condensed among themselves, at least one ring not being a six-membered ring having three carbocyclic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C65/00Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
    • C07C65/21Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups containing ether groups, groups, groups, or groups

Description

COOHCOOH

in der X Halogen, Methoxy oder Amino und η 1, 2,3 oder 4 bedeuten, wobei Methoxy und Halogen oder Amino und Halogen oder Methoxy, Amino und Halogen gleichzeitig vorliegen können. in which X is halogen, methoxy or amino and η is 1, 2, 3 or 4, it being possible for methoxy and halogen or amino and halogen or methoxy, amino and halogen to be present at the same time.

Herbizid
Ausscheidung aus Patentanmeldung P 22 17 722.6-41
herbicide
Separation from patent application P 22 17 722.6-41

Die vorliegende Erfindung betrifft ein Herbizid, das eine Mischung aus zwei Wirkstoffen enthältThe present invention relates to a herbicide that contains a mixture of two active substances

Es ist bekannt, daß substituierte Benzoesäure?! und Benzthiothiadiazinone eine herbizide Wirkung haben. Ihre herbizide Wirkung ist jedoch schlechtIt is known that substituted benzoic acid ?! and Benzthiothiadiazinones have herbicidal effects. However, their herbicidal effect is poor

Es wurde gefunden, daß eine Mischung ausIt has been found that a mixture of

a) einer Verbindung der Formel
O
a) a compound of the formula
O

in der X Halogen, Methoxy oder Amino und η 1,2,3 oder 4 bedeuten, wobei Methoxy und Halogen oder Amino und Halogen oder Methoxy, Amino und Halogen gleichzeitig vorliegen können.in which X is halogen, methoxy or amino and η 1, 2, 3 or 4, it being possible for methoxy and halogen or amino and halogen or methoxy, amino and halogen to be present at the same time.

in der R einen niederen Alkylrest mit bis zu 4 C-Atomen bedeutet, oder deren Salzen, wie Alkali-, Erdalkali-, Ammonium-, Hydroxyalkyl- oder Alkylammonium- und Hydrazinsalze, beispielsweise Salze mit Natrium. Lithium, Kalium. Calcium, Eisen, Methylammonium. Trimethylammonium. Äthylammonium. Diäthanoiammonium, Äthanolammonium, Dimethylamin, Dimcthyläthanolamin, Hydrazin oder F'hcnylhydrazin. undin which R is a lower alkyl radical with up to 4 carbon atoms, or their salts, such as alkali, Alkaline earth, ammonium, hydroxyalkyl or alkylammonium and hydrazine salts, e.g. salts with sodium. Lithium, potassium. Calcium, iron, Methylammonium. Trimethylammonium. Ethylammonium. Diethanoiammonium, Ethanolammonium, Dimethylamine, dimethylethanolamine, hydrazine or F'hcnylhydrazine. and

eine bessere herbizide Wirkung als die Einzelwirkstoffe hathas a better herbicidal effect than the individual active ingredients

is Die Wirkstoffe a und b können in Mengen von 0,5 bis 5 kg/ha angewandt werden.is The active ingredients a and b can be used in amounts from 0.5 to 5 kg / ha can be applied.

Das Mischungsverhältnis der Wirkstoffe a : b beträgtThe mixing ratio of the active ingredients a: b is

5 :1 bis I : 5, vorzugsweise 3 :1 bis I : 3 Gewichtsteile.5: 1 to I: 5, preferably 3: 1 to I: 3 parts by weight.

Die Mischungen sind geeignet in Nutzpfinzenkultu-The mixtures are suitable in crop cultivation

ren, z. B. Getreide, Reis, Soja, Mais, Kartoffeln, Erbsen und Bohnen, unerwünschte Pflanzen, beispielsweise dikotyle Samenunkräuter, monokotyle Samenungräser oder Cypcracccn zu bekämpfen.ren, e.g. B. cereals, rice, soy, corn, potatoes, peas and beans, undesirable plants such as dicot seed weeds, monocot seed weeds or to fight Cypcrack.

Die Mischungen können im Vorauflaufverfahren und/oder im N achauflauf verfahren angewandt werden. Die neuen Mischungen können a« Herbizide in Form von Lösungen, Emulsionen, Suspensionen, Stäubemitteln oder Granulaten angewendet werden. Die Anwendungsformen richten sich ganz nach den Verwendungszwecken; sie sollen in jedem Fall eine feine Verteilung der wirksamen Substanzen gewährleisten.The mixtures can be used pre-emergence and / or post-emergence. The new mixtures can be herbicides in the form of solutions, emulsions, suspensions, dusts or granules are used. The forms of application depend entirely on the intended use; they should ensure a fine distribution of the active substances in each case.

Zur Herstellung von direkt versprühbaren Lösungen kommen Mineralölfraktionen von mittlerem bis hohem Siedepunkt wie Kerosin oder Dieselöl, ferner Kohlenteeröle sowie öle pflanzlichen oder tierischen Ursprungs, außerdem cyclische Kohlenwasserstoffe, wie Tetrahydronaphthalin. und alkylierte Naphthaline in Betracht.Medium to high mineral oil fractions are used to produce solutions that can be sprayed directly Boiling point such as kerosene or diesel oil, as well as coal tar oils and oils of vegetable or animal origin, also cyclic hydrocarbons, such as tetrahydronaphthalene. and alkylated naphthalenes in Consideration.

Wäßrige Anwendungsformen können aus Emulsionskonzentraten. Pasten oder netzbaren Pulvern (Spritzpulvern) durch Zusatz von Wasser bereitet werden. Zur Herstellung von Emulsionen können die Substanzen als solche oder in einem Lösungsmittel gelöst, mittels Netzoder Dispergiermittel in Wasser homogenisiert werden. Es können aber auch aus wirksame. Substanz. Emulgier- oder Dispergiermittel und eventuell Lösungsmittel bestehende Konzentrate hergestellt werden, die zur Verdünnung mit Wasser geeignet sind. Zu fertigen Spritzbrühen können öle verschiedenen Typs zugesetzt werden.Aqueous use forms can be obtained from emulsion concentrates. Pastes or wettable powders (wettable powders) can be prepared by adding water. To produce emulsions, the substances can be used as such or dissolved in a solvent, by means of a network or Dispersants are homogenized in water. But it can also be effective. Substance. Emulsifying or dispersants and possibly solvents existing concentrates are prepared, which for Dilution with water are suitable. Oils of various types can be added to finished spray mixtures will.

Stäubemittel können durch Mischen oder gemeinsames Vermählen der wirksamen Substanzen mit einem festen Trägerstoff hergestellt werden.Dusts can be produced by mixing or grinding together the active substances with one solid carrier material are produced.

Granulate können durch Bindung der Wirkstoffe an feste Trägerstoffe hergestellt werden.Granules can be produced by binding the active ingredients to solid carriers.

Außerdem können mit Ölen direkt versprühbare Dispersionen hergestellt werden.In addition, dispersions that can be sprayed directly with oils can be produced.

Die Mischungen können mit Düngemitteln. Insektiziden. Fungiziden oder anderen Herbiziden gemischt werden.The mixtures can be made with fertilizers. Insecticides. Fungicides or other herbicides.

Beispiel 1example 1

Die Pflanzen Weizen (Triticum aestivum), Klcbkraut (Galium aparine). echte Kamille (Matricaria chamomil-Ia). Ackerfuchsschwanzgras (Alopecunis myosuroides) und einjähriges Rispengras (Poa annua) wurden beiThe plants wheat (Triticum aestivum), Klcbkraut (Galium aparine). real chamomile (Matricaria chamomil-Ia). Foxtail grass (Alopecunis myosuroides) and annual bluegrass (Poa annua) were at

einer Wuchshöhe von 4 bis 20 cm mit den nachfolgenden Einzelprodukten und Mischungen, jeweils emulgiert oder dispergiert in 500 Liter Wasser je Hektar, behandelt:a height of 4 to 20 cm with the following individual products and mixtures, each emulsified or dispersed in 500 liters of water per hectare, treated:

C 2-Methoxy-3,6-dichlor-benzoesäure 14 und 2 kg/ha aktive SubstanzC 2-methoxy-3,6-dichloro-benzoic acid 14 and 2 kg / ha of active substance

B + A 0,5 + 1,5 kg/ha aktive Substanz C+A 14+04 kg/ha aktive SubstanzB + A 0.5 + 1.5 kg / ha of active substance C + A 14 + 04 kg / ha of active substance

A 3- Isopropyl-2,13-benzo-thiadiazinon-(4)-
2^-dioxid, 04, t, 14,2 und 3 kg/ha
aktive Substanz
B 23,6-Trichlor-benzoesäure,
04 und 2 kg/ha aktive Substanz
A 3- isopropyl-2,13-benzo-thiadiazinon- (4) -
2 ^ -dioxide, 04, t, 14.2 and 3 kg / ha
active substance
B 23,6-trichlorobenzoic acid,
04 and 2 kg / ha of active substance
Wirkstoff
B
Active ingredient
B.
CC. 1010 kg/ha aktive Substanz
04 2 1,5 2
kg / ha of active substance
04 2 1.5 2
2020th 1010 1515th Aus nachfolgender Tabelle ist zu entnehmen, daß die
Mischungen nach 8 bis 14 Tagen gegenüber den
Einzelkomponenten eine bessere Gesamtwirkung bei
günstiger Kulturpflanzenverträglichkeit zeigen.
The table below shows that the
Mixtures after 8 to 14 days versus the
Individual components have a better overall effect
show favorable crop plant tolerance.
11 00 1414th 22 33 00 B +B + A C +AA C + A
Tabelle 1Table 1 00 8585 6060 8585 4040 00 00 8080 0404 M4 14 + 0,5M4 14 + 0.5 2525th 9595 6565 9090 AA. 5050 6060 7070 9595 00 1010 3030th 9595 4545 8080 0.50.5 55 6060 9090 1515th 100100 9595 Triticum aestivumTriticum aestivum 5050 100100 6060 9595 00 55 1515th 1010 1010 100100 9595 Galium aparineGalium aparine 5555 3030th 55 55 8080 7575 Matricaria chamomillaMatricaria chamomilla 3535 8080 8080 Alopecurus myosucndesAlopecurus myosucndes 55 Poa annuaPoa annua 55 0 - ohne Schädigung0 - without damage 100 - totale Schädigung.100 - total damage.

Beispiel 2Example 2

In Freiland werden nach dem Auflaufen die Kulturpflanzen Soja (Soja hispida) und Mais (Zea mays) und die unerwünschten Pflanzen Hühnerhirse (Echinochloa crus galli). große Borstenhirse (Setaria faberii). Erdmandel (Cyperus esculentus), Ackersenf (Sinapis arvensis), pennsylvaiüsche Spitzklette vXanthium pensylvanicum), Klebkraut (Galium ayarine), echte Kamille (Matricaria chamomilla), englisches Raugras (Lolium perenne), gemeines Rispengras (Poa trivialis) mit folgenden Einzelwirkstoffen und deren MischungenIn the open field, after emergence, the crop plants soy (Soja hispida) and maize (Zea mays) and the undesired plants barn millet (Echinochloa crus galli) are grown. great millet (Setaria faberii). Tigernut (Cyperus esculentus), field mustard (Sinapis arvensis), pennsylvaiüsche pointed burdock v Xanthium pensylvanicum), glutinous herb (Galium ayarine), real chamomile (Matricaria chamomilla), English ragweed (Lolium perenne), common panicle grass (Poa trivialis) with the following single active ingredients Mixtures

3-lsopropyl-2,13-benzo-thiadiazinon-(4)-2,2-dioxid 0,7 und 2 kg/ha aktive Substanz3-Isopropyl-2,13-benzo-thiadiazinon- (4) -2,2-dioxide 0.7 and 2 kg / ha of active substance

Tabelle 2Table 2

4040

D 3-Amino-24-dichlor-benzoesäure 13 und 2 kg/ha aktive SubstanzD 3-Amino-24-dichloro-benzoic acid 13 and 2 kg / ha of active substance

A + D °'7 und U kS/ha^tlve Substan* behandelt A + D ° ' 7 and U k S / ha ^ tlve Substan * treated

Nach 10 bis 14 Tagen wurde festgestellt, daß die Mischung A+D eine bessere Verträglichkeit an den Kulturpflanzen und eine bessere herbizide Wirkung zeigt als die Einzelwirkstoffe A und D.After 10 to 14 days it was found that the mixture A + D was better tolerated by the Cultivated plants and shows a better herbicidal effect than the individual active ingredients A and D.

Das Versuchsergebnis ist aus nachfolgender Tabelle zu ersehen.The test result can be seen from the table below.

WirkstoffActive ingredient Substanzsubstance 00 DD. 22 A + DA + D AA. 22 00 1010 kg/ha aktivekg / ha active 1010 1,31.3 1515th 0,7 + U0.7 + U 0,70.7 2020th 00 8080 00 Soja hispidaSoy hispida 00 7575 00 8080 00 Zea maysZea mays 00 8080 5050 1010 8585 EchinochJoa cms galliEchinochJoa cms galli 1010 9090 4545 3030th 9090 Setaria faberiiSetaria faberii 1515th 8080 1010 1010 9090 Cyperus esculentusCyperus esculentus 4040 8080 2020th 1010 100100 SiiupU anrensisSiiupU anrensis 4040 00 55 1010 100100 Xanthium pensylvanicumXanthium pensylvanicum 5050 00 1010 7070 8585 Galium aparineGalium aparine 4545 55 8080 9595 Matriaria chamomillaMatriaria chamomilla 5050 4040 7070 Lolium pcrenneLolium pcrenne 00 5050 9090 Foa trivialisFoa trivialis 00

0 = ohne Schädigung.
100 - totale Schädigung.
0 = without damage.
100 - total damage.

Beispiel 3Example 3

Im Gewächshaus werden die Pflanzen und der Erdboden nach dem Auflaufen von Gerste (Hordeum vulgäre), Roggen (Seeale cereale) und Weizen (Triticuni aestivutn) und den unerwünschten Pflanzen Klebkrau/ (Galium aparine) und Ackerfuchsschwanz (Aiopecurus myosuroides) mit folgenden Einzel wirkstoff?'"! und deren Mischungen behandelt:In the greenhouse the plants and the soil are after the emergence of barley (Hordeum vulgar), rye (Seeale cereale) and wheat (Triticuni aestivutn) and the undesirable plants sticky weed / (Galium aparine) and black foxtail (Aiopecurus myosuroides) with the following single active ingredients? '"! and their mixtures dealt with:

A 3-lsopropyl-2,l ,3-benzo-thiadiazinon-(4}·
2^2-dioxid 0,5,0,75.1.0 und 1,5 kg/ha
aktive Substanz
A 3-isopropyl-2, l, 3-benzo-thiadiazinon- (4} ·
2 ^ 2-dioxide 0,5,0,75.1.0 and 1.5 kg / ha
active substance

B 2,5-Dichlor-ß-nieinoxyberiZoesäure
(Dimethylammoniumsalz)
0,5.0,75,1,0 und 1,5 kg/ha aktive Substanz
B 2,5-dichloro-β-nieinoxyberzoic acid
(Dimethylammonium salt)
0.5, 0.75, 1.0 and 1.5 kg / ha of active substance

A + B 0,5+1,0,1,0+0,5,0,75 + 0,75 kg/haA + B 0.5 + 1.0.1.0 + 0.5, 0.75 + 0.75 kg / ha

Nach 10 bis 14 Tagen wurde festgestellt, daß die Mischungen eine bessere herbizide Wirkung bei gleicher Verträglichkeit an den Kulturpflanzen zeigten. Das Versuchsergebnis ist aus nachfolgender Tabelle zu ersehen:After 10 to 14 days it was found that the mixtures had a better herbicidal effect showed the same compatibility on the crop plants. The test result is shown in the table below see:

Tabelle 3Table 3

Wirkstoff
A
Active ingredient
A.

kg/ha aktive Substanz
0,5 0,75 1,0 1,5
kg / ha of active substance
0.5 0.75 1.0 1.5

A + BA + B

0,5 0,75 1,0 1T5 0,5 + 1,0 1,0 + 04 0,75 + 0,750.5 0.75 1.0 1 T 5 0.5 + 1.0 1.0 + 04 0.75 + 0.75

Hordeum vulgäre
Seeale cereale
Triticum aestivutn
Galium aparine
AJopec. myos.
Hordeum vulgar
Seeale cereale
Triticum aestivutn
Galium aparine
AJopec. myos.

00 00 00 00 00 00 00 1010 00 00 00 00 00 00 00 00 00 00 1010 00 UU 00 00 00 00 00 00 00 00 1010 00 00 00 3030th 3535 4040 6060 3737 4545 5050 6060 100100 100100 1Ö01Ö0 22 55 55 1010 2525th SOSO 3535 4545 8787 8080 8080

0 = ohne Schädigung.
100 = totale Schädigung.
0 = without damage.
100 = total damage.

Claims (1)

Patentanspruch:Claim: Herbizid, enthaltend eine Mischung aus
a) einer Verbindung der Formel
Herbicide containing a mixture of
a) a compound of the formula
b) einer Verbindung der Formelb) a compound of the formula COOHCOOH in der R einen niederen Alkylrest mit bis zu 4 C-Atomen bedeutet, oder deren Salzen und b) einer Verbindung der Formelin which R is a lower alkyl radical with up to 4 carbon atoms, or their salts and b) a compound of the formula
DE19722265665 1972-04-13 1972-04-13 herbicide Expired DE2265665C2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DE19722265665 DE2265665C2 (en) 1972-04-13 1972-04-13 herbicide

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19722265665 DE2265665C2 (en) 1972-04-13 1972-04-13 herbicide
DE2217722A DE2217722C2 (en) 1972-04-13 1972-04-13 herbicide

Publications (1)

Publication Number Publication Date
DE2265665C2 true DE2265665C2 (en) 1983-01-05

Family

ID=25763057

Family Applications (1)

Application Number Title Priority Date Filing Date
DE19722265665 Expired DE2265665C2 (en) 1972-04-13 1972-04-13 herbicide

Country Status (1)

Country Link
DE (1) DE2265665C2 (en)

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1937551A1 (en) * 1969-07-24 1971-02-11 Basf Ag herbicide

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1937551A1 (en) * 1969-07-24 1971-02-11 Basf Ag herbicide

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
Klimmer, O.R.: Pflanzenschutz- und Schädlings- bekämpfungsmittel, 2. Auflage, 1971, Seiten 87 bis 95 *

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