CH247387A - Method of controlling insects and fungal diseases of plants. - Google Patents
Method of controlling insects and fungal diseases of plants.Info
- Publication number
- CH247387A CH247387A CH247387DA CH247387A CH 247387 A CH247387 A CH 247387A CH 247387D A CH247387D A CH 247387DA CH 247387 A CH247387 A CH 247387A
- Authority
- CH
- Switzerland
- Prior art keywords
- compound
- plants
- fungal diseases
- controlling insects
- organic
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 8
- 241000238631 Hexapoda Species 0.000 title claims description 4
- 208000031888 Mycoses Diseases 0.000 title claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 11
- 239000000839 emulsion Substances 0.000 claims description 5
- BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 claims description 2
- 239000003085 diluting agent Substances 0.000 claims description 2
- 239000000843 powder Substances 0.000 claims description 2
- 125000004122 cyclic group Chemical group 0.000 description 3
- 235000013399 edible fruits Nutrition 0.000 description 3
- 241000196324 Embryophyta Species 0.000 description 2
- 241001363490 Monilia Species 0.000 description 2
- 235000009827 Prunus armeniaca Nutrition 0.000 description 2
- 244000018633 Prunus armeniaca Species 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 241000258916 Leptinotarsa decemlineata Species 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 230000001154 acute effect Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- UKLJMHXGZUJRTL-UHFFFAOYSA-L calcium;n-cyclohexylsulfamate Chemical compound [Ca+2].[O-]S(=O)(=O)NC1CCCCC1.[O-]S(=O)(=O)NC1CCCCC1 UKLJMHXGZUJRTL-UHFFFAOYSA-L 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 235000021395 porridge Nutrition 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
Procédé de lutte contre les insectes et les maladies cryptogamiques des végétaux. La présente invention concerne un pro <B>cédé de</B> lutte, contre les insectes et les mala dies cryptogamiques des végétaux, caracté risé en<B>ce</B> qu'on utilise un composé halogéno- sulfuré organique, avantageusement incor poré<B>à</B> un agent diluant.
On peut employer comme composé halo- t, créno-sulfuré organique un composé halogéno- .sulfuré comportant deux groupes, de préfé rence symétriques, reliés l'un<B>à</B> l'autre par des atomes de soufre, ce composé halogéno- sulfuré étant obtenu, par exemple, en faisant agir un composé inorganique sulfuré, avan- tagefflement ùu sulfure alcalin en solution,
sur un composé organique chloré, de préfé-: rence cyclique et saturé.
Ce dernier composé est avantaigeuspment constitué par<B>de</B> Fliexachlorocyclollexane ou un cyclane halogéné <B>à</B> un ou plusieurs royaux ou un dérivé halogéné d'un cyclane <B>à</B> fonctions multiples.
On peut utiliser notamment comme coin- posés halogéno-sulfurés organiques les pro duits suivants: a) 'un disulfure de pentachlorocyclollexyle constitué de deux groupes cycliques halogénés et saturés et reliés l'un<B>à</B> l'autre par une seule liaison<B>à</B> deux atomes de soufre-.
EMI0001.0031
<B>b)</B> un dérivé dans lequel les deux groupes cycliques halogénés sont reliés l'un<B>à</B> l'autre par deux liaisons, chacune de ces liaisons étant constituée par deux atomes<B>de</B> soufre, tel que par exemple:
EMI0001.0033
Ces composés halogéno-suffurés et notam ment le disulfure de pentachlorocycloliexyle peuvent avantageusement être utilisés sous forme d'émulsions dans lalcool.
Cette émulsion, additionnée de produits mouillants et adhésifs, constitue un insecti cide, a-ntieryptogamique et fongicide extrê mement actif, n'ayant aucune action fâcheuse ni sur<B>le</B> feuillage ni sur les fruits, même les plus délicats, par exemple les abricots au voisinage de la maturité.
<B>Il</B> est connu que certaines variétés de fruits, les abricots notamment, sont très su jettes<B>à</B> la pourriture causée par un champi gnon du type ,Monilia". Une pulvérisation très fine de l'émulsion précitée arrête rapi dement l'évolution de la monilia et permet d'avoir des fruits sains.
L'émulsion précitée, qui ressemble<B>à</B> un véritable lait, possède une action toxique très marquée sur les doryphores, larves et adultes, qui sont tués au bout<B>de</B> 20<B>* à 30</B> heures. Une teneur de<B>0,5 à 1</B> gramme de disulfure par litre suffit.
Ori peut aussi, si le composé halogéno- suIfLirA- a été préparé en présence d'un sol- -#ant non aqueux, distiller la solution obtenue pour recouvrer ce solvant et pour obtenir le composé désiré et employer celui-ci -sous forme de poudre, après dilution par des corps inertes. On peut également s'en servir sous forme<B>de</B> bouillie ou sous toutes autres formes appropriées.
Method of controlling insects and fungal diseases of plants. The present invention relates to a <B> given </B> process against insects and fungal diseases of plants, characterized in <B> this </B> that an organic halosulfide compound is used, advantageously incorporated <B> in </B> a diluting agent.
As an organic halo, creno-sulphide compound, a halo-sulphide compound comprising two groups, preferably symmetrical, linked one <B> to </B> the other by sulfur atoms, can be used. halosulfur compound being obtained, for example, by causing an inorganic sulfur compound to act, advantageously of alkali sulfide in solution,
on a chlorinated organic compound, preferably cyclic and saturated.
This last compound is before acute constituted by <B> of </B> Fliexachlorocyclollexane or a halogenated cyclane <B> with </B> one or more royals or a halogenated derivative of a cyclan <B> with </B> multiple functions .
The following products can in particular be used as organic halogeno-sulphides: a) a pentachlorocyclollexyl disulphide consisting of two halogenated and saturated cyclic groups and linked to one <B> to </B> the other by a single bond <B> to </B> two atoms of sulfur-.
EMI0001.0031
<B> b) </B> a derivative in which the two halogenated cyclic groups are linked to one <B> to </B> the other by two bonds, each of these bonds being constituted by two atoms <B> of </B> sulfur, such as for example:
EMI0001.0033
These halogenosulfur compounds and in particular pentachlorocycloliexyl disulphide can advantageously be used in the form of emulsions in alcohol.
This emulsion, with the addition of wetting and adhesive products, constitutes an extremely active insecticide, antieryptogamic and fungicide, having no detrimental action either on <B> the </B> foliage or on the fruits, even the most delicate. , for example apricots near maturity.
<B> It </B> is known that certain varieties of fruit, especially apricots, are very prone to <B> </B> rot caused by a fungus of the type, Monilia ". A very fine spray of the aforementioned emulsion quickly stops the development of monilia and makes it possible to have healthy fruits.
The aforementioned emulsion, which resembles <B> </B> real milk, has a very marked toxic action on the Colorado beetle, larvae and adults, which are killed after <B> </B> 20 <B> * at 30 </B> hours. A content of <B> 0.5 to 1 </B> gram of disulfide per liter is sufficient.
Or, if the halo-suIfLirA- compound has been prepared in the presence of a non-aqueous sol- - #ant, it is also possible to distill the obtained solution to recover this solvent and to obtain the desired compound and to employ this in the form of powder, after dilution with inert bodies. It can also be used as a <B> </B> porridge or in any other suitable form.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR247387X | 1943-07-26 | ||
| FR151143X | 1943-11-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH247387A true CH247387A (en) | 1947-03-15 |
Family
ID=26213786
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH247387D CH247387A (en) | 1943-07-26 | 1944-05-03 | Method of controlling insects and fungal diseases of plants. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH247387A (en) |
-
1944
- 1944-05-03 CH CH247387D patent/CH247387A/en unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0806895B2 (en) | Insecticidal combinations including an insecticide from the chloronicotinyl family and an insecticide having a pyrazole, pyrrole or phenylimidazole group | |
| US8092817B2 (en) | Biorational insecticide and fungicide and method of application | |
| DE69214805T2 (en) | FUNGICIDE AGENTS BASED ON FATTY ACID, WITH LASTING EFFECT | |
| FR2517176A1 (en) | INSECTICIDE AND ACARICIDE ASSOCIATION OF PYRETHROID | |
| RU2593306C2 (en) | Novel method of processing plant products with phosphonic acid and essential oil before or after harvesting | |
| US20080070787A1 (en) | Adjuvant composition for use with herbicides, pesticides, insecticides, ovicides and fungicides and method of application | |
| AU2004324869B2 (en) | An adjuvant composition for use with herbicides, pesticides, insecticides, ovicides and fungicides and method of application | |
| FR2923356A1 (en) | USE OF MINT OR L-CARVONE SOLUTIONS FOR FUNGICIDE AND / OR ANTI -MINMINATION TREATMENT OF BULBS AND / OR TUBERS | |
| DE60315839T2 (en) | TEA TREE OIL-CONTAINING FUNGICIDAL COMPOSITION | |
| FR2684519A1 (en) | ASSOCIATION OF A FUNGICIDE OF THE TRIAZOLE FAMILY AND IMIDACLOPRID. | |
| EP0629345B1 (en) | Insecticidal/acaricidal composition based on anionic surfactant(s), and semiochemical(s), and method for combatting arthropods using this composition | |
| CA2470395C (en) | Biorational insecticide/fungicide and method of application | |
| CH427400A (en) | Fungicidal composition | |
| DE69627302T2 (en) | ENVIRONMENTALLY FRIENDLY PESTICIDE AND PLANT GROWTH ACCELERATOR | |
| CH247387A (en) | Method of controlling insects and fungal diseases of plants. | |
| US2381082A (en) | Insect repellent | |
| EP0840549B1 (en) | Insecticidal combinations of an oxime carbamate with an insecticide having a pyrazole, pyrrole or phenylimidazole group | |
| US2389427A (en) | Insect repellents | |
| JP4183723B2 (en) | Fruit bag | |
| EP2030506A1 (en) | Pesticide treatment of stored foodstuff, enclosures, structures and works of art using sulphur compounds | |
| FR2577385A1 (en) | Process and means for controlling the eudemis moth | |
| US2943977A (en) | Insecticidal composition comprising 2, 2, 4,-4, 6, 6-tris (tetramethylene)-1, 3, 5-trithiane and 2, 2, 4, 4, 6, 6 tris (pentamethylene) 1, 3, 5-trithiane | |
| BE897484A (en) | COMPOSITE PRODUCT ATTRACTING INSECTS, FOR MALE Y-SILVER BUTTERFLIES | |
| FR2520197A1 (en) | ETHION AND PYRETHROID-BASED INSECTICIDE AND ACARICIDE COMPOSITIONS AND PROCESS FOR TREATING ARTHROPODIC VEGETABLES USING THE SAME | |
| BE476254A (en) |