Synergistic fungicidal composition containing 5-fluorocytosine for fungal control in cereals

A synergistic and fungicidal technology, applied in the field of synergistic fungicidal compositions containing 5-fluorocytosine for fungal control in grains, capable of solving problems such as resistance to fungicides

Inactive Publication Date: 2013-01-02
DOW AGROSCIENCES LLC
View PDF1 Cites 3 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] However, no single fungicide is useful in all situations, and repeated use

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Synergistic fungicidal composition containing 5-fluorocytosine for fungal control in cereals
  • Synergistic fungicidal composition containing 5-fluorocytosine for fungal control in cereals
  • Synergistic fungicidal composition containing 5-fluorocytosine for fungal control in cereals

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0033] Representative organic liquids that may be employed in the preparation of the emulsifiable concentrates of the present invention are aromatic liquids such as xylene and propylbenzene fractions; or mixed naphthalene fractions, mineral oils, substituted aromatic organic liquids such as phthalates Dioctyl formate; kerosene; dialkylamides of various fatty acids, especially dimethylamides of fatty diols and diol derivatives such as n-butyl, ethyl or methyl ethers of diethylene glycol Ether and methyl ether of triethylene glycol, etc. Mixtures of two or more organic liquids are also suitably employed in the preparation of emulsifiable concentrates. Preferred organic liquids are xylene and propylbenzene fractions, with xylene being most preferred. Surface active dispersants are typically employed in liquid formulations and are present in an amount of 0.1 to 20 wt%, based on the combined weight of the surface active dispersant and synergistic composition. The formulations may...

Embodiment

[0047] Fungicide mixture against spot blight of wheat (Gremina graminearum; anamorph: Septoria tritici; Bayer coded as: SEPTTR) evaluation of therapeutic agent and protective agent activity

[0048] Wheat plants (var. Yuma) were grown from seed in a greenhouse in plastic pots with a surface area of ​​27.5 square centimeters (cm2) containing a 50% mineral soil / 50% soilless Metro mix, 8-12 seeds per pot. The plants were used for testing when the first leaves had fully emerged (this usually required 7 to 8 days after planting). The test plants were inoculated with an aqueous spore suspension of Septoria tritici 3-days before (3-day treatment test; 3DC) or 1-day after (1-day protectant test; 1DP) of fungicide treatment. After inoculation, the plants were kept at 100% relative humidity (1 day in a dark dew chamber, then two days in a lighted mist chamber) to allow spores to germinate and infect the leaves. The plants were then transferred to the greenhouse until the disease ha...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

PropertyMeasurementUnit
Surface areaaaaaaaaaaa
Login to view more

Abstract

A fungicidal composition containing a fungicidally effective amount of a) a compound of Formula I and (b) at least one fungicide selected from the group consisting of epoxiconazole, prothioconazole, azoxystrobin, pyraclostrobin, penthiopyrad, isopyrazam, bixafen, boscalid, chlorothalonil and isobutyric acid (3S,6S,7R,8R)-8-benzyl-3-[(3-isobutyryloxymethoxy-4-methoxypyridine-2-carbonyl)-amino]-6-methyl-4,9-dioxo-[1,5]dioxonan-7-yl ester provides synergistic control of selected fungi.

Description

[0001] Cross-references to related applications [0002] This application claims the benefit of U.S. Provisional Patent Application 61 / 249,475, filed October 7, 2009, which provisional application is expressly incorporated by reference into this application. Technical field [0003] The present invention relates to synergistic fungicidal compositions containing (a) a compound of formula I, and (b) at least one fungicide selected from the group consisting of epoxiconazole, prothioconazole, and azoxystrobin. esters, pyraclostrobin, pyritiostrobin, isopyrazam, bixafen, nicotinamide, chlorothalonil and isobutyric acid (3S,6S,7R,8R)-8-benzyl-3-[(3-isobutyryl Oxymethoxy-4-methoxypyridin-2-carbonyl)-amino]-6-methyl-4,9-dioxa-[1,5]dioxacyclononan-7-yl ester . Background technique [0004] Fungicides are compounds of natural or synthetic origin that are used to protect plants from damage caused by fungi. Current agricultural methods rely heavily on the use of fungicides. In fact...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
IPC IPC(8): A61K31/505
CPCA01N43/54A01N37/34A01N43/22A01N43/40A01N43/56A01N43/653A01N45/02A01N47/24A01N2300/00A01N43/48
Inventor B.洛斯巴赫A.梅特尔W.J.欧文姚成林
Owner DOW AGROSCIENCES LLC
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap