Advances in Weed Management (2015)
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2,4-Dichlorophenoxyacetic Acid
2,4-Dichlorophenoxyacetic acid 2,4-Dichlorophenoxyacetic acid IUPAC (2,4-dichlorophenoxy)acetic acid name 2,4-D Other hedonal names trinoxol Identifiers CAS [94-75-7] number SMILES OC(COC1=CC=C(Cl)C=C1Cl)=O ChemSpider 1441 ID Properties Molecular C H Cl O formula 8 6 2 3 Molar mass 221.04 g mol−1 Appearance white to yellow powder Melting point 140.5 °C (413.5 K) Boiling 160 °C (0.4 mm Hg) point Solubility in 900 mg/L (25 °C) water Related compounds Related 2,4,5-T, Dichlorprop compounds Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) 2,4-Dichlorophenoxyacetic acid (2,4-D) is a common systemic herbicide used in the control of broadleaf weeds. It is the most widely used herbicide in the world, and the third most commonly used in North America.[1] 2,4-D is also an important synthetic auxin, often used in laboratories for plant research and as a supplement in plant cell culture media such as MS medium. History 2,4-D was developed during World War II by a British team at Rothamsted Experimental Station, under the leadership of Judah Hirsch Quastel, aiming to increase crop yields for a nation at war.[citation needed] When it was commercially released in 1946, it became the first successful selective herbicide and allowed for greatly enhanced weed control in wheat, maize (corn), rice, and similar cereal grass crop, because it only kills dicots, leaving behind monocots. Mechanism of herbicide action 2,4-D is a synthetic auxin, which is a class of plant growth regulators. -
WO 2012/125779 Al 20 September 2012 (20.09.2012) P O P C T
(12) INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (10) International Publication Number (43) International Publication Date WO 2012/125779 Al 20 September 2012 (20.09.2012) P O P C T (51) International Patent Classification: CA, CH, CL, CN, CO, CR, CU, CZ, DE, DK, DM, DO, A01N 43/90 (2006.01) DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, HN, HR, HU, ID, IL, IN, IS, JP, KE, KG, KM, KN, KP, KR, (21) International Application Number: KZ, LA, LC, LK, LR, LS, LT, LU, LY, MA, MD, ME, PCT/US20 12/029 153 MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, (22) International Filing Date: OM, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SC, SD, 15 March 2012 (15.03.2012) SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW. (25) Filing Language: English (84) Designated States (unless otherwise indicated, for every (26) Publication Language: English kind of regional protection available): ARIPO (BW, GH, (30) Priority Data: GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, SZ, TZ, 61/453,202 16 March 201 1 (16.03.201 1) US UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, MD, RU, TJ, TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, (71) Applicant (for all designated States except US) : DOW DK, EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LT, LU, AGROSCIENCES LLC [US/US]; 9330 Zionsville Road, LV, MC, MK, MT, NL, NO, PL, PT, RO, RS, SE, SI, SK, Indianapolis, IN 46268 (US). -
Solventless Formulation of Triclopyr Butoxyethyl
(19) & (11) EP 1 983 829 B1 (12) EUROPEAN PATENT SPECIFICATION (45) Date of publication and mention (51) Int Cl.: of the grant of the patent: A01N 43/40 (2006.01) A01N 25/30 (2006.01) 13.01.2010 Bulletin 2010/02 A01N 25/04 (2006.01) A01P 13/00 (2006.01) (21) Application number: 06837962.7 (86) International application number: PCT/US2006/044751 (22) Date of filing: 17.11.2006 (87) International publication number: WO 2007/094836 (23.08.2007 Gazette 2007/34) (54) SOLVENTLESS FORMULATION OF TRICLOPYR BUTOXYETHYL ESTER LÖSUNGSMITTELFREIE FORMULIERUNG VON TRICLOPYR-BUTOXYETHYLESTER FORMULE SANS SOLVANT D’ESTER DE BUTOXYETHYLE DU TRICYCLOPYR (84) Designated Contracting States: • POMPEO, Michael, P. DE ES FR GB IT Sumter, SC 29150 (US) (30) Priority: 15.02.2006 US 773417 P (74) Representative: Weiss, Wolfgang Weickmann & Weickmann (43) Date of publication of application: Patentanwälte 29.10.2008 Bulletin 2008/44 Postfach 86 08 20 81635 München (DE) (73) Proprietors: • Dow AgroSciences LLC (56) References cited: Indianapolis, WO-A-96/28027 WO-A-2004/093546 Indiana 46268-1054 (US) US-A1- 5 466 659 • Jensen, Jeffrey, Lee Brownsburg IN 46112 (US) • BOVEY RODNEY W ET AL: "Honey mesquite (Prosopis glandulosa) control by synergistic (72) Inventors: action of clopyralid: Triclopyr mixtures" WEED • JENSEN, Jeffrey, Lee SCIENCE, vol. 40, no. 4, 1992, pages 563-567, Brownsburg, IN 46112 (US) XP009080681 ISSN: 0043-1745 • KLINE, William, N., III • BEBAWI F F ET AL: "Impact of foliar herbicides Duluth, GA 30096 (US) on pod and seed behaviour of rust-infected • BURCH, Patrick, L. rubber vine (Cryptostegia grandiflora) plants" Christiansburg, VA 24073 (US) PLANT PROTECTION QUARTERLY, vol. -
Manuka Oil As a Potential Natural Herbicide
Manuka Oil as a Potential Natural Herbicide Franck E. Dayan and Daniel K. Owens USDA-ARS Natural Products Utilization Research Unit P.O. Box 8048, University, MS 38677 [email protected] In 1977, Gray observed that bottlebrush plant (Callistemon citrinus) repressed the growth of plants in its surroundings. Crude extracts from this plant caused the bleaching of grass weeds. He identified the active component as leptospermone, a natural triketone structure with no known biological activity that had been reported in a number of Australasian shrubs. Leptospermone was moderately active in greenhouse tests, controlling mostly small-seeded grass weeds. This natural product and a small number of synthetic structural analogs were patented as herbicides in 1980. A few years later, a separate group at the Western Research Center was generating analogs of the cyclohexanedione herbicide sethoxydim, an inhibitor or acetyl- coenzyme-A carboxylase. Some of the second generation herbicidal derivatives with a dimedone backbone caused bleaching symptoms similar to leptospermone. Combination of the syncarpic acid of leptospermone to this chemistry ultimately served as the basis for the development of the triketone synthetic herbicides (Fig. 1). Fig. 1. Struct ure s of the n a tural trik et o n e leptosperm one a nd t w o s y nthetic analogues that are sold as commer ci a l he r bic ides. Natural β-triketones are common in many Australasian woody plants (e.g., Leptospermum, Eucalyptus, Melaceuca, etc...). Steam distilled manuka oil account for 0.3% of the dried weight of L. scoparium. However, the amount of β-triketone present in these oils varies wildly across New Zealand. -
Managing Pesticide Drift1 F
PI232 Managing Pesticide Drift1 F. M. Fishel and J. A. Ferrell2 Introduction may drift and whether it is harmful depends on interrelated factors that can be complex. The drift of spray from pesticide applications can expose people, plants and animals, and the environment to Drift is a significant legal concern in Florida. During pesticide residues that can cause health and environmental 2009–2010, the Florida Department of Agriculture and effects and property damage. Agricultural practices are Consumer Services (FDACS), which is the state pesticide poorly understood by the public, which causes anxiety and regulatory agency, initiated 39 investigations in response sometimes overreaction to a situation. Even the application to allegations of drift. Where significant drift does occur, of fertilizers or biological pesticides, like Bt or pheromones, it can damage or contaminate sensitive crops, poison bees, can be perceived as a danger to the general public. Drift pose health risks to humans and animals, and contaminate can lead to litigation, financially damaging court costs, soil and water in adjacent areas (Figure 1). Applicators are and appeals to restrict or ban the use of crop protection legally responsible for the damages resulting from the off- materials. Urbanization has led to much of Florida’s agri- target movement of pesticides. It is impossible to eliminate cultural production being in areas of close proximity to the drift totally, but it is possible to reduce it to a legal level. general public, including residential subdivisions, assisted The purpose of this guide is to discuss factors influencing living facilities, hospitals, and schools. Such sensitive sites drift and provide common-sense solutions for minimizing heighten the need for drift mitigation measures to be taken potential drift problems. -
Jamesdanieljonesiiithesis.Doc-After Defense
The Evaluation of HPPD-Inhibitors for Full-Season Control of Morningglory (Ipomoea) Species in Corn (Zea mays L.) by James Daniel Jones III A thesis submitted to the Graduate Faculty of Auburn University in partial fulfillment of the requirements for the Degree of Master of Science Auburn, Alabama December 15, 2018 Keywords: Ipomoea, corn, HPPD, postemergence Approved by Dr. Dennis Delaney, Chair, Extension Specialist, Crop, Soil, and Environmental Sciences Dr. Andrew Price, Affiliate Associate Professor, Crop, Soil, and Environmental Sciences Dr. Audrey Gamble, Assistant Professor and Extension Specialist, Crop, Soil, and Environmental Sciences i Abstract Due to late-season morningglory harvest interference concerns in corn, field studies were conducted in 2017 and 2018 at the Prattville Agricultural Research Unit in Prattville, Alabama and at the Sand Mountain Research and Extension Center in Crossville, Alabama to evaluate late season control of morningglory species using HPPD- inhibitors postemergence (POST) applied alone, following atrazine preemergence (PRE), or in combination with atrazine. Additionally, Amaranthus spp. and Senna spp. were evaluated for control. An incomplete randomized design with a split-plot treatment arrangement with four replications was utilized. The trial was divided into two sections: one with a PRE application of atrazine and a second without a preemergence application of atrazine. Eleven herbicides were applied POST without atrazine including: tembotrione; mesotrione; topramezone+dimethenamid; mesotrione+S- metolachlor+glyphosate; tembotrione+thiencarbazone; topramezone; mesotrione+S- metolachlor+atrazine; mesotrione+S-metolachlor+atrazine+bicyclopyrone; mesotrione+nicosulfuron; isoxaflutole; isoxaflutole+thiencarbazone-methyl; non-treated with atrazine applied PRE, and a true non-treated check. The same herbicides, excluding the two treatments that contain atrazine in the premixture, were also applied with atrazine. -
Signs and Symptoms of Pesticide Poisoning
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Historical Materials from University of Nebraska-Lincoln Extension Extension 1997 EC97-2505 Signs and Symptoms of Pesticide Poisoning Larry D. Schulze University of Nebraska - Lincoln, [email protected] Clyde Ogg University of Nebraska - Lincoln, [email protected] Edward F. Vitzthum University of Nebraska - Lincoln, [email protected] Follow this and additional works at: https://digitalcommons.unl.edu/extensionhist Part of the Agriculture Commons, and the Curriculum and Instruction Commons Schulze, Larry D.; Ogg, Clyde; and Vitzthum, Edward F., "EC97-2505 Signs and Symptoms of Pesticide Poisoning" (1997). Historical Materials from University of Nebraska-Lincoln Extension. 1225. https://digitalcommons.unl.edu/extensionhist/1225 This Article is brought to you for free and open access by the Extension at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Historical Materials from University of Nebraska-Lincoln Extension by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. University of Nebraska Cooperative Extension EC97-2505-A Signs and Symptoms of Pesticide Poisoning Larry D. Schulze, Extension Pesticide Coordinator Clyde L. Ogg, Extension Assistant, Pesticide Training Edward F. Vitzthum, Coordinator, Environmental Programs z Manage Your Risk z Signal Words z Read the pesticide Label z Routes of Exposure z Pesticide Toxicity z Recognizing Signs and Symptoms of Poisoning z Recognizing Common pesticide Poisonings { Organophosphate and Carbamate Insecticides { Organochlorine Insecticides { Synthetic Pyrethroid Insecticides { Plant-derived Insecticides { Inorganic Insecticides { Microbial Insecticides { DEET Repellent { Bipyridyl Herbicides { Chlorophenoxy Herbicides { Arsenical Herbicides { Wood Preservatives { Fumigants { Rodenticides { Fungicides z What To Do When Pesticide Poisoning Occurs z References z Pesticide Safety Telephone Numbers Accidental exposure or overexposure to pesticides can have serious implications. -
US EPA, Pesticide Product Label, AC 801,757 3EC MITICIDE
OZlKl UNITED STATES ENVIRONMENTAL PROTECTION AGENCY WASHINGTON, D.C. 20460 OFFICE OF CHEMICAL SAFETY AND POLLUTION PREVENTION' Mr. Kenneth Chisholm Nichino America, Inc, 4550 New Linden Hill Road, Suite 501 FEB 1 4 2013 Wilmington, DE 19808 fc ',"- ;•- Subject: Label Amendment AC 801, 757 3 EC Miticide-Insecticide EPA Registration Number: 71711 -23 Application Dated: September 20, 2012 Decision: 473901 Dear Mr. Chisholm: The label referred to above, submitted in connection with registration under the Federal Insecticide, Fungicide, and Rodenticide Act, as amended, is acceptable. A stamped copy is enclosed for your records. If you have any questions, please contact Melody Banks on 703 305-5413 or via E-mail @ [email protected]. Sincerely >uarez Insecticide Branch Product Manager Registration Division (7504P) Enclosure: Stamped Accepted Copy of Product Label NICHING AMERICA GROUP INSECTICIDE AC 801,757 SEC miticide/insecticide For Use on Ornamental Crops Grown in Commercial Greenhouses ACTIVE INGREDIENT: Tebufenpyrad: Pyrazole, 5-carboxamide, N-(p-tert-butylbenzyl)-4- chloro-3-ethyl-1-methyl 34.6% OTHER INGREDIENTS* .65.4% TOTAL 100.0% 1 Gallon contains-3.0 Ibs. of active ingredient, "contains petroleum distillates EPA Reg No. 71711-23 EPA Est. No. KEEP OUT OF REACH OF CHILDREN WARNING - AVSSO Si usted no entiende la etiqueta, busque a alguien para que se la explique a usted en detalle. (If you do not understand the label, find someone to explain it to you in detail.) FIRST AID If swallowed: • Immediately call a poison control center or doctor. • Do not induce vomiting unless told to do so by a poison control center or doctor. -
Sound Management of Pesticides and Diagnosis and Treatment Of
* Revision of the“IPCS - Multilevel Course on the Safe Use of Pesticides and on the Diagnosis and Treatment of Presticide Poisoning, 1994” © World Health Organization 2006 All rights reserved. The designations employed and the presentation of the material in this publication do not imply the expression of any opinion whatsoever on the part of the World Health Organization concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. Dotted lines on maps represent approximate border lines for which there may not yet be full agreement. The mention of specific companies or of certain manufacturers’ products does not imply that they are endorsed or recommended by the World Health Organization in preference to others of a similar nature that are not mentioned. Errors and omissions excepted, the names of proprietary products are distinguished by initial capital letters. All reasonable precautions have been taken by the World Health Organization to verify the information contained in this publication. However, the published material is being distributed without warranty of any kind, either expressed or implied. The responsibility for the interpretation and use of the material lies with the reader. In no event shall the World Health Organization be liable for damages arising from its use. CONTENTS Preface Acknowledgement Part I. Overview 1. Introduction 1.1 Background 1.2 Objectives 2. Overview of the resource tool 2.1 Moduledescription 2.2 Training levels 2.3 Visual aids 2.4 Informationsources 3. Using the resource tool 3.1 Introduction 3.2 Training trainers 3.2.1 Organizational aspects 3.2.2 Coordinator’s preparation 3.2.3 Selection of participants 3.2.4 Before training trainers 3.2.5 Specimen module 3.3 Trainers 3.3.1 Trainer preparation 3.3.2 Selection of participants 3.3.3 Organizational aspects 3.3.4 Before a course 4. -
AP-42, CH 9.2.2: Pesticide Application
9.2.2PesticideApplication 9.2.2.1General1-2 Pesticidesaresubstancesormixturesusedtocontrolplantandanimallifeforthepurposesof increasingandimprovingagriculturalproduction,protectingpublichealthfrompest-bornediseaseand discomfort,reducingpropertydamagecausedbypests,andimprovingtheaestheticqualityofoutdoor orindoorsurroundings.Pesticidesareusedwidelyinagriculture,byhomeowners,byindustry,andby governmentagencies.Thelargestusageofchemicalswithpesticidalactivity,byweightof"active ingredient"(AI),isinagriculture.Agriculturalpesticidesareusedforcost-effectivecontrolofweeds, insects,mites,fungi,nematodes,andotherthreatstotheyield,quality,orsafetyoffood.Theannual U.S.usageofpesticideAIs(i.e.,insecticides,herbicides,andfungicides)isover800millionpounds. AiremissionsfrompesticideusearisebecauseofthevolatilenatureofmanyAIs,solvents, andotheradditivesusedinformulations,andofthedustynatureofsomeformulations.Mostmodern pesticidesareorganiccompounds.EmissionscanresultdirectlyduringapplicationorastheAIor solventvolatilizesovertimefromsoilandvegetation.Thisdiscussionwillfocusonemissionfactors forvolatilization.Thereareinsufficientdataavailableonparticulateemissionstopermitemission factordevelopment. 9.2.2.2ProcessDescription3-6 ApplicationMethods- Pesticideapplicationmethodsvaryaccordingtothetargetpestandtothecroporothervalue tobeprotected.Insomecases,thepesticideisapplieddirectlytothepest,andinotherstothehost plant.Instillothers,itisusedonthesoilorinanenclosedairspace.Pesticidemanufacturershave developedvariousformulationsofAIstomeetboththepestcontrolneedsandthepreferred -
Use of Mesotrione for Annual Bluegrass (Poa Annua L.) at Cool
USE OF MESOTRIONE FOR ANNUAL BLUEGRASS (POA ANNUA L.) AT COOL- SEASON TURFGRASS ESTABLISHMENT by KATELYN A. VENNER A Thesis submitted to the Graduate School-New Brunswick Rutgers, The State University of New Jersey in partial fulfillment of the requirements for the degree of Master of Science Graduate Program in Plant Biology written under the direction of Stephen E. Hart Ph.D. and approved by ________________________ ________________________ ________________________ New Brunswick, New Jersey October, 2011 ABSTRACT OF THE THESIS USE OF MESOTRIONE AT COOL-SEASON TURFGRASS ESTABLISMENT By Katelyn Anne Venner Thesis director: Stephen E. Hart Annual bluegrass is a problematic weed in highly maintained turfgrass environments, and is difficult to control due to its adaptability to highly maintained turfgrass environments and lack of highly effective chemical control options. Mesotrione is a relatively new herbicide which has been found to show some level of control of annual bluegrass, and is safe to use at cool season turfgrass establishment. Thus, mesotrione has potential to be utilized for weed control in cultivated sod production. The objectives of this research were to evaluate mesotrione to determine: 1) tolerance of selected tall fescue cultivars, an important turfgrass species cultivated for sod, to applications of mesotrione; 2) the length of residual of mesotrione versus prodiamine, bensulide and dithiopyr for control of annual bluegrass; and 3) potential of mesotrione to control winter annual broadleaf weeds at Kentucky bluegrass establishment. Tall fescue cultivars were found to be tolerant to mesotrione applications made preemergence and preemergence plus 4 weeks after emergence at higher rates than required for weed control. -
Pesticide Application Procedures
CHAPTER 11 Pesticide ApplicAtion Procedures LEARNING OBJECTIVES After studying this chapter, you should be able to: • Name several different application procedures and types of equipment. • Discuss appropriate safety systems (e.g., closed mixing and loading, enclosed cab, and pesticide containment). • Identify the factors (e.g., nozzles, volumes, pressures, and speeds) that affect calibration. • Explain the importance of calibrating application equipment. • Show how to calculate the size of the application area. • Indicate how to determine the pesticide application rate. • Demonstrate how to determine the amount of pesticide concentrate and diluent to use. • Explain how to choose appropriate drift reduction practices. oday’s pest management practices be matched to the pesticide as well as to Trequire modern equipment to apply the size and type of the job. To make an a variety of pesticides. Pesticides may be effective, safe, and efficient application, applied as sprays, dusts, granules, gases read the label first. In addition, you (vapors), fogs, baits, rubs, or dips. The must properly select, operate, calibrate, vast array of application equipment must and maintain your equipment. APPLICATION METHODS he pesticide application method you equipment, and cost and efficiency of Tchoose depends on the nature and alternative methods. Your choice is habits of the target pest, characteristics often predetermined by one or more of of the target site, properties of the these factors. The following are some pesticide, suitability of the application common application methods: PESTICIDE APPLICATION PROCEDURES 157 • Crack-and-crevice application —placing small amounts of pes- ticide into cracks and crevices in buildings, such as along base- boards and in cabinets.