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,EXTOXNET I'll'-Ii Fi3EPf ION (7)ttp://ace.orst.edu/cgi-6in/mt's/0l/pipsrethephon,iiim <br /> t <br /> EXTOXNET <br /> Extension Toxicology Network <br /> S <br /> Pesticide Information Profiles <br /> i <br /> A Pesticide Information Project of Cooperative Extension Offices of Cornell University, Oregon State <br /> University, the University of Idaho, and the University of California at Davis and the Institute for <br /> Environmental Toxicology, Michigan State University. Major support and funding was provided by the <br /> USDA/Extension Service/National Agricultural Pesticide Impact Assessment Program. <br /> I EXTOXNET primary files maintained and archived at Oregon State University <br /> Revised 9/95. <br /> h <br /> ETHEPHON <br /> TRADE OR OTHER NAMES: The active ingredient ethephon is found in a variety of commercial <br /> herbicides. Trade names for products containing ethephon include Arvest, Bromeflor, Etheverse, r <br /> Flordimex, Flordimex T-Extra, Cerone, Etherel, Chipco Flores Pro and Prep (223, 316). <br /> REGULATORY STATUS: Ethephon is a general use pesticide (GUP). Check with specific state ' <br /> regulations for local restrictions that may apply. Products containing ethephon carry the Signal Words <br /> I <br /> "Danger", "Warning", or "Caution" depending on the product (223). <br /> I CHEMICAL CLASS: organic phosphorus compound /ethylene generator/plant growth regulator <br /> INTRODUCTION: Ethephon is a plant growth regulator. Its use varies with plant species, chemical <br /> concentration, and time of application. Ethephon regulates phases of plant growth and development by <br /> application to various growth sites (1). It is currently registered in the U.S. for use on apples, barley, <br /> blackberries, bromeliads, cantaloupes, cherries, coffee, cotton, cucumbers, grapes, guava, macadamia <br /> nuts, ornamentals, peppers, pineapples, rye, squash, sugarcane, tobacco, tomatoes, walnuts, wheat, etc. <br /> (1, 223, 207). Ethephon's mode of action acts via liberation of ethylene, which is absorbed by the plant <br /> and interferes in the growth process (1). It is also used in the acceleration of ripening of fruits and <br /> vegetables (302). Ethephon comes in RTU (ready-to-use), emulsifiable concentrate and aqueous solution <br /> formulations (223, 316). It may also be used in combination with Terpal (with mepiquat-chloride) and <br /> Terpal C (chlormequat-chloride) (223). <br /> TOXICOLOGICAL EFFECTS <br /> Acute Toxicity: The amount of ethephon that is lethal to one-half(50%) of experimental animals <br /> fed the material is referred to as its acute oral lethal dose fifty, or L1350. The acute oral toxicity of <br /> ethephon in rats ranged from 3400 mg/kg (313) to 4229 mg/kg (242, 223, 302). Acute animal <br /> toxicity studies in a few species show that via the oral and dermal routes, ethephon is relatively <br /> non-toxic except in hens. An acute study with rats showed an oral LD50 of 1.6 g/kg (EPA toxicity <br /> category III). An acute dermal study using rabbits showed a dermal LD50 of greater than 5 g/kg <br /> (EPA toxicity category III) (315). In a rat study, ethephon was administered by gavage for 13 weeks <br /> i <br /> i <br /> of 4 1/26,00 8:58 ANE <br />