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・ Chloroxylenol
・ Chloroxylon
・ Chloroxymorphamine
・ Chlorozancla
・ Chlorozotocin
・ Chlorphenamine
・ Chlorphenesin
・ Chlorphenoxamine
・ Chlorphentermine
・ Chlorproethazine
・ Chlorproguanil
・ Chlorproguanil hydrochloride-dapsone-artesunate
・ Chlorproguanil/dapsone
・ Chlorpromazine
・ Chlorpropamide
Chlorpropham
・ Chlorprothixene
・ Chlorpyrifos
・ Chlorquinaldol
・ Chlortalidone
・ Chlortetracycline
・ Chlorthiamide
・ Chlorthiophos
・ Chlortoluron
・ Chlorurus
・ Chlorurus bleekeri
・ Chlorurus bowersi
・ Chlorurus capistratoides
・ Chlorurus enneacanthus
・ Chlorurus microrhinos


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Chlorpropham : ウィキペディア英語版
Chlorpropham

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Chlorpropham (commercial names: Bud Nip, Taterpex, Preventol, Elbanil, Metoxon, Nexoval, Stickman Pistols, Preweed, Furloe, Stopgerme-S, Sprout Nip, Mirvale, Bygran, ChlorIPC, CHLOROPROPHAM, Spud-Nic, Spud-Nie, Chloro-IFK, Chloro-IPC, Keim-stop, Triherbicide CIPC) is a plant growth regulator and herbicide used as a sprout suppressant for grass weeds, alfalfa, lima and snap beans, blueberries, cane fruit, carrots, cranberries, ladino clover, garlic, seed grass, onions, spinach, sugar beets, tomatoes, safflower, soybeans, gladioli and woody nursery stock. It is also used to inhibit potato sprouting and for sucker control in tobacco. Chlorpropham is available in emulsifiable concentrate and liquid formulations.
Chlorpropham is within the maximum residue limit regulation in Germany germination inhibitors approved for the treatment of potatoes for the purpose of preservation after harvest. Chlorpropham products are approved as a germination inhibitor for potatoes in Germany, Austria and Switzerland.
==Toxicity==
''Chlorpropham'' displays a low level toxicity profile, with no signs of acute toxicity after exposure of less than 1000 mg/kg/day. Long term exposure at high doses (≥ 1000 mg/kg/day) could cause reduction of body weight gain, decrease in hematocrit and hemoglobin, and increase in blood reticulocytes.
Regarding the carginogenic risk, chlorpropham is classified by the EPA as group E (non-carcinogenic). However, one of its metabolites (3-chloroaniline, for which there are no carcinogenicity data available) is structurally similar to the known carcinogen 4-chloroaniline.
The acceptable daily intake ranges from 0.03 mg/Kg (FAO 2001) to 0.05 mg/Kg (EPA 1996〔 and EC 2003).

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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