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5-(2-Chloro-4-(trifluoro-methyl)phenoxy)-2-nitro-benzoic acid sodium salt

 структура
62476-59-9
CAS №
62476-59-9
английское имя:
5-(2-Chloro-4-(trifluoro-methyl)phenoxy)-2-nitro-benzoic acid sodium salt
Синонимы:
Blazer;tackle 2as;LS 80.1213;Scifluorfen;Aciuorfen sodiuM;Sodium acifluorfen;ACIFLUORFEN SODIUM;ACIFLUORFENSODIUMSALT;Acifluorfen Sodium (Patented-No-Supply);SODIUM5-(2-CHLORO-A,A,A-TRIFLUORO-P-TOLYLOXY)-2-NITROBENZOA
CBNumber:
CB8455648
Формула:
C14H6ClF3NNaO5
молекулярный вес:
383.64
MOL File:
62476-59-9.mol

5-(2-Chloro-4-(trifluoro-methyl)phenoxy)-2-nitro-benzoic acid sodium salt атрибут

Температура плавления: 124-125°C
Температура кипения: >100 °C
плотность: 1.26 g/cm3(Temp: 23 °C)
форма: Твердый
FDA UNII: 6H07I1G902
Предложение 65 Список: Acifluorfen Sodium
Система регистрации веществ EPA: Acifluorfen, sodium salt (62476-59-9)
безопасность
  • Заявления о рисках и безопасности
  • код информации об опасности(GHS)
кода HS 29252900
Банк данных об опасных веществах 62476-59-9(Hazardous Substances Data)
символ(GHS) GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
сигнальное слово Danger
Заявление об опасности
пароль Заявление об опасности Класс опасности категория сигнальное слово пиктограмма предупреждение
H302 Вредно при проглатывании. Острая токсичность, пероральная Категория 4 Предупреждение GHS hazard pictograms P264, P270, P301+P312, P330, P501
H315 При попадании на кожу вызывает раздражение. Разъедание/раздражение кожи Категория 2 Предупреждение GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H318 При попадании в глаза вызывает необратимые последствия. Серьезное повреждение/раздражение глаз Категория 1 Опасность GHS hazard pictograms P280, P305+P351+P338, P310
H410 Чрезвычайно токсично для водных организмов с долгосрочными последствиями. Опасность для водной среды, долгосрочная опасность Категория 1 Предупреждение GHS hazard pictograms P273, P391, P501
Внимание
P264 После работы тщательно вымыть кожу.
P270 При использовании продукции не курить, не пить, не принимать пищу.
P273 Избегать попадания в окружающую среду.
P280 Использовать перчатки/ средства защиты глаз/ лица.
P301+P312 ПРИ ПРОГЛАТЫВАНИИ: Обратиться за медицинской помощью при плохом самочувствии.
P302+P352 ПРИ ПОПАДАНИИ НА КОЖУ: Промыть большим количеством воды.
P305+P351+P338 ПРИ ПОПАДАНИИ В ГЛАЗА: Осторожно промыть глаза водой в течение нескольких минут. Снять контактные линзы, если Вы ими пользуетесь и если это легко сделать. Продолжить промывание глаз.
P310 Немедленно обратиться за медицинской помощью.
P332+P313 При возникновении раздражения кожи: обратиться за медицинской помощью.
P501 Удалить содержимое/ контейнер на утвержденных станциях утилизации отходов.

5-(2-Chloro-4-(trifluoro-methyl)phenoxy)-2-nitro-benzoic acid sodium salt MSDS


5-(2-Chloro-4-(trifluoro-methyl)phenoxy)-2-nitro-benzoic acid sodium salt

5-(2-Chloro-4-(trifluoro-methyl)phenoxy)-2-nitro-benzoic acid sodium salt химические свойства, назначение, производство

Описание

Sodium acifluorfen was first registered in the United States in 1980 as the herbicide Blazer, by the Rohm and Haas Company. In 1987, the BASF Corporation purchased the registration and supporting data. In 2003, the US Environmental Protection Agency (EPA) conducted an assessment to determine if pesticide products containing the active ingredient sodium acifluorfen were eligible for pesticide reregistration. Results of the US EPA assessment were explained in the Reregistration Eligibility Decision (RED) of sodium acifluorfen. The RED document determined pesticides with the active ingredient of sodium acifluorfen were eligible for reregistration provided certain stipulations listed in the RED document were met, which included additional label requirements to limit the potential for drift. Under the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA) Section 3, all new pesticides used in the United States must be registered by the Administrator of the US EPA. There are 12 registrations for sodium acifluorfen.

Химические свойства

A diphenyl ether, is a combustible, off-white, light tan or brown solid.

Использование

Sodium acifluorfen is a member of a diphenyl ether group of light-dependent peroxidizing herbicides. Sodium acifluorfen is also a member of the nitrophenyl ether class of herbicides. This class of herbicides can cause rapid disruption of cell membranes in plants. Acifluorfen penetrates into the cytoplasm and causes the formation of peroxides and free electrons (requires light), ultimately destroying the cell membrane. Destruction of the cell membrane prevents translocation to other regions of the plant. In the environment, sodium acifluorfen degrades to acifluorfen (or acifluorfen acid). Additionally, acifluorfen acid is a degradation product of lactofen, another herbicide used on agricultural crops and in forestry. Sodium acifluorfen can be used alone or formulated with similar herbicides. Various formulation types include liquid, ready-to-use, and soluble concentrates. Agricultural crop applications are conducted by aircraft and by broadcast and band treatment using ground equipment. A trigger spray bottle for spot treatment is used by both agricultural and residential applicators. Sodium acifluorfen is primarily used on agricultural crops as a nonselective herbicide for pre- and postemergent control of annual broadleaf weeds and grasses. From 2001 to 2007, the annual US agricultural consumption of sodium acifluorfen was estimated at 300 000 pounds. An estimated 200 000 pounds of the agricultural consumption was applied to soybean crops. Sodium acifluorfen is also used on the agricultural crops peanuts, rice, peas, and strawberries. Sodium acifluorfen is registered for residential use; however, it is limited to spot treatment with ready-to-use formulations. Residential application of sodium acifluorfen is minor compared to agricultural, since it is a nonselective herbicide that kills both weeds and grasses.

Общее описание

White powder. Melting point 255- 257°F (124-125°C). Irritates skin and eyes. Used as a herbicide.

Реакции воздуха и воды

Water soluble.

Возможный контакт

A potential danger to those involved in the manufacture, formulation and application of this selective preemergence and postemergence herbicide used to control weeds and grass in soybean and peanut crops

Экологическая судьба

Acifluorfen inhibits the enzyme protoporphyrinogen oxidase, which catalyzes the dehydrogenation of protoporphyrinogen IX to protoporphyrin IX. In the presence of light, accumulated protoporphyrin can generate highly reactive oxygen species and induce membrane lipid peroxidation. The peroxidation of the lipid can result in a chain reaction and cause fragmentation and destruction of the lipid. The consequence of lipid peroxidation for a cell is loss of the membrane function. The primary target organs for sodium acifluorfen are the liver and kidneys. However, there are limited data that suggest cells can synthesize cytochrome P450 for detoxification of sodium acifluorfen. Further study is needed to confirm this.

Перевозки

UN2588 Pesticides, solid, toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required. UN3077 Environmentally hazardous substancessolid, n.o.s., Hazard class: 9; Labels: 9-Miscellaneous hazardous material, Technical Name Required

Несовместимости

Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides. Avoid contact with all sources of ignition.

Утилизация отходов

In accordance with 40CFR165, follow recommendations for the disposal of pesticides and pesticide containers.

5-(2-Chloro-4-(trifluoro-methyl)phenoxy)-2-nitro-benzoic acid sodium salt препаратная продукция и сырье

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