플루아지포프-뷰틸

한글명:플루아지포프-뷰틸

카스 번호69806-50-4

상품명:Fluazifop-butyl

CBNumberCB4670528

분자식C19H20F3NO4

포뮬러 무게383.36

MOL 파일69806-50-4.mol

동의어(한글)

플루아지포프-뷰틸

플루아지풉

풀루아지포프-부틸

화학적 성질

녹는점	13°C
끓는 점	bp0.05 167°
밀도	1.2100
인화점	2 °C
저장 조건	0-6°C
산도 계수 (pKa)	0.78±0.22(Predicted)
수용성	536.6ug/L(온도 미표시)
Merck	13,4142
EPA	Fluazifop-butyl (69806-50-4)

위험 및 안전 성명

위험품 표기	T,N,Xn,F
위험 카페고리 넘버	61-50/53-36-20/21/22-11
안전지침서	53-45-60-61-36-26-16
유엔번호(UN No.)	UN3082 9/PG 3
WGK 독일	3
RTECS 번호	UA3000000
HS 번호	29333990
유해 물질 데이터	69806-50-4(Hazardous Substances Data)

그림문자(GHS)

플루아지포프-뷰틸 화학적 특성, 용도, 생산

화학적 성질
Pale straw-colored, odorless liquid.
용도
Fluazifop-butyl-d9 is the labeled version of Fluazifop-butyl (F407433), which is often found in herbicidal and fungicidal mixture compositions.
일반 설명
A pale straw colored liquid. Selective herbicide.
공기와 물의 반응
Slightly soluble in water.
반응 프로필
FLUAZIFOP-BUTYL is a trimethyl phenoxy pyridine ester. May react with acids to liberate heat. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. May generate heat with caustic solutions. Genreates flammable hydrogen with alkali metals and hydrides.
위험도
Moderately toxic by ingestion.
농업용
Herbicide: Fluazifop-butyl is a selective post-emergence herbicide. Its principal uses in California is on rights-of-way, landscapes, almonds, cotton, and outdoor container nurseries. Not approved for use in EU countries. Not registered for use in the U.S. Used in southeast Asia. There are 18 global suppliers.
상품명
FUSILADE®[C]; FUSILADE® MAX (P-butyl); FUSION®; GRASS-B-GONE®; Greencrop; HACHE UNO SUPER®; HORIZON®; ICI-A0009®; ONESIDE®; ONESIDE EC®; ORNAMEC®; PP 009®; SL-236®; TF 1169®; TS-7236®; TORNADO®
잠재적 노출
Fluazifop-butyl is a selective post emergence aryloxyphenoxypropionate/organofluorine herbi cide. Its principal uses In California is on rights-of-way, landscapes, almonds, cotton, and outdoor container nurseries.
신진 대사 경로
Fluazifop butyl as a thin film on glass is photorearranged by UV irradiation to the isomer butyl-(RS)-2-[4-hydroxy-3-(5-trifluoromethyl-2- pyridyl)phenoxy]propionate. Plants of both resistant and susceptible populations of Digitaria sanguinalis rapidly hydrolyze 14C-fluazifop butyl to corresponding acid in leaves, but fluazifop acid is metabolized to other compounds at a more rapid rate in the resistant plants. An enhanced metabolism of toxophore, fluazifop acid is a likely mechanism of resistance in this population. The plants of putative resistant and susceptible population of Digitaria sanguinalis (L.) Scop had survived the application of 212 g/ha fluazifop-P-butyl in the year of collection.
폐기물 처리
In accordance with 40CFR165, follow recommendations for the disposal of pesticides and pesticide containers. Containers must be dis posed of properly by following package label directions or by contacting your local or federal environmental control agency, or by contacting your regional EPA office.

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