LD50 in male, female rats (mg/kg): >5000, 2028 orally; in rats (mg/kg): >2000 dermally; LC50 in bobwhite quail, mallard duck (mg/kg): >5200, >5200 dietary (Mercer)
그림문자(GHS):
신호 어:
Warning
유해·위험 문구:
암호
유해·위험 문구
위험 등급
범주
신호 어
그림 문자
P- 코드
H312
피부와 접촉하면 유해함
급성 독성 물질 - 경피
구분 4
경고
P280,P302+P352, P312, P322, P363,P501
H410
장기적 영향에 의해 수생생물에 매우 유독함
수생 환경유해성 물질 - 만성
구분 1
경고
P273, P391, P501
예방조치문구:
P273
환경으로 배출하지 마시오.
P280
보호장갑/보호의/보안경/안면보호구를 착용하시오.
P391
누출물을 모으시오.
P501
...에 내용물 / 용기를 폐기 하시오.
FENAMIDONE C화학적 특성, 용도, 생산
개요
Fenamidone (13; RPA 407213; (S)-5-methyl-2-methylthio-
5-phenyl-3-phenylamino-3,4-dihydroimidazol-4-one) is a complex III inhibitor
that does not derive from the strobilurins but rather
belongs to the imidazolinone chemical class. Fenamidone is a white woolly powder, with the
following characteristics: mp = 137 ?C; water solubility =
7.8 mg/L; logP = 2.8, and vp = 3.4×10?7 Pa. It was
first described by Mercer et al. (39) in 1998. Only the
S-enantiomer shows antifungal activity, thus offering a
reduction in application rates over the racemic mixture.
용도
Fungicide.
정의
ChEBI: A member of the class of imidazolones that is 3,5-dihydroimidazol-4-one substituted at position 2 by a methylthiogroup, at position 3 by an anilino group and at position 5 by phenyl and methyl groups (the S-enantiomer). A fungicide effecti
e against Oomycete diseases such as downy mildew and certain leaf spot diseases.
위험도
Moderately toxic by ingestion and skin contact. Low toxicity by inhalation.
