LD50 in rats, mice, rabbits (mg/kg): >5000 orally; LD50 dermally in rats: >2000 mg/kg; LC50 (4 hr) in rats: >1502 mg/m3 by inhalation (Nevill)
그림문자(GHS):
신호 어:
Warning
유해·위험 문구:
암호
유해·위험 문구
위험 등급
범주
신호 어
그림 문자
P- 코드
H332
흡입하면 유해함
급성 독성 물질 흡입
구분 4
경고
P261, P271, P304+P340, P312
예방조치문구:
P261
분진·흄·가스·미스트·증기·...·스프레이의 흡입을 피하시오.
P271
옥외 또는 환기가 잘 되는 곳에서만 취급하시오.
FENPICLONIL C화학적 특성, 용도, 생산
개요
Fenpiclonil is the
first phenylpyrrole fungicide developed by Ciba Geigy
(now belonging to the portfolio of Syngenta Crop Protection
AG) for seed treatment. Different formulation
types have been used for its commercialization either
in solo (trade name “Beret”) or in mixture with other
fungicides, as for instance, imazalil (“Beret Special”) or
carboxin + imazalil (“Beret Universal”).
용도
Fenpiclonil is a systemic and contact fungicide that provides protective
control of seed-borne pathogens of cereals such as snow mould
and bunt caused by Fusarium spp., Tilletia caries, Septoria nodorum, etc. It
also controls leaf spot, brown foot rot and ear blight in non-cereal crops.
정의
ChEBI: A member of the class of pyrroles carrying cyano and 2,3-dichlorophenyl substituents at positions 3 and 4 respectively. A fungicide used mainly to control seed-borne pathogens in cereal crops.
일반 설명
Fenpiclonil is a phenylpyrrole fungicide and a structural analogue of the antibiotic pyrrolnitrin found to be toxic to representatives of Ascomycetes, Basidiomycetes, and Deuteromycetes.
신진 대사 경로
Limited data are available in the open literature. Information presented in
this summary was abstracted from the data evaluation published by the
Pesticide Safety Directorate (PSD, 1993). Fenpiclonil is stable to hydrolytic
and soil degradation. Photolytic degradation is rapid. Hydroxylation
and oxidation of the pyrrole ring are the primary metabolic reactions in
plants and animals (Scheme 1).
