FE나RIM올

한글명:FE나RIM올

카스 번호60168-88-9

상품명:Fenarimol

CBNumberCB9431616

분자식C17H12Cl2N2O

포뮬러 무게331.2

MOL 파일60168-88-9.mol

동의어(한글)

FE나RIM올

FE나RIM올(FENARIMOL)

페나리몰

화학적 성질

녹는점	117-119°C
끓는 점	0°C
밀도	1.3886 (rough estimate)
증기압	6.5 x 10^-5 Pa at 25 °C
굴절률	1.5490 (estimate)
인화점	0°C
저장 조건	0-6°C
용해도	클로로포름(약간 용해됨), 메탄올(약간 용해됨)
산도 계수 (pKa)	2.58
수용성	14.6 mg l^-1 (pH 3), 13.7 mg l^-1 (pH 7), 13.8 mg l^-1 (pH 10) at 25 °C
색상	황백색에서 밝은 노란색까지
Merck	13,3986
BRN	5972869
CAS 데이터베이스	60168-88-9(CAS DataBase Reference)
NIST	5-Pyrimidinemethanol, «alpha»-(2-chlorophenyl)-«alpha»-(4-chlorophenyl)-(60168-88-9)
EPA	Fenarimol (60168-88-9)

위험 및 안전 성명

위험품 표기	Xn;N,N,Xn
위험 카페고리 넘버	51/53-62-63-64
안전지침서	36/37-61
유엔번호(UN No.)	UN 3017/3077
WGK 독일	2
RTECS 번호	UV9279400
독성	LD50 in mice, rats (mg/kg): 4500, 2500 orally (Beraud)

그림문자(GHS)

FE나RIM올 MSDS

FE나RIM올 화학적 특성, 용도, 생산

용도
Fenarimol is a broad spectrum pyrimidine carbinol fungicide with protective, curative and eradicative activities against powdery mildew (Erysiphe spp., Pudusphaera leucutricha, Uncinula necatur, Sphaerutheca spp., Leveillula spp.) and scab (Venturia spp.) in many crops. It also controls powdery mildew (Sphaerutheca pannusa) in ornamentals and Fusarium patch (Micruduccium niuale), Take-all patch (Laefisaria fuciformis), Dollar spot (Sderutina humeucavpa) and red thread (Gaeumannumyces graminis) in turf and amenity grasses.
일반 설명
Pure white crystalline solid. Used as a fungicide. Irritates skin and mucous membranes.
반응 프로필
Fenarimol produces toxic gases when heated to decomposition.
Safety Profile
Moderately toxic by ingestion. Experimental reproductive effects. Mutation data reported. When heated to decomposition it emits toxic fumes of Cland NOx.
신진 대사 경로
The primary dissipation mechanism of fenarimol in the environment involves photolysis on plants/soil surfaces and water. More than 80 photoproducts have been observed, resulting from the reduction of the pyrimidine ring, hydrolysis, ring migration and cleavage of the phenyl and pyrimidine ring moieties. Under laboratory conditions in the dark, fenarimol is relatively persistent in soil, but a more rapid dissipation was observed under field conditions with DT₅₀ values of 18-140 days, attributed to photolysis of fenarimol on the soil surface. Fenarimol degrades in/on plant foliage/fruit surfaces mainly by photochemical processes. In animals, fenarimol is metabolised extensively to yield hydroxylated, cleavage and dechlorination products. The primary photolytic and metabolic pathways of fenarimol are presented in Schemes 1 and 2.

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