이프로다이온

이프로다이온
이프로다이온 구조식 이미지
카스 번호:
36734-19-7
한글명:
이프로다이온
동의어(한글):
이프로다이온;이프로디온;이프로다이온(IPRODIONE)
상품명:
Iprodione
동의어(영문):
IPRODION;3-(3,5-dichlorophenyl)-1-iso-propylcarbamoylhydantion;3-(3,5-Dichlorophenyl)-N-(1-methylethyl)-2,4-dioxo-1-imidazolidinecarboxamide;KIDAN;ROVER;anfor;rovrol;ROVRAL;330.16;fa2071
CBNumber:
CB7131064
분자식:
C13H13Cl2N3O3
포뮬러 무게:
330.17
MOL 파일:
36734-19-7.mol

이프로다이온 속성

녹는점
130-134 °C(lit.)
밀도
1.6223 (rough estimate)
증기압
5 x 10-7 Pa (25 °C)
굴절률
1.6140 (estimate)
인화점
2 °C
저장 조건
Sealed in dry,Room Temperature
용해도
DMSO: 100 mg/mL (302.87 mM)
산도 계수 (pKa)
9.19±0.20(Predicted)
수용성
0.0013g/100mL
Merck
13,5096
BRN
895003
LogP
3.000
CAS 데이터베이스
36734-19-7(CAS DataBase Reference)
NIST
Iprodione(36734-19-7)
EPA
Iprodione (36734-19-7)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xn,N,F
위험 카페고리 넘버 40-50/53-36-20/21/22-11
안전지침서 36/37-60-61-36-26-16
유엔번호(UN No.) UN 3077 9/PG 3
WGK 독일 3
RTECS 번호 NI8870000
HS 번호 29332900
유해 물질 데이터 36734-19-7(Hazardous Substances Data)
독성 LD50 in mice, rats (g/kg): 4, 3.5 orally (Lacroix, 1980)
기존화학 물질 KE-10192
그림문자(GHS): GHS hazard pictogramsGHS hazard pictograms
신호 어: Warning
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H351 암을 일으킬 것으로 의심됨 (노출되어도 암을 일으키지 않는다는 결정적인 증거가 있는 노출경로가 있다면 노출경로 기재) 발암성 물질 구분 2 경고 P201, P202, P281, P308+P313, P405,P501
H410 장기적 영향에 의해 수생생물에 매우 유독함 수생 환경유해성 물질 - 만성 구분 1 경고 GHS hazard pictograms P273, P391, P501
예방조치문구:
P202 모든 안전 조치 문구를 읽고 이해하기 전에는 취급하지 마시오.
P273 환경으로 배출하지 마시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P308+P313 노출 또는 접촉이 우려되면 의학적인 조치· 조언를 구하시오.
P391 누출물을 모으시오.
P405 밀봉하여 저장하시오.

이프로다이온 MSDS


3-(3,5-Dichlorophenyl)-2,4-dioxo-N-isopropylimidazolidine-1-carboxamide

이프로다이온 C화학적 특성, 용도, 생산

용도

Iprodione is a non-systemic fungicide that exhibits both protectant and eradicant activities against the spores and mycelium of a number of parasitic fungi. It is effective against Alternaria, Botrytis, Corticium, Fusarium, Helminthosporium, Monilinia, Phoma, Pleiochaeta, Rhizoctonia and Sclerotinia, etc. in nut crops, fruit trees (stone and pome fruit), vines, berries, vegetables, cereals, oilseed rape, cotton and ornamentals. Iprodione also controls various summer and winter turf diseases.

정의

ChEBI: An imidazolidine-2,4-dione in which the nitrogen at position 1 is substituted by an N-(isopropyl)carboxamide group while that at position 3 is substituted by a 3,5-dichlorophenyl group. A contact fungicide, it blocks the growth of the fu gal mycelium and inhibits the germination of fungal spores. It is used on fruit and vegetable crops affected by various fungal diseases. It is also used as a nematicide.

생산 방법

The synthesis uses 3,5-dichloroaniline which is coupled with glycine and phosgene. The urea substructure is formed by reaction with isopropylamine and phosgene. Many fungicide mixtures with Iprodione are on the market.

Safety Profile

Moderately toxic by ingestion. When heated to decomposition it emits very toxic fumes of NOx and Cl-.

환경귀착

Soil. Readily degrades in soil (half-life 20 to 160 days) releasing carbon dioxide 3,5dichloroaniline (Walker, 1987) and (Hartley and Kidd, 1987; Worthing and Hance, 1991). The rate of degradation increases with repeated applications of this fungicide. In a clay loam, the half-life was 1 week. After the second and third applications, the half-lives were 5 and 2 days, respectively (Walker et al., 1986).
Plant. Translocation and uptake by potato plants were reported (Cayley and Hide, 1980). Iprodione is rapidly metabolized in plants to 3,5-dichloroaniline (Cayley and Hide, 1980; Hartley and Kidd, 1987).
Chemical/Physical. In an aqueous solution at pH 8.7, iprodione hydrolyzed to N-(3,5dichloroanilinocarbonyl)-N-(isopropylaminocarbonyl)glycine (Belafdal et al., 1986). At pH 8.7, complete hydrolysis occurred after 14 hours (Cayley and Hide, 1980).
Gomez et al. (1982) studied the pyrolysis of iprodione in an helium atmosphere at 400–1,000°C. Decomposition began at 300°C producing isopropyl isocyanate and 3-(3,5dichlorophenyl)hydantoin. Above 600°C, the hydantoin ring began to decompose forming the following products: 3-chloroaniline, 3,5-dichloroaniline, chlorinated benzenes and benzonitrile. From 800 to 1,000°C, the hydantoin ring was completed destroyed whichled to the formation of aryl isocyanates, anilines and the corresponding diarylureas, namely 3-(3,5-dichlorophenyl)urea and 1-(3-chlorophenyl)-3-(3,5-dichlorophenyl)urea (Gomez et al., 1982).

신진 대사 경로

The opening and rearrangement of the dioxoimidazolidine ring is the initial and major degradation/metabolic reaction for iprodione. Iprodione degrades in soil via cleavage of the dioxoimidazolidine-carboxamide linkage, followed by ring opening to yield 3,5-dichloroaniline and CO2. In plants and animals, primary degradation reactions include N-dealkylation of the isopropyl moiety, ring opening and aryl hydroxylation (Scheme 1).

이프로다이온 준비 용품 및 원자재

원자재

준비 용품


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