QUINOXYFEN

QUINOXYFEN 구조식 이미지
카스 번호:
124495-18-7
상품명:
QUINOXYFEN
동의어(영문):
Quinoxyphen;Quintec;QUINOXYFEN;FORTRESS(R);Legend Elios;Quinoxyfen 0.1;Quinoxyfen >Legend (fungicide);Quinoxyfen Standard;C16715000 Quinoxyfen
CBNumber:
CB7757516
분자식:
C15H8Cl2FNO
포뮬러 무게:
308.13
MOL 파일:
124495-18-7.mol
MSDS 파일:
SDS

QUINOXYFEN 속성

녹는점
105-106°
끓는 점
423℃
밀도
1.430
증기압
1.2 x 10-5 Pa (20 °C)
인화점
>100 °C
저장 조건
0-6°C
용해도
클로로포름(약간 용해됨), 메탄올(약간 용해됨)
물리적 상태
Solid
수용성
0.12mg l-1(20°C)
산도 계수 (pKa)
2.87±0.50(Predicted)
색상
흰색에서 밝은 노란색
Merck
14,8079
LogP
5.1 at 20℃
해리상수
3.56
EPA
Quinoxyfen (124495-18-7)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xi,N
위험 카페고리 넘버 43-50/53
안전지침서 24-37-46-60-61
유엔번호(UN No.) UN3077 9/PG 3
WGK 독일 3
RTECS 번호 VB4287500
위험 등급 9
포장분류 III
HS 번호 38220090
유해 물질 데이터 124495-18-7(Hazardous Substances Data)
독성 LD50 orally in rats: >5000 mg/kg; dermally in rabbits: >2000 mg/kg; by inhalation in rats: >3.38 mg/l (Longhurst)
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
H317 알레르기성 피부 반응을 일으킬 수 있음 피부 과민성 물질 구분 1 경고 GHS hazard pictograms P261, P272, P280, P302+P352,P333+P313, P321, P363, P501
H410 장기적 영향에 의해 수생생물에 매우 유독함 수생 환경유해성 물질 - 만성 구분 1 경고 GHS hazard pictograms P273, P391, P501
예방조치문구:
P261 분진·흄·가스·미스트·증기·...·스프레이의 흡입을 피하시오.
P272 작업장 밖으로 오염된 의복을 반출하지 마시오.
P273 환경으로 배출하지 마시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P302+P352 피부에 묻으면 다량의 물로 씻으시오.
P333+P313 피부자극성 또는 홍반이 나타나면 의학적인 조치·조언를 구하시오.

QUINOXYFEN C화학적 특성, 용도, 생산

화학적 성질

Off-White Solid

용도

Quinoxyfen is under development for the control of powdery mildew in cereals and grapes.

정의

ChEBI: A member of the class of quinolines carrying two chloro substituents at positions 5 and 7 together with a 4-fluorophenoxy substituent at position 4. A fungicide used mainly to control powdery mildew in cereals.

환경귀착

The stability of quinoxyfen in the soil has been shown to vary depending on soil type and source. DT50 values obtained in the field varied from 5 to 454 days for a range of soil types. The strong adsorptive properties of quinoxyfen reduce its soil dissipation rate, but result in no leaching potential of this fungicide into waterways or groundwater. The primary metabolite formed in the soil is 3-hydroxyquinoxyfen . A secondary soil metabolite is 5,7-dichloro-4-hydroxyquinoline (DCHQ). DCHQ was also found not to leach, even in sandy soils. Under acidic aqueous conditions, DCHQ was the primary metabolite found, and this was produced in greater quantities at acidic pHs. An additional metabolite was isolated from both water and the sediment in an aqueous clay loam system. Although not positively identified, it is suspected to be 6-hydroxyquinoxyfen.
A similar hydrolysis profile is observed in water as in soil (3). The primary product produced under acidic conditions in the absence of light was DCHQ. However, in the presence of light, photolysis was greatly increased and dose dependent on the amount of sunlight received. The primary photolysis product was 2-chloro-10- fluoro[1]benzopyrano[2,3,4-de]quinoline (CFBPQ).

신진 대사 경로

Quinoxyfen is a novel fungicide for the control of powdery mildew in cereals. Its mode of action is unknown but it appears to differ from those of current fungicides and thus may be novel (Longhurst et al., 1996). Quinoxyfen is tightly bound to soil components and is somewhat persistent in this medium but in aqueous solution it is subject to rapid photodecomposition. Photodegradation is therefore likely to be an important process in its immediate removal from the environment. Plant metabolites have not been reported but unchanged quinoxyfen has been confirmed as the major residue.
The compound is rapidly metabolised and eliminated following ingestion by rats and goats. Metabolism involves mainly hydroxylation of the intact quinoxyfen, cleavage at the ether bond and conjugation of the resulting metabolites. The information presented below was obtained from two sources (DowElanco, 1996; Reeves et al., 1996).

QUINOXYFEN 준비 용품 및 원자재

원자재

준비 용품


QUINOXYFEN 공급 업체

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