Diniconazole

Diniconazole 구조식 이미지
카스 번호:
83657-24-3
상품명:
Diniconazole
동의어(영문):
DINICONAZOL;DINIT;XF 779;ACIDAN;sumi-8;ALYANS;s-3308l;xe-779l;DINIZOL;enazole
CBNumber:
CB1105036
분자식:
C15H17Cl2N3O
포뮬러 무게:
326.22
MOL 파일:
83657-24-3.mol
MSDS 파일:
SDS

Diniconazole 속성

녹는점
134~156℃
끓는 점
501.1±60.0 °C(Predicted)
밀도
1.32
증기압
2.93 x l0-3 Pa (20 °C)
저장 조건
Inert atmosphere,Room Temperature
용해도
DMSO:100.0(Max Conc. mg/mL);306.54(Max Conc. mM)
Water:0.67(Max Conc. mg/mL);2.05(Max Conc. mM)
물리적 상태
고체
수용성
4mg l-1(25°C)
산도 계수 (pKa)
12.89±0.20(Predicted)
CAS 데이터베이스
83657-24-3(CAS DataBase Reference)
EPA
1H-1,2,4-Triazole-1-ethanol, .beta.-[(2,4-dichlorophenyl)methylene]-.alpha.-(1,1-dimethylethyl)-, (.beta.E)- (83657-24-3)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
독성 LD50 in male, female rats (mg/kg): 639, 474 orally; >5000, >5000 dermally (Takano)
기존화학 물질 KE-10185
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
H302 삼키면 유해함 급성 독성 물질 - 경구 구분 4 경고 GHS hazard pictograms P264, P270, P301+P312, P330, P501
H410 장기적 영향에 의해 수생생물에 매우 유독함 수생 환경유해성 물질 - 만성 구분 1 경고 GHS hazard pictograms P273, P391, P501
예방조치문구:
P264 취급 후에는 손을 철저히 씻으시오.
P264 취급 후에는 손을 철저히 씻으시오.
P270 이 제품을 사용할 때에는 먹거나, 마시거나 흡연하지 마시오.
P273 환경으로 배출하지 마시오.
P301+P312 삼켜서 불편함을 느끼면 의료기관(의사)의 진찰을 받으시오.
P391 누출물을 모으시오.
P501 ...에 내용물 / 용기를 폐기 하시오.
NFPA 704
0
2 0

Diniconazole C화학적 특성, 용도, 생산

용도

Diniconazole is used to control leaf and ear diseases in cereals, powdery mildew in vines, rust and black spot in roses, leaf spot in peanuts, Sigatoka disease in bananas, and Uredinales in coffee. It is also used on fruit, vegetables and ornamentals.

신진 대사 경로

Diniconazole is a mixture of four isomers, which are derived from a chiral carbon atom and a double bond in the molecule. Diniconazole M [( E)-( S)-1-(2 ,4-dichlorophenyl)-4,4-dimethyl-2-1(H -1,2,4-triazol-l-yl)pent- 1-en-3-ol] is more potent than diniconazole. The major metabolic pathways of diniconazole involve oxidative attack on the pentenol side chain to give products which may form conjugates. In mammals, sulfurcontaining metabolites may be formed.

Degradation

Diniconazole is stable to heat, light and moisture. It undergoes photolysis and irradiation of a solution in methanol with light from a high-pressure mercury lamp for 8 hours gave three major and seven minor products, 2- 11 (Scheme 1). The major photoproduct was identified as the 2-isomer (2). The other major products (5 and 6) were formed by photooxidation of the CHOH group to a carbonyl group.
When diniconazole was irradiated as a thin film under ultraviolet light (254 nm), the major product was identified as the Z-isomer. On the surface of a sandy loam soil, under the same irradiation conditions rapid degradation occurred with the formation of 2, 5 and 6. A thin film of diniconazole applied to a glass plate degraded very slowly in the dark. When the plate was placed in the sunhght, 70% of the applied material disappeared after 5 days exposure and isomerisation occurred to give the Z-isomer (65%). The DT50 in sunlight was 2.5 days. Under ultraviolet light (254 mn), the Z-isomer was formed after 15 minutes irradiation, and after 5 hours 90% of the material had isomerised (Dureja and Walia, 1992).

Diniconazole 준비 용품 및 원자재

원자재

준비 용품


Diniconazole 공급 업체

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+8618523575427
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Longyan Tianhua Biological Technology Co., Ltd
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CHINA 2783 58

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