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氟环唑

氟环唑用途

Epoxiconazole 是一种杀菌剂,是麦角固醇生物合成途径的去甲基化抑制剂。Epoxiconazole 对耐多菌灵和耐苯甲酰胺的菌株均表现出强大的抑制作用,可用于控制多种农作物病害。

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氟环唑名称

[ CAS 号 ]:
133855-98-8

[ 中文名 ]:
氟环唑

[ 英文名 ]:
Epoxiconazole

[英文别名 ]:

Opal 7.5 EC
OPUS
Epoxiconazole

氟环唑生物活性

[ 描述 ]:

[ 相关类别 ]:

研究领域 >> 感染

信号通路 >> 抗感染 >> 真菌

[参考文献]

[1]. Yabing Duan, et al. Impact of Epoxiconazole on Fusarium Head Blight Control, Grain Yield and Deoxynivalenol Accumulation in Wheat. Pestic Biochem Physiol. 2018 Nov;152:138-147.

氟环唑物理化学性质

[ 密度 ]:
1.4±0.1 g/cm3

[ 沸点 ]:
463.1±55.0 °C at 760 mmHg

[ 熔点 ]:
125°C (lit.)

[ 分子式 ]:
C₁₇H₁₃ClFN₃O

[ 分子量 ]:
329.756

[ 闪点 ]:
233.9±31.5 °C

[ 精确质量 ]:
329.073120

[ PSA ]:
43.24000

[ LogP ]:
3.44

[ 外观性状 ]:
固体

[ 蒸汽压 ]:
0.0±1.1 mmHg at 25°C

[ 折射率 ]:
1.659

[ 储存条件 ]:
室温

氟环唑MSDS

详细MSDS(安全技术说明书)

氟环唑安全信息

[ 符号 ]:

GHS08, GHS09

[ 信号词 ]:
Danger

[ 危害声明 ]:
H351-H360Df-H411

[ 警示性声明 ]:
P201-P273-P308 + P313-P391-P501

[ 危害码 (欧洲) ]:
Xn: Harmful;N: Dangerous for the environment;

[ 风险声明 (欧洲) ]:
R40;R51/53;R62;R63

[ 安全声明 (欧洲) ]:
36/37-46-61

[ 危险品运输编码 ]:
UN 3077

[ RTECS号 ]:
XZ4500100

[ 海关编码 ]:
2933199090

氟环唑海关

[ 海关编码 ]: 2933199090

[ 中文概述 ]:
2933199090. 其他结构上有非稠合吡唑环化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%

[ 申报要素 ]: 品名, 成分含量, 用途, 乌洛托品请注明外观, 6－己内酰胺请注明外观, 签约日期

[ Summary ]:
2933199090. other compounds containing an unfused pyrazole ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

氟环唑文献

Molecular modelling of the emergence of azole resistance in Mycosphaerella graminicola.

PLoS ONE 6(6) , e20973, (2011)

A structural rationale for recent emergence of azole (imidazole and triazole) resistance associated with CYP51 mutations in the wheat pathogen Mycosphaerella graminicola is presented, attained by homo...

Enantiomeric separation of triazole fungicides with 3-μm and 5-μml particle chiral columns by reverse-phase high-performance liquid chromatography.

Chirality 23(6) , 479-86, (2011)

This study used chiral columns packed with 3-μm and 5-μm particles to comparatively separate enantiomers of 9 triazole fungicides, and Lux Cellulose-1 columns with chiral stationary phase of cellulose...

Inhibition of efflux transporter-mediated fungicide resistance in Pyrenophora tritici-repentis by a derivative of 4'-hydroxyflavone and enhancement of fungicide activity.

Appl. Environ. Microbiol. 71(6) , 3269-75, (2005)

Populations of the causal agent of wheat tan spot, Pyrenophora tritici-repentis, that are collected from fields frequently treated with reduced fungicide concentrations have reduced sensitivity to str...

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氟环唑