CAS: 83121-18-0; N-((3,5-Dichloro-2,4-Difluorophenyl)Carbamoyl)-2,6-Difluorobenzamide
该化合物是一种化学化合物,被归类为苯甲醚昆虫生长调节器,主要用于农业用途,以控制虫害;其作用方式是抑制昆虫的合成,干扰昆虫的生长和发育,特别是在脱叶过程中;Teflubenzuron的特点是其对哺乳动物和鸟类的毒性相对较低,使其成为综合虫害管理系统的首选;通常用于乳油或颗粒等配方;该化合物在正常环境条件下保持稳定,但若暴露于极端pH水平或高温,则可能降解;其功效受温度,湿度和目标虫害生命阶段等因素的影响;此外,Teflubenzuron的免疫潜力较低,这有利于其环境安全性特征;然而,与所有农药一样,它应该用于标注指令,以尽量减少非目标生物和生态系统的潜在风险.
- 英文名称N-((3,5-Dichloro-2,4-Difluorophenyl)Carbamoyl)-2,6-Difluorobenzamide
- 中文名称氟苯脲
- IUPAC名称N-((3,5-dichloro-2,4-difluorophenyl)carbamoyl)-2,6-difluorobenzamide
- 其它别名Nomolt; N-(((3,5-Dichloro-2,4-Difluorophenyl)Amino)Carbonyl)-2,6-Difluorobenzamide; Diaract; Unii-Fs9P57Vl74; Teflubenzuron [iso]; N-(3,5
- CAS编号83121-18-0
- MFCD编号:MFCD00068254
- EINECS号:617-441-5
- FDA UNII编号:FS9P57VL74
- 分子式:C14H6Cl2F4N2O2
- 分子量:381.11
- 产品CID: 1820312
- 产品分类化学农药原药 → 杀虫剂 → 有机氯杀虫剂
物理性质
- 熔点221-224°
- 沸点539.6±60.0 °C at 760 mmHg
- 闪点280.2±32.9 °C
- 密度1.6±0.1 g/cm3
- pKa:8.16±0.46(预测)
- PSA:58.2
- LogP:4.84
- 折射率1.582
- 蒸汽压0.0±1.5 mmHg at 25°C
- 溶解性DMSO (Slightly), Methanol (Slightly, Heated, Sonicated)
- 敏感性常温下贮存稳定，50°C时水解半衰期为5d（pH值7）、4h(pH值9），土壤中半衰期2～6周。对家兔眼睛、皮肤有轻度刺激。
- 外观形态白色至类白色
- 储存条件0-6°C
- 产品应用该化合物用于控制莱皮多拉,科洛佩特拉,迪普泰拉,阿利罗德,希门诺彼拉,普西里达和希米特拉幼虫在葡萄树,小麦,柑橘,蔬菜,大豆,烟草和棉花上的控制,它还控制了蝗虫的苍蝇和蚊虫幼虫和不成熟的阶段.
MSDS等安全信息
欧盟法规
[欧盟农药活性物质上下游产品
CAS号60731-73-9 2,6-二氟苯甲酰异氰酸酯 | CAS号83121-15-7 3,5-二氯-2,4-二氟苯胺合成工艺路线路线简述
- 合成目标产物 Teflubenzuron 主要起始原料 2,6-Difluorobenzoyl Isocyanate And 2,4-Difluoro-3,5-Dichloroaniline
- 83121-15-7 + 60731-73-9 = 83121-18-0
反应条件:1.1 Solvents: 1,2-Dichloroethane; 5 - 6 H,Reflux
标题:Synthesis Of The Benzoylurea Insecticide Teflubenzuron
作者:Lu,Yang; Et Al
参考文献:Xiandai Nongyao 日期:2006 卷标:5(2) 页码:14-16]
= 83121-18-0
反应条件:1.1 Catalysts: Dimethyl Sulfoxide
标题:Preparation Of Benzoylurea Insecticides Such As Teflubenzuron By Oxidation Of Benzoylthioureas
参考文献:United Kingdom]
18063-03-1 + 83121-16-8 = 83121-18-0
反应条件:1.1 Solvents: Toluene; Rt -> Reflux; 7 - 8 H,Reflux
标题:Synthesis Of The Benzoylurea Insecticide Teflubenzuron
作者:Tu,Sai-Fei; Et Al
参考文献:Guangzhou Huagong 日期:2013 卷标:41(4) 页码:107-108]
1194-65-6 = 83121-18-0
反应条件:1.1 Reagents: Potassium Fluoride Solvents: Sulfolane; 8 H,230 °C1.2 Reagents: Sulfuric Acid Solvents: Water; 5 H,60 °C2.1 Solvents: 1,2-Dichloroethane; 5 H,Reflux2.2 Solvents: Toluene; Rt -> 100 °C; 6 H,Reflux
标题:Synthesis Of Insecticide Triflubenzuron
作者:Liu,Chang-Chun
参考文献:Jingxi Huagong Zhongjianti 日期:2001 卷标:31(6) 页码:28-29]
15952-70-2 = 83121-18-0
反应条件:1.1 Reagents: Acetic Acid,Iron,Ammonium Chloride Solvents: Ethanol,Water; 1 H,Reflux1.2 5 - 6 H1.3 Reagents: Sodium Carbonate Solvents: Water; Ph 92.1 Solvents: 1,2-Dichloroethane; 5 - 6 H,Reflux
标题:Synthesis Of The Benzoylurea Insecticide Teflubenzuron
作者:Lu,Yang; Et Al
参考文献:Xiandai Nongyao 日期:2006 卷标:5(2) 页码:14-16]
15952-70-2 = 83121-18-0
反应条件:1.1 Reagents: Acetic Acid,Iron Solvents: Ethanol,Water; 1 H,Reflux1.2 5 - 6 H,Reflux1.3 Reagents: Sodium Carbonate Solvents: Water; Ph 92.1 Solvents: 1,2-Dichloroethane; Rt -> Reflux; 5 - 6 H,Reflux
标题:New Technique For Synthesis Of Benzoylurea Insecticide Teflubenzuron
作者:Lu,Yang; Et Al
参考文献:Yingyong Huagong 日期:2006 卷标:35(1) 页码:54-56]
83121-15-7 + 333-20-0 + 18063-02-0 = 83121-18-0
反应条件:1.1 -2.1 Catalysts: Dimethyl Sulfoxide
标题:Preparation Of Benzoylurea Insecticides Such As Teflubenzuron By Oxidation Of Benzoylthioureas
参考文献:United Kingdom]
18063-03-1 = 83121-18-0
反应条件:1.1 Solvents: Toluene; 30 Min,Rt; 3 - 4 H,Reflux2.1 Solvents: 1,2-Dichloroethane; Rt -> Reflux; 5 - 6 H,Reflux
标题:New Technique For Synthesis Of Benzoylurea Insecticide Teflubenzuron
作者:Lu,Yang; Et Al
参考文献:Yingyong Huagong 日期:2006 卷标:35(1) 页码:54-56]
18063-03-1 = 83121-18-0 [标题:Reaction Conditions
标题:Urea Derivatives And Their Use
参考文献:European Patent Organization]
385-00-2 = 83121-18-0
反应条件:1.1 Reagents: Thionyl Chloride2.1 -3.1 Catalysts: Dimethyl Sulfoxide
标题:Preparation Of Benzoylurea Insecticides Such As Teflubenzuron By Oxidation Of Benzoylthioureas
参考文献:United Kingdom]
446-35-5 = 83121-18-0
反应条件:1.1 Reagents: Chlorine Solvents: Dimethyl Sulfoxide; 8 - 10 H,120 - 130 °C2.1 Reagents: Acetic Acid,Iron,Ammonium Chloride Solvents: Ethanol,Water; 1 H,Reflux2.2 5 - 6 H2.3 Reagents: Sodium Carbonate Solvents: Water; Ph 93.1 Solvents: 1,2-Dichloroethane; 5 - 6 H,Reflux
标题:Synthesis Of The Benzoylurea Insecticide Teflubenzuron
作者:Lu,Yang; Et Al
参考文献:Xiandai Nongyao 日期:2006 卷标:5(2) 页码:14-16]
446-35-5 = 83121-18-0
反应条件:1.1 Catalysts: Iodine Solvents: Dimethyl Sulfoxide; Rt -> 130 °C1.2 Reagents: Chlorine; 8 - 10 H,120 - 130 °C2.1 Reagents: Acetic Acid,Iron,Ammonium Chloride Solvents: Ethanol,Water; Rt -> 100 °C; 1 H,90 - 100 °C2.2 90 - 100 °C; 5 - 6 H,90 - 100 °C2.3 Reagents: Sodium Carbonate Solvents: Water; Ph 93.1 Solvents: 1,2-Dichloroethane; Reflux; 5 - 6 H,Reflux
标题:New Technique For Synthesis Of Insecticide Teflubenzuron,One Kind Of Benzoylureas
作者:Lu,Yang; Et Al
参考文献:Jingxi Yu Zhuanyong Huaxuepin 日期:2006 卷标:14(6) 页码:18-19]
83121-15-7 + 60731-73-9 = 83121-18-0
反应条件:1.1 Solvents: 1,2-Dichloroethane; Reflux; 5 - 6 H,Reflux
标题:New Technique For Synthesis Of Insecticide Teflubenzuron,One Kind Of Benzoylureas
作者:Lu,Yang; Et Al
参考文献:Jingxi Yu Zhuanyong Huaxuepin 日期:2006 卷标:14(6) 页码:18-19]
83121-15-7 + 18063-03-1 = 83121-18-0
反应条件:1.1 Solvents: 1,2-Dichloroethane; 5 H,Reflux1.2 Solvents: Toluene; Rt -> 100 °C; 6 H,Reflux
标题:Synthesis Of Insecticide Triflubenzuron
作者:Liu,Chang-Chun
参考文献:Jingxi Huagong Zhongjianti 日期:2001 卷标:31(6) 页码:28-29]
101513-70-6 = 83121-18-0
反应条件:1.1 Reagents: Sodium Azide Solvents: Toluene; 3 H,67 - 75 °C; 75 °C -> Reflux; 4 H,Reflux2.1 Solvents: Toluene; Rt -> Reflux; 7 - 8 H,Reflux
标题:Synthesis Of The Benzoylurea Insecticide Teflubenzuron
作者:Tu,Sai-Fei; Et Al
参考文献:Guangzhou Huagong 日期:2013 卷标:41(4) 页码:107-108]
1194-65-6 = 83121-18-0
反应条件:1.1 Reagents: Potassium Fluoride Catalysts: 2,4-Dinitrotoluene,Polyethylene Glycol Solvents: Sulfolane; 4 - 6 H,240 °C2.1 Reagents: Sulfuric Acid Solvents: Water; 5 H,70 - 80 °C3.1 Solvents: Toluene; 3 - 4 H,Reflux4.1 Solvents: 1,2-Dichloroethane; 5 - 6 H,Reflux
标题:Synthesis Of The Benzoylurea Insecticide Teflubenzuron
作者:Lu,Yang; Et Al
参考文献:Xiandai Nongyao 日期:2006 卷标:5(2) 页码:14-16]
15952-70-2 = 83121-18-0
反应条件:1.1 Reagents: Acetic Acid,Iron,Ammonium Chloride Solvents: Ethanol,Water; Rt -> 100 °C; 1 H,90 - 100 °C1.2 90 - 100 °C; 5 - 6 H,90 - 100 °C1.3 Reagents: Sodium Carbonate Solvents: Water; Ph 92.1 Solvents: 1,2-Dichloroethane; Reflux; 5 - 6 H,Reflux
标题:New Technique For Synthesis Of Insecticide Teflubenzuron,One Kind Of Benzoylureas
作者:Lu,Yang; Et Al
参考文献:Jingxi Yu Zhuanyong Huaxuepin 日期:2006 卷标:14(6) 页码:18-19]
18063-03-1 = 83121-18-0
反应条件:1.1 Solvents: Toluene; 3 - 4 H,Reflux2.1 Solvents: 1,2-Dichloroethane; 5 - 6 H,Reflux
标题:Synthesis Of The Benzoylurea Insecticide Teflubenzuron
作者:Lu,Yang; Et Al
参考文献:Xiandai Nongyao 日期:2006 卷标:5(2) 页码:14-16]
18063-03-1 = 83121-18-0
反应条件:1.1 Solvents: Toluene; 30 Min,Rt; Rt -> Reflux; 3 - 4 H,Reflux2.1 Solvents: 1,2-Dichloroethane; Reflux; 5 - 6 H,Reflux
标题:New Technique For Synthesis Of Insecticide Teflubenzuron,One Kind Of Benzoylureas
作者:Lu,Yang; Et Al
参考文献:Jingxi Yu Zhuanyong Huaxuepin 日期:2006 卷标:14(6) 页码:18-19]
1897-52-5 = 83121-18-0
反应条件:1.1 Reagents: Sulfuric Acid Solvents: Water; 5 H,70 - 80 °C2.1 Solvents: Toluene; 3 - 4 H,Reflux3.1 Solvents: 1,2-Dichloroethane; 5 - 6 H,Reflux
标题:Synthesis Of The Benzoylurea Insecticide Teflubenzuron
作者:Lu,Yang; Et Al
参考文献:Xiandai Nongyao 日期:2006 卷标:5(2) 页码:14-16]
1897-52-5 = 83121-18-0
反应条件:1.1 Reagents: 2,4-Dinitrotoluene,Potassium Fluoride Solvents: Sulfolane; 4 - 6 H,230 - 240 °C1.2 Reagents: Sulfuric Acid Solvents: Water; 5 H,70 - 80 °C2.1 Solvents: Toluene; 30 Min,Rt; Rt -> Reflux; 3 - 4 H,Reflux3.1 Solvents: 1,2-Dichloroethane; Reflux; 5 - 6 H,Reflux
标题:New Technique For Synthesis Of Insecticide Teflubenzuron,One Kind Of Benzoylureas
作者:Lu,Yang; Et Al
参考文献:Jingxi Yu Zhuanyong Huaxuepin 日期:2006 卷标:14(6) 页码:18-19]
42221-52-3 = 83121-18-0
反应条件:1.1 Reagents: Potassium Fluoride Solvents: Dimethylformamide; Rt -> 135 °C; 4 H,130 - 135 °C2.1 Reagents: Sodium Azide Solvents: Toluene; 3 H,67 - 75 °C; 75 °C -> Reflux; 4 H,Reflux3.1 Solvents: Toluene; Rt -> Reflux; 7 - 8 H,Reflux
标题:Synthesis Of The Benzoylurea Insecticide Teflubenzuron
作者:Tu,Sai-Fei; Et Al
参考文献:Guangzhou Huagong 日期:2013 卷标:41(4) 页码:107-108]
446-35-5 = 83121-18-0
反应条件:1.1 Reagents: Chlorine; 8 - 10 H,120 - 130 °C2.1 Reagents: Acetic Acid,Iron Solvents: Ethanol,Water; 1 H,Reflux2.2 5 - 6 H,Reflux2.3 Reagents: Sodium Carbonate Solvents: Water; Ph 93.1 Solvents: 1,2-Dichloroethane; Rt -> Reflux; 5 - 6 H,Reflux
标题:New Technique For Synthesis Of Benzoylurea Insecticide Teflubenzuron
作者:Lu,Yang; Et Al
参考文献:Yingyong Huagong 日期:2006 卷标:35(1) 页码:54-56]
879-39-0 = 83121-18-0
反应条件:1.1 Reagents: Potassium Fluoride2.1 -3.1 -
标题:Urea Derivatives And Their Use
参考文献:European Patent Organization]
89-69-0 = 83121-18-0
反应条件:1.1 Reagents: Chlorine; Rt -> 70 °C; 10 H,50 - 70 °C1.2 Reagents: Potassium Fluoride Solvents: Dimethyl Sulfoxide; 10 H,Reflux2.1 Reagents: Iron,Ammonium Chloride Solvents: Water; Rt -> 90 °C; 60 Min,90 - 95 °C; 2 H,90 - 95 °C3.1 Solvents: 1,2-Dichloroethane; 5 H,Reflux3.2 Solvents: Toluene; Rt -> 100 °C; 6 H,Reflux
标题:Synthesis Of Insecticide Triflubenzuron
作者:Liu,Chang-Chun
参考文献:Jingxi Huagong Zhongjianti 日期:2001 卷标:31(6) 页码:28-29]
= 83121-18-0
反应条件:1.1 Reagents: Sulfuric Acid,Nitric Acid; Rt -> 50 °C; 2 H,50 °C2.1 Reagents: Chlorine; Rt -> 70 °C; 10 H,50 - 70 °C2.2 Reagents: Potassium Fluoride Solvents: Dimethyl Sulfoxide; 10 H,Reflux3.1 Reagents: Iron,Ammonium Chloride Solvents: Water; Rt -> 90 °C; 60 Min,90 - 95 °C; 2 H,90 - 95 °C4.1 Solvents: 1,2-Dichloroethane; 5 H,Reflux4.2 Solvents: Toluene; Rt -> 100 °C; 6 H,Reflux
标题:Synthesis Of Insecticide Triflubenzuron
作者:Liu,Chang-Chun
参考文献:Jingxi Huagong Zhongjianti 日期:2001 卷标:31(6) 页码:28-29
敌草腈置于potassium Fluoride,四丁基溴化铵,双氧水体系中,用 氯仿,甲苯 作为反应溶剂,化学反应 24.0H,反应生成 氟苯脲
参考文献:一种杀虫剂伏虫隆及其中间体2,6-二氟苯甲酰胺的合成方法
标题:一种杀虫剂伏虫隆及其中间体2,6-二氟苯甲酰胺的合成方法
摘要:本发明公开了一种杀虫剂伏虫隆及其中间体2,6‑二氟苯甲酰胺的合成方法,属于杀虫剂领域,一种杀虫剂伏虫隆及其中间体2,6‑二氟苯甲酰胺的合成方法,包括以下步骤:步骤一,制备2,6‑二氯苄叉二氯:配制二氯甲苯和五氯化磷的悬浊液,并通入氯气,而后利用气液分离器对物料分层,收集粗品,对粗品精馏得到2,6‑二氯苄叉二氯;步骤二,制备2,6‑二氯苯腈:将2,6‑二氯苄叉二氯,乙酸,氯化锌,盐酸羟胺和醋酸钠混合,升温至回流反应,反应完全后,降温搅拌,过滤,烘干得到2,6‑二氯苯腈,它采用"一锅法"完成,反应路线缩短,总收率从现有的55.4%提升至67.3%;成本大大减少.
海关参考信息
- 2903919090-氯苯
2912110000-甲醛
2912210000-苯甲醛
2924199090-其他无环酰胺 - 💡 提示：海关信息按照顺序优先匹配，如需确认的海关信息，请参考相关资料。
- 详情请参考：📖 海关编码查询和海关进出口税则
专利信息
专利号:WO-2025056767-A1
优先权日:2023-09-15
标题 :Process for the preparation of enantiomerically enriched aliphatic amines
发明人：BOU HAMDAN FARHAN; GODINEAU EDOUARD; SMEJKAL TOMAS; DUMEUNIER RAPHAEL; BOUSSEMGHOUNE MOHAMED ABDELOUAHAB; BLUM MATHIAS
权利人:SYNGENTA CROP PROTECTION AG
摘要:The present invention relates to a process for the preparation of enantiomerically enriched cyclobutylamines of formula (I) from α-tertiary cyclobutanones and reacting said enantiomerically enriched cyclobutylamines to enantiomerically enriched cyclobutylamides. Such compounds are useful intermediates in the synthesis of microbiocidal thiazole compounds.
专利号:WO-2011067757-A1
优先权日:2009-12-06
标题 :INSECTICIDAL COMPOSITIONS OF CHITIN SYNTHESIS INHIBITORS (CSIs) AND THE ENTOMOPATHOGENIC FUNGUS NOMURAEA RILEYI
发明人：APPLEBAUM SHALOM W; ICHELCZIK DANA; BARAZANI AVNER
权利人:MAKHTESHIM CHEM WORKS LTD; YISSUM RES DEV CO; APPLEBAUM SHALOM W; ICHELCZIK DANA; BARAZANI AVNER
摘要:The present invention discloses a pesticidal composition comprising a combination of a chitin synthesis inhibitor (CSI) and the fungus Nomuraea rileyi, wherein this composition is insecticidally effective and contains an insecticidally effective amount of a chitin synthesis inhibitor and an insecticidally effective amount of the fungus Nomuraea rileyi. Also are disclosed a method of treating or preventing pest infestation in a plant or in an environment in which this plant is grown, by contacting the plant or environment with the pesticidal composition of the invention, and a method for reducing the amount of CSI required to control insects, and the use of the pesticidal composition of the invention in controlling insects in a plant or an environment of the plant.
专利号:US-10906880-B2
优先权日:2016-01-26
标题:Kind of isothiazole oxime ether-containing strobilurin derivatives and its preparation methods and application
发明人：FAN ZHIJIN; CHEN LAI; GUO XIAOFENG; ZHU YUJIE; QIAN XIAOLIN; MA LIUYONG; ZHANG NAILOU; WANG HAIXIA; ZHANG ZHIMING; XU JINGHUA; SONG YINQI
权利人:UNIV NANKAI
摘要:The present invention is that provided a synthesis method of a series of isothiazole oxime ether containing strobilurin derivatives IV. The present invention relates to 3,4-dichloroisothiazolyl oxime ether strobilurin derivatives, and their chemical structural formula is as shown by IV. n n n n n n n n n n The invention discloses the structural formula of the above compound, the synthesis method and the use as an insecticide, a fungicide, an anti-plant virus agent, and an agriculturally acceptable auxiliary or synergist and a commercial insecticide. The use of a fungicide, an anti-plant virus agent and an acaricide in combination for controlling agricultural, forestry, horticultural plant pests, diseases, virus diseases and preparation methods.
专利号:US-7628979-B1
优先权日:2005-04-20
标题 :Use of calco oil blue V in bait formulations for marking and controlling subterranean termites
发明人：MORALES-RAMOS JUAN A; ROJAS MARIA G
权利人:US AGRICULTURE
摘要:Termite bait matrix containing cellulose, calco oil blue V (solvent blue 58 or 9,10-anthracenedione, 1,4-bis[(2-ethylhexyl)amino]), and optionally a termite toxicant (e.g., chitin synthesis inhibitor). Methods of monitoring termite activity in a region involving placing a termite bait matrix in the region and assessing the presence of termites at the site of the termite matrix, the termite bait matrix contains cellulose and 9,10-anthracenedione, 1,4-bis[(2-ethylhexyl)amino]. Methods of killing termites, involving placing a termite bait matrix in a termite habitat and allowing termites to feed on the bait matrix, the termite bait matrix contains cellulose, 9,10-anthracenedione, 1,4-bis[(2-ethylhexyl)amino], and a termite toxicant (e.g., chitin synthesis inhibitor).
专利号:WO-02087337-A3
优先权日:2001-05-01
标 题:Pesticidal compositions comprising a chitin synthesis inhibitor and piperonyl butoxide
发明人：VERBRUGGEN LUC ROSALIA MICHAEL
权利人:JANSSEN PHARMACEUTICA NV; VERBRUGGEN LUC ROSALIA MICHAEL
摘要:The present invention relates to pesticide compositions and particularly to compositions which are able to provide an improved protecting effect against invertebrates such as insects and acari. More particularly, the present invention relates to synergistic pesticide compositions comprising a chitin synthesis inhibitor and piperonyl butoxide for protecting any living or non-living material, such as crops, plants, fruits, seeds, building parts made of wood, thatch or the like, biodegradable material and textiles against deterioration due to the action of pests such as insects and for treating animals, especially mammals, gallinaceae and anatidae, against such harmful invertebrates. This invention thus relates to the field of protection of plants, crops, warm-blooded animals, food, building materials and textiles through the control of pests. The chitin biosynthesis inhibitors are specifically, bistrifluron, buprofezin, chlorfluazuron, diflubenzuron, flucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, teflubenzuron or triflumuron. Preferred is flufenoxuron.
专利号:EP-1306084-B1
优先权日:1998-06-09
标 题 :Compositions for the control of parasitic infestations in fish
发明人：ALEXANDER SVEIN; EVENSEN OYSTEIN; SYVERTSEN CHRISTIAN; MARTINSEN BERNT
权利人:PHARMAQ AS
摘要:Injectable compositions comprising antiparasitically active chitin synthesis inhibitor substances are described, for controlling parasitic infestations including infestations with sea lice and isopod species in farmed fish. The compositions are optionally formulated in a fish vaccine. The antiparasitically active chitin synthesis inhibitor substances protect the fish against parasites for a substantial period of time after injection. Useful embodiments include compositions with lufenuron that confer protection against new parasitic infestation for an extended period of time after treatment.
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供应商参考报价(招募中)
品牌试剂参考报价(招募中)
📌 第三方产品分析报告
主要参考文献
1: Reshuffling of Aspergillus fumigatus Cell Wall Components Chitin and β-Glucan under the Influence of Caspofungin or Nikkomycin Z Alone or in Combination Patricia E. B. Verwer, M. L. van Duijn, M. Tavakol, Irma A. J. M. Bakker-Woudenberg, Wendy W. J. van de Sande Antimicrob Agents Chemother. 2012 Mar; 56(3): 1595–1598. doi: 10.1128/AAC.05323-11 An overview and outlook with emphasis on efficacy, usage and resistance Pablo Junquera, Barry Hosking, Marta Gameiro, Alicia Macdonald Parasite. 2019;
26: 26. Published online 2019 May 1. doi: 10.1051/parasite/2019026 2019; 14(9): e0222520. Published online 2019 Sep 23. doi: 10.1371/journal.pone.0222520 Toé, Laurence Gamet-Payrastre, Pierre I. Guissou Toxicol Rep. 2014;
1: 474–489. Published online 2014 Jul 25. doi: 10.1016/j.toxrep.2014.07.008 Poley, Laura M. Braden, Amber M. Messmer, Okechukwu O. Igboeli, Shona K. Whyte, Alicia Macdonald, Jose Rodriguez, Marta Gameiro, Lucien Rufener, Jacques Bouvier, Dorota W. Wadowska, Ben F. Koop, Barry C. Hosking, Mark D. Fast Int J Parasitol Drugs Drug Resist. 2018 Aug; 8(2): 174–188. Published online 2018 Mar 13. doi: 10.1016/j.ijpddr.2018.02.007 2013 Mar; 36(3): 171–194. Published online 2013 Jan 13. doi: 10.1111/jfd.12061 Meagher, Jr., Neil Miller, Lambert Kanga, Muhammad Haseeb, José Eduardo Serrão, Carlos Frederico Wilcken, José Cola Zanuncio PLoS One. 2018; 13(11): e0206789. Published online 2018 Nov 8. doi: 10.1371/journal.pone.0206789 2015;
合成参考文献
摘要:Nippon Noyaku Gakkaishi. Journal of the Pesticide Science Society of Japan., 18(S15), 1993
参考文献:10.1186/1471-2148-14-108
摘要:Ljungfeldt LER, Espedal PG, Nilsen F, Skern-Mauritzen M, Glover KA. A common-garden experiment to quantify evolutionary processes in copepods: the case of emamectin benzoate resistance in the parasitic sea louse Lepeophtheirus salmonis. BMC Ecology and Evolution. 2014 May 19;14(1):108. doi: 10.1186/1471-2148-14-108.
参考文献:10.1007/s10646-020-02261-w
摘要:Souza JR, Moreira LB, Lima LLR, Silva TG, Braga PPM, Carvalho GA. Susceptibility of Chrysoperla externa (Hagen, 1861) (Neuroptera: Crysopidae) to insecticides used in coffee crops. Ecotoxicology. 2020 Nov;29(9):1306–14. doi: 10.1007/s10646-020-02261-w.
摘要:Ohtake C. [First drafts of the Environmental Health Criteria (EHC) circulated for comments by IPCS in 1995-1996]. Eisei Shikenjo Hokoku. 1996;(114):95–8.
参考文献:10.1021/jf980846a
摘要:Aplada-Sarlis PG, Miliadis GE, Tsiropoulos NG. Dissipation of teflubenzuron and triflumuron residues in field-sprayed and cold-stored pears. J Agric Food Chem. 1999 Jul;47(7):2926–9. doi: 10.1021/jf980846a.
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