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32510

Supelco

氯虫酰胺

PESTANAL®, analytical standard

别名:

3-溴-4′-氯-1-(3-氯-2-吡啶)-2′-甲基-6′-(甲氨基甲酰基)吡唑-5--甲酰苯胺, 3-溴-N-[4-氯-2-甲基-6-[(甲氨基)羰基]苯基]-1-(3-氯-2-吡啶基)-1H-吡唑-5-甲酰胺, DPX E2Y45

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About This Item

经验公式(希尔记法):
C18H14BrCl2N5O2
分子量:
483.15
MDL编号:
UNSPSC代码:
41116107
PubChem化学物质编号:
NACRES:
NA.24

CN¥1,132.57


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等级

analytical standard

质量水平

产品线

PESTANAL®

保质期

limited shelf life, expiry date on the label

技术

HPLC: suitable
gas chromatography (GC): suitable

应用

agriculture
environmental

包装形式

neat

SMILES字符串

CNC(=O)c1cc(Cl)cc(C)c1NC(=O)c2cc(Br)nn2-c3ncccc3Cl

InChI

1S/C18H14BrCl2N5O2/c1-9-6-10(20)7-11(17(27)22-2)15(9)24-18(28)13-8-14(19)25-26(13)16-12(21)4-3-5-23-16/h3-8H,1-2H3,(H,22,27)(H,24,28)

InChI key

PSOVNZZNOMJUBI-UHFFFAOYSA-N

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此商品
SPEIROMAEIIIRONOTIRO
Sma I from Serratia marcescens Sb

SMAIRO

Sma I

Spe I from Sphaerotilus species

SPEIRO

Spe I

Mae III from Methanococcus aeolicus PL-15/H

MAEIIIRO

Mae III

Not I from Nocardia otitidis-caviarum

NOTIRO

Not I

biological source

Serratia marcescens

biological source

bacterial (Sphaerotilus spp.)

biological source

bacterial (Methanococcus aeolicus PL-15/H)

biological source

bacterial (Nocardia otitidis-caviarum)

specific activity

10000 U/mL

specific activity

10000 U/mL

specific activity

-

specific activity

-

suitability

suitable for molecular biology

suitability

suitable for molecular biology

suitability

-

suitability

-

concentration

<0.1 % (w/w)

concentration

-

concentration

-

concentration

-

application(s)

life science and biopharma

application(s)

life science and biopharma
sample preparation

application(s)

-

application(s)

-

一般描述

氯虫苯甲酰胺是一种新型的邻氨基苯甲酰胺杀虫剂,属于选择性ryanodine受体激动剂。它是对肌肉收缩至关重要的昆虫ryanodine受体(RyRs)的选择性和有效激活剂。它对于控制鳞翅目害虫以及双翅目、半翅目和鞘翅目中的某些物种非常有效。[1][2]

应用

有关合适的仪器技术的更多信息,请参阅产品′的检验报告。想要获得更多支持,请联系技术服务部。

生化/生理作用

氯虫苯甲酰胺激活昆虫中的RyRs,从而通过细胞中内部钙的不受调节的释放来影响钙稳态,导致昆虫停止进食,肌肉瘫痪,困倦,最终死亡。[2]

法律信息

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

象形图

Environment

警示用语:

Warning

危险声明

预防措施声明

危险分类

Aquatic Acute 1 - Aquatic Chronic 1

储存分类代码

11 - Combustible Solids

WGK

WGK 3

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

农药列管产品

  • 历史批次信息供参考:

    分析证书(COA)

    Lot/Batch Number

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    Jun Zhao et al.
    International journal of molecular sciences, 20(5) (2019-03-03)
    Uridine diphosphate glycosyltransferases (UGTs) are multifunctional detoxification enzymes, which are involved in metabolizing various chemicals and contribute to the development of insecticide resistance. However, the possible roles of UGTs in chlorantraniliprole resistance in Chilo suppressalis have rarely been studied in
    Feeding cessation effects of chlorantraniliprole, a new anthranilic diamide insecticide, in comparison with several insecticides in distinct chemical classes and mode-of-action groups.
    Hannig, Greg T., Melissa Ziegler, and Paula G. Marcon.
    Pest Management Science, 65 (9), 969-974 (2009)
    Su Liu et al.
    Pesticide biochemistry and physiology, 143, 102-110 (2017-12-01)
    Insect glutathione S-transferases (GSTs) play essential roles in the detoxification of insecticides and other xenobiotic compounds. The cabbage white butterfly, Pieris rapae, is an economically important agricultural pest. In this study, 17 cDNA sequences encoding putative GSTs were identified in
    Effects of chlorantraniliprole on eggs and larvae of Lobesia botrana (Denis & Schiffermuller)(Lepidoptera: Tortricidae).
    Ioriatti, Claudio, et al.
    Pest Management Science, 65 (6), 717-722 (2009)
    Llewellyn Green et al.
    Proceedings of the National Academy of Sciences of the United States of America, 116(21), 10424-10429 (2019-05-09)
    Insecticide resistance is a paradigm of microevolution, and insecticides are responsible for the strongest cases of recent selection in the genome of Drosophila melanogaster Here we use a naïve population and a novel insecticide class to examine the ab initio

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