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Merck
CN

32506

乙螨唑

PESTANAL®, analytical standard

别名:

(RS)-5-叔丁基-2-[2-(2,6-二氟苯基)-4,5-二氢-1,3-氧氮杂茂-4-基]苯乙醚, 4-(4-叔丁基-2-乙氧基苯基)-2-(2,6-二氟苯基)-4,5-二氢噁唑

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关于此项目

经验公式(希尔记法):
C21H23F2NO2
化学文摘社编号:
分子量:
359.41
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
8930214
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产品名称

乙螨唑, PESTANAL®, analytical standard

InChI key

IXSZQYVWNJNRAL-UHFFFAOYSA-N

SMILES string

CCOc1cc(ccc1C2COC(=N2)c3c(F)cccc3F)C(C)(C)C

InChI

1S/C21H23F2NO2/c1-5-25-18-11-13(21(2,3)4)9-10-14(18)17-12-26-20(24-17)19-15(22)7-6-8-16(19)23/h6-11,17H,5,12H2,1-4H3

grade

analytical standard

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

Quality Level

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

General description

Etoxazole is an organofluorine pesticide and an alternative for carbamates, organochlorines and other miticides. It is a commonly used acaricide, for flowers, fruits, vegetables, tea, cotton etc.

Legal Information

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

pictograms

Environment

signalword

Warning

hcodes

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

854.6 °F

flash_point_c

457 °C

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

法规信息

农药列管产品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Dali Sun et al.
Chemosphere, 226, 782-790 (2019-04-10)
Etoxazole is a newly registered and widely used acaricide. However, its metabolites were not fully understood and might exhibit similar or even higher toxicity than parent compound. Therefore, in this study, the metabolites of etoxazole in citrus, soil and earthworms
Dali Sun et al.
Environmental science and pollution research international, 23(24), 24731-24738 (2016-09-24)
The stereoselective cytotoxicity of new chiral acaricide etoxazole and its dissipation in citrus and soil were investigated for the first time. Enantioselective toxicity and oxidative stress of etoxazole toward MCF-7 cells was conducted. The phenomenon of dose- and form-dependent cytotoxicity
High resolution genetic mapping uncovers chitin synthase-1 as the target-site of the structurally diverse mite growth inhibitors clofentezine, hexythiazox and etoxazole in Tetranychus urticae.
Demaeght P, et al.
Insect Biochemistry and Molecular Biology, 51, 52-61 (2014)
Evaluation of etoxazole toxicity in the liver of Oreochromis niloticus.
Sevgiler Y, et al.
Pesticide Biochemistry and Physiology, 78(1), 1-8 (2004)
Weixia Chang et al.
Journal of agricultural and food chemistry, 67(24), 6708-6715 (2019-05-30)
This is the first systemic assessment of the stereoselectivity of etoxazole enantiomers. Etoxazole's stereoselective bioactivity was assessed against target organisms ( Tetranychus urticae eggs and Tetranychus cinnabarinus eggs), and its acute toxicity was assessed toward nontarget aquatic organisms ( Daphnia

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