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Merck
CN

34343

苯氧威

PESTANAL®, analytical standard

别名:

2-(4-苯氧基苯氧基)乙基氨基甲酸乙酯

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关于此项目

经验公式(希尔记法):
C17H19NO4
化学文摘社编号:
分子量:
301.34
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
276-696-7
Beilstein/REAXYS Number:
6932817
MDL number:
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产品名称

苯氧威, PESTANAL®, analytical standard

InChI

1S/C17H19NO4/c1-2-20-17(19)18-12-13-21-14-8-10-16(11-9-14)22-15-6-4-3-5-7-15/h3-11H,2,12-13H2,1H3,(H,18,19)

InChI key

HJUFTIJOISQSKQ-UHFFFAOYSA-N

SMILES string

CCOC(=O)NCCOc1ccc(Oc2ccccc2)cc1

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

Fenoxycarb is a neurotoxic carbamate, insect growth regulator or public health insecticide, which can exhibit potent insect juvenile hormone-mimic activity, which causes disturbance in the development, reproduction and behaviour of insects. It can be used to control a wide variety of insect pests, basically in agriculture, forestry, and stored products.

Legal Information

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

hcodes

pictograms

Health hazardEnvironment

signalword

Warning

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

农药列管产品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Synthesis of haptens and protein conjugates for the development of immunoassays for the insect growth regulator fenoxycarb
Szurdoki F, et al.
Journal of Agricultural and Food Chemistry, 50, 29-40 (2002)
Quang Dang Nong et al.
Scientific reports, 7(1), 13521-13521 (2017-11-04)
Sexually dimorphic traits are common and widespread among animals. The expression of the Doublesex-/Mab-3-domain (DM-domain) gene family has been widely studied in model organisms and has been proven to be essential for the development and maintenance of sex-specific traits. However
David Jarriault et al.
Hormones and behavior, 56(1), 185-191 (2009-05-05)
Male moths use sex pheromones to find their mating partners. In the moth, Agrotis ipsilon, the behavioral response and the neuron sensitivity within the primary olfactory centre, the antennal lobe (AL), to sex pheromone increase with age and juvenile hormone
R Bober et al.
Insect molecular biology, 19(1), 77-86 (2009-12-17)
Sex pheromone production in Helicoverpa armigera is regulated by pheromone-biosynthesis-activating neuropeptide (PBAN), which binds to a G-protein coupled receptor at the pheromone gland. We demonstrate the temporal differential expression levels of the PBAN receptor (PBAN-R) gene, reaching peak levels at
Takeru Matsumoto et al.
Chemosphere, 72(3), 451-456 (2008-04-02)
It was reported that males daphnid Daphnia magna that have been induced by methyl farnesoate exposure exhibit higher tolerance to chemical compounds such as potassium dichromate and pentachlorophenol than females. Male neonates are also known to be induced by exposure

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