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Merck
CN
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安全信息

45495

Supelco

氰戊菊酯

PESTANAL®, analytical standard

别名:

α-氰基-3-苯氧基苄基-α-(4-氯苯基)-3-甲基丁酸酯

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About This Item

经验公式（希尔记法）:
C25H22ClNO3
CAS号:
51630-58-1
分子量:
419.90
Beilstein:
2025982
EC 号:
257-326-3
MDL编号:
MFCD00055324
UNSPSC代码:
41116107
PubChem化学物质编号:
329756787
NACRES:
NA.24

等级

analytical standard

质量水平

100

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

CC(C)C(C(=O)OC(C#N)c1cccc(Oc2ccccc2)c1)c3ccc(Cl)cc3

InChI

1S/C25H22ClNO3/c1-17(2)24(18-11-13-20(26)14-12-18)25(28)30-23(16-27)19-7-6-10-22(15-19)29-21-8-4-3-5-9-21/h3-15,17,23-24H,1-2H3

InChI key

NYPJDWWKZLNGGM-UHFFFAOYSA-N

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应用

有关合适的仪器技术的更多信息，请参阅产品的分析证书。想要获得更多支持，请联系技术服务部。

生化/生理作用

II 型拟除虫菊酯。强效钙调磷酸酶（蛋白磷酸酶 2B）抑制剂。

法律信息

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

象形图

Skull and crossbonesEnvironment
GHS06,GHS09

警示用语：

Danger

危险分类

Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

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
BCCM5344
BCCD3529
BCCC6546

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Saskia Knillmann et al.
Global change biology, 19(5), 1598-1609 (2013-03-19)
Considerable research efforts have been made to predict the influences of climate change on species composition in biological communities. However, little is known about how changing environmental conditions and anthropogenic pollution can affect aquatic communities in combination. We investigated the
Saskia Knillmann et al.
Ecotoxicology (London, England), 21(4), 1039-1049 (2012-02-09)
Xenobiotics alter the balance of competition between species and induce shifts in community composition. However, little is known about how these alterations affect the recovery of sensitive taxa. We exposed zooplankton communities to esfenvalerate (0.03, 0.3, and 3 μg/L) in
Tao Tang et al.
Pest management science, 68(11), 1501-1511 (2012-06-13)
The function of cytochrome P450 proteins (P450s) in the metabolism of a variety of compounds by oxidation and reduction is well elucidated, but its interactions with other electron transfer components in the pyrethroid resistance of insect pests have been a
Fang B Yu et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 48(3), 198-207 (2013-01-30)
A fenvalerate-degrading bacterial strain F-7 was isolated from long-term contaminated sludge. Based on morphological, physiological and biochemical characterization, and phylogenetic analysis of 16S rRNA gene sequence, strain F-7 was identified as Sphingomonas sp. The bacterium could utilize fenvalerate as the
Xiaohua Gao et al.
American journal of physiology. Endocrinology and metabolism, 303(8), E1025-E1035 (2012-08-02)
Previously, we reported that fenvalerate (Fen) promotes proliferation of human uterine leiomyoma (UtLM) cells by enhancing progression of cells from G(0)-G(1) to S phase through molecular mechanisms independent of estrogen receptor-α and -β. The cyclin-dependent kinase (CDK) inhibitor p27, which
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