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Merck

14657

Supelco

trans-Cypermethrin-(phenoxy-d5)

PESTANAL®, analytical standard

别名:

(1R,3S)-rel-3-(2,2-Dichloroethenyl)-2,2-dimethylcyclopropanecarboxylic acid cyano[3-(phenoxy-d5)phenyl]methyl ester, trans-Cypermethrin-d5

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About This Item

经验公式(希尔记法):
C22D5H14Cl2NO3
分子量:
421.33
分類程式碼代碼:
41116107
PubChem物質ID:
NACRES:
NA.24

等級

analytical standard

品質等級

產品線

PESTANAL®

化驗

≥95.0% (HPLC)

儲存期限

limited shelf life, expiry date on the label

應用

agriculture

格式

neat

儲存溫度

2-8°C

相关类别

一般說明

trans-Cypermethrin-(phenoxy-d5) is an isotope-labeled analog of the trans-isomeric form of cypermethrin , a synthetic pyrethroid insecticide wherein all the phenyl protons are replaced by deuterium.

應用

Isotope-labeled compounds are increasingly used in isotope dilution mass spectrometry (IDMS) for the quantitative analysis of pesticides. The main advantage of using the IDMS technique is because isotope-labeled compounds have nearly the same physical properties as their non-labeled counterpart analog, and thus show identical behavior during the workup and sample preparation process. This helps in overcoming the problems of matrix effects generally encountered in the usual LC-MS/GC-MS analysis potentially resulting in biased results. By spiking the sample before workup with its isotope labeled analog, the loss of analyte that leads to matrix effects can be determined and compensated.

法律資訊

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

訊號詞

Danger

危險分類

Acute Tox. 3 Oral - Acute Tox. 4 Inhalation - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT RE 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

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

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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分析证书(COA)

Lot/Batch Number

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Toxicity of cypermethrin in Labeo rohita fingerlings: biochemical, enzymatic and haematological consequences
Das BK, et al.
Comparative Biochemistry and Physiology. C, Comparative Pharmacology and Toxicology, 134(1), 109-121 (2003)

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