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Merck

CRM69091

Supelco

呋虫胺

certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

别名:

(RS)-N-甲基-N′-硝基-N″-(四氢-3-呋喃甲基)胍

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About This Item

经验公式(希尔记法):
C7H14N4O3
分子量:
202.21
MDL號碼:
分類程式碼代碼:
41116107
NACRES:
NA.24

等級

certified reference material
TraceCERT®

品質等級

產品線

TraceCERT®

儲存期限

limited shelf life, expiry date on the label

製造商/商標名

Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

格式

neat

儲存溫度

2-8°C

SMILES 字串

CN\C(N[N+]([O-])=O)=N/CC1CCOC1

InChI

1S/C7H14N4O3/c1-8-7(10-11(12)13)9-4-6-2-3-14-5-6/h6H,2-5H2,1H3,(H2,8,9,10)

InChI 密鑰

YKBZOVFACRVRJN-UHFFFAOYSA-N

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一般說明

This certified reference material (CRM) is produced and certified in accordance with ISO/IEC 17025 and ISO 17034. This CRM is traceable to primary material from an NMI, e.g. NIST or NMIJ.
Certified content by quantitative NMR incl. uncertainty and expiry date are given on the certificate.
Download your certificate at: http://www.sigma-aldrich.com
Dinotefuran is a third-generation chiral neonicotinoid insecticide, used against sucking, biting, and public health insects such as mosquitoes, ticks, beetles, aphids, whiteflies, and leaf hoppers. It disrupts the insect nervous system by exhibiting agonistic activity towards the nicotinic acetylcholine (ACh) receptors (nAChR) and affecting the cholinergic synaptic transmission.
Under the Regulation (EC) No 1107/2009 and revoking the Council Directives 79/117/EEC and 91/414/EEC, dinotefuran is not approved for its use as a plant protection agent in the European Union (EU). But a default maximum residue limit (MRL) of 0.01 mg/kg is set for dinotefuran in accordance with Art 18(1)(b) Reg 396/2005.

應用

The certified reference material (CRM) is intended to be used as a calibrant for chromatography and other analytical techniques.
The dinotefuran CRM may also find given below uses:
  • Development of a method to simultaneously determine dinotefuran and its 3 polar metabolites in plum samples using dispersive-solid phase extraction procedure (d-SPE) followed by liquid chromatography-tandem mass spectrometry (LC-MS/MS)
  • Potentiometric determination of dinotefuran residues in soil and cucumber samples by using novel molecularly imprinted polymeric (MIP) material based sensors
  • Evaluation of an ultra high-performance liquid chromatography-tandem triple quadrupole mass spectrometry based method for the detection and quantification of dinotefuran and its metabolites in products of plant (watermelon, cucumber, rice) and animal (milk, egg, and pork) origin and also environmental samples of soil and water
  • Multi-residue analysis of pyridaben, dinotefuran, and metabolites of dinotefuran in soil and eggplant samples with a modified QuEChERS based sample extraction and rapid resolution liquid chromatography-triple quadrupole-tandem mass spectrometry (RRLC-QqQ-MS/MS)
  • Quantitative analysis of dinotefuran and its two metabolites in rice plant samples by high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS)
  • Development of a method to determine residues of dinotefuran and its two major metabolites in apple samples by QuEChERS based sample pre-treatment and liquid chromatography-tandem mass spectrometry (LC-MS/MS)

法律資訊

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

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2

儲存類別代碼

11 - Combustible Solids

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)

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Xiaoxin Chen et al.
Chemosphere, 195, 245-251 (2017-12-23)
A sensitive method for simultaneous determination of pyridaben, dinotefuran, DN and UF in eggplant ecosystem was established and validated through rapid resolution liquid chromatography triples quadrupole tandem mass spectrometry (RRLC-QqQ-MS/MS). Matrix-matched external calibrations were introduced to check matrix effects. Limits
Md Musfiqur Rahman et al.
Food chemistry, 239, 1235-1243 (2017-09-07)
A simple and effective method was developed for analyzing dinotefuran and its three metabolites (MNG, UF, and DN) in plum using liquid chromatography-tandem mass spectrometry (LC-MS/MS). Due to the polarity and high water miscibility, dinotefuran and some of its metabolites
Zenglong Chen et al.
Environment international, 130, 104854-104854 (2019-06-15)
In last decade, there has been a concerted effort to reduce the potential threats of honeybees' population due to exposure to neonicotinoid pesticides. A new perspective was put forward to reduce the potential ecological toxicity of neonicotinoid dinotefuran to honeybee

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