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Merck

90622

Supelco

环唑醇

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

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About This Item

经验公式(希尔记法):
C15H18ClN3O
CAS号:
分子量:
291.78
Beilstein:
8396421
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

形式

neat

儲存溫度

-10 to -25°C

SMILES 字串

CC(C1CC1)C(O)(Cn2cncn2)c3ccc(Cl)cc3

InChI

1S/C15H18ClN3O/c1-11(12-2-3-12)15(20,8-19-10-17-9-18-19)13-4-6-14(16)7-5-13/h4-7,9-12,20H,2-3,8H2,1H3

InChI 密鑰

UFNOUKDBUJZYDE-UHFFFAOYSA-N

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相关类别

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.

Cyproconazole is a systemic triazole fungicide, typically applied as foliar sprays to control diseases caused by ascomycetes, basidiomycetes, and deuteromycetes in cereals, sugar beets, peanut, oilseed rape, coffee, fruit tree, and grapes. Cyproconazole inhibits C-14α-demethylase enzyme biosynthesis of pathogenic fungi.

Cyproconazole has to be monitored in the Multiannual Control Programme for Pesticides Residues (MACP), run within the EU and EFTA in/on products of plant origin.

As per Regulation (EC) No 1107/2009, cyproconazole is not approved in European Union. Maximum residue levels (MRLs) for Cyproconazole have been set according to Regulation (EU) No 2018/70 from 0.05 to 0.5 mg/kg for various products of plant and animal origin.

應用

It is intended to be used as a certified reference material (CRM) for calibration in chromatography and other analytical techniques. Cyproconazole CRM may also find its use as described below:
  • To investigate stereoselective degradation of the fungicides, epoxiconazole, and cyproconazole in different soils
  • Study the inhibition effect of cyproconazole as corrosion inhibitor of copper in sulphuric acid solution
  • Evaluation of stereoselective metabolism of cyproconazole in rat liver microsomes through chiral LC-MS/MS method
  • Development and validation of QuEChERS method for the enantioseparation and detection of cyproconazole stereoisomers in food and environmental samples (wheat flour, cucumber, pear, soil) using HPLC
  • To investigate stereoselective quantification and degradation of cyproconazole in different matrices using chiral liquid chromatography-tandem mass spectrometry (LC-MS/MS) method

法律資訊

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

訊號詞

Danger

危險分類

Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 1B - STOT RE 2

標靶器官

Liver

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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Zongzhe He et al.
The Analyst, 144(17), 5193-5200 (2019-07-28)
Cyproconazole, a chiral triazole fungicide, has been diffusely used and analyzed. The development of an effective analytical method for cyproconazole enantiomers can support their residual monitoring and risk assessment. In the present study, the absolute configuration of the cyproconazole enantiomers
Rujian He et al.
Chemosphere, 264(Pt 2), 128495-128495 (2020-10-11)
The vast usage of agrochemicals enhances food security globally but may pose challenge to understand the risk assessment to non-target organisms and human beings, and liver microsomes are responsible for metabolism of these agrochemicals in vivo. In this study, stereoselective
Ignaz J Buerge et al.
Environmental science & technology, 40(17), 5443-5450 (2006-09-27)
Many pesticides are chiral and consist of two or more enantiomers/stereoisomers, which may differ in biological activity, toxicity, effects on nontarget organisms, and environmental fate. In the last few years, several racemic compounds have been substituted by enantiomer-enriched or single-isomer

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