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Fontos dokumentumok
90622
Cyproconazol
certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland
Bejelentkezésa Szervezeti és Szerződéses árazás megtekintéséhez
Összes fotó(1)
About This Item
Tapasztalati képlet (Hill-képlet):
C15H18ClN3O
CAS-szám:
Molekulatömeg:
291.78
Beilstein:
8396421
MDL-szám:
UNSPSC kód:
41116107
NACRES:
NA.24
Javasolt termékek
grade
certified reference material
TraceCERT®
Minőségi szint
termékcsalád
TraceCERT®
eltarthatósági idő
limited shelf life, expiry date on the label
gyártó/kereskedő neve
Manufactured by: Sigma-Aldrich Production GmbH, Switzerland
Formátum
neat
tárolási hőmérséklet
-10 to -25°C
SMILES string
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
Nemzetközi kémiai azonosító kulcs
UFNOUKDBUJZYDE-UHFFFAOYSA-N
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Általános leírás
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.
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.
Alkalmazás
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
Jogi információk
TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany
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Figyelmeztetés
Danger
Figyelmeztető mondatok
Óvintézkedésre vonatkozó mondatok
Veszélyességi osztályok
Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 1B - STOT RE 2
Célzott szervek
Liver
Tárolási osztály kódja
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
Lobbanási pont (F)
Not applicable
Lobbanási pont (C)
Not applicable
Analitikai tanúsítványok (COA)
Analitikai tanúsítványok (COA) keresése a termék sarzs-/tételszámának megadásával. A sarzs- és tételszámok a termék címkéjén találhatók, a „Lot” vagy „Batch” szavak után.
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Az Ön által nemrégiben megvásárolt termékekre vonatkozó dokumentumokat a Dokumentumtárban találja.
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
Rujian He et al.
Journal of agricultural and food chemistry, 67(38), 10782-10790 (2019-09-07)
Systematic investigation of cyproconazole, including absolute stereochemistry, fungicidal activity, quantification in two matrixes, and stereoselective degradation in cucumber, are conducted in this study. By virtue of vibrational circular dichroism (VCD) spectroscopy, absolute configurations of four stereoisomers were identified to be
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
Tudóscsoportunk valamennyi kutatási területen rendelkezik tapasztalattal, beleértve az élettudományt, az anyagtudományt, a kémiai szintézist, a kromatográfiát, az analitikát és még sok más területet.
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