CRM04984
Ethalfluralin
certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland
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About This Item
Empirical Formula (Hill Notation):
C13H14F3N3O4
CAS Number:
Molecular Weight:
333.26
Beilstein/REAXYS Number:
2907084
MDL number:
UNSPSC Code:
41116107
NACRES:
NA.24
Recommended Products
grade
certified reference material
TraceCERT®
Quality Level
product line
TraceCERT®
shelf life
limited shelf life, expiry date on the label
manufacturer/tradename
Manufactured by: Sigma-Aldrich Production GmbH, Switzerland
format
neat
storage temp.
2-8°C
SMILES string
CCN(CC(C)=C)c1c(cc(cc1[N+]([O-])=O)C(F)(F)F)[N+]([O-])=O
InChI
1S/C13H14F3N3O4/c1-4-17(7-8(2)3)12-10(18(20)21)5-9(13(14,15)16)6-11(12)19(22)23/h5-6H,2,4,7H2,1,3H3
InChI key
PTFJIKYUEPWBMS-UHFFFAOYSA-N
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General description
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
Ethalfluralin is a pre-plant soil applied herbicide that belongs to the class of 2,6-dinitroaniline compounds. It has a low aqueous solubility and is highly volatile. It acts by inhibiting the mitotic cell divisions in plant root and shoot tips. It is used to protect crops such as cotton, maize, soya beans, peppers, tomatoes, lentils, peanuts, and sunflowers against pre-emergence of a wide spectrum of annual grasses and broad-leaf weeds.
Ethalfluralin is not allowed for use in the European Union and the decision to not include it in Annex I of Directive 91/414/EEC came to force on 12 December 2008. But a maximum residue limit (MRLs) of 0.01 mg/kg has been set according to Reg (EU) No 777/2013 for the presence of ethalfluralin in various products of plant and animal origin.
Certified content by quantitative NMR incl. uncertainty and expiry date are given on the certificate.
Download your certificate at: http://www.sigma-aldrich.com
Ethalfluralin is a pre-plant soil applied herbicide that belongs to the class of 2,6-dinitroaniline compounds. It has a low aqueous solubility and is highly volatile. It acts by inhibiting the mitotic cell divisions in plant root and shoot tips. It is used to protect crops such as cotton, maize, soya beans, peppers, tomatoes, lentils, peanuts, and sunflowers against pre-emergence of a wide spectrum of annual grasses and broad-leaf weeds.
Ethalfluralin is not allowed for use in the European Union and the decision to not include it in Annex I of Directive 91/414/EEC came to force on 12 December 2008. But a maximum residue limit (MRLs) of 0.01 mg/kg has been set according to Reg (EU) No 777/2013 for the presence of ethalfluralin in various products of plant and animal origin.
Application
It is intended to be used as a certified reference material (CRM) for calibration in chromatography and other analytical techniques.
Ethalfluralin CRM can also be used as described below:
Ethalfluralin CRM can also be used as described below:
- Simultaneous determination of seven dinitroaniline herbicide residues using a modified QuEChERS method coupled with gas chromatography-negative chemical ionization–mass spectrometry (GC-NCI/MS) from complex food matrices
- Analysis of 35 multiclass pesticides in honey samples by solid phase extraction and gas chromatography-mass spectrometry
- Development of a multiresidue method for the analysis of 200 pesticides, their degradation products, and 13 polychlorinated biphenyls (PCBs) in water samples by liquid chromatography-tandem mass spectrometry (LC-MS/MS) and gas chromatography-tandem mass spectrometry (GC-MS/MS)
- Study the atmospheric degradation of ethalfluralin in order to understand the consequences of ethalfluralin emissions into the atmosphere
- Identification and measurement of 160 pesticides in surface water, stemflow, and throughfall samples, adjacent to agricultural fields by GC-MS
Recommended products
Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.
Legal Information
TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Inhalation - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2
Storage Class
11 - Combustible Solids
wgk_germany
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
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A new multiresidue method for the determination of multiclass pesticides, degradation products and PCBs in water using LC-MS/MS and GC-MS (n) systems
Charalampous A C, et al.
International Journal of Environmental Analytical Chemistry, 1283-1298 null
Nazia Rafique et al.
Environmental monitoring and assessment, 190(11), 666-666 (2018-10-24)
Analytical method for the monitoring of residues of multiclass pesticides (variable chemical structure and chromatographic behavior) in honey has been optimized and in-house validated in the present study. Chemical confirmation of 35 selected pesticides (in-hive-treated pesticides and pesticides applied for
Analysis of 7 dinitroaniline residues in complex food matrices by GC-NCI/MS
Xia G, et al.
Chromatographia, 493-499 null
Donna A Glinski et al.
Chemosphere, 209, 496-507 (2018-06-26)
To study spray drift contributions to non-targeted habitats, pesticide concentrations in stemflow (water flowing down the trunk of a tree during a rain event), throughfall (water from tree canopy only), and surface water in an agriculturally impacted wetland area near
Amalia Muñoz et al.
Chemosphere, 95, 395-401 (2013-10-22)
The gas-phase degradation of ethalfluralin, N-ethyl-α,α,α-trifluoro-N-(2-methylallyl)-2,6-dinitro-p-toluidine, a widely used herbicide, was investigated under atmospheric conditions at the large outdoor European simulation chamber (EUPHORE) in Valencia, Spain. The photolysis of ethalfluralin was investigated under solar radiation and the mean photolysis rate
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