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经验公式(希尔记法):
C9H10BrClN2O2
化学文摘社编号:
分子量:
293.54
NACRES:
NA.24
UNSPSC Code:
41116107
Beilstein/REAXYS Number:
2128736
MDL number:
产品名称
氯溴隆, certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland
SMILES string
CON(C)C(=O)Nc1ccc(Br)c(Cl)c1
InChI
1S/C9H10BrClN2O2/c1-13(15-2)9(14)12-6-3-4-7(10)8(11)5-6/h3-5H,1-2H3,(H,12,14)
InChI key
NLYNUTMZTCLNOO-UHFFFAOYSA-N
grade
certified reference material
TraceCERT®
product line
TraceCERT®
shelf life
limited shelf life, expiry date on the label
manufacturer/tradename
Manufactured by: Sigma-Aldrich Production GmbH, Switzerland
storage temp.
2-8°C
Quality Level
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相关类别
Application
The certified reference material (CRM) is intended to be used as a calibrant for chromatography and other analytical techniques.
Chlorobromouron CRM can also be used as below:
Chlorobromouron CRM can also be used as below:
- Method development for the quantification of 25 polar pesticides in fruit, vegetable, and water samples using high-performance liquid chromatography(HPLC)
- Separation and determination of 12 substituted phenylurea herbicides by HPLC in the study to assess the leaching of the herbicides in two agricultural soil samples
- Development of an HPLC method with diode array detection following dispersive liquid-liquid microextraction to determine 11 phenylurea herbicides in natural waters
- Investigation of 1,6-hexanediol ethoxylate diacrylate (HEDA)-based polymeric monoliths as a sorbent for the extraction of phenylurea herbicides from water samples
- Multi-residue analysis of 250 pesticides in surface water samples using liquid chromatography- quadrupole-Orbitrap high resolution tandem mass spectrometry
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
Chlorbromouron is an obsolete systemic phenylurea herbicide used for pre- and post- emergence control of annual grasses (e.g. foxtail) and broad leafed weeds (e.g. chickweed) on a variety of crops. It inhibits photosynthesis by interfering with the electron transfer in photosystem II. As per the commission regulation no 1107/2009, repealing the council directive 91/414/EEC, chlorobromouron is not approved for use in the European Union. A default maximum residue limit (MRL) of 0.01 mg/kg is set for chlorbromuron as per regulation (EC) no. 396/2005.
Certified content by quantitative NMR incl. uncertainty and expiry date are given on the certificate.
Download your certificate at: http://www.sigma-aldrich.com
Chlorbromouron is an obsolete systemic phenylurea herbicide used for pre- and post- emergence control of annual grasses (e.g. foxtail) and broad leafed weeds (e.g. chickweed) on a variety of crops. It inhibits photosynthesis by interfering with the electron transfer in photosystem II. As per the commission regulation no 1107/2009, repealing the council directive 91/414/EEC, chlorobromouron is not approved for use in the European Union. A default maximum residue limit (MRL) of 0.01 mg/kg is set for chlorbromuron as per regulation (EC) no. 396/2005.
Legal Information
TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Inhalation - Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
Determination of polar pesticides in water, vegetables, and fruits by high performance liquid chromatography
Amelin V G, et al.
Moscow University Chemistry Bulletin, 67(6), 275- 282 (2012)
Simón Navarro et al.
Journal of agricultural and food chemistry, 60(21), 5279-5286 (2012-05-15)
In this study, the potential groundwater pollution of 12 substituted phenylurea herbicides (chlorbromuron, chlorotoluron, diuron, fenuron, fluometuron, isoproturon, linuron, metobromuron, metoxuron, monolinuron, Monuron, and neburon) was investigated under laboratory conditions. For this purpose, leaching studies were conducted using disturbed soil
Abiotic and biotic processes governing the fate of phenylurea herbicides in soils: a review
Hussain S, et al.
Critical reviews in environmental science and technology, 45(18), 1947- 1998 (2015)
Dispersive liquid-liquid microextraction for the determination of herbicides of urea derivatives family in natural waters by HPLC
Amelin VG, et al.
Journal of Analytical Chemistry, 68(9), 822- 830 (2013)
Shu-Ling Lin et al.
Talanta, 147, 199-206 (2015-11-26)
In this study, recently developed 1,6-hexanediol ethoxylate diacrylate (HEDA)-based polymeric monoliths were utilized as sorbents for efficient extraction of phenylurea herbicides (PUHs) from water samples. The HEDA-based monolithic sorbents were prepared in a fused silica capillary (0.7mm i.d., 4.5-cm long)
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