46318
磺草酮
PESTANAL®, analytical standard
别名:
2-[2-氯-4-(甲磺酰)苯甲酰基]-1,3-环己二酮
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关于此项目
经验公式（希尔记法）:
C14H13ClO5S
化学文摘社编号:
分子量:
328.77
Beilstein:
8155739
MDL编号:
UNSPSC代码:
41116107
PubChem化学物质编号:
NACRES:
NA.24
等级
analytical standard
质量水平
产品线
PESTANAL®
保质期
limited shelf life, expiry date on the label
技术
HPLC: suitable
gas chromatography (GC): suitable
应用
agriculture
environmental
包装形式
neat
SMILES字符串
CS(=O)(=O)c1ccc(c(Cl)c1)C(=O)C2C(=O)CCCC2=O
InChI
1S/C14H13ClO5S/c1-21(19,20)8-5-6-9(10(15)7-8)14(18)13-11(16)3-2-4-12(13)17/h5-7,13H,2-4H2,1H3
InChI key
PQTBTIFWAXVEPB-UHFFFAOYSA-N
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一般描述
Sulcotrione is a herbicide belonging to the triketone class, commonly used in corn production.
应用
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Sulcotrione may be used as an analytical reference standard for the quantification of the analyte in environmental samples using liquid chromatography coupled to tandem mass spectrometry.
其他说明
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.
法律信息
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
警示用语：
Warning
危险分类
Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 2 - Skin Sens. 1A - STOT RE 2
储存分类代码
11 - Combustible Solids
WGK
WGK 2
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
法规信息
农药列管产品
此项目有
Richard Cherrier et al.
Pest management science, 61(9), 899-904 (2005-07-26)
A soil column experiment under outdoor conditions was performed to monitor the fate of 14C-ring-labelled sulcotrione, 2-(2-chloro-4-mesylbenzoyl)cyclohexane-1,3-dione and atrazine, 6-chloro-N2-ethyl-N4-isopropyl-1,3,5-triazine-2,4-diamine, in water leachates and in the ploughed horizon of a sandy loam soil. Two months after treatment, the cumulative amounts
Minir Murati et al.
Environmental science and pollution research international, 19(5), 1563-1573 (2011-11-26)
The degradation and mineralization of two triketone (TRK) herbicides, including sulcotrione and mesotrione, by the electro-Fenton process (electro-Fenton using Pt anode (EF-Pt), electro-Fenton with BDD anode (EF-BDD) and anodic oxidation with BDD anode) were investigated in acidic aqueous medium. The
P D Fraser et al.
The Plant journal : for cell and molecular biology, 24(4), 551-558 (2000-12-15)
The application of high-performance liquid chromatography (HPLC) using a C30 reverse-phase stationary matrix has enabled the simultaneous separation of carotenes, xanthophylls, ubiquinones, tocopherols and plastoquinones in a single chromatogram. Continuous photodiode array (PDA) detection ensured identification and quantification of compounds
Sophia Keller et al.
PloS one, 6(10), e26604-e26604 (2011-11-03)
The opportunistic human pathogenic fungus Aspergillus fumigatus is able to produce the dark brown pigment pyomelanin by degradation of L-tyrosine. Pyomelanin was shown to protect the fungus against reactive oxygen intermediates as well as cell wall disturbing compounds and is
Boris Eyheraguibel et al.
Journal of agricultural and food chemistry, 59(9), 4868-4873 (2011-03-24)
Pesticide reactivity toward light is rarely considered at the leaf surface after crop treatment; regardless, these degradation reactions directly impact the pesticide effectiveness. The use of sunscreen adjuvants to overcome photodegradation has presented some limitations so far. Raw hydroalcoholic plant
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