45434
二氯萘醌
PESTANAL®, analytical standard
别名:
2,3-二氯-1,4-萘醌, 二氯萘醌
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关于此项目
经验公式（希尔记法）:
C10H4Cl2O2
化学文摘社编号:
分子量:
227.04
Beilstein:
1073511
EC 号:
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
mp
194-197 °C (lit.)
应用
agriculture
environmental
包装形式
neat
SMILES字符串
ClC1=C(Cl)C(=O)c2ccccc2C1=O
InChI
1S/C10H4Cl2O2/c11-7-8(12)10(14)6-4-2-1-3-5(6)9(7)13/h1-4H
InChI key
SVPKNMBRVBMTLB-UHFFFAOYSA-N
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一般描述
Dichlon is an agricultural fungicide of the quinone class, widely used against a variety of plant pathogenic fungi.
应用
Dichlon may be used as an analytical reference standard for the quantification of the analyte in food matrices using supercritical fluid extraction (SFE) and supercritical fluid chromatography (SFC).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
法律信息
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
警示用语：
Danger
危险分类
Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Irrit. 2
储存分类代码
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
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
危险化学品
此项目有
Thin-layer chromatography of some substituted naphthoquinones
Agricultural and Biological Chemistry, 30(9), 935-936 (1966)
Pesticide residues in canned foods, fruits, and vegetables: The application of supercritical fluid extraction and chromatographic techniques in the analysis
EL-Saeid.HM
TheScientificWorldJournal, 3(3), 1314-1326 (2003)
Chemistry and Biology of Water, Air and Soil: Environmental Aspects
Studies in Environmental Science, 53(3), 1314-1326 (1993)
Ibrahim A Darwish
Journal of AOAC International, 88(1), 38-45 (2005-03-12)
Three simple and sensitive spectrophotometric methods were developed and validated for determination of the hydrochloride salts of fluoxetine, sertraline, and paroxetine in their pharmaceutical dosage forms. These methods were based on the reaction of the N-alkylvinylamine formed from the interaction
C A Pritsos et al.
Biochemical pharmacology, 33(23), 3771-3777 (1984-12-01)
The addition of 2,3-dichloro-1,4-naphthoquinone (CNQ) to substrate-depleted, GSH-supplemented rat liver mitochondria resulted in a dose-dependent depletion of reactable suflhydryl groups and a concomitant increase in mitochondrial disulfide content at a ratio of 2 thiols depleted/disulfide generated. The molar ratio of
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