InChI key
OBLNWSCLAYSJJR-UHFFFAOYSA-N
InChI
1S/C10H6ClNO2/c11-7-8(12)10(14)6-4-2-1-3-5(6)9(7)13/h1-4H,12H2
SMILES string
NC1=C(Cl)C(=O)c2ccccc2C1=O
grade
analytical standard
product line
PESTANAL®
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
application(s)
agriculture
environmental
format
neat
Quality Level
General description
Quinoclamine belongs to the class of naphthoquinone compounds.
Application
Quinoclamine may be used as an analytical reference standard for the determination of the analyte in:
- Honeybees by dispersive solid-phase extraction (dSPE), followed by liquid and gas chromatography coupled with tandem mass spectrometry (LC-MS/MS and GC-MS/MS).
- Chlorophyll-containing matrix by dSPE and GC-MS/MS.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Other Notes
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
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Eye Irrit. 2 - Repr. 2 - Skin Sens. 1A - STOT RE 2
target_organs
Blood,Kidney
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
法规信息
农药列管产品
此项目有
Lijie Hou et al.
Dalton transactions (Cambridge, England : 2003), 48(25), 9234-9242 (2019-06-05)
Green and renewable organic redox molecules are greatly advantageous over conventional inorganic intercalation electrode materials in terms of electrochemical reversibility and cycling stability. However, their electrical insulation prevents them from being used alone as electrode materials for supercapacitors. Herein, 2-amino-3-chloro-1,4-naphthoquinone
H Kwon et al.
Research communications in molecular pathology and pharmacology, 97(2), 215-227 (1997-08-01)
Naphthoquinone compounds have various pharmacological effects such as antiviral, antifungal and anticancer activities. We demonstrated the differentiation of the inducing effect of a naphthoquinone derivative, 2-chloro-3-amino-1,4-nahpthoquinone (NQCA) on the human leukemia cell line U-937. When U-937 cells were treated with
Two-step dispersive-solid phase extraction strategy for pesticide multiresidue analysis in a chlorophyll-containing matrix by gas chromatography-tandem mass spectrometry.
Walorczyk S, et al.
Journal of Chromatography A, 1412(2), 22-32 (2015)
Application of bioactivity database of Chinese herbal medicine on the therapeutic prediction, drug development, and safety evaluation.
Cheng HM, et al.
Journal of Ethnopharmacology, 132(2), 429-437 (2010)
K A Bae et al.
Biological & pharmaceutical bulletin, 19(6), 824-827 (1996-06-01)
There are some highly cytotoxic anticancer compounds inducing differentiation of cancer cells to normal cells at below highly cytotoxic concentration. Naphthoquinone derivatives having cytotoxic effects on cancer cell were tested to learn whether they have differentiation inducing activity in human
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