36521
Quinchlorac
PESTANAL®, analytical standard
Synonym(s):
3,7-Dichloro-8-quinolinecarboxylic acid
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About This Item
Empirical Formula (Hill Notation):
C10H5Cl2NO2
CAS Number:
Molecular Weight:
242.06
Beilstein:
7761858
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24
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grade
analytical standard
Quality Level
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
SMILES string
OC(=O)c1c(Cl)ccc2cc(Cl)cnc12
InChI
1S/C10H5Cl2NO2/c11-6-3-5-1-2-7(12)8(10(14)15)9(5)13-4-6/h1-4H,(H,14,15)
InChI key
FFSSWMQPCJRCRV-UHFFFAOYSA-N
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General description
Quinchlorac is a postemergence herbicide, used for the control of broadleaf weeds, especially white clover (Trifolium repens L.) and Veronica filiformis.
Application
Quinchlorac may be used as an analytical reference standard for the quantification of the analyte in environmental samples using high-performance liquid chromatography with ultraviolet detection (HPLC-UV).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
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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
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Sens. 1
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Development and validation of a high-performance liquid chromatographic procedure for the determination of herbicide residues in surface and agriculture waters
Zanella R, et al.
Journal of Separation Science, 26(9-10), 935-938 (2003)
N Mito et al.
Plant physiology, 109(1), 293-297 (1995-09-01)
The effect of a tomato (Lycopersicon esculentum) mutation, diageotropica (dgt), on the accumulation of mRNA corresponding to tomato homologs of three auxin-regulated genes, LeAux, LeSAUR, and Lepar, was examined. The dgt mutation inhibited the induction of LeAux and LeSAUR mRNA
Zhenmei Lü et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 38(6), 771-782 (2003-12-03)
Strain WZI capable of degrading quinclorac was isolated from a pesticide manufactory soil and considered to be Burkholderia cepacia, belonged to bacteria, Proteobacteria, beta-Proteobacteria, based on morphology, physio-biochemical properties, whole cell fatty acid analysis and a partial sequencing of 16S
Zhen-Mei Lu et al.
Biomedical and environmental sciences : BES, 16(4), 314-322 (2004-03-12)
To investigate the potential effects of herbicide quinclorac (3,7-dichloro-8-quinoline-carboxylic) on the culturable microorganisms in flooded paddy soil. Total soil aerobic bacteria, actinomycetes and fungi were counted by a 10-fold serial dilution plate technique. Numbers of anaerobic fermentative bacteria (AFB), denitrifying
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