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Quinchlorac

PESTANAL®, analytical standard

Synonyme(s) :

3,7-Dichloro-8-quinolinecarboxylic acid

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About This Item

Formule empirique (notation de Hill):
C10H5Cl2NO2
Numéro CAS:
84087-01-4
Poids moléculaire :
242.06
Numéro Beilstein :
7761858
Numéro CE :
402-780-1
Numéro MDL:
MFCD00072495
Code UNSPSC :
41116107
ID de substance PubChem :
329755372
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

Gamme de produits

PESTANAL®

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

agriculture
environmental

Format

neat

Chaîne SMILES 

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)

Clé InChI

FFSSWMQPCJRCRV-UHFFFAOYSA-N

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Catégories apparentées

Description générale

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.

Produits recommandés

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.

Informations légales

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H317

Classification des risques

Skin Sens. 1

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Certificats d'analyse (COA)

Lot/Batch Number
BCCJ7729
BCBZ3257
SZBD324XV
SZB8324XV
SZE8324X

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Consulter la Bibliothèque de documents

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
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
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

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