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About This Item
Linear Formula:
Cl2C6H3O(CH2)3CO2H
CAS Number:
Molecular Weight:
249.09
NACRES:
NA.24
PubChem Substance ID:
UNSPSC Code:
12352209
EC Number:
202-366-9
MDL number:
Beilstein/REAXYS Number:
1976809
SMILES string
COc1ccc(cc1OC)[C@H](CC(O)=O)NC(=O)OC(C)(C)C, OC(=O)CCCOc1ccc(Cl)cc1Cl
InChI key
YIVXMZJTEQBPQO-UHFFFAOYSA-N
InChI
1S/C10H10Cl2O3/c11-7-3-4-9(8(12)6-7)15-5-1-2-10(13)14/h3-4,6H,1-2,5H2,(H,13,14)
grade
analytical standard
product line
PESTANAL®
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
mp
118-120 °C (lit.)
application(s)
agriculture
environmental
format
neat
Quality Level
Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
wgk
WGK 2
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2
Storage Class
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
农药列管产品
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Martin Fulda et al.
The Plant cell, 16(2), 394-405 (2004-01-27)
In plants and other eukaryotes, long-chain acyl-CoAs are assumed to be imported into peroxisomes for beta-oxidation by an ATP binding cassette (ABC) transporter. However, two genes in Arabidopsis thaliana, LACS6 and LACS7, encode peroxisomal long-chain acyl-CoA synthetase (LACS) isozymes. To
The DEG15 serine protease cleaves peroxisomal targeting signal 2-containing proteins in Arabidopsis.
Holger Schuhmann et al.
Plant physiology, 148(4), 1847-1856 (2008-10-28)
Two distinct peroxisomal targeting signals (PTSs), the C-terminal PTS1 and the N-terminal PTS2, are defined. Processing of the PTS2 on protein import is conserved in higher eukaryotes. Recently, candidates for the responsible processing protease were identified from plants (DEG15) and
F Mariana et al.
Journal of microbiological methods, 82(1), 42-48 (2010-04-14)
The environmental fate and, in particular, biodegradation rates of hydrophobic organic compounds (HOC) are of high interest due to the ubiquity, persistence, and potential health effects of these compounds. HOC tend to interact with bioreactor materials and sampling devices and
Virginia Cuadrado et al.
Applied microbiology and biotechnology, 77(6), 1371-1378 (2007-11-16)
The dissipation of 4-(2,4-dichlorophenoxy) butyric acid (2,4-DB) in high-humic-matter-containing soils from agricultural fields of the Argentinean Humid Pampa region was studied, employing soil microcosms under different experimental conditions. The added herbicide was dissipated almost completely by soils with and without
Meliha Lekić et al.
Medicinski arhiv, 59(3), 147-151 (2005-07-07)
Derivatives of chlorophenoxy carboxylic acids have been the first class of herbicides in continuous use since 1947. The main interest for these substances is due to their evident chronic toxicity and carcinogenic effect. On the other hand, they can cause
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