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Merck
CN

45420

2,4-DB

PESTANAL®, analytical standard

Synonym(s):

4-(2,4-Dichlorophenoxy)butyric acid, 2,4-DB

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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
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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

pictograms

Exclamation markEnvironment

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
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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