25890
4-Chlorophenoxyacetic acid
≥98.0% (T)
Sinónimos:
4-CPA
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Acerca de este artículo
Fórmula empírica (notación de Hill):
C8H7ClO3
Número CAS:
Peso molecular:
186.59
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-581-3
Beilstein/REAXYS Number:
1211804
MDL number:
Assay:
≥98.0% (T)
Form:
powder
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Permítanos ayudarleNombre del producto
4-Chlorophenoxyacetic acid, ≥98.0% (T)
InChI key
SODPIMGUZLOIPE-UHFFFAOYSA-N
InChI
1S/C8H7ClO3/c9-6-1-3-7(4-2-6)12-5-8(10)11/h1-4H,5H2,(H,10,11)
SMILES string
OC(=O)COc1ccc(Cl)cc1
assay
≥98.0% (T)
form
powder
functional group
carboxylic acid
chloro
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Categorías relacionadas
Application
- Innovative adsorbents for chemical analysis: The application of three-dimensional material CZIF-8/CS-MS was explored as adsorbents for the determination of plant growth regulators including 4-Chlorophenoxyacetic acid in traditional Chinese medicine, improving the precision and efficiency of chemical residue analysis (Zhang et al., 2024).
General description
4-Chlorophenoxyacetic acid is a herbicide. Degradation of 4-chlorophenoxyacetic acid in aqueous medium by advanced electrochemical oxidation processes, using an undivided cell containing a Pt anode has been reported.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
Clase de almacenamiento
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Two miniaturized sample preparation techniques, ultrasound-assisted emulsification microextraction (USAEME) and micro-solid-phase extraction (μ-SPE) have been integrated for the pre-concentration of four polar chlorophenoxy acid (CPA) herbicides from environmental aqueous samples. An metal-organic framework, MIL-101(Cr), characterized by its high porosity and
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A novel solvent-loaded dispersive solid-phase extraction (SL-DSPE) method integrated with liquid-phase microextraction (LPME) has been developed by the direct loading of solvent into the pores of a metal-organic framework (MOF), MIL-101(Cr)-NH2. Despite numerous advantages of MOFs, they are usually highly hydrophobic
Sonia Traverso et al.
The Journal of general physiology, 122(3), 295-306 (2003-08-13)
Opening of CLC chloride channels is coupled to the translocation of the permeant anion. From the recent structure determination of bacterial CLC proteins in the closed and open configuration, a glutamate residue was hypothesized to form part of the Cl--sensitive
Xiao-Dong Zhang et al.
The Journal of general physiology, 133(1), 59-68 (2008-12-18)
Intracellularly applied amphiphilic molecules, such as p-chlorophenoxy acetate (CPA) and octanoate, block various pore-open mutants of CLC-0. The voltage-dependent block of a particular pore-open mutant, E166G, was found to be multiphasic. In symmetrical 140 mM Cl(-), the apparent affinity of
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