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About This Item
Linear Formula:
Cl2C6H3CH2CO2H
CAS Number:
Molecular Weight:
205.04
Beilstein:
1948767
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
99%
form
solid
mp
129-131 °C (lit.)
functional group
carboxylic acid
chloro
SMILES string
OC(=O)Cc1ccc(Cl)cc1Cl
InChI
1S/C8H6Cl2O2/c9-6-2-1-5(3-8(11)12)7(10)4-6/h1-2,4H,3H2,(H,11,12)
InChI key
GXMWLJKTGBZMBH-UHFFFAOYSA-N
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Application
2,4-Dichlorophenylacetic acid has been used as internal standard in:
- determination of phenoxyalkanoic acid herbicides in blood by GC with electron-capture detection
- determination of 2-methyl-4-chlorophenoxyacetic acid (herbicide) in soils by GC technique
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Jiaqin Wang et al.
Analytica chimica acta, 996, 20-28 (2017-11-16)
A high throughput, low environmental impact methodology for rapid determination of phenoxy carboxylic acids (PCAs) in water samples was developed by combing dispersive solid phase extraction (DSPE) using velvet-like graphitic carbon nitride (V-g-C
Derivatization and Determination of MCPA in Soil by GC.
Cai K, et al.
Chromatographia, 72(9-10), 933-939 (2010)
The Toxoplasma effector TEEGR promotes parasite persistence by modulating NF-κB signalling via EZH2.
Laurence Braun et al.
Nature microbiology, 4(7), 1208-1220 (2019-05-01)
The protozoan parasite Toxoplasma gondii has co-evolved with its homeothermic hosts (humans included) strategies that drive its quasi-asymptomatic persistence in hosts, hence optimizing the chance of transmission to new hosts. Persistence, which starts with a small subset of parasites that
Guobin Xin et al.
Se pu = Chinese journal of chromatography, 26(1), 116-118 (2008-04-29)
A method for the determination of three phenoxyalkanoic acid herbicides, 2,4-dichlorophenoxyacetic acid (2,4-D), 2-(2,4-dichlorophenoxy)-propanoic acid (2,4-DP), and 4-chloro-2-methylphenoxy-acetic acid (MCPA), in blood was developed. The blood sample was diluted with 0.1 mol/L hydrochloric acid, and extracted by solid-phase extraction using
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