158518
Phenoxyacetic acid
98%
Synonym(s):
Glycolic acid phenyl ether
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All Photos(2)
About This Item
Linear Formula:
C6H5OCH2CO2H
CAS Number:
Molecular Weight:
152.15
Beilstein:
907949
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
98%
form
solid
mp
98-100 °C (lit.)
solubility
ethanol: soluble 10%, clear, colorless
SMILES string
OC(=O)COc1ccccc1
InChI
1S/C8H8O3/c9-8(10)6-11-7-4-2-1-3-5-7/h1-5H,6H2,(H,9,10)
InChI key
LCPDWSOZIOUXRV-UHFFFAOYSA-N
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General description
Phenoxyacetic acid is a herbicide and its photodegradation using TiO2 as photocatalyst has been studied. Selective separation of penicillin V from phenoxyacetic acid using liquid membranes consisting of 1,2-dichloroethane and Amberlite LA-2 as carrier has been studied.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - 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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Rudina Bleta et al.
Langmuir : the ACS journal of surfaces and colloids, 30(39), 11812-11822 (2014-09-16)
A series of mesoporous titania photocatalysts with tailorable structural and textural characteristics was prepared in aqueous phase via a colloidal self-assembly approach using various cyclodextrins (CDs) as structure-directing agents. The photocatalysts and the structure-directing agents were characterized at different stages
Photocatalyzed Degradation of Phenol, 2, 4-Dichlorophenol, Phenoxyacetic Acid and 2, 4-Dichlorophenoxyacetic Acid over SupportedTiO2 in a Flow System.
Trillas M, et al.
Journal of Chemical Technology and Biotechnology, 67(3), 237-242 (1996)
Selective separation of penicillin V from phenoxyacetic acid using liquid membranes.
Cascaval D, et al.
Biochemical Engineering Journal, 55(1), 45-50 (2000)
Mohamed Ashraf Ali et al.
Bioorganic & medicinal chemistry, 15(5), 1896-1902 (2007-01-26)
A series of 2-{4-[1-amino (thioxo) methyl-5-(substituted phenyl)-4,5-dihydro-1H-3-pyrazolyl]-2-methoxyphenoxy}acetic acid and 2-{4-[1-carbamoyl-5-(substituted phenyl)-4,5-dihydro-1H-3-pyrazolyl]-2-methoxyphenoxy}acetic acid were synthesized and the in vitro activity of the synthesized compounds against Mycobacterium tuberculosis H37Rv (MTB) and INH-resistant M. tuberculosis (INHR-MTB) was studied. Among the synthesized compounds, compound
Discovery of carboranes as inducers of 20S proteasome activity.
Hyun Seung Ban et al.
ChemMedChem, 5(8), 1236-1241 (2010-05-13)
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