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About This Item
Empirical Formula (Hill Notation):
C9H7Cl3O3
CAS Number:
Molecular Weight:
269.51
EC Number:
202-271-2
UNSPSC Code:
41116107
PubChem Substance ID:
Beilstein/REAXYS Number:
1985768
MDL number:
InChI key
ZLSWBLPERHFHIS-UHFFFAOYSA-N
InChI
1S/C9H7Cl3O3/c1-4(9(13)14)15-8-3-6(11)5(10)2-7(8)12/h2-4H,1H3,(H,13,14)
SMILES string
CC(Oc1cc(Cl)c(Cl)cc1Cl)C(O)=O
grade
analytical standard
packaging
ampule of 250 mg
manufacturer/tradename
Chem Service, Inc. PS-47
application(s)
agriculture
environmental
General description
Silvex®(2-(2,4,5-trichlorophenoxy)-propionic acid) is a chlorophenoxy acid pesticide. It is used to control annual and perennial broadleaf weeds.
Application
2-(2,4,5-Trichlorophenoxy)propionic acid may be used as a reference standard for the determination of Silvex® (2-(2,4,5-Trichlorophenoxy)propionic acid), in soil and water samples by enzyme-linked immunosorbent assay (ELISA).
Legal Information
Silvex is a registered trademark of Silberline Manufacturing Co., Inc.
signalword
Warning
hcodes
pcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Irrit. 2
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Assessment of enzyme-linked immunosorbent assay for the determination of 2,4,5-TP in water and soil.
Sergi Morais et al.
Analytical and bioanalytical chemistry, 374(2), 262-268 (2002-09-27)
A highly sensitive and specific indirect enzyme-linked immunosorbent assay is described for Silvex, 2-(2,4,5 trichlorophenoxy)propionic acid, (2,4,5-TP). One specific feature of the immunoassay is the use of simple chemical activation of chlorophenoxy acids to prepare both the immunizing and coating
Emeline L Maillet et al.
Journal of medicinal chemistry, 52(21), 6931-6935 (2009-10-13)
We show that phenoxyauxin herbicides and lipid-lowering fibrates inhibit human but not rodent T1R3. T1R3 as a coreceptor in taste cells responds to sweet compounds and amino acids; in endocrine cells of gut and pancreas T1R3 contributes to glucose sensing.
Lourdes Santana et al.
Journal of medicinal chemistry, 51(21), 6740-6751 (2008-10-07)
The work provides a new model for the prediction of the MAO-A and -B inhibitor activity by the use of combined complex networks and QSAR methodologies. On the basis of the obtained model, we prepared and assayed 33 coumarin derivatives
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