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45691

Supelco

2-(2,4,5-Trichlorophenoxy)propionic acid

PESTANAL®, analytical standard

Synonym(s):

2,4,5-TP, Fenoprop, Silvex®

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About This Item

Empirical Formula (Hill Notation):
C9H7Cl3O3
CAS Number:
93-72-1
Molecular Weight:
269.51
Beilstein:
1985768
EC Number:
202-271-2
MDL number:
MFCD00002646
UNSPSC Code:
41116107
PubChem Substance ID:
329756904
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

CC(Oc1cc(Cl)c(Cl)cc1Cl)C(O)=O

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)

InChI key

ZLSWBLPERHFHIS-UHFFFAOYSA-N

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
Silvex is a registered trademark of Silberline Manufacturing Co., Inc.

Pictograms

Exclamation markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H302 - H315 - H410

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Irrit. 2

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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Certificates of Analysis (COA)

Lot/Batch Number
BCCK6693
BCCG8898
BCBZ9087
SZBF103XV
SZBB174XV

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I Voskoboinik et al.
Toxicology letters, 87(2-3), 147-155 (1996-10-01)
We have investigated the effects of peroxisome proliferators silvex, nafenopin and diethylhexylphthalate (DEHP) on rat liver glutathione S-transferase (GST) isoenzyme activities and patterns. Silvex was a more potent in vitro GST inhibitor than nafenopin and DEHP. After 14 days oral
I Voskoboinik et al.
Toxicology, 122(1-2), 81-91 (1997-09-26)
Peroxisome proliferators are known to modulate the activity of xenobiotic-metabolising enzymes, including glutathione S-transferase (GST) and cytochrome P-450 (CYP). In this study the effect of peroxisome proliferators silvex and di(2-ethylhexyl)phthalate (DEHP) on the formation of (+)-anti-benzo(a)pyrene -7,8-dihydrodiol-9,10-epoxide (BPDE)-DNA adducts from
P Schmitt-Kopplin et al.
Electrophoresis, 22(1), 77-87 (2001-02-24)
By transforming the time-based x-axis of electropherograms in capillary zone electrophoresis (CZE) into the corresponding effective mobility-scale, we propose a simple and robust data representation for a better qualitative and quantitative capillary electrophoresis (CE) analysis. The time scale of the
E K Arnold et al.
Veterinary and human toxicology, 31(2), 121-125 (1989-04-01)
The chlorinated phenoxy acid herbicides (CPAHs) appear to have similar pharmacokinetics. They are rapidly and almost completely absorbed from an oral dose. They distribute to other tissues and are highly protein-bound in the plasma. The CPAHs are rapidly eliminated unchanged
R B Geerdink et al.
Journal of chromatography, 547(1-2), 478-483 (1991-06-28)
Novel clean-up techniques for a polymeric precolumn (PLRP-S) for the subsequent determination of bentazone and eight phenoxy acid herbicides in surface water samples are described. After preconcentration of the components at pH 3 on a 10 x 2 mm I.D.
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