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45691

Supelco

Acide 2-(2,4,5-trichlorophénoxy)propionique

PESTANAL®, analytical standard

Synonyme(s) :

2,4,5-TP, Fenoprop, Silvex®

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About This Item

Formule empirique (notation de Hill):
C9H7Cl3O3
Numéro CAS:
93-72-1
Poids moléculaire :
269.51
Numéro Beilstein :
1985768
Numéro CE :
202-271-2
Numéro MDL:
MFCD00002646
Code UNSPSC :
41116107
ID de substance PubChem :
329756904
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

Gamme de produits

PESTANAL®

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

agriculture
environmental

Format

neat

Chaîne SMILES 

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)

Clé InChI

ZLSWBLPERHFHIS-UHFFFAOYSA-N

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Catégories apparentées

Application

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

Produits recommandés

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Informations légales

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

Pictogrammes

Exclamation markEnvironment
GHS07,GHS09

Mention d'avertissement

Warning

Mentions de danger

H302 - H315 - H410

Classification des risques

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

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves

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Certificats d'analyse (COA)

Lot/Batch Number
BCCK6693
BCCG8898
BCBZ9087
SZBF103XV
SZBB174XV

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Silvex (2,4,5-TP).
Reviews of environmental contamination and toxicology, 104, 195-202 (1988-01-01)
E Herrero-Hernández et al.
Analytica chimica acta, 650(2), 195-201 (2009-09-02)
An extraction-preconcentration procedure based on the use of a molecularly imprinted polymer (MIP) as selective sorbent has been developed for the determination of several phenolic compounds (bisphenol-A, bisphenol-F and 4-nitrophenol) and phenoxyacid herbicides (2,4-D, 2,4,5-T and 2,4,5-TP) in honey samples.
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
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
F A Nicholls-Grzemski et al.
Journal of biochemical and molecular toxicology, 14(6), 335-345 (2000-11-18)
Pretreatment with peroxisome proliferators protects mice against various hepatotoxicants. Since our previous work suggested that the hepatoprotection may involve an increased ability to cope with oxidative stress, the present work directly addressed this possibility. Several observations indicated a heightened defense
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