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Supelco

2,3,4,6-Tetrachlorophenol

analytical standard

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About This Item

Formule empirique (notation de Hill):
C6H2Cl4O
Numéro CAS:
58-90-2
Poids moléculaire :
231.89
Numéro CE :
200-402-8
Numéro MDL:
MFCD00019979
Code UNSPSC :
12000000
eCl@ss :
32150233
ID de substance PubChem :
24867777

Qualité

analytical standard

CofA (certificat d'analyse)

current certificate can be downloaded

Conditionnement

ampule of 100 mg

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

environmental

Format

neat

Température de stockage

2-30°C

Chaîne SMILES 

Oc1c(Cl)cc(Cl)c(Cl)c1Cl

InChI

1S/C6H2Cl4O/c7-2-1-3(8)6(11)5(10)4(2)9/h1,11H

Clé InChI

VGVRPFIJEJYOFN-UHFFFAOYSA-N

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Catégories apparentées

Description générale

2,3,4,6-Tetrachlorophenol belongs to the class of substituted phenol compounds, which are widely used in industrial applications such as synthesis of pesticides, dyes, drugs, plastics, etc. Due to their extensive usage, they are commonly found in environmental samples as pollutants.

Application

2,3,4,6-Tetrachlorophenol may be used as an analytical reference standard for the determination of the analyte in landfill leachates, aqueous samples, and environmental samples by various chromatographic techniques.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pictogrammes

Skull and crossbonesEnvironment
GHS06,GHS09

Mention d'avertissement

Danger

Mentions de danger

H301 + H311,H315,H319,H410

Classification des risques

Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Irrit. 2

Code de la classe de stockage

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

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

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

Faites votre choix parmi les versions les plus récentes :

Certificats d'analyse (COA)

Lot/Batch Number
LRAD6074
LRAC9464
LRAC4175
LRAB8148
LC25849V

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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

D A Kalman
Journal of chromatographic science, 22(10), 452-455 (1984-10-01)
A method for the determination of pentachlorophenol, 2,3,4,6-tetrachlorophenol, and their salts or hydrolyzable biological conjugates in urine, water, serum, or fish tissue is reported. The method utilizes fused silica capillary gas chromatography (GC) with electron capture detection of the free
M K Männisto et al.
Water research, 35(10), 2496-2504 (2001-06-08)
The composition and chlorophenol-degrading potential of groundwater bacterial community in a permanently cold, oxygen-deficient chlorophenol contaminated aquifer at Kärkölä, Finland was studied with the aim of evaluating in situ bioremediation potential. The groundwater contained from 10(4) to 10(7) microscopically counted
J H Langwaldt et al.
Applied microbiology and biotechnology, 49(6), 663-668 (1998-07-31)
Air-lift percolator experiments simulated in situ subsurface degradation of 2,4,6-trichlorophenol, 2,3,4,6-tetrachlorophenol and pentachlorophenol, in mixtures and individually, by indigenous microorganisms from a chlorophenol-contaminated aquifer. Inoculation with a chlorophenol(CP)-degrading gram-positive isolate from the CP-contaminated groundwater did not significantly increase CP degradation
H Huang et al.
Chemosphere, 41(6), 943-951 (2000-06-23)
A kinetic model is developed for PCDD formation from chlorophenol catalysed by incinerator fly ash. The key step in the model is a Langmuir-Hinshelwood type elementary step for the coupling of two adsorbed chlorophenol species to PCDD. Kinetic expression is
Pavel Smejtek et al.
The Journal of chemical physics, 120(3), 1383-1394 (2004-07-23)
We studied the effect of segmented solvent molecules on the free energy of transfer of small molecules from water into alkanes (hexane, heptane, octane, decane, dodecane, tetradecane, and hexadecane). For these alkanes we measured partition coefficients of benzene, 3-methylindole (3MI)
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Protocoles

GC Analysis of Phenols in Water

Analytical standard separation of various phenols for research and industrial applications.

GC Analysis of Phenols in Water

Analytical standard separation of various phenols for research and industrial applications.

GC Analysis of Phenols in Water

Analytical standard separation of various phenols for research and industrial applications.

GC Analysis of Phenols in Water

Analytical standard separation of various phenols for research and industrial applications.

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