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Merck
CN

48264

Supelco

2,3,4,6-Tetrachlorophenol solution

new

certified reference material, 5000 μg/mL in methanol

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About This Item

Empirical Formula (Hill Notation):
C6H2Cl4O
CAS Number:
58-90-2
Molecular Weight:
231.89
Beilstein:
779754
MDL number:
MFCD00019979
UNSPSC Code:
12352200
PubChem Substance ID:
24871838

Key Documents

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grade

certified reference material
TraceCERT®

product line

TraceCERT®

CofA

current certificate can be downloaded

packaging

ampule of 1 mL

concentration

5000 μg/mL in methanol

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

environmental

format

single component solution

storage temp.

2-8°C

SMILES string

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

InChI

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

InChI key

VGVRPFIJEJYOFN-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.

Other Notes

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

Legal Information

TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 3 - Flam. Liq. 2 - STOT SE 1

Target Organs

Eyes,Central nervous system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

51.8 °F - closed cup

Flash Point(C)

11 °C - closed cup

Regulatory Information

危险化学品
This item has

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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)
Acute and short-term toxicity of 2,3,4,6-tetrachlorophenol in rats.
M L Hattula et al.
Bulletin of environmental contamination and toxicology, 26(6), 795-800 (1981-06-01)
J S Karns et al.
Applied and environmental microbiology, 46(5), 1176-1181 (1983-11-01)
Resting cells of 2,4,5-trichlorophenoxyacetic acid-grown Pseudomonas cepacia AC1100 were able to completely and rapidly dechlorinate several chlorine-substituted phenols, including 2,4,5-trichlorophenol, 2,3,4,6-tetrachlorophenol, and pentachlorophenol. Several other trichlorophenols were only partially dechlorinated. The evidence suggests that 2,4,5-trichlorophenol is an intermediate in the
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
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