34379

Supelco

1,2,4,5-Tetrachlorobenzene

PESTANAL®, analytical standard

Empirical Formula (Hill Notation):
C6H2Cl4
CAS Number:
Molecular Weight:
215.89
Beilstein/REAXYS Number:
1618315
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.04
Pricing and availability is not currently available.

Quality Level

grade

analytical standard

product line

PESTANAL®

form

neat

CofA

certificate is enclosed in each package

shelf life

limited shelf life, expiry date on the label

application(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

240-246 °C (lit.)

mp

138-140 °C (lit.)

Featured Industry

Agriculture
Environmental

format

neat

SMILES string

Clc1cc(Cl)c(Cl)cc1Cl

InChI

1S/C6H2Cl4/c7-3-1-4(8)6(10)2-5(3)9/h1-2H

InChI key

JHBKHLUZVFWLAG-UHFFFAOYSA-N

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Related Categories

Application

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

Legal Information

PESTANAL is a registered trademark of Sigma-Aldrich International GmbH

Pictograms

Exclamation markEnvironment

Signal Word

Warning

Hazard Statements

Precautionary Statements

Personal Protective Equipment

dust mask type N95 (US),Eyeshields,Gloves

Hazard Codes

Xn,N

Risk Statement

22-36/37/38-51/53

Safety Statement

26-36-61

RIDADR

UN 3077 9 / PGIII

WGK Germany

WGK 3

Flash Point(F)

320.0 °F - closed cup

Flash Point(C)

160 °C - closed cup

Lin Xiao et al.
Environmental science & technology, 41(8), 2750-2755 (2007-05-31)
We observed that the presence of transition metal ion, Ag+, Cu2+, or Fe3+, at a concentration of 3 mg L(-1) increases sorption of two nonpolar hydrophobic organic compounds (HOCs), phenanthrene (PHEN), and 1,2,4,5-tetrachlorobenzene (TeCB) by 1.5-4 times to Gram-negative bacteria...
Motoki Terashima et al.
Chemosphere, 57(6), 439-445 (2004-09-08)
Solubilizing abilities of aggregates of humic acid (HA) to chlorinated benzenes (CBs) were investigated by means of the apparent water solubility enhancement. Both the water solubilities of 1,4-dichlorobenzene (DCB) and 1,2,4,5-tetrachlorobenzene (TeCB) linearly increased with increasing concentration of HA above...
S Beil et al.
Journal of bacteriology, 180(21), 5520-5528 (1998-10-29)
The TecA chlorobenzene dioxygenase and the TodCBA toluene dioxygenase exhibit substantial sequence similarity yet have different substrate specificities. Escherichia coli cells producing recombinant TecA enzyme dioxygenate and simultaneously eliminate a halogen substituent from 1,2,4,5-tetrachlorobenzene but show no activity toward benzene...
Hun-Young Wee et al.
Journal of hazardous materials, 155(1-2), 1-9 (2007-12-07)
Palladium-catalyzed hydrodehalogenation (HDH) was applied for destroying 1,2,4,5-tetrachlorobenzene (TeCB) in mixtures of water and ethanol. This investigation was performed as a critical step in the development of a new technology for clean-up of soil contaminated by halogenated hydrophobic organic contaminants....
Oxygen consumption of juvenile rainbow trout (Oncorhynchus mykiss) exposed to sublethal concentrations of 1,2,4,5-tetrachlorobenzene and tetrachloroguaiacol.
R Yang et al.
Bulletin of environmental contamination and toxicology, 59(3), 479-485 (1997-09-01)
Protocols
US EPA Method 8270 (Appendix IX): GC Analysis of Semivolatiles on Equity®-5 (30 m x 0.25 mm I.D., 0.50 μm)
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