1,2,4,5-Tetrachlorobenzene

1,2,4,5-Tetrachlorobenzene Basic information
Product Name:1,2,4,5-Tetrachlorobenzene
Synonyms:I,2,4,5-Tetrachlorbenzol;Rcra waste number U207;rcrawastenumberu207;s-Tetrachlorobenzene;Melting point 140.0 to 143.0 deg-C;Purity(GC) min. 99.0 %;1,2,4,5-Tetrachlorobenzne;1,2,4,5-TETRACHLOROBENZENE, 1X1ML, ACN 1 000UG/ML
CAS:95-94-3
MF:C6H2Cl4
MW:215.89
EINECS:202-466-2
Product Categories:Organics;Chlorine Compounds;Pesticides&Metabolites;Aryl;C6;Halogenated Hydrocarbons;Alpha Sort;TA - TE;T-ZAlphabetic;Volatiles/ Semivolatiles;Q-ZAlphabetic
Mol File:95-94-3.mol
1,2,4,5-Tetrachlorobenzene Structure
1,2,4,5-Tetrachlorobenzene Chemical Properties
Melting point 139 °C
Boiling point 240-246 °C(lit.)
density 1.858
vapor pressure 5 at 25 °C (extrapolated, Mackay et al., 1982)
refractive index 1.5348 (estimate)
Fp >230 °F
storage temp. 0-6°C
solubility 0.0003g/l
form Crystalline Solid
color Light pink to gray
Water Solubility insoluble. <0.1 g/100 mL at 21 ºC
BRN 1618315
Henry's Law Constant0.10 at 20 °C (gas stripping-GC, Oliver, 1985)
Stability:Stable. Combustible. Incompatible with strong oxidizing agents. Reacts explosively with alkaline methanol solutions.
CAS DataBase Reference95-94-3(CAS DataBase Reference)
NIST Chemistry ReferenceBenzene, 1,2,4,5-tetrachloro-(95-94-3)
EPA Substance Registry System1,2,4,5-Tetrachlorobenzene (95-94-3)
Safety Information
Hazard Codes Xn,T,F,N
Risk Statements 22-36/37/38-23/24/25-11-36-20/21/22-51/53
Safety Statements 26-36-45-27-16-36/37-61
RIDADR UN 3077 9/PG 3
WGK Germany 3
RTECS DB9450000
TSCA Yes
HazardClass 9
HS Code 29036990
Hazardous Substances Data95-94-3(Hazardous Substances Data)
ToxicityAcute oral LD50 for rats 1,500 mg/kg, mice 1,035 mg/kg (quoted, RTECS, 1985).
MSDS Information
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1,2,4,5-Tetrachlorobenzene English
SigmaAldrich English
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1,2,4,5-Tetrachlorobenzene Usage And Synthesis
Chemical Propertieswhite solid
UsesIntermediate for herbicides and defoliants, insecticide, impregnant for moisture resistance, electrical insulation.
Uses1,2,4,5-Tetrachlorobenzene was used to study the environmental behavior of hexachlorobutadiene (HCBD).
DefinitionChEBI: A tetrachlorobenzene carrying chloro groups at positions 1, 2, 4 and 5.
Environmental fateBiological. A mixed culture of soil bacteria or a Pseudomonas sp. transformed 1,2,4,5- tetrachlorobenzene to 2,3,5,6-tetrachlorophenol (Ballschiter and Scholz, 1980). After incubation in sewage sludge for 32 d under anaerobic conditions, 1,2,4,5-tetrachlorobenzene did not biodegrade (Kirk et al., 1989).
In an enrichment culture derived from a contaminated site in Bayou d’Inde, LA, 1,2,4,5- tetrachlorobenzene underwent reductive dechlorination to 1,2,4-trichlorobenzene. The maximum dechlorination rate, based on the recommended Michaelis-Menten model, was 5.5 nM/d (Pavlostathis and Prytula, 2000).
Photolytic. Irradiation (λ ≥285 nm) of 1,2,4,5-tetrachlorobenzene (1.1–1.2 mM/L) in an acetonitrile-water mixture containing acetone (0.553 mM) as a sensitizer gave the following products (% yield): 1,2,4-trichlorobenzene (25.3), 1,3-dichlorobenzene (8.1), 1,4-dichlorobenzene (3.6), 2,2′,3,4′,5,5′,6-heptachlorobiphenyl (4.19), four hexachlorobiphenyls (6.78), four pentachlorobiphenyls (2.33), one tetrachlorobiphenyl (0.32), 2,4,5-trichloroacetophenone, and (2,4,5- trichlorophenyl)acetonitrile (Choudhry and Hutzinger, 1984). Without acetone, the identified photolysis products (% yield) included 1,2,4-trichlorobenzene (27.7), 1,3-dichlorobenzene (0.3), 1,4-dichlorobenzene (8.5), pentachlorobenzene (trace), 1,2,3,4-tetrachlorobenzene (0.45), 1,2,3,5- tetrachlorobenzene (1.11), 2,2′,3,4′,5,5′,6-heptahlorobiphenyl (1.24), three hexachlorobiphenyls (1.19), and four pentachlorobiphenyls (0.56) (Choudhry and Hutzinger, 1984). The sunlight irradiation of 1,2,4,5-tetrachlorobenzene (20 g) in a 100-mL borosilicate glass-stoppered Erlenmeyer flask for 28 d yielded 26 ppm heptachlorobiphenyl (Uyeta et al., 1976).
Chemical/Physical. Based on an assumed base-mediated 1% disappearance after 16 d at 85 °C and pH 9.70 (pH 11.26 at °C), the hydrolysis half-life was estimated to be >900 yr (Ellington et al., 1988).
Purification MethodsCrystallise it from EtOH, ether, *benzene, *benzene/EtOH or carbon disulfide. [Beilstein 5 IV 668.]
1,4-Bis(chloromethyl)-2,3,5,6-tetrachlorobenzene,1,4-Bis(chloromethyl)tetrachlorobenzene 1,2,4,6-tetrachlorobenzen 2,3,5,6-TETRACHLORO-P-XYLENE-A,A'-DIOL 2,3,5,6-TETRACHLORO-P-XYLYLENEDIAMINE 2,3,5,6-TETRACHLOROTHIOANISOLE Quintozine PENTACHLOROBENZENE Chlorthal p-Dichlorobenzene 1,2,4,5-Tetrachlorobenzene 1,2,4-Trichlorobenzene 1,3-Dichlorobenzene Chlorphenamine maleate HexanitrodiphenylaMine 2,4-Dichlorobenzyl chloride 1,2-Dichlorobenzene 2-Chlorobenzaldehyde TECNAZENE

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