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About This Item
Empirical Formula (Hill Notation):
C6H2Cl4O
CAS Number:
Molecular Weight:
231.89
UNSPSC Code:
41116107
PubChem Substance ID:
EC Number:
200-402-8
MDL number:
InChI key
VGVRPFIJEJYOFN-UHFFFAOYSA-N
InChI
1S/C6H2Cl4O/c7-2-1-3(8)6(11)5(10)4(2)9/h1,11H
SMILES string
Oc1c(Cl)cc(Cl)c(Cl)c1Cl
grade
analytical standard
packaging
vial of 1 g
manufacturer/tradename
Cerilliant®
application(s)
environmental
forensics and toxicology
format
neat
storage temp.
room temp
Legal Information
CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Danger
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Irrit. 2
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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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
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)
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 Männistö et al.
Biodegradation, 12(5), 291-301 (2002-05-09)
Effects of low temperature and low oxygen partial pressure on the occurrence and activity of 2,3,4,6-tetrachlorophenol degrading bacteria in a boreal chlorophenol contaminated groundwater and a full-scale fluidized-bed bioreactor were studied using four polychlorophenol degrading bacterial isolates of different phylogenetic
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
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