CAS 74472-36-9
:2,3,3′,5,6-Pentachlorobiphenyl
Description:
2,3,3′,5,6-Pentachlorobiphenyl, with the CAS number 74472-36-9, is a member of the polychlorinated biphenyl (PCB) family, which are synthetic organic chemicals known for their environmental persistence and potential toxicity. This compound consists of two connected benzene rings with five chlorine atoms substituted at specific positions on the biphenyl structure. Its physical properties include a high melting point and low solubility in water, making it more soluble in organic solvents and oils. 2,3,3′,5,6-Pentachlorobiphenyl is characterized by its stability and resistance to degradation, which contributes to its accumulation in the environment and living organisms. Due to its potential for bioaccumulation and associated health risks, including endocrine disruption and carcinogenic effects, its use has been heavily regulated or banned in many countries. Analytical methods such as gas chromatography-mass spectrometry (GC-MS) are commonly employed to detect and quantify this compound in environmental samples. Overall, 2,3,3′,5,6-Pentachlorobiphenyl exemplifies the environmental and health concerns associated with PCBs.
Formula:C12H5Cl5
InChI:InChI=1S/C12H5Cl5/c13-7-3-1-2-6(4-7)10-11(16)8(14)5-9(15)12(10)17/h1-5H
InChI key:InChIKey=NTKSJAPQYKCFPP-UHFFFAOYSA-N
SMILES:ClC1=C(C(Cl)=C(Cl)C=C1Cl)C2=CC(Cl)=CC=C2
Synonyms:- 1,1'-Biphenyl, 2,3,3',5,6-Pentachloro-
- 1,1′-Biphenyl, 2,3,3′,5,6-pentachloro-
- 2,3,3',5,6-Pcb
- 2,3,3',5,6-Pentachloro-1,1'-biphenyl
- 2,3,3′,5,6-Pentachloro-1,1′-biphenyl
- 2,3,3′,5,6-Pentachlorobiphenyl
- 2,3,5,6,3′-Pentachlorobiphenyl
- 74472-36-9
- Pcb 112
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Found 3 products.
PCB No. 112 10 µg/mL in Isooctane
CAS:Controlled ProductFormula:C12H5Cl5Color and Shape:Single SolutionMolecular weight:326.432,3,3',5,6-Pentachlorobiphenyl
CAS:Controlled Product<p>2,3,3',5,6-Pentachlorobiphenyl is a compound that contains chlorine atoms attached to the biphenyl structure. It is used in various applications such as controlled products and catalysts. This compound has been studied for its photophysical properties and its potential use as an electrode material. Additionally, 2,3,3',5,6-Pentachlorobiphenyl has shown promising results in gene therapy research as it can enhance the efficiency of adeno-associated virus-mediated gene transfer. It has also demonstrated inhibitory effects on enzymes involved in arachidonic acid metabolism and dopamine synthesis. Furthermore, this compound has shown potential as an intraocular drug delivery system due to its ability to form stable complexes with certain proteins. Overall, 2,3,3',5,6-Pentachlorobiphenyl exhibits a wide range of characteristics and applications that make it a valuable compound in various fields.</p>Formula:C12H5Cl5Purity:Min. 95%Molecular weight:326.43 g/mol

