Cas no 93952-23-9 (3,3',4,4'-Tetrachlorobiphenyl-d6)
3,3',4,4'-Tetrachlorobiphenyl-d6 Chemical and Physical Properties
Names and Identifiers
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- 1,1'-Biphenyl-2,2',3,3',6,6'-d6,4,4',5,5'-tetrachloro- (9CI)
- 3,3',4,4'-TETRACHLORODIPHENYL-D6
- 93952-23-9
- F91347
- HY-W140545S
- 3,3',4,4'-Tetrachloro-1,1'-biphenyl-d6
- 3,3',4,4'-TETRACHLOROBIPHENYL-D6
- 1,2-Dichloro-3,4,6-trideuterio-5-(3,4-dichloro-2,5,6-trideuteriophenyl)benzene
- CS-0566698
- 1ST3676D6-100L
- 3,3',4,4'-Tetrachlorobiphenyl-d6 Solution in Dichloromethane, 100ug/mL
- DB-304002
- 1,1'-Biphenyl-2,2',3,3',6,6'-d6, 4,4',5,5'-tetrachloro- (9CI); 3,3',4,4'-Tetrachlorobiphenyl-2,2',5,5',6,6'-d6; PCB 77-d6; PCB 77 d6;
- 3,3',4,4'-Tetrachlorobiphenyl-d6
-
- Inchi: 1S/C12H6Cl4/c13-9-3-1-7(5-11(9)15)8-2-4-10(14)12(16)6-8/h1-6H/i1D,2D,3D,4D,5D,6D
- InChI Key: UQMGJOKDKOLIDP-MZWXYZOWSA-N
- SMILES: ClC1=C(C([2H])=C([2H])C(=C1[2H])C1C([2H])=C([2H])C(=C(C=1[2H])Cl)Cl)Cl
Computed Properties
- Exact Mass: 297.957071g/mol
- Monoisotopic Mass: 295.960021g/mol
- Isotope Atom Count: 6
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 0
- Heavy Atom Count: 16
- Rotatable Bond Count: 1
- Complexity: 209
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 6.6
- Topological Polar Surface Area: 0?2
3,3',4,4'-Tetrachlorobiphenyl-d6 Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | T889976-5mg |
3,3',4,4'-Tetrachlorobiphenyl-d6 |
93952-23-9 | 5mg |
$ 607.00 | 2023-09-05 | ||
| TRC | T889976-10mg |
3,3',4,4'-Tetrachlorobiphenyl-d6 |
93952-23-9 | 10mg |
$ 1016.00 | 2023-09-05 |
3,3',4,4'-Tetrachlorobiphenyl-d6 Related Literature
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Karl Crowley,Eimer O'Malley,Aoife Morrin,Malcolm R. Smyth,Anthony J. Killard Analyst, 2008,133, 391-399
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2. An autonomous self-optimizing flow machine for the synthesis of pyridine–oxazoline (PyOX) ligands?Eric Wimmer,Daniel Cortés-Borda,Solène Brochard,Elvina Barré,Charlotte Truchet,Fran?ois-Xavier Felpin React. Chem. Eng., 2019,4, 1608-1615
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Yang Xu,Min Wang,Donghui Wei,Rongqiang Tian,Zheng Duan,Fran?ois Mathey Dalton Trans., 2019,48, 5523-5526
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Jialiang Yuan,Ran Dong,Yuan Li,Yang Liu,Zhuo Zheng,Yuxia Liu,Yan Sun,Benhe Zhong,Zhenguo Wu,Xiaodong Guo Chem. Commun., 2021,57, 13004-13007
Additional information on 3,3',4,4'-Tetrachlorobiphenyl-d6
Recent Advances in the Study of 3,3',4,4'-Tetrachlorobiphenyl-d6 (CAS: 93952-23-9)
3,3',4,4'-Tetrachlorobiphenyl-d6 (CAS: 93952-23-9) is a deuterated analog of the polychlorinated biphenyl (PCB) congener 3,3',4,4'-tetrachlorobiphenyl (PCB-77). This compound has gained significant attention in recent years due to its utility as an internal standard in environmental and toxicological studies. The deuterated form enhances the accuracy of mass spectrometry-based analyses, enabling precise quantification of PCB-77 in complex matrices such as biological tissues and environmental samples.
Recent studies have focused on the environmental persistence and toxicological effects of PCB-77, which is classified as a dioxin-like PCB due to its structural similarity to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). Research has demonstrated that PCB-77 binds to the aryl hydrocarbon receptor (AhR), triggering a cascade of biochemical responses that can lead to oxidative stress, endocrine disruption, and carcinogenesis. The use of 3,3',4,4'-Tetrachlorobiphenyl-d6 has been instrumental in elucidating these mechanisms, as it allows for the differentiation of exogenous PCB-77 from endogenous compounds in experimental systems.
One notable advancement is the application of 3,3',4,4'-Tetrachlorobiphenyl-d6 in high-resolution mass spectrometry (HRMS) techniques. A 2023 study published in Environmental Science & Technology utilized this compound to develop a novel method for the simultaneous detection of PCB-77 and its metabolites in human serum. The method achieved a detection limit of 0.1 pg/mL, significantly improving upon previous techniques. This breakthrough has important implications for biomonitoring and risk assessment in populations exposed to PCBs.
In addition to its role in analytical chemistry, 3,3',4,4'-Tetrachlorobiphenyl-d6 has been employed in mechanistic studies of PCB toxicity. A recent investigation published in Toxicological Sciences used the deuterated compound to track the distribution and metabolism of PCB-77 in a rodent model. The study revealed that PCB-77 preferentially accumulates in adipose tissue and the liver, where it undergoes cytochrome P450-mediated oxidation to form reactive metabolites. These findings underscore the potential health risks associated with chronic PCB exposure and highlight the need for targeted remediation strategies.
Another area of research has explored the use of 3,3',4,4'-Tetrachlorobiphenyl-d6 in environmental fate studies. A 2022 paper in Chemosphere reported on the degradation kinetics of PCB-77 in soil microcosms, using the deuterated analog to distinguish between biotic and abiotic transformation pathways. The results indicated that microbial degradation plays a dominant role in the breakdown of PCB-77 under aerobic conditions, with half-lives ranging from 30 to 90 days depending on soil properties. This work provides valuable insights for the development of bioremediation approaches for PCB-contaminated sites.
Looking ahead, the continued use of 3,3',4,4'-Tetrachlorobiphenyl-d6 is expected to drive further advancements in PCB research. Emerging applications include its incorporation into stable isotope probing (SIP) studies to trace PCB fluxes in food webs and its use in metabolomics platforms to identify novel biomarkers of PCB exposure. As analytical technologies continue to evolve, the precision and versatility offered by deuterated standards like 3,3',4,4'-Tetrachlorobiphenyl-d6 will remain indispensable for advancing our understanding of PCB toxicology and environmental behavior.
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