93951-97-4
93951-97-4
Chemical Structure
Acenaphthylene-d8
Synonym(s): Acenaphthylene-d8
- CAS No.: 93951-97-4
- Formula:C12D8
- Molecular Weight:160.24
IUPAC Name: acenaphthylene-d8
InChIKey: HXGDTGSAIMULJN-PGRXLJNUSA-N
SMILES: [2H]C1=C([2H])C([2H])=C2C([2H])=C([2H])C([2H])=C3C([2H])=C([2H])C1=C32
Biological Activity: Acenaphthylene-d8 is the deuterium labeled Acenaphthylene[1]. Acenaphthylene is a polycyclic aromatic hydrocarbon (PAH). PAHs are derived naturally from coal and tar deposits, and produced by incomplete combustion of organic matter[2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Acenaphthylene-d8 | 99.48% | Acenaphthylene-d8 is the deuterium labeled Acenaphthylene. Acenaphthylene is a polycyclic aromatic hydrocarbon (PAH). PAHs are derived naturally from coal and tar deposits, and produced by incomplete combustion of organic matter. | ||||||||||||||||||||
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Acenaphthylene (Standard) | ≥98% | Acenaphthylene (Standard) is the analytical standard of Acenaphthylene. This product is intended for research and analytical applications. Acenaphthylene is a polycyclic aromatic hydrocarbon (PAH). PAHs are derived naturally from coal and tar deposits, and produced by incomplete combustion of organic matter. | ||||||||||||||||||||
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Acenaphthylene | 99.62% | Acenaphthylene is a polycyclic aromatic hydrocarbon (PAH). PAHs are derived naturally from coal and tar deposits, and produced by incomplete combustion of organic matter. | ||||||||||||||||||||
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References
- [1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-216. [Content Brief]
- [2]. Fabienne Reisen, et al. Reactions of hydroxyl radicals and ozone with acenaphthene and acenaphthylene. Environ Sci Technol. 2002 Oct 15;36(20):4302-11. [Content Brief]
