Determine the necessary mass, volume, or concentration for preparing a solution.
for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
5-Methylchrysene can be activated by several isoenzymes of cytochrome P450 into mutagenic metabolites.
| Canonical Smiles | CC1=CC2=CC=CC=C2C3=C1C4=CC=CC=C4C=C3 |
|---|---|
| IUPAC Name | 5-methylchrysene |
| InChIKey | GOHBXWHNJHENRX-UHFFFAOYSA-N |
| INCHI | 1S/C19H14/c1-13-12-15-7-3-4-8-16(15)18-11-10-14-6-2-5-9-17(14)19(13)18/h2-12H,1H3 |
| Isomeric SMILES | CC1=CC2=CC=CC=C2C3=C1C4=CC=CC=C4C=C3 |
| WGK Germany | 3 |
| PubChem CID | 19427 |
| Molecular Weight | 242.31 |
| Beilstein | 2048519 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
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View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Phenanthrenes and derivatives |
| Subclass | Chrysenes |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Chrysenes |
| Alternative Parents | Naphthalenes Aromatic hydrocarbons Polycyclic hydrocarbons Unsaturated hydrocarbons |
| Molecular Framework | Aromatic homopolycyclic compounds |
| Substituents | Chrysene - Naphthalene - Aromatic hydrocarbon - Polycyclic hydrocarbon - Unsaturated hydrocarbon - Hydrocarbon - Aromatic homopolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as chrysenes. These are compounds containing the polyaromatic chrysene moiety, which consists of a benzene ring fused to a phenanthrene ring system to form Benzo[a]phenanthrene. |
| External Descriptors | carbopolycyclic compound |