218-01-9

Chrysene Chemical Structure
218-01-9

Chemical Structure

Chrysene

  • CAS No.: 218-01-9
  • Formula:C18H12
  • Molecular Weight:228.29

IUPAC Name: chrysene

InChIKey: WDECIBYCCFPHNR-UHFFFAOYSA-N

SMILES: C12=CC=CC=C1C=CC3=C4C=CC=CC4=CC=C23

Biological Activity: Chrysene is a high molecular weight (HMW), polycyclic aromatic hydrocarbon (PAH) known for its recalcitrance and carcinogenic properties[1].

Cat. No. Nom du produit Pureté Description Pricing
HY-121107
Chrysene 99.49% Chrysene is a high molecular weight (HMW), polycyclic aromatic hydrocarbon (PAH) known for its recalcitrance and carcinogenic properties.
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HY-121107R
Chrysene (Standard) ≥98% Chrysene (Standard) is the analytical standard of Chrysene. This product is intended for research and analytical applications. Chrysene is a high molecular weight (HMW), polycyclic aromatic hydrocarbon (PAH) known for its recalcitrance and carcinogenic properties.
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HY-121107S
Chrysene-d12 99.71% Chrysene-d12 is the deuterium labeled Chrysene. Chrysene is a high molecular weight (HMW), polycyclic aromatic hydrocarbon (PAH) known for its recalcitrance and carcinogenic properties.
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HY-133986
6-Methylchrysene 97.0% 6-Methylchrysene, a tobacco smoke constituent, is a weak carcinogen.
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HY-B1727
Phenanthrene 99.82% Phenanthrene is an orally active polycyclic aromatic hydrocarbon (PAH) that induces inflammation, oxidative stress, and apoptosis. Additionally, phenanthrene is commonly used to detect or assess PAH pollution in the environment.
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HY-N10021
Benzo[e]pyrene Benzo[e]pyrene occurs in fossil fuels and is a highly toxic member of a family of compounds called polyaromatic hydrocarbons (PAHs).
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HY-W012277
Benzo[c]phenanthrene Benzo[c]phenanthrene has carcinogenic activity. Benzo[c]phenanthrene can be used as a substrate or intermediate.
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HY-W012278
Benz[a]anthracene 99.90% Benz[a]anthracene (Tetraphene) is a polycyclic aromatic hydrocarbon pollutant and also a ligand of aryl hydrocarbon receptor 2 (AHR2), with a pIC50 of 7.319. Benz[a]anthracene can be detected in spruce needles near aluminum smelters. Exposure to Benz[a]anthracene during zebrafish embryonic stage activates the AHR-CYP1A signaling pathway and induces AHR2 expression, leading to social behavioral deficits that persist into adulthood, accompanied by impaired neuro-immune interaction, while anxiety levels remain unaffected. Benz[a]anthracene can be used in studies related to PAH environmental toxicology, developmental neurotoxicity and biodegradation.
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HY-W013053R
Dibenz[a,h]anthracene (Standard) ≥98% Dibenz[a,h]anthracene (Standard) is the analytical standard of Dibenz[a,h]anthracene. This product is intended for research and analytical applications. Dibenz[a,h]anthracene (DBA) is a polycyclic aromatic hydrocarbon (PAH) of considerable tumorigenicity. Dibenz[a,h]anthracene results in DNA adduct formation leading to the activation of a DNA damage response. Dibenz[a,h]anthracene induces cell cycle arrest and apoptosis via both Tp53-dependent and Tp53-independent mechanisms.
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HY-W013423
5-Methylchrysene 5-Methylchrysene can be activated by several isoenzymes of cytochrome P450 into mutagenic metabolites.
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HY-W096907
Picene Picene is a polycyclic aromatic hydrocarbon of environmental relevance. Picene can be widely distributed in the environment as the result of incomplete combustion of organic matter. Picene is found to be inactive as complete carcinogen, while it acts in a high dose as a weak tumor initiator.
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HY-W777456
Phenanthrene-13C6 99.9% Phenanthrene-13C6 is the 13C labeled Phenanthrene (HY-B1727). Phenanthrene is an orally active polycyclic aromatic hydrocarbon (PAH) that induces inflammation, oxidative stress, and apoptosis. Additionally, phenanthrene is commonly used to detect or assess PAH pollution in the environment.
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HY-W778162
Phenanthrene-13C2 Phenanthrene-13C2 is the 13C-labeled Phenanthrene (HY-B1727). Phenanthrene is an orally active polycyclic aromatic hydrocarbon (PAH) that induces inflammation, oxidative stress, and apoptosis. Additionally, phenanthrene is commonly used to detect or assess PAH pollution in the environment.
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References