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CAS 191-30-0
:Dibenzo[a,l]pyrene
Description:
Dibenzo[a,l]pyrene is a polycyclic aromatic hydrocarbon (PAH) characterized by its complex fused ring structure, consisting of five benzene rings. It is known for its high molecular weight and is classified as a potent carcinogen. This compound is typically found in products of incomplete combustion, such as tobacco smoke, grilled meats, and various industrial processes. Dibenzo[a,l]pyrene is insoluble in water but soluble in organic solvents, which influences its environmental persistence and bioaccumulation potential. Its chemical structure contributes to its stability and resistance to degradation, making it a concern for environmental health. The compound has been studied for its mutagenic and carcinogenic properties, particularly in relation to DNA damage and the formation of adducts. Due to its hazardous nature, dibenzo[a,l]pyrene is subject to regulatory scrutiny, and its presence in the environment is monitored to mitigate potential health risks. Understanding its behavior and effects is crucial for assessing environmental contamination and human exposure.
Formula:C24H14
InChI:InChI=1S/C24H14/c1-2-8-18-16(6-1)14-17-13-12-15-7-5-11-20-19-9-3-4-10-21(19)24(18)23(17)22(15)20/h1-14H
InChI key:InChIKey=JNTHRSHGARDABO-UHFFFAOYSA-N
SMILES:C12=C3C=4C(C=5C1=C(C=CC2=CC=6C3=CC=CC6)C=CC5)=CC=CC4
Synonyms:- 1,2,9,10-Dibenzopyrene
- 1,2:3,4-Dibenzopyrene
- 2,3:4,5-Dibenzpyrene
- 4,5,6,7-Dibenzpyrene
- 7A,10A-Dihydronaphtho[1,2,3,4-Pqr]Tetraphene
- Ba 51-090462
- Dibenzo(A,L)Pyrene
- Dibenzo[a,l]pyrene (purity)
- Dibenzo[def,p]chrysene
- NSC 90324
- Naphtho[1,2,3,4-Pqr]Tetraphene
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Found 12 products.
Dibenzo[a,l]pyrene 10 µg/mL in Acetonitrile
CAS:Formula:C24H14Color and Shape:Single SolutionMolecular weight:302.37Dibenzo[a,l]pyrene 10 µg/mL in Cyclohexane
CAS:Formula:C24H14Color and Shape:ColourlessMolecular weight:302.37Dibenzo[def,p]chrysene
CAS:Controlled Product<p>Applications An active metabolite from inhalation and dermal exposure to polycyclic aromatics hydrocarbons found in hot mix asphalt paving workers. DBC is the most potent tumorigen that has been identified to date. Dibenzo[def,p]chrysene (DBC) is a carcinogen and should be handled with caution.<br>References Anderson, L., et al.: Toxicol. Appl. Pharmacol., 199, 85 (2004), Yu, Z., et al.: Cancer Res., 66, 755 (2006), Shen, J., et al.: Toxicol. Sci., 95, 313 (2007),<br></p>Formula:C24H14Color and Shape:Off-WhiteMolecular weight:302.37Dibenzo[def,p]chrysene-d14 (Major)
CAS:Controlled Product<p>Applications Labelled Dibenzo[a,l]pyrene (D416945). An active metabolite from inhalation and dermal exposure to polycyclic aromatics hydrocarbons in hot mix asphalt paving workers. DBC is the most potent tumorigen that has been identified to date. Dibenzo[def,p]chrysene (DBC) is a carcinogen and should be handled with appropriate caution.<br>References Anderson, L., et al.: Toxicol. Appl. Pharmacol., 199, 85 (2004), Yu, Z., et al.: Cancer Res., 66, 755 (2006), Shen, J., et al.: Toxicol. Sci., 95, 313 (2007),<br></p>Formula:C24D14Color and Shape:NeatMolecular weight:316.45Dibenzo[def,p]chrysene-d8 (Major)
CAS:Controlled Product<p>Applications Labelled Dibenzo[a,l]pyrene (D416945). An active metabolite from inhalation and dermal exposure to polycyclic aromatics hydrocarbons in hot mix asphalt paving workers. DBC is the most potent tumorigen that has been identified to date. Dibenzo[def,p]chrysene (DBC) is a carcinogen and should be handled with appropriate caution.<br>References Anderson, L., et al.: Toxicol. Appl. Pharmacol., 199, 85 (2004), Yu, Z., et al.: Cancer Res., 66, 755 (2006), Shen, J., et al.: Toxicol. Sci., 95, 313 (2007),<br></p>Formula:C24H6D8Color and Shape:NeatMolecular weight:310.42Dibenzo[def,p]chrysene
CAS:<p>Dibenzo[def,p]chrysene is a polycyclic aromatic hydrocarbon (PAH) that has been shown to be genotoxic and carcinogenic in animals. It has also been found to have potential as a biomarker for exposure. The toxic effects of dibenzo[def,p]chrysene are due to its ability to induce oxidative stress and cause DNA damage, leading to cell death. Dibenzo[def,p]chrysene inhibits transcriptional regulation by binding to the polymerase chain reaction (PCR) enzyme, cytochrome p450, and pro-apoptotic protein. Dibenzo[def,p]chrysene can also activate detoxification enzymes such as glutathione S-transferases and quinone reductases. This PAH is metabolized through phase II conjugation with glutathione or glucuronides. Listed below are some biological properties of diben</p>Formula:C24H14Purity:Min. 95%Molecular weight:302.37 g/mol
![Dibenzo[def,p]chrysene](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2FIN%2Fthumb%2FDA002EZK.jpg&w=3840&q=75)
![Dibenzo[a,l]pyrene 10 µg/mL in Acetonitrile](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F04%2Fthumb%2FL20725000AL.jpg&w=3840&q=75)
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