TargetMol

Retene

Product Code:
 
TAR-T34298
Product Group:
 
Inhibitors and Activators
Supplier:
 
TargetMol
Regulatory Status:
 
RUO
Shipping:
 
cool pack
Storage:
 
-20℃
1 / 1
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CodeSizePrice
TAR-T34298-1mg1mg£201.00
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TAR-T34298-5mg5mg£400.00
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TAR-T34298-10mg10mg£550.00
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TAR-T34298-25mg25mg£852.00
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TAR-T34298-50mg50mg£1,107.00
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TAR-T34298-100mg100mg£1,492.00
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Quantity:
TAR-T34298-500mg500mg£2,922.00
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This product comes from: United States.
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Further Information

Bioactivity:
Retene is a polycyclic aromatic hydrocarbon present in the coal tar fraction, boiling above 360 ?C.
CAS:
483-65-8
Formula:
C18H18
Molecular Weight:
234.342
Purity:
0.98
SMILES:
CC(C)c1ccc2c(ccc3c(C)cccc23)c1

References

Bandowe BAM, et al. A 150-year record of polycyclic aromatic compound (PAC) deposition from high Andean Cajas National Park, southern Ecuador. Sci Total Environ. 2018;621:1652-1663. De Oliveira Alves N, et al. Biomass burning in the Amazon region causes DNA damage and cell death in human lung cells. Sci Rep. 2017;7(1):10937. Sun H, et al. Direct determination of surfactant effects on the uptake of gaseous parent and alkylated PAHs by crop leaf surfaces. Ecotoxicol Environ Saf. 2018;154:206-213. Oikari A, et al. Bioavailability to juvenile rainbow trout (Oncorynchus mykiss) of retene and other mixed-function oxygenase-active compounds from sediments. Environ Toxicol Chem. 2002;21(1):121-128. Maria VL, et al. Anguilla anguilla L. liver EROD induction and genotoxic responses after retene exposure. Ecotoxicol Environ Saf. 2005;61(2):230-238. H?kkinen J, et al. Histopathological responses of newly hatched larvae of whitefish (Coregonus lavaretus s.l.) to UV-B induced toxicity of retene. Aquat Toxicol. 2003;63(2):159-171. Geier MC, et al. Systematic developmental neurotoxicity assessment of a representative PAH Superfund mixture using zebrafish. Toxicol Appl Pharmacol. 2018;41(18)30121-30122.