1,6-Diphenyl-1,3,5-hexatriene (Highly Pure)


Catalog Number: B2012303 (100 mg)
1,6-Diphenyl-1,3,5-hexatriene (Highly Pure) is a high quality 1,6-Diphenyl-1,3,5-hexatriene used as a probe for lipid mono- and bilayers. This product has been used as molecular tool for various biochemical applications. It has also been used in a wide array of other chemical and immunological applications. Custom bulk amounts of this product are available upon request.

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1,6-Diphenyl-1,3,5-hexatriene (Highly Pure)
Catalog number: B2012303
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 100 mg
Molecular Weight or Concentration: 232.3 g/mol
Supplied as: Powder
Applications: molecular tool for various biochemical applications
Storage: -20C
Keywords: Diphenylhexatriene, DPH, NSC 90479
Grade: Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um.

1: Ma L, Morgan JC, Stancill WE, Allen WE. Phosphorylated 1,6-diphenyl-1,3,5-hexatriene Bioorg Med Chem Lett. 2004 Mar 8;14(5):1075-8.
2: Caudron E, Zhou JY, England P, Ollivon M, Prognon P. Some insights about 1,6-diphenyl-1,3,5-hexatriene-lipid supramolecular assemblies by steady-state fluorescence measurements Appl Spectrosc. 2007 Sep;61(9):963-9.
3: Makwana PK, Jethva PN, Roy I. Coumarin 6 and 1,6-diphenyl-1,3,5-hexatriene (DPH) as fluorescent probes to monitor protein aggregation Analyst. 2011 May 21;136(10):2161-7.
4: Li MH, Manathunga L, London E, Raleigh DP. The Fluorescent Dye 1,6-Diphenyl-1,3,5_hexatriene Binds to Amyloid Fibrils Formed by Human Amylin and Provides a New Probe of Amylin Amyloid Kinetics Biochemistry. 2021 Jun 29;60(25):1964-1970.
5: Hitzemann RJ, Harris RA. Developmental changes in synaptic membrane fluidity: a comparison of 1,6-diphenyl-1,3,5_hexatriene (DPH) and 1-[4-(trimethylamino)phenyl]-6-phenyl-1,3,5-hexatriene (TMA-DPH) Brain Res. 1984 May;316(1):113-20.
6: Straume M, Litman BJ. Equilibrium and dynamic structure of large, unilamellar, unsaturated acyl chain phosphatidylcholine vesicles. Higher order analysis of 1,6-diphenyl_1,3,5-hexatriene and 1-[4-(trimethylammonio)phenyl]- 6-phenyl-1,3,5-hexatriene anisotropy decay Biochemistry. 1987 Aug 11;26(16):5113-20.
7: Turek AM, Saltiel J, Krishna TR, Krishnamoorthy G. Resolution of conformer-specific all-trans-1,6-diphenyl-1,3,5-hexatriene UV absorption spectra J Phys Chem A. 2012 Jun 7;116(22):5353-67.
8: Fiorini R, Valentino M, Wang S, Glaser M, Gratton E. Fluorescence lifetime distributions of 1,6-diphenyl-1,3,5-hexatriene in phospholipid vesicles Biochemistry. 1987 Jun 30;26(13):3864-70.
9: Wang S, Beechem JM, Gratton E, Glaser M. Orientational distribution of 1,6-diphenyl-1,3,5-hexatriene in phospholipid vesicles as determined by global analysis of frequency domain fluorimetry data Biochemistry. 1991 Jun 4;30(22):5565-72.
10: Ibrahim H, Jurcic K, Wang JS, Whitehead SN, Yeung KK. 1,6-Diphenyl-1,3,5-hexatriene (DPH) as a Novel Matrix for MALDI MS Imaging of Fatty Acids, Phospholipids, and Sulfatides in Brain Tissues Anal Chem. 2017 Dec 5;89(23):12828-12836.

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