Para Red

Product Description

Para Red
Catalog number: B2027083
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 100 mg
Molecular Weight or Concentration: 293.28
Supplied as: Solid
Storage: RT
Keywords: Pigment Red 1, CI 12070, 1-(4-Nitrophenylazo)-2-naphthol

References:
1. Chalmers J. G., Crowfoot D. The elimination of 3:4-benzpyrene from the animal body after subcutaneous injection: Changed benzpyrene. Biochem J. 1941 Nov;35(10-11):1270–1275.
2. Chalmers J. G., Peacock P. R. Further evidence regarding the elimination of certain polycyclic hydrocarbons from the animal body. Biochem J. 1936 Jul;30(7):1242–1248.1.
3. FLYNN F. V., DE MAYO P. Microelectrophoresis of protein on filter-paper. Lancet. 1951 Aug 11;2(6676):235–239.
4. HEIDELBERGER C., WEISS S. M. The distribution of radioactivity in mice following administration of 3,4-benzpyrene-5-C14 and 1,2,5,6-dibenzanthracene-9,10-C14. Cancer Res. 1951 Nov;11(11):885–891.
5. SCHULTZ J., JAMISON W., SHAY H., GRUENSTEIN M. The influence of methylcholanthrene on serum protein synthesis in the rat. Arch Biochem Biophys. 1954 May;50(1):124–133.
6. WIEST W. G., HEIDELBERGER C. The interaction of carcinogenic hydrocarbons with tissue constituents. II. 1,2,5,6-Dibenzanthracene-9,10-C14 in skin. Cancer Res. 1953.
7. Nakajima-Shimada J., et al. Effects of purine and pyrimidine analogs on the infection rate and growth of Trypanosoma cruzi. Mem Inst Oswaldo Cruz. 1996.
8. Aguiar, A.L.G.d. New Boron-Dipyrromethene (BODIPY) Molecules As Suitable Electron-Donors for Organic Photovoltaic Cells. Ph.D. Thesis, University of Coimbra, Coimbra, Portugal, 2019.
9. Loudet, A.; Burgess, K. BODIPY Dyes and Their Derivatives: Syntheses and Spectroscopic Properties. Chem. Rev. 2007.
10. Boens, N.; Leen, V.; Dehaen, W. Fluorescent Indicators Based on BODIPY. Chem. Soc. Rev. 2012.
Benzopurpurin 4B 

Products Related to Para Red can be found at Dyes