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Ethyl Red Dye

$395.00

Catalog Number: B2012279 (100 mg)
Ethyl Red Dye is a high quality Ethyl Red Dye. 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.

Live enquiry about this product via Text/SMS: 1-858-900-3210.

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Description

Ethyl Red Dye
Catalog number: B2012279
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 100 mg
Molecular Weight or Concentration: 297.4 g/mol
Supplied as: Powder
Applications: molecular tool for various biochemical applications
Storage: -20C
Keywords: 4-(Diethylamino)azobenzene-2′-carboxylic Acid, Diethyl Red
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.

References:
1: Akita H, Fujimoto S, Wada K, Takeda N, Iwasaki Y, Fujii T, Matsushika A. Performance of Burkholderia multivorans CCA53 for ethyl red degradation J Gen Appl Microbiol. 2020 Sep 30;66(4):220-227.
2: Sun C, Li Y, Song P, Ma F. An Experimental and Theoretical Investigation of the Electronic Structures and Photoelectrical Properties of Ethyl Red and Carminic Acid for DSSC Application Materials (Basel). 2016 Oct 1;9(10):813.
3: Lang W, Kumagai Y, Sadahiro J, Maneesan J, Okuyama M, Mori H, Sakairi N, Kimura A. Different molecular complexity of linear-isomaltomegalosaccharides and β-cyclodextrin on enhancing solubility of azo dye ethyl red: towards dye biodegradation Bioresour Technol. 2014 Oct;169:518-524.
4: Heath RL. Ethyl red as a probe into the mechanism of light-driven proton translocation by isolated chloroplasts. I. The spectral shift of ethyl red and membrane conformational changes Biochim Biophys Acta. 1973 Feb 22;292(2):444-58.
5: Ren MX, Wu W, Cai W, Pi B, Zhang XZ, Xu JJ. Reconfigurable metasurfaces that enable light polarization control by light Light Sci Appl. 2017 Jun 2;6(6):e16254.
6: Heath RL, Hind G. Bromocresol purple and ethyl red as indicators of events linked to changes in the energization of chloroplast membranes J Biol Chem. 1972 May 10;247(9):2917-25.
7: Matsumoto K, Mukai Y, Ogata D, Shozui F, Nduko JM, Taguchi S, Ooi T. Characterization of thermostable FMN-dependent NADH azoreductase from the moderate thermophile Geobacillus stearothermophilus Appl Microbiol Biotechnol. 2010 May;86(5):1431-8.
8: Fang H, Xu B, Li X, Kuhn DL, Zachary Z, Tian G, Chen V, Chu R, DeLacy BG, Rao Y, Dai HL. Effects of Molecular Structure and Solvent Polarity on Adsorption of Carboxylic Anchoring Dyes onto TiO(2) Particles in Aprotic Solvents Langmuir. 2017 Jul 18;33(28):7036-7042.
9: Clemen M, Grotemeyer J. Subsequent radical fragmentation reactions of N, N-diethylamino-substituted azobenzene derivatives in a Fourier transform ion cyclotron resonance mass spectrometer using collision-induced dissociation and photodissociation Eur J Mass Spectrom (Chichester). 2017 Dec;23(6):359-368.
10: Soe G, Nishi N, Kakuno T, Yamashita J. Reversible conversion from Ca(2)+-ATPase activity to Mg(2)+- and Mn(2)+-ATPase activities of coupling factor purified from acetone powder of Rhodospirillum rubrum chromatophores J Biochem. 1978 Oct;84(4):805-14.

Products Related to Ethyl Red Dye can be found at Substrates

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