Catalog Number: B2012255 (1 g)
Thioindigo Dye is a high quality Thioindigo 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.
Catalog number: B2012255
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 1 g
Molecular Weight or Concentration: 296.4 g/mol
Supplied as: Powder
Applications: molecular tool for various biochemical applications
Keywords: Fluorescent Red Dye, Vat Red 41
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: Ibrahim M, El-Nahass MM, Kamel MA, El-Barbary AA, Wagner BD, El-Mansy MA. On the spectroscopic analyses of thioindigo dye Spectrochim Acta A Mol Biomol Spectrosc. 2013 Sep;113:332-6.
2: Koeppe B, Römpp F. Reversible Spatial Control in Aqueous Media by Visible Light: A Thioindigo Photoswitch that is Soluble and Operates Efficiently in Water Chemistry. 2018 Sep 25;24(54):14382-14386.
3: Konarev DV, Kuzmin AV, Khasanov SS, Fatalov AM, Yudanova EI, Lyubovskaya RN. Coordination Complexes of Titanium(IV) and Indium(III) Phthalocyanines with Carbonyl-Containing Dyes: The Formation of Singly Bonded Anionic Squarylium Dimers Chemistry. 2018 Jun 12;24(33):8415-8423.
4: Jacquemin D, Preat J, Wathelet V, Fontaine M, Perpète EA. Thioindigo dyes: highly accurate visible spectra with TD-DFT J Am Chem Soc. 2006 Feb 15;128(6):2072-83.
5: Ross DL. Photochromic Indigoids. III: A Photochromic Element Based on the cis-trans Photoisomerization of a Thioindigo Dye Appl Opt. 1971 Mar 1;10(3):571-6.
6: Perpète EA, Preat J, André JM, Jacquemin D. An ab initio study of the absorption spectra of indirubin, isoindigo, and related derivatives J Phys Chem A. 2006 May 4;110(17):5629-35.
7: Polette-Niewold LA, Manciu FS, Torres B, Alvarado M Jr, Chianelli RR. Organic/inorganic complex pigments: ancient colors Maya Blue J Inorg Biochem. 2007 Nov;101(11-12):1958-73.
8: Bressler DC, Fedorak PM. Purification, stability, and mineralization of 3-hydroxy-2- formylbenzothiophene, a metabolite of dibenzothiophene Appl Environ Microbiol. 2001 Feb;67(2):821-6.
9: Dittmann M, Graupner FF, Maerz B, Oesterling S, de Vivie-Riedle R, Zinth W, Engelhard M, Lüttke W. Photostability of 4,4′-dihydroxythioindigo, a mimetic of indigo Angew Chem Int Ed Engl. 2014 Jan 7;53(2):591-4.
10: Kihara Y, Tani S, Higashi Y, Teramoto T, Nagasawa Y. Ultrafast Excited State Dynamics of Forward and Reverse trans-cis Photoisomerization of Red-Light-Absorbing Indigo Derivatives J Phys Chem B. 2022 May 19;126(19):3539-3550.
Products Related to Thioindigo Dye can be found at Dyes
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