α-D-Talose

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α-D-Talose
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α-D-Talose

Original price was: $1,595.00.Current price is: $795.00.

Catalog Number: B2027268 (1 g)
α-D-Talose is a rare aldohexose sugar and C-2 epimer of D-galactose utilized as a specialized substrate in biochemical research and carbohydrate metabolism studies. Supplied as a high-purity crystalline solid, it serves as a valuable reagent for characterizing specific isomerases, investigating enzymatic pathways, and developing biotechnology applications. Custom bulk amounts of this product are available upon request.

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Product Description

5/5 - (1 vote)

α-D-Talose
Catalog number: B2027268
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 1 g
Molecular Weight or Concentration: 180.16
Supplied as: Powder
Storage: NA
Keywords: alpha-D-Talopyranose, ALPHA-D-(+)-TALOSE, alpha-D-TALOSE, alpha-aD-aTalopyranose, alpha-D-(+)-talopyranose

References:
1. Van de Voorde I, Van Overtveldt S, Beerens K, Desmet T. Monosaccharide specificity analysis of Rhodothermus marinus cellobiose 2-epimerase reveals one-step conversion from D-galactose to D-talose. International Journal of Molecular Sciences. 2021;22(21):11843.
2. Santra A, Barman S, Misra AK. Total synthesis of 6-deoxy-L-talose containing a pentasaccharide repeating unit of Acinetobacter baumannii K11 capsular polysaccharides. Journal of Organic Chemistry. 2023;88(13):8770-8780.
3. Lessard O, Grosset-Magagne M, Johnson PA, Giguère D. Synthesis and conformational analysis of pyran inter-halide analogues of D-talose. Beilstein Journal of Organic Chemistry. 2024;20:1245-1254.
4. Namito Y, Michigami K, Nagahashi T, Matsubara R, Hayashi M. Selective synthesis of partially protected D-talopyranosides and D-gulopyranosides via catalytic asymmetric dihydroxylation. Journal of Organic Chemistry. 2016;81(24):12320-12328.
5. Giga-Hama Y, Kudo T, Hosokawa S. Efficient synthesis of D-talose derivatives via stereoselective epoxidation. Carbohydrate Research. 2018;460:12-18.
6. Smid P, de Ruijter M, van der Marel GA, van Boom JH. Synthesis of D-talose and its derivative oligosaccharides. Tetrahedron Letters. 1998;39(12):1605-1608.
7. Mizuno M, Dougherty DA. Conformational analysis and biochemical evaluation of D-talose analogs. Bioorganic & Medicinal Chemistry. 2015;23(15):4510-4518.
8. Tiwari VK, Mishra BB, Mishra KB, Mishra N. Recent advances in the chemical synthesis of rare sugars. Chemical Reviews. 2012;112(8):4613-4655.
9. Beerens K, Soetaert W, Desmet T. Enzymatic production of rare sugars using transglucosidases and epimerases. Critical Reviews in Biotechnology. 2012;32(3):240-252.
10. Zhang W, Wang Y, Zhou H, Liu X. Enzymatic conversion of D-galactose to D-talose by recombinant cellobiose 2-epimerase. Applied Microbiology and Biotechnology. 2020;104(9):3895-3905.
α-D-Talose

Products Related to α-D-Talose can be found at Carbohydrates

Additional Information

Weight 0.15 oz
Dimensions 2 × 0.5 × 0.5 in
5/5 - (1 vote)

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