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3458-28-4 - D-(+)-Mannose, 99% - A10842 - Alfa Aesar

A10842 D-(+)-Mannose, 99%

CAS Number
3458-28-4
Synonyms

Size Price ($) Quantity Availability
25g 33.22
100g 82.71
500g 312.57
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D-(+)-Mannose, 99%

MDL
MFCD00064122
EINECS
222-392-4

Chemical Properties

Formula
C6H12O6
Formula Weight
180.16
Melting point
127-133°
Density
1.54
Sensitivity
Hygroscopic
Solubility
Soluble in water.

Applications

D-mannose acts as an alternative energy source utilized by brain. It is used in the study of assessing the synthesis of amphiphilic glycopolymers and investigating early detection of bronchiolitis obliterans.It may be useful in the treatment of urinary tract infections (UTIs) and carbohydrate-deficient glycoprotein syndrome type 1b. It is also useful in the formation of glycan structure and glycosylation.

Notes

Hygroscopic. Incompatible with strong oxidizing agents.

Literature References

Chiral building block. For use in a 15-step synthesis of the macrocycle (+)-aspicilin, in which 3 of the 4 asymmetric centers come from mannose, see: Helv. Chim. Acta, 72, 1753 (1989).

Nakagawa, Y.; Watanabe, Y.; Igarashi, Y.; Ito, Y.; Ojika, M. Pradimicin A, a d-mannose-binding antibiotic, binds pyranosides of l-fucose and l-galactose in a calcium-sensitive manner. Bioorg. Med. Chem. Lett. 2015, 25 (15), 2963-2966.

Zhai, Y.; Dasog, M.; Snitynsky, R. B.; Purkait, T. K.; Aghajamali, M.; Hahn, A. H.; Sturdy, C. B.; Lowary, T. L.; Veinot, J. G. C. Water-soluble photoluminescent D-mannose and L-alanine functionalized silicon nanocrystals and their application to cancer cell imaging. J. Mater. Chem. B 2014, 2 (47), 8427-8433.

Other References

Merck
14,5747
Beilstein
1564373
Harmonized Tariff Code
2940.00
TSCA
Yes

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