Gulose

d-Gulose^[1]
Names
	IUPAC name (3R,4R,5R,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol
Identifiers
CAS Number	4205-23-6 (d) ; 6027-89-0 (l) ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:37695 ;
ChemSpider	146783 ;
DrugBank	DB01914 ;
PubChem CID	167792;
UNII	25008KX916 (d) ; J96E9Q45N7 (l) ;
	show InChI
	show SMILES
Properties
Chemical formula	C6H12O6
Molar mass	180.156 g·mol−1
Melting point	syrup
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	(what is ?)
	Infobox references

Gulose is an aldohexose sugar. It is a monosaccharide that is very rare in nature, but has been found in archaea, bacteria and eukaryotes.^[2] It also exists as a syrup with a sweet taste. It is soluble in water and slightly soluble in methanol. Neither the d- and l-forms are fermentable by yeast.

Gulose is a C-3 epimer of galactose and a C-5 epimer of mannose.^[3]

References[]

^ Merck Index, 11th Edition, 4490
^ Swain, M., Brisson, J. R., Sprott, G. D., Cooper, F. P. and Patel, G. B. (1997). "Identification of β-L-gulose as the sugar moiety of the main polar lipid Thermoplasma acidophilum". Biochim. Biophys. Acta. 1345 (1): 56–64. doi:10.1016/s0005-2760(96)00163-4. PMID 9084501.CS1 maint: multiple names: authors list (link)
^ Zhang, Qingju; et al. "On the Reactivity of Gulose and Guluronic Acid Building Blocks in the Context of Alginate Assembly". European Journal of Organic Chemistry. 2016 (14): 2393–2397. doi:10.1002/ejoc.201600336.

This article about an organic compound is a stub. You can help Wikipedia by .

[1] Merck Index, 11th Edition, 4490

[2] Swain, M., Brisson, J. R., Sprott, G. D., Cooper, F. P. and Patel, G. B. (1997). "Identification of β-L-gulose as the sugar moiety of the main polar lipid Thermoplasma acidophilum". Biochim. Biophys. Acta. 1345 (1): 56–64. doi:10.1016/s0005-2760(96)00163-4. PMID 9084501.CS1 maint: multiple names: authors list (link)

[3] Zhang, Qingju; et al. "On the Reactivity of Gulose and Guluronic Acid Building Blocks in the Context of Alginate Assembly". European Journal of Organic Chemistry. 2016 (14): 2393–2397. doi:10.1002/ejoc.201600336.

[1]

[2]

[3]