L-Glucose

l-Glucose

Haworth projection of α-l-glucopyranose
Fischer projection of α-l-glucose
Names
IUPAC name l-Glucose
Identifiers
CAS Number	921-60-8 Y
3D model (JSmol)	Interactive image
Abbreviations	L-Glc
ChEBI	CHEBI:37627 Y
ChemSpider	2006622 Y
EC Number	213-068-3
PubChem CID	2724488
UNII	02833ISA66 Y
InChI InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5-,6?/m0/s1 Y Key: WQZGKKKJIJFFOK-ZZWDRFIYSA-N Y InChI=1/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5-,6?/m0/s1 Key: WQZGKKKJIJFFOK-ZZWDRFIYBQ
SMILES O[C@@H]1[C@@H](O)[C@@H](OC(O)[C@H]1O)CO
Properties
Chemical formula	C6H12O6
Molar mass	180.156 g·mol−1
Density	1.54 g/cm3
Solubility in water	91 g/100 mL
Hazards
Safety data sheet (SDS)	ICSC 0865
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references

l-Glucose is an organic compound with formula C₆H₁₂O₆ or O=CH[CH(OH)]₅H, specifically one of the aldohexose monosaccharides. As the l-isomer of glucose, it is the enantiomer of the more common d-glucose.

l-Glucose does not occur naturally in living organisms, but can be synthesized in the laboratory. l-Glucose is indistinguishable in taste from d-glucose,^[1] but cannot be used by living organisms as a source of energy because it cannot be phosphorylated by hexokinase, the first enzyme in the glycolysis pathway. One of the known exceptions is in Burkholderia caryophylli, a plant pathogenic bacterium, which contains the enzyme d-threo-aldose 1-dehydrogenase which is capable of oxidizing l-glucose.^[2]

Like the d-isomer, l-glucose usually occurs as one of four cyclic structural isomers—α- and β-l-glucopyranose (the most common, with a six-atom ring), and α- and β-l-glucofuranose (with a five-atom ring). In water solution, these isomers interconvert in matters of hours, with the open-chain form as an intermediate stage.