Glyceraldehyde

Glyceraldehyde

Names
IUPAC name Glyceraldehyde
Systematic IUPAC name 2,3-Dihydroxypropanal
Other names Glyceraldehyde Glyceric aldehyde Glyceral
Identifiers
CAS Number	56-82-6 (racemic) Y 453-17-8 (R) Y 497-09-6 (S) Y
3D model (JSmol)	Interactive image Interactive image
ChemSpider	731 Y
ECHA InfoCard	100.000.264
PubChem CID	751
UNII	DI19XSG16H (racemic) Y 41A680M0WB (R) Y GI7U82BL5A (S) Y
CompTox Dashboard (EPA)	DTXSID90861586
InChI InChI=1S/C3H6O3/c4-1-3(6)2-5/h1,3,5-6H,2H2 Y Key: MNQZXJOMYWMBOU-UHFFFAOYSA-N Y InChI=1/C3H6O3/c4-1-3(6)2-5/h1,3,5-6H,2H2 Key: MNQZXJOMYWMBOU-UHFFFAOYAU
SMILES O=CC(O)CO OCC(O)C=O
Properties[1]
Chemical formula	C3H6O3
Molar mass	90.078 g·mol−1
Density	1.455 g/cm3
Melting point	145 °C (293 °F; 418 K)
Boiling point	140 to 150 °C (284 to 302 °F; 413 to 423 K) at 0.8 mmHg
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

Glyceraldehyde (glyceral) is a triose monosaccharide with chemical formula C₃H₆O₃. It is the simplest of all common aldoses. It is a sweet, colorless, crystalline solid that is an intermediate compound in carbohydrate metabolism. The word comes from combining glycerol and aldehyde, as glyceraldehyde is glycerol with one alcohol group oxidized to an aldehyde.

Glyceraldehyde has one chiral center and therefore exists as two different enantiomers with opposite optical rotation:

• In the D/L nomenclature, either D from Latin Dexter meaning "right", or L from Latin Laevo meaning "left"
• In the R/S nomenclature, either R from Latin Rectus meaning "right", or S from Latin Sinister meaning "left"

	D-glyceraldehyde (R)-glyceraldehyde (+)-glyceraldehyde	L-glyceraldehyde (S)-glyceraldehyde (−)-glyceraldehyde
Fischer projection
Skeletal formula
Ball-and-stick model

While the optical rotation of glyceraldehyde is (+) for R and (−) for S, this is not true for all monosaccharides. The stereochemical configuration can only be determined from the chemical structure, whereas the optical rotation can only be determined empirically (by experiment).

It was by a lucky guess that the molecular D- geometry was assigned to (+)-glyceraldehyde in the late 19th century, as confirmed by X-ray crystallography in 1951.^[2]

In the D/L system, glyceraldehyde is used as the configurational standard for carbohydrates.^[3] Monosaccharides with an absolute configuration identical to (R)-glyceraldehyde at the last stereocentre, for example C5 in glucose, are assigned the stereo-descriptor D-. Those similar to (S)-glyceraldehyde are assigned an L-.

Glyceraldehyde can be prepared, along with dihydroxyacetone, by the mild oxidation of glycerol, for example with hydrogen peroxide^[4] and a ferrous salt as catalyst.^{[citation needed]}

Its cyclohexylidene acetal can also be produced by oxidative cleavage of the bis(acetal) of mannitol.^[5]

The enzyme glycerol dehydrogenase (NADP⁺) has two substrates, glycerol and NADP⁺, and 3 products, D-glyceraldehyde, NADPH and H+.^[6]

The interconversion of the phosphates of glyceraldehyde (glyceraldehyde 3-phosphate) and dihydroxyacetone (dihydroxyacetone phosphate), catalyzed by the enzyme triosephosphate isomerase, is an intermediate step in glycolysis.

• Stereoisomerism