ChemicalBook--->CAS DataBase List--->3646-73-9

3646-73-9

3646-73-9 Structure

3646-73-9 Structure
IdentificationBack Directory
[Name]

C00984
[CAS]

3646-73-9
[Synonyms]

C00984
α-D-Galactose
alpha-D-Galactose
α-D-galactopyranose
[Molecular Formula]

C6H12O6
[MOL File]

3646-73-9.mol
[Molecular Weight]

180.16
Chemical PropertiesBack Directory
[Melting point ]

169-170oC
[storage temp. ]

Refrigerator, Under Inert Atmosphere
[solubility ]

Water (Slightly)
[form ]

neat
[color ]

White to Off-White
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P280-P301+P312-P302+P352-P305+P351+P338
Hazard InformationBack Directory
[Uses]

α-D-Galactose is the alpha anomer of D-Galactose (G155250), the C-4 epimer of Glucose (G595000). D-Galactose is found in milk and sugar beets as well as being synthesized by the body.
[Definition]

ChEBI: Alpha-D-galactose is d-Galactopyranose having alpha-configuration at the anomeric centre. It has a role as a mouse metabolite. It is an enantiomer of an alpha-L-galactose.
[Purification Methods]

-D-Galactose is crystallised twice from aqueous 80% EtOH at -10o, then dried in a vacuum oven at 90o over P2O5 for 10hours. [Link Biochemical Preparations 3 75 1953, Hansen et al. Biochemical Preparations 4 2 1955.] Also purify it by recrystallising the dried solid (150g) in hot H2O (150mL), then adding hot MeOH (250mL) and hot EtOH (500mL), stirring to mix, filtering through a bed of charcoal, and the clear filtrate is stirred to initiate crystallisation. After standing overnight at 10o, the crystals of the -anomer are filtered off by suction, washed with MeOH, then EtOH, and dried (yield 130g), and more can be obtained by evaporation of the filtrate and washing as before. [Wolfrom & Thompson Methods in Carbohydrate Chemistry I 120 1962, Academic Press, Beilstein 1 IV 4336.]
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