D-Galactose

D-Galactose Chemical Properties
Melting point 168-170 °C(lit.)
Boiling point 232.96°C (rough estimate)
alpha +79.0~+81.0°(D/20℃) (c=10, dil. NH4OH)
density 1,5 g/cm3
refractive index 80 ° (C=10, H2O)
storage temp. room temp
solubility H2O: 100 mg/mL
form powder
pkapK1:12.35 (25°C)
color White
OdorOdorless
PH Range5 - 7 at 180 g/l at 25 °C
PH4.5-6.0 (H2O)Aqueous solution
optical activity[α]20/D +80±1°, 24 hr, c = 5% in H2O
Water Solubility Soluble in water.
Merck 14,4335
BRN 1724619
InChIKeyGZCGUPFRVQAUEE-DPYQTVNSSA-N
LogP-2.490 (est)
CAS DataBase Reference59-23-4(CAS DataBase Reference)
NIST Chemistry ReferenceD-Galactose(59-23-4)
EPA Substance Registry SystemD-Galactose (59-23-4)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 22-24/25-36/37/39-27-26
WGK Germany 3
RTECS LW5490000
3
TSCA Yes
HS Code 29400090
MSDS Information
ProviderLanguage
D-Galactose English
D-Galactose Usage And Synthesis
DescriptionD-Galactose is a monosaccharide sugar that serves as an energy source and glycosylation component. It is a C-4 epimer of glucose and often used as a source of carbon in culture media. Galactose is a component of the disaccharide lactose and released upon hydrolysis by β-galactosidase enzymes. It is converted to glucose via the Leloir pathway or metabolized via an alternative pathway, such as the DeLey-Doudoroff pathway.
DescriptionD-Galactose is a natural aldohexose and C-4 epimer of glucose. D-galactose is converted enzymatically into D-glucose for metabolism or polysaccharides for storage. Chronic, systemic exposure to D-galactose accelerates senescence in invertebrates and mammals and has been used as a model for aging. In bacteria, D-galactose is imported by a methyl-galactoside transport system to drive chemotaxis.
Chemical PropertiesWhite powder
UsesGalactose is a simple monosaccharide used as a component of the galactosyltransferase labeling buffer. It serves as an energy source and an important constituent of glycolipids and glycoproteins. Since it is a component of antigens, it plays a vital role in the determination of blood type within the ABO blood group system.
UsesA C-4 epimer of Glucose (G595000) found in milk and sugar beets as well as being synthesized by the body. Potential use in oral therapy for nephrotic syndrome in focal and segmental glomerulosclerosis.
UsesD-Galactose is suitable for use in cell culture systems requiring sugar additives.
DefinitionA monosaccharide commonly occurring in milk sugar or lactose.
ApplicationGalactose has been used:
as a component of galactosyltransferase labeling buffer.
as a supplement in MRS broth for the growth of thermophilic lactobacilli.
to induce the expression of uncoupling protein (UCP) in yeast transformants.
General DescriptionGalactose is a constituent of lactose. It is one of the main nutrients for newborn infants and young children. It is produced in the body for the formation of lactose and is also a component of glycolipids (cerebrosides) and glycoproteins.
Biological ActivityGalactose is a simple monosaccharide that serves as an energy source and as an essential component of glycolipids and glycoproteins. Galactose contributes to energy metabolism via its conversion to glucose by the enzymes that constitute the Leloir pathway. Defects in the genes encoding these proteins lead to the metabolic disorder galactosemia.
Biochem/physiol ActionsGalactose is a simple monosaccharide that serves as an energy source and as an essential component of glycolipids and glycoproteins. Galactose contributes to energy metabolism via its conversion to glucose by the enzymes that constitute the Leloir pathway. Defects in the genes encoding these proteins lead to the metabolic disorder galactosemia.
Purification MethodsD-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.]
ALPHA-D-GALACTURONIC ACID HYDRATE GALACTOSE,GALACTOSE, D-(+)- ALPHA-1-D-GALACTOPYRANOSYL-4-O-[1-(2-OCTADECYLTHIOETHYL)-(BETA-D-GALACTOPYRANOSIDE)] 1,2,3,4,6-PENTA-O-ACETYL-ALPHA-D-GALACTOPYRANOSE 1-O-ETHYL-[A-1-D-GALACTOPYRANOSYL-(4-(BETA-1-D-GALACTOPYRANOSIDE))] 1,2:3,4-Di-O-isopropylidene-D-galactopyranose DEXTROSE Centchroman 4-O-(A-D-GALACTOPYRANOSYL)-D-GALACTOSE FUCOSE ALPHA1,2-GALACTOSE BETA1,4-N-ACETYLGLUCOSAMINE ALPHA-D-GALACTOPYRANOSYLPHENYL ISOTHIOCYANATE STACHYOSE 6-O-ACETYL-1,2:3,4-DI-O-ISOPROPYLIDENE-ALPHA-D-GALACTOPYRANOSE GALACTOSE 1-PHOSPHATE, DISODIUM SALT, D-[14C(U)]- L-GALACTOSE-1-PHOSPHATE ALPHA-D-GALACTURONIC ACID 1-PHOSPHATE LITHIUM SALT (4-NITRO)PHENYL-2,3,4,6-TETRA-O-ACETYL-ALPHA-D-GALACTOPYRANOSIDE O-2,3,4,6-tetra-O-acetyl-alpha-D-galactopyranosyl-(1->6)-1,3,4-tri-O-acetyl-beta-D-fructofuranosyl-alpha-D-glucopyranoside tetraacetate

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