| Identification | More | [Name]
D-Galactose | [CAS]
59-23-4 | [Synonyms]
BETA-D-(+)-GALACTOSE
d-galactos
brain sugar
D(+)-Glactose
Dextrogalactose
Lactoglucose
alpha-Galactose(D)
D(+)galactose minimum 98%
D(+)galactose minimum 99%
D(+)GALACTOSE SIGMA GRADE
D(+)galactose sigmaultra
Gal
galactose, pure
D(+)-GALACTOSE ANHYDROUS CELL CULTURE*TE STED
D(+)-GALACTOSE, FOR BIOTECHNOLOGICAL PUR POSES
D-(+)-GALACTOSE, BIOTECH
GALACTOSE, USP STANDARD
GALACTOSE, EP STANDARD
D-GalactoseExtraPure
MaltaseHydrate | [EINECS(EC#)]
200-416-4 | [Molecular Formula]
C6H12O6 | [MDL Number]
MFCD00871336 | [Molecular Weight]
180.16 | [MOL File]
59-23-4.mol |
| Chemical Properties | Back Directory | [Definition]
A monosaccharide commonly occurring in milk
sugar or lactose. | [Appearance]
White powder | [Melting point ]
168-170 °C(lit.)
| [alpha ]
+79.0～+81.0°(D/20℃) (c=10, dil. NH4OH) | [Boiling point ]
232.96°C (rough estimate) | [density ]
1,5 g/cm3 | [refractive index ]
80 ° (C=10, H2O) | [storage temp. ]
Store at RT. | [solubility ]
H2O: 100 mg/mL
| [form ]
powder
| [pka]
pK1:12.35 (25°C) | [color ]
White | [Odor]
Odorless | [PH]
4.5-6.0 (H2O)Aqueous solution | [PH Range]
5 - 7 at 180 g/l at 25 °C | [optical activity]
[α]20/D +80±1°, 24 hr, c = 5% in H2O | [Water Solubility ]
Soluble in water. | [Detection Methods]
HPLC(Differential) | [Merck ]
14,4335 | [BRN ]
1724619 | [InChIKey]
GZCGUPFRVQAUEE-DPYQTVNSSA-N | [LogP]
-2.490 (est) | [CAS DataBase Reference]
59-23-4(CAS DataBase Reference) | [NIST Chemistry Reference]
D-Galactose(59-23-4) | [EPA Substance Registry System]
59-23-4(EPA Substance) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S27:Take off immediately all contaminated clothing .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . | [WGK Germany ]
3
| [RTECS ]
LW5490000
| [F ]
3 | [TSCA ]
Yes | [HS Code ]
29400090 |
| Hazard Information | Back Directory | [Description]
D-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. | [Chemical Properties]
White powder | [Uses]
A 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. | [Uses]
D-Galactose is suitable for use in cell culture systems requiring sugar additives. | [Application]
Galactose 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 Description]
Galactose 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 Activity]
Galactose 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 Actions]
Galactose 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. | [storage]
Store at RT | [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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