| Identification | More | [Name]
2-Deoxy-D-galactose | [CAS]
1949-89-9 | [Synonyms]
2-DEOXY-BETA-D-GALACTOSE
2-DEOXY-BETA-D-LYXO-HEXOSE
2-DEOXY-D-GALACTOPYRANOSE
2-DEOXY-D-GALACTOSE
2-DEOXY-D-LYXOHEXOSE
2-DEOXYGALACTOSE
DEOXY-D-GALACTOSE,2-
2-Deoxy-D-galactose (1.24798)
Deoxygalactose
D-lyxo-Hexose, 2-deoxy-
2-DEOXY-B-D-LYXO-HEXOSE, 99% MIN., HPLC
2-DEOXYGALACTOSE extrapure
(3R,4R,5R)-3,4,5,6-Tetrahydroxyhexanal | [EINECS(EC#)]
217-765-3 | [Molecular Formula]
C6H12O5 | [MDL Number]
MFCD00014649 | [Molecular Weight]
164.16 | [MOL File]
1949-89-9.mol |
| Chemical Properties | Back Directory | [Appearance]
White Crystalline Solid | [Melting point ]
107-110 °C(lit.) | [alpha ]
57 º (c=3.7, H20 NH3) | [Boiling point ]
211.61°C (rough estimate) | [density ]
1.1738 (rough estimate) | [refractive index ]
1.4230 (estimate) | [storage temp. ]
Sealed in dry,2-8°C | [solubility ]
Methanol, Water | [form ]
Powder | [pka]
13.47±0.20(Predicted) | [color ]
White to Off-white | [Optical Rotation]
[α]20/D +59.7°, c = 2 in H2O | [Water Solubility ]
Soluble in water. | [BRN ]
1723333 | [InChI]
1S/C6H12O5/c7-2-4-6(10)3(8)1-5(9)11-4/h3-10H,1-2H2/t3-,4-,5?,6-/m1/s1 | [InChIKey]
PMMURAAUARKVCB-DUVQVXGLSA-N | [SMILES]
OC[C@H]1OC(O)C[C@@H](O)[C@H]1O | [LogP]
-3.070 (est) | [CAS DataBase Reference]
1949-89-9(CAS DataBase Reference) | [EPA Substance Registry System]
1949-89-9(EPA Substance) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi,Xn | [Risk Statements ]
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S24/25:Avoid contact with skin and eyes .
S37/39:Wear suitable gloves and eye/face protection .
S36:Wear suitable protective clothing .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . | [WGK Germany ]
3
| [F ]
3-10 | [HS Code ]
29400090 | [Storage Class]
11 - Combustible Solids |
| Hazard Information | Back Directory | [Chemical Properties]
White Crystalline Solid | [Uses]
2-Deoxy-D-galactose is used as an inhibitor of fucosylation, which is a process of adding hexose deoxy sugar units to a molecule. It is used for studying galactose uptake into Escherichia coli and also for competitive elution of Anadarin P lectin (a galactosyl-binding lectin from blood clam). | [Definition]
ChEBI: 2-deoxy-D-galactose is a deoxygalactose. It is functionally related to an aldehydo-D-galactose and a D-galactose. | [General Description]
2-Deoxy-D-galactose is a glucose analog that shows a wide range of biological activities such as inhibition of glycolysis and thereby tumor growth, interference with the biosynthetic processing of glycoproteins, antiviral activity, and hepatotoxicity. It is being extensively studied as trapping agents for phosphate and uridylate in mammalian cells due to its ability to interfere in the phosphate and nucleotide metabolism. | [Purification Methods]
Crystallise 2-deoxy-D-galactose from MeOH or diethyl ether. The aniline derivative has m 142-143o, [ ] D 16.5 -149o (c 0.8, pyridine). [Overend et al. J Chem Soc 671, 675 1950 and 992 1951.] A 30% equilibrium solution at 31o in D2O contains 40% -pyranose, 44% pyranose, 8% -furanose and 8% -furanose forms as estimated by 1HNMR spectroscopy [Angyal & Pickles Aust J Chem 25 1711 1972]. [Beilstein 1 IV 4283.] |
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