| Identification | More | [Name]
alpha-L-Rhamnose | [CAS]
3615-41-6 | [Synonyms]
6-DEOXY-L-MANNOSE
ALPHA-RHAMNOSE
ISO-DULCITE
ISODULCITOL
L-MANNOMETHYLOSE
L-(+)-RHAMNOSE
L-RHAMNOSE
RHAMNOSE
6-Deoxyhexopyranose
6-deoxy-l-mannos
6-Deoxymannose
Isoducitol
L-Mannopyranose, 6-deoxy-
Locaose
Mannose, 6-deoxy-
Rhamnopyranose
Rhamnopyranose, L-
L-Mannose, 6-deoxy-
(3R,4R,5S,6S)-6-methyloxane-2,3,4,5-tetrol
6-Deoxy-L-mannose | [EINECS(EC#)]
222-793-4 | [Molecular Formula]
C6H12O5 | [MDL Number]
MFCD00136036 | [Molecular Weight]
164.16 | [MOL File]
3615-41-6.mol |
| Chemical Properties | Back Directory | [Appearance]
White crystals. For
equilibrium mixture optical rotation is +9.18
degrees. Very soluble in water and in methanol;
soluble in absolute alcohol.
| [Melting point ]
91-95°C | [Boiling point ]
251.61°C (rough estimate) | [density ]
1.3058 (rough estimate) | [FEMA ]
3730 | [refractive index ]
1.6400 (estimate) | [storage temp. ]
Sealed in dry,2-8°C | [pka]
12.50±0.20(Predicted) | [Odor]
at 100.00 %. odorless | [Odor Type]
odorless | [Water Solubility ]
521.5g/L(40 ºC) | [Merck ]
8172 | [LogP]
-2.17 at 25℃ | [Uses]
Synthetic sweetener research. | [CAS DataBase Reference]
3615-41-6(CAS DataBase Reference) | [NIST Chemistry Reference]
L-Mannose, 6-deoxy-(3615-41-6) | [EPA Substance Registry System]
3615-41-6(EPA Substance) |
| Hazard Information | Back Directory | [Chemical Properties]
L-Rhamnose has no odor, but has a very sweet taste. | [Chemical Properties]
White crystals. For
equilibrium mixture optical rotation is +9.18
degrees. Very soluble in water and in methanol;
soluble in absolute alcohol.
| [Definition]
ChEBI: The acyclic form of L-rhamnose. | [Flammability and Explosibility]
Notclassified | [Purification Methods]
Crystallise the rhamnose from H2O or EtOH. It crystallises easily as the monohydrate by evaporating a solution in MeOH (90%) and H2O (10%). It is also purified by dissolving in a small volume of EtOH, adding a few drops of H2O and cooling. 1H NMR in D2O at 44o contains 60% -pyranose and 40% -pyranose forms [Angyal Adv Carbohydr Chem 42 15 1984.] [Smith J Chem Soc 1035 1940, McGeachin & Beevers Acta Cryst 10 227,230 197, Beilstein 1 IV 4261.] |
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