| Identification | More |  [Name]
  L(+)-Rhamnose monohydrate |  [CAS]
  10030-85-0 |  [Synonyms]
  6-DEOXY-L-MANNOSE 6-DEOXY-L-MANNOSE HYDRATE 6-DEOXY-L-MANNOSE MONOHYDRATE ISODULCIT ISODULCIT MONOHYDRATE L-RHA H2O L-(+)-RHAMMNOSE MONOHYDRATE L-(+)-RHAMNOPYRANOSE, MONOHYDRATE L-(+)-RHAMNOSE L-(+)-RHAMNOSE HYDRATE L-(+)-RHAMNOSE MONOHYDRATE L-RHAMNOSE MONOHYDRATE RHAMNOSE, L-(+)- Rhamnose,monohydrate L-Rhamnegin L-RhamnoseForBiochemistry L (+) RHAMNOSE GR FOR BIOCHEMISTRY L-Mannose, 6-deoxy-, monohydrate RHAMNOSE, L-(+)-(RG) Rhamnose,monohydrate iso-Ducitol |  [EINECS(EC#)]
  222-793-4 |  [Molecular Formula]
  C6H14O6 |  [MDL Number]
  MFCD00149363 |  [Molecular Weight]
  182.17 |  [MOL File]
  10030-85-0.mol |  
 | Chemical Properties | Back Directory |  [Appearance]
  White crystals or crystalline powder |  [Melting point ]
  90-95 °C(lit.) 
 |  [alpha ]
  8.2 º (c=4.5,H2O) |  [density ]
  1.47 |  [storage temp. ]
  Inert atmosphere,Room Temperature |  [solubility ]
  H2O: 0.1 g/mL, clear, colorless 
 |  [form ]
  Crystals or Crystalline Powder |  [color ]
  White |  [Odor]
  Odorless |  [PH Range]
  7.8 - 8.6 |  [biological source]
  oranges |  [Optical Rotation]
  [α]20/D +8±0.5°, 2 hr, c = 5% in H2O |  [Water Solubility ]
  300 g/L (20 ºC) |  [Merck ]
  14,8172 |  [BRN ]
  5988592 |  [Stability:]
  Stable at RT |  [InChIKey]
  BNRKZHXOBMEUGK-FGASXDGJSA-N |  [CAS DataBase Reference]
  10030-85-0(CAS DataBase Reference) |  
 | Safety Data | Back Directory |  [Hazard Codes ]
  Xi |  [Risk Statements ]
  R36/38:Irritating to eyes and skin . |  [Safety Statements ]
  S24/25:Avoid contact with skin and eyes . S37/39:Wear suitable gloves and eye/face protection . S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . |  [WGK Germany ]
  3 
 |  [F ]
  3 |  [TSCA ]
  Yes |  [HS Code ]
  29400010 |  
 | Hazard Information | Back Directory |  [Chemical Properties]
  White crystals or crystalline powder |  [Uses]
  Composition of plum leaf polysaccharides. |  [Uses]
  L-Rhamnose monohydrate is a deoxy sugar in plants and bacteria. It is a component of plant cell walls that helps maintain structure. L-Rhamnose monohydrate is used as a starting material for the production of furanones. It is an important material involved in the reaction of flavors developed during the preparation of various foods like bread, grilled meats, etc. |  [Biological Functions]
  L-Rhamnose is a part of plant cell wall polysaccharides, rhamnogalacturonan I and rhamnogalacturonan.It is also present in bacterial cell walland a major antigenic determinant contributing to its pathogenicity.L-rhamnose is non-absorbable in humans but is fermented by intestinal microbes. Supplementation of L-rhamnose slows down gastric emptying. L-rhamnose monosaccharide conjugated immunogens have applications in cancer immunotherapies. Intake of L-rhamnose elevates serum propionate levels. 
L-Rhamnose monohydrate has been used: 
in biofilm enhancement assay in S.pneumonia. 
as a sugar drink in humans undergoing intestinal barrier permeability test. 
for the standard curve generation in high performance liquid chromatography(HPLC). |  [General Description]
 
 L-Rhamnose is a part of plant cell wall polysaccharides, rhamnogalacturonan I and rhamnogalacturonan. It is also present in bacterial cell walland a major antigenic determinant contributing to its pathogenicity. L-rhamnose is non-absorbable in humans but is fermented by intestinal microbes. Supplementation of L-rhamnose slows down gastric emptying. L-rhamnose monosaccharide conjugated immunogens have applications in cancer immunotherapies. Intake of L-rhamnose elevates serum propionate levels.  |  [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.] |  
  
             | 
            
            
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
                
             |