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609-06-3

609-06-3 Structure

609-06-3 Structure
IdentificationMore
[Name]

L-XYLOSE
[CAS]

609-06-3
[Synonyms]

L-XYL
L-(-)-XYLOSE
L-XYLOSE
XYLOSE
XYLOSE, L
L-(-)-Xylose, 99+%, mixture of anomers
L(-)XYLOSE 99%
L-Xylose (9CI)
L-Xylose,99%
l-(-)-xylose, mixture of anomers
XYLOSE, L-(RG)
[EINECS(EC#)]

210-174-1
[Molecular Formula]

C5H10O5
[MDL Number]

MFCD00151096
[Molecular Weight]

150.13
[MOL File]

609-06-3.mol
Chemical PropertiesBack Directory
[Appearance]

WHITE FINE CRYSTALLINE POWDER
[Melting point ]

150-152 °C(lit.)
[Boiling point ]

191.65°C (rough estimate)
[density ]

1.525
[refractive index ]

-20 ° (C=10, H2O)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[solubility ]

H2O: 0.1 g/mL, clear, colorless
[form ]

Crystalline Powder
[pka]

12.46±0.20(Predicted)
[color ]

White to off-white
[optical activity]

[α]24/D 18.7°, c = 4 in H2O
[Water Solubility ]

within almost transparency
[Sensitive ]

Hygroscopic
[BRN ]

1723080
[InChIKey]

SRBFZHDQGSBBOR-VVZXFQNISA-N
[LogP]

-2.390 (est)
[CAS DataBase Reference]

609-06-3(CAS DataBase Reference)
[EPA Substance Registry System]

L-Xylose (609-06-3)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S24/25:Avoid contact with skin and eyes .
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
[TSCA ]

Yes
[HS Code ]

29400090
Raw materials And Preparation ProductsBack Directory
[Raw materials]

L-xylulose
[Preparation Products]

acrylonitrile fiber oil 1^<#^>-->1,2-O-Isopropylidene-a-L-xylofuranose
Hazard InformationBack Directory
[Chemical Properties]

WHITE FINE CRYSTALLINE POWDER
[Uses]

L-Xylose is used in the synthesis of L-Xylose derivatives as selective sodium-dependent glucose cotransporter 2 (SGLT2) inhibitors for the treatment of type 2 diabetes.
[Application]

l-Xylose is a suitable starting material for the production of L-ribonucleosides. L- Xylose can be converted into an L-ribose derivative via oxidation and reduction steps. This product is then glycosylated to give L-ribonucleosides: L-uridine, L-cytidine, L- adenosine and L-guanosine (Moyroud and Strazewski, 1999; Chelain et al., 1995).
L-Xylose can also be used as a starting material for the production of polyhydroxypyrrolidines and related analogues. These compounds have many biological activities. They are shown to have anti-HIV effects, inhibit tumor growth, and also act as ?- and ?-glucosidase inhibitors, which is of relevance for the development of diabetes drugs (Behr and Guillerm, 2007).
[Definition]

ChEBI: A xylose of ring-opened form having L-configuration.
[Preparation]

L-Xylose can be produced from L-xylulose by isomerization. This can be achieved either enzymatically or chemically under alkaline conditions. The equilibrium of the reaction between D-xylose and D-xylulose in an aqueous solution has been determined at pH 6.8-7.4 and at 25 °C to be 85:15 in favor of D-xylose (Tewari et al., 1985).
Spectrum DetailBack Directory
[Spectrum Detail]

L-xylose(609-06-3)MS
L-xylose(609-06-3)IR1
L-xylose(609-06-3)IR2
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

L(-)-Xylose, 99+%(609-06-3)
[Alfa Aesar]

L-(-)-Xylose, 99%(609-06-3)
[Sigma Aldrich]

609-06-3(sigmaaldrich)
[TCI AMERICA]

L-(-)-Xylose,>97.0%(T)(609-06-3)
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