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A propos de cet article
Formule empirique (notation de Hill) :
C5H10O5
Numéro CAS:
Poids moléculaire :
150.13
UNSPSC Code:
12352201
NACRES:
NA.21
PubChem Substance ID:
EC Number:
200-400-7
Beilstein/REAXYS Number:
1562108
MDL number:
Service technique
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Laissez-nous vous aiderbiological source
cell culture
Quality Segment
assay
≥99% (HPLC)
form
powder
optical activity
[α]20/D 18.2 to 19.4 °, c = 4% (w/v) in water
technique(s)
gas chromatography (GC): suitable
color
white
useful pH range
6.0-6.5 (20 °C, 100 g/L)
mp
154-158 °C (lit.)
solubility
water: 50 mg/mL, clear, colorless
storage temp.
room temp
SMILES string
O[C@@H]1COC(O)[C@H](O)[C@H]1O
InChI
1S/C5H10O5/c6-2-1-10-5(9)4(8)3(2)7/h2-9H,1H2/t2-,3+,4-,5?/m1/s1
InChI key
SRBFZHDQGSBBOR-IOVATXLUSA-N
General description
Xylose is a five-carbon sugar that contributes to lignocellulose in plants. Xylose is predominantly found in hardwoods and agricultural residues.
Application
D-(+)-Xylose has been used:
- as one of the component to stimulate microbial activity
- for the enhancement of biofilm formation
- as a part of biochemical tests for the identification of B. cereus group
- for substrate screening characterization
Biochem/physiol Actions
Estimation of xylose in the urine after oral administration, is useful in diagnosing absorption of carbohydrates and malabsorption of non-pancreatic molecules. Xylose plays a significant role in the biologically conversion of plant biomass to fuels and chemicals.
Other Notes
To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.
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Classe de stockage
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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