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About This Item
Empirical Formula (Hill Notation):
C5H10O5
CAS Number:
Molecular Weight:
150.13
UNSPSC Code:
12352201
NACRES:
NA.25
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1723052
InChI key
LQXVFWRQNMEDEE-PYHARJCCSA-N
SMILES string
OCC1(O)OC[C@H](O)[C@H]1O
InChI
1S/C5H10O5/c6-2-5(9)4(8)3(7)1-10-5/h3-4,6-9H,1-2H2/t3-,4+,5?/m0/s1
assay
≥95% (HPLC)
form
syrup
technique(s)
HPLC: suitable
color
faintly yellow
solubility
water: 50 mg/mL, clear, faintly yellow to yellow
storage temp.
−20°C
Quality Level
Biochem/physiol Actions
D-xylulose is a monosaccharide, converted from xylitol in the glucuronate pathway.
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.
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
Regulatory Information
涉药品监管产品
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Nichole F Huntley et al.
PloS one, 13(10), e0205913-e0205913 (2018-10-26)
It is important to understand if, and to what extent, the pig can utilize xylose as an energy source if xylanase releases free xylose in the small intestine. The experimental objectives were to determine the effects of industry-relevant dietary xylose
Tien Anh Ngo et al.
Journal of the American Chemical Society, 138(9), 3012-3021 (2016-02-18)
We report the construction of an artificial enzyme cascade based on the xylose metabolic pathway. Two enzymes, xylose reductase and xylitol dehydrogenase, were assembled at specific locations on DNA origami by using DNA-binding protein adaptors with systematic variations in the
Mingyong Xiong et al.
Bioresource technology, 102(19), 9206-9215 (2011-08-13)
A K270R mutation of xylose reductase (XR) was constructed by site-direct mutagenesis. Fermentation results of the F106X and F106KR strains, which carried wild type XR and K270R respectively, were compared using different substrate concentrations (from 55 to 220 g/L). After
Yu Yang et al.
ChemSusChem, 5(2), 405-410 (2012-02-09)
Furfural was prepared in high yields (75 %) from the reaction of xylose in a water-tetrahydrofuran biphasic medium containing AlCl(3)·6H2O and NaCl under microwave heating at 140 °C. The reaction profile revealed the formation of xylulose as an intermediate en
Biosynthesis of monoethylene glycol in Saccharomyces cerevisiae utilizing native glycolytic enzymes.
Boonsom Uranukul et al.
Metabolic engineering, 51, 20-31 (2018-10-01)
Monoethylene glycol (MEG) is an important commodity chemical with applications in numerous industrial processes, primarily in the manufacture of polyethylene terephthalate (PET) polyester used in packaging applications. In the drive towards a sustainable chemical industry, bio-based production of MEG from
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