Date published: 2026-3-6

1-800-457-3801

SCBT Portrait Logo
Seach Input

D-(-)-Lyxose (CAS 1114-34-7)

0.0(0)
Write a reviewAsk a question

Alternate Names:
D-Lyxopyranose
Application:
D-(−)-Lyxose is a chiral building block
CAS Number:
1114-34-7
Purity:
≥98%
Molecular Weight:
150.13
Molecular Formula:
C5H10O5
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

D-(−)-Lyxose is a rare deoxy sugar naturally found in small quantities in various organisms. It belongs to the ketopentose family, which is a group of monosaccharides containing five carbon atoms and a ketone group. This sugar′s unique structure, lacking one oxygen atom compared to its pentose counterparts, makes it an interesting subject for biochemical and synthetic research. In scientific studies, D-(−)-Lyxose is used to investigate the roles and metabolic pathways of rare sugars in organisms, providing insights into their biological significance and evolutionary aspects. Research applications have leveraged D-(−)-Lyxose in the synthesis of complex carbohydrates and glycoconjugates due to its ability to introduce structural diversity into these molecules. This has implications for understanding carbohydrate-mediated biological recognition and signaling processes. Furthermore, D-(−)-Lyxose is studied in the context of enzymatic reactions involving rare sugars, aiding in the discovery and engineering of enzymes with novel functionalities or specificities. These studies contribute to a broader understanding of carbohydrate chemistry and enzyme catalysis, emphasizing the exploration of biochemical pathways and molecular interactions that govern cellular functions and biochemical diversity.


D-(-)-Lyxose (CAS 1114-34-7) References

  1. Evaluation of analyte protectants to improve gas chromatographic analysis of pesticides.  |  Anastassiades, M., et al. 2003. J Chromatogr A. 1015: 163-84. PMID: 14570329
  2. Analysis of sugars in environmental samples by gas chromatography-mass spectrometry.  |  Medeiros, PM. and Simoneit, BR. 2007. J Chromatogr A. 1141: 271-8. PMID: 17207493
  3. Metabolic footprinting of Lactobacillus buchneri strain LA1147 during anaerobic spoilage of fermented cucumbers.  |  Johanningsmeier, SD. and McFeeters, RF. 2015. Int J Food Microbiol. 215: 40-8. PMID: 26325599
  4. Exploring the chemical space for freeze-drying excipients.  |  Meng-Lund, H., et al. 2019. Int J Pharm. 566: 254-263. PMID: 31145963
  5. Conversion of alcohols to methylene acetals by reaction with dimethyl sulfoxide-bromine  |  Munavu, R. M. 1980. The Journal of Organic Chemistry. 45(16): 3341-3343.
  6. Excess enthalpies of aqueous solutions of monosaccharides at 298.15 K: pentoses and 2-deoxy sugars  |  Barone, G., Castronuovo, G., Doucas, D., Elia, V., & Mattia, C. A. 1983. The Journal of Physical Chemistry. 87(11): 1931-1937.
  7. Selective Binding of Sugar to β‐Cyclodextrin: A Prototype for Sugar–Sugar Interactions in Water  |  Aoyama, Y., Nagai, Y., Otsuki, J. I., Kobayashi, K., & Toi, H. 1992. Angewandte Chemie International Edition in English. 31(6): 745-747.
  8. Qualitative and quantitative analysis of characteristic sugars in three colored quinoas based on untargeted and targeted metabolomics  |  Song, J., & Peng, J. 2024. Journal of Food Composition and Analysis. 126: 105880.
  9. Characterization of the key aroma compounds in a novel Qingke baijiu of Tibet by GC-MS, GC× GC-MS and GC-O-MS  |  Zhao, Y., Liao, P., Chen, L., Zhang, Y., Wang, X., Kang, Q.,.. & Sun, J. 2024. Food Chemistry Advances. 4: 100589.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

D-(-)-Lyxose, 5 g

sc-221457
5 g
$65.00