Date published: 2026-4-20

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Chitobiose Octaacetate (CAS 41670-99-9)

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Alternate Names:
2-(Acetylamino)-2-deoxy-4-O-[3,4,6-tri-O-acetyl-2-(acetylamino)-2-deoxy-β-D- glucopyranosyl]-D-glucopyranose 1,3,6-Triacetate; Peracetylchitobiose
Application:
Chitobiose Octaacetate is a chitin derivative
CAS Number:
41670-99-9
Molecular Weight:
676.62
Molecular Formula:
C28H40N2O17
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Chitobiose Octaacetate is a chemically modified form of chitobiose, a disaccharide composed of two glucosamine units linked by a β-(1→4) bond, extensively acetylated to enhance its chemical stability and solubility for use in research applications. This derivative is particularly valuable in the study of chitinase enzymes, which play crucial roles in the degradation of chitin, a major component of the exoskeletons of arthropods and the cell walls of fungi. The octaacetate modification of chitobiose serves as a protective mechanism, preventing premature hydrolysis and allowing researchers to explore enzyme-substrate interactions with greater specificity and control. By studying how chitinases interact with this substrate, scientists can gain insights into the catalytic mechanisms of these enzymes, which is essential for understanding natural chitin degradation processes and developing synthetic routes to mimic or inhibit these reactions. In research, Chitobiose Octaacetate is used primarily to investigate the kinetics and dynamics of chitinase action, helping to explain factors that influence enzyme specificity and activity. This research is crucial for advancing our understanding of biochemical pathways involved in fungal and microbial ecology, as well as in agricultural applications where chitinase enzymes are targeted to combat fungal infections. These studies are strictly scientific, focusing solely on the biochemical and enzymological aspects.


Chitobiose Octaacetate (CAS 41670-99-9) References

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  2. The chitinase system of a strain of Streptomyces griseus.  |  BERGER, LR. and REYNOLDS, DM. 1958. Biochim Biophys Acta. 29: 522-34. PMID: 13584354
  3. Synthesis of a peripheral trisaccharide sequence of lutropin, a pituitary glycoprotein hormone; use of chitobiose as a key starting material.  |  Nishimura, S. and Kuzuhara, H. 1990. Carbohydr Res. 206: 207-17. PMID: 2073633
  4. Synthesis and X-ray crystallographic investigation of N-(β-D-glycosyl)butanamides derived from GlcNAc and chitobiose as analogs of the conserved chitobiosylasparagine linkage of N-glycoproteins.  |  Mathiselvam, M., et al. 2013. Carbohydr Res. 380: 37-44. PMID: 23916853
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  6. Alg mannosyltransferases: From functional and structural analyses to the lipid-linked oligosaccharide pathway reconstitution.  |  Wang, N., et al. 2022. Biochim Biophys Acta Gen Subj. 1866: 130112. PMID: 35217128
  7. The stereospecificity of human, hen, and papaya lysozymes.  |  Dahlquist, FW., et al. 1969. Biochemistry. 8: 694-700. PMID: 5815782
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  9. Selective cleavage of the glycosidic bond in acetylated 2-acetamido-2-deoxy-. beta.-D-glucopyranosides by a chemical transglycosylation  |  Salo W L, Fletcher Jr H G. 1968. The Journal of Organic Chemistry. 33: 3585-3588.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Chitobiose Octaacetate, 100 mg

sc-211065
100 mg
$388.00