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Open Access Articles- Top Results for Cellobiose

Cellobiose

Cellobiose
Cellobiose
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528-50-7 7pxN
ChEBI CHEBI:17057 7pxN
ChEMBL ChEMBL1614877 7pxN
ChemSpider 388323 7pxN
DrugBank DB02061 7pxY
Jmol-3D images Image
KEGG C00185 7pxN
PubChem Template:Chembox PubChem/formatTemplate:Chembox PubChem/format
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This page is a soft redirect. Properties

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C12H22O11
Molar mass Lua error in Module:Math at line 495: attempt to index field 'ParserFunctions' (a nil value). g·mol−1
Appearance white, hard powder
Odor odorless
Density 1.768 g/mL
Melting point Script error: No such module "convert". (decomposes)
12 g/100mL
Solubility very slightly soluble in alcohol
insoluble in ether, chloroform
log P -5.03
Acidity (pKa) 12.39
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SDS Sigma-Aldrich
NFPA 704

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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Cellobiose is a disaccharide with the formula [HOCH2CHO(CHOH)3]2O. Cellobiose, a reducing sugar, consists of two glucose molecules linked by a β(1→4) bond. It can be hydrolyzed to glucose enzymatically or with acid.[1] Cellobiose has eight free alcohol (OH) groups, one acetal linkage and one hemiacetal linkage, which give rise to strong inter- and intra-molecular hydrogen bonds. It can be obtained by enzymatic or acidic hydrolysis of cellulose and cellulose rich materials such as cotton, jute, or paper.

Treatment of cellulose with acetic anhydride and sulfuric acid, gives cellobiose octoacetate, which cannot engage in hydrogen bonding and is soluble in nonpolar organic solvents.[2]

References

  1. Cancerweb.ncl.ac.uk
  2. Braun, G. (1943). "α-Cellobiose Octaacetate" (PDF). Organic Syntheses. Collected Volume 2: 124.  and Braun, G. (1937). "α-Cellobiose Octaacetate". Organic Syntheses 17: 36. 

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