Cellotriose

Base Information

• Chemical Name: Cellotriose
• CAS No.: 33404-34-1
• Deprecated CAS: 2640-12-2
• Molecular Formula: C18H32O16
• Molecular Weight: 504.442
• Hs Code.: 29400090
• Nikkaji Number: J1.028.426K
• Wikidata: Q27096269
• Metabolomics Workbench ID: 53053
• Mol file: 33404-34-1.mol

Synonyms:D-glucose, O-D-glucopyranosyl;D-glucose,O-beta-D-glucopyranosyl

Chemical Property of Cellotriose

Chemical Property:

• Appearance/Colour: white solid
• Vapor Pressure: 6.5E-35mmHg at 25°C
• Melting Point: > 165 °C
• Refractive Index: 1.673
• Boiling Point: 865.164 °C at 760 mmHg
• Flash Point: 477.034 °C
• PSA: 268.68000
• Density: 1.81 g/cm³
• LogP: -7.57300
• Storage Temp.: −20°C
• Sensitive.: Hygroscopic
• Solubility.: H2O: soluble50mg/mL, clear, colorless
• Water Solubility.: Soluble in water at 50mg/ml /n
• XLogP3: -6.9
• Hydrogen Bond Donor Count: 11
• Hydrogen Bond Acceptor Count: 16
• Rotatable Bond Count: 7
• Exact Mass: 504.16903493
• Heavy Atom Count: 34
• Complexity: 641

Purity/Quality:

98%, ^*data from raw suppliers

D-Cellotriose ^*data from reagent suppliers

Safty Information:

• Safety Statements: 22-24/25

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(OC(C(C3O)O)O)CO)CO)O)O)O)O
• Isomeric SMILES: C([C@@H]1[C@H]([C@@H]([C@H]([C@@H](O1)O[C@@H]2[C@H](O[C@H]([C@@H]([C@H]2O)O)O[C@@H]3[C@H](OC([C@@H]([C@H]3O)O)O)CO)CO)O)O)O)O
• Recent ClinicalTrials: Cellodextrin Tolerability Study
• Uses: C255901 is a 13C labeled D-(+)-Cellotriose(C255900) which may be used in saccharification and ethanol fermentation research.

Technology Process of Cellotriose

There total 21 articles about Cellotriose which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 50.0%

Pinus cellulose → cellotriose (33404-34-1) + 5-hydroxymethyl-2-furfuraldehyde (67-47-0) + D-glucose (50-99-7) + cellotetraose (6918-41-8,34612-38-9,38819-01-1,51327-76-5,51841-90-8,59862-03-2,60755-09-1,60755-10-4,61237-57-8,70399-65-4,72165-13-0,73062-57-4,95336-74-6,102031-44-7,107595-47-1,146491-17-0,150668-99-8) + cellobiose (528-50-7)

Guidance literature:

Pinus cellulose; With choline chloride; oxalic acid; 1-butyl-3-methylimidazolium chloride; at 120 ℃; for 6h;

With water; at 120 ℃; for 4h;

DOI:10.1002/open.201900283

Reference yield: 48.0%

Eucalyptus cellulose → cellotriose (33404-34-1) + 5-hydroxymethyl-2-furfuraldehyde (67-47-0) + D-glucose (50-99-7) + cellobiose (528-50-7)

Guidance literature:

Eucalyptus cellulose; With choline chloride; oxalic acid; 1-butyl-3-methylimidazolium chloride; at 120 ℃; for 6h;

With water; at 120 ℃; for 4h;

DOI:10.1002/open.201900283

Reference yield: 46.0%

Pinus cellulose, unbleached → cellotriose (33404-34-1) + 5-hydroxymethyl-2-furfuraldehyde (67-47-0) + D-glucose (50-99-7) + cellotetraose (6918-41-8,34612-38-9,38819-01-1,51327-76-5,51841-90-8,59862-03-2,60755-09-1,60755-10-4,61237-57-8,70399-65-4,72165-13-0,73062-57-4,95336-74-6,102031-44-7,107595-47-1,146491-17-0,150668-99-8) + cellobiose (528-50-7)

Guidance literature:

Pinus cellulose, unbleached; With choline chloride; oxalic acid; 1-butyl-3-methylimidazolium chloride; at 120 ℃; for 6h;

With water; at 120 ℃; for 4h;

DOI:10.1002/open.201900283

upstream raw materials:

cellotetraose

cellopentaose

Sucrose

D-maltose

Downstream raw materials:

D-glucose

C₄₅H₆₃NO₁₉S

C₄₄H₆₅N₅O₂₀

cellobiose

Refernces

• 1、 Bodachivskyi, Iurii,Kuzhiumparambil, Unnikrishnan,Bradley G. Williams. "High Yielding Acid-Catalysed Hydrolysis of Cellulosic Polysaccharides and Native Biomass into Low Molecular Weight Sugars in Mixed Ionic Liquid Systems". . p. 1316 - 1324. Retrieved 2019/11/11.
• 2、 Miranda-Molina, Alfonso,Marquina-Bahena, Silvia,Alvarez, Laura,Lopez-Munguia, Agustin,Castillo, Edmundo. "Regioselective glucosylation of inositols catalyzed by Thermoanaerobacter sp. CGTase". . p. 93 - 101,9. Retrieved 2020/08/20.