b-D-Fructofuranosyl-(2->1)-b-D-fructofuranosyl-(2->1)-b-D-fructofuranosyl a-D-glucopyranoside, 9CI

Base Information

• Chemical Name: b-D-Fructofuranosyl-(2->1)-b-D-fructofuranosyl-(2->1)-b-D-fructofuranosyl a-D-glucopyranoside, 9CI
• CAS No.: 13133-07-8
• Molecular Formula: C24H42 O21
• Molecular Weight: 666.585
• Hs Code.: 29400090
• Wikidata: Q104996976
• Mol file: 13133-07-8.mol

Synonyms:SCHEMBL12608174;.alpha.-D-Glucopyranoside, O-.beta.-D-fructofuranosyl-(2.fwdarw.1)-O-.beta.-D-fructofuranosyl-(2.fwdarw.1)-.beta.-D-fructofuranosyl;FT-0697542;b-D-Fructofuranosyl-(2->1)-b-D-fructofuranosyl-(2->1)-b-D-fructofuranosyl a-D-glucopyranoside, 9CI

Chemical Property of b-D-Fructofuranosyl-(2->1)-b-D-fructofuranosyl-(2->1)-b-D-fructofuranosyl a-D-glucopyranoside, 9CI

Chemical Property:

• Vapor Pressure: 0mmHg at 25°C
• Melting Point: 130-133℃
• Refractive Index: 10 ° (C=4, H2O)
• Boiling Point: 1075.7°Cat760mmHg
• PKA: 12.76±0.70(Predicted)
• Flash Point: 604.3°C
• PSA: 347.83000
• Density: 1.84g/cm³
• LogP: -9.74400
• Storage Temp.: 2-8°C
• XLogP3: -7.4
• Hydrogen Bond Donor Count: 14
• Hydrogen Bond Acceptor Count: 21
• Rotatable Bond Count: 13
• Exact Mass: 666.22185834
• Heavy Atom Count: 45
• Complexity: 964

Purity/Quality:

97% ^*data from raw suppliers

Fungitetraose ^*data from reagent suppliers

Safty Information:

• Safety Statements: 24/25

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)COC3(C(C(C(O3)CO)O)O)COC4(C(C(C(O4)CO)O)O)CO)O)O)O)O
• Uses: Fungitetraose is a part of the sugar mixture of Neosugar, sweetner.

Technology Process of b-D-Fructofuranosyl-(2->1)-b-D-fructofuranosyl-(2->1)-b-D-fructofuranosyl a-D-glucopyranoside, 9CI

There total 20 articles about b-D-Fructofuranosyl-(2->1)-b-D-fructofuranosyl-(2->1)-b-D-fructofuranosyl a-D-glucopyranoside, 9CI 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: 30.2%

Sucrose (57-50-1) → 1-fructofuranosylnystose (59432-60-9) + D-glucose (50-99-7) + 1-kestose (470-69-9) + nystose (13133-07-8)

Guidance literature:

With Aspergillus niger ATCC 20611 FopA(A₁₇₈P)-overexpression strain; In aq. buffer; at 50 ℃; for 5h; pH=5.5; Reagent/catalyst; Time; Microbiological reaction;

DOI:10.1016/j.jbiotec.2017.03.021

Reference yield: 29.5%

Sucrose (57-50-1) → D-glucose (50-99-7) + 1-kestose (470-69-9) + nystose (13133-07-8)

Guidance literature:

With Aspergillus niger ATCC 20611; In aq. buffer; at 50 ℃; for 5h; pH=5.5; Time; Microbiological reaction;

DOI:10.1016/j.jbiotec.2017.03.021

Reference yield: 22.1%

N-Acetyl-D-glucosamine (7512-17-6,72-87-7,1136-42-1,1136-44-3,6082-29-7,6730-06-9,7772-94-3,10036-64-3,14131-60-3,14131-64-7,14131-68-1,14215-68-0,62057-49-2,62057-50-5,62057-51-6,62057-52-7,62057-53-8,62057-54-9,62057-55-0,62057-56-1,62075-50-7,62137-54-6,134451-97-1,134522-12-6,148347-16-4) + Sucrose (57-50-1) → β-D-fructofuranosyl-(2->1)-2-acetamido-2-deoxy-α-D-glucopyranoside (84039-32-7) + 1-kestose (470-69-9) + nystose (13133-07-8)

Guidance literature:

With Aspergillus oryzae NBRC₁₀₀₉₅₉ mycelia; In citrate buffer; at 30 ℃; for 8h; pH=5.5; Enzymatic reaction;

DOI:10.1016/j.carres.2012.03.037

upstream raw materials:

Sucrose

1-kestose

lactosucrose

1-fructofuranosylnystose

Downstream raw materials:

D-fructose

1-kestose