Sucrose octastearate

Base Information

• Chemical Name: Sucrose octastearate
• CAS No.: 34816-22-3
• Molecular Formula: C156H294O19
• Molecular Weight: 2474.04
• European Community (EC) Number: 252-225-0
• UNII: CR8AD002QQ
• DSSTox Substance ID: DTXSID001111193
• Nikkaji Number: J289.842J
• Wikidata: Q27275686
• Mol file: 34816-22-3.mol

Synonyms:sucrose octastearate;34816-22-3;UNII-CR8AD002QQ;CR8AD002QQ;EINECS 252-225-0;1,3,4,6-Tetrakis-O-(1-oxooctadecyl)-beta-D-fructofuranosyl-alpha-D-glucopyranoside tetrastearate;NSC-192748;C156H294O19;C156-H294-O19;DTXSID001111193;NSC 192748;Q27275686;beta-D-Fructofuranosyl alpha-D-glucopyranoside octastearate;alpha-D-Glucopyranoside, 1,3,4,6-tetrakis-O-(1-oxooctadecyl)-beta-D-fructofuranosyl, 2,3,4,6-tetraoctadecanoate

Chemical Property of Sucrose octastearate

Chemical Property:

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Density: g/cm³
• XLogP3: 66.3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 19
• Rotatable Bond Count: 149
• Exact Mass: 2473.20729198
• Heavy Atom Count: 175
• Complexity: 3480

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCCCCCCCCC(=O)OCC1C(C(C(C(O1)OC2(C(C(C(O2)COC(=O)CCCCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCCCC
• Isomeric SMILES: CCCCCCCCCCCCCCCCCC(=O)OC[C@@H]1[C@H]([C@@H]([C@H]([C@H](O1)O[C@]2([C@H]([C@@H]([C@H](O2)COC(=O)CCCCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCCCC

Technology Process of Sucrose octastearate

There total 3 articles about Sucrose octastearate 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:

Methyl stearate (112-61-8) + sucrose octaacetate (126-14-7) → (tetra-O-stearoyl-β-D-fructofuranosyl)-(tetra-O-stearoyl-α-D-glucopyranoside) (34816-22-3)

Guidance literature:

With sodium; at 110 ℃; for 2h; under 5 Torr;

DOI:10.1016/S0009-3084(00)00222-X

Reference yield:

Stearoyl chloride (112-76-5) + Sucrose (57-50-1) → (tetra-O-stearoyl-β-D-fructofuranosyl)-(tetra-O-stearoyl-α-D-glucopyranoside) (34816-22-3)

Guidance literature:

With pyridine; chloroform;

Reference yield:

→ (tetra-O-stearoyl-β-D-fructofuranosyl)-(tetra-O-stearoyl-α-D-glucopyranoside) (34816-22-3)

Guidance literature:

Sucroseoctaacetat, Methylstearat, NaOMe;

DOI:10.1016/0009-3084(78)90042-7

upstream raw materials:

Stearoyl chloride

Sucrose

Methyl stearate

sucrose octaacetate

Refernces