Sucrose octapalmitate

Base Information

• Chemical Name: Sucrose octapalmitate
• CAS No.: 39024-75-4
• Molecular Formula: C140H262O19
• Molecular Weight: 2249.61
• European Community (EC) Number: 254-251-8
• UNII: JE1NY6BUOI
• DSSTox Substance ID: DTXSID501110990
• Nikkaji Number: J319.888J
• Wikidata: Q27281464
• Mol file: 39024-75-4.mol

Synonyms:sucrose octapalmitate;39024-75-4;JE1NY6BUOI;UNII-JE1NY6BUOI;EINECS 254-251-8;NSC 97431;1,3,4,6-Tetrakis-O-(1-oxohexadecyl)-beta-D-fructofuranosyl-alpha-D-glucopyranoside tetrapalmitate;((2S,3S,4R,5R)-4-Hexadecanoyloxy-2,5-bis(hexadecanoyloxymethyl)-2-((2R,3R,4S,5R,6R)-3,4,5-tri(hexadecanoyloxy)-6-(hexadecanoyloxymethyl)oxan-2-yl)oxyoxolan-3-yl) hexadecanoate;NSC-97431;C140H262O19;C140-H262-O19;SCHEMBL597451;DTXSID501110990;Q27281464;alpha-D-Glucopyranoside, 1,3,4,6-tetrakis-O-(1-oxohexadecyl)-beta-D-fructofuranosyl, 2,3,4,6-tetrahexadecanoate

Chemical Property of Sucrose octapalmitate

Chemical Property:

• XLogP3: 57.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 19
• Rotatable Bond Count: 133
• Exact Mass: 2248.95689096
• Heavy Atom Count: 159
• Complexity: 3180

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCCCCCCC(=O)OCC1C(C(C(C(O1)OC2(C(C(C(O2)COC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCC
• Isomeric SMILES: CCCCCCCCCCCCCCCC(=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)CCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCC

Technology Process of Sucrose octapalmitate

There total 3 articles about Sucrose octapalmitate 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:

hexadecanoic acid methyl ester (112-39-0) + sucrose octaacetate (126-14-7) → (tetra-O-palmitoyl-β-D-fructofuranosyl)-(tetra-O-palmitoyl-α-D-glucopyranoside) (39024-75-4)

Guidance literature:

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

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

Reference yield:

Sucrose (57-50-1) + n-hexadecanoyl chloride (112-67-4) → (tetra-O-palmitoyl-β-D-fructofuranosyl)-(tetra-O-palmitoyl-α-D-glucopyranoside) (39024-75-4)

Guidance literature:

With pyridine; chloroform;

Reference yield:

→ (tetra-O-palmitoyl-β-D-fructofuranosyl)-(tetra-O-palmitoyl-α-D-glucopyranoside) (39024-75-4)

Guidance literature:

Sucroseoctaacetat, Methylpalmitat, NaOMe;

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

upstream raw materials:

Sucrose

n-hexadecanoyl chloride

hexadecanoic acid methyl ester

sucrose octaacetate

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