Sucrose monolaurate

Base Information

• Chemical Name: Sucrose monolaurate
• CAS No.: 13039-40-2
• Molecular Formula: C₂₄H₄₄O₁₂
• Molecular Weight: 524.606
• UNII: 2AN420DS8I
• DSSTox Substance ID: DTXSID90156500
• Nikkaji Number: J643.751F
• Wikidata: Q27254485
• ChEMBL ID: CHEMBL4060183
• Mol file: 13039-40-2.mol

Synonyms:beta-fructofuranosyl-alpha-D-glucopyranoside monododecanoate;L-1690;sucrose laurate;sucrose monododecanoate;sucrose monolaurate

Chemical Property of Sucrose monolaurate

Chemical Property:

• XLogP3: 1.5
• Hydrogen Bond Donor Count: 7
• Hydrogen Bond Acceptor Count: 12
• Rotatable Bond Count: 17
• Exact Mass: 524.28327683
• Heavy Atom Count: 36
• Complexity: 636

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

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

Technology Process of Sucrose monolaurate

There total 23 articles about Sucrose monolaurate 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: 96.0%

methyl n-dodecanoate (111-82-0) + Sucrose (57-50-1) → 6-O-sucrose monolaurate (13039-40-2)

Guidance literature:

With MBC-01; In N,N-dimethyl-formamide; at 110 ℃; for 8h; under 3.75038 Torr; Reagent/catalyst;

Reference yield: 88.0%

lauric acid (143-07-7) + Sucrose (57-50-1) → 6-O-sucrose monolaurate (13039-40-2)

Guidance literature:

With MAC-01; In N,N-dimethyl-formamide; at 120 ℃; for 6h; under 3.75038 Torr;

Reference yield: 70.0%

n-dodecanoyl chloride (112-16-3) + Sucrose (57-50-1) → 3-O-lauroyl sucrose (146270-43-1) + 6-O-sucrose monolaurate (13039-40-2)

Guidance literature:

Sucrose; With di(n-butyl)tin oxide; In methanol; for 3h; Heating;

n-dodecanoyl chloride; With triethylamine; In N,N-dimethyl-formamide; at 4 - 20 ℃; for 96h;

DOI:10.1080/07328309708006506

upstream raw materials:

methyl n-dodecanoate

Sucrose

3-dodecanoyl-5-methyl-1,3,4-thiadiazole-(3H)-2-thione

2-O-sucrosyl laurate

Downstream raw materials:

D-fructose

6-O-Dodecanoyl-α-D-glucose