Sorbitan monolaurate

Base Information

Chemical Name:Sorbitan monolaurate
CAS No.:5959-89-7
Deprecated CAS:53528-77-1,55070-12-7,76011-50-2,8028-02-2,507483-77-4
Molecular Formula:C₁₈H₃₄O₆
Molecular Weight:346.464
Hs Code.:
European Community (EC) Number:227-729-9,215-663-3,617-034-2
UNII:6W9PS8B71J
DSSTox Substance ID:DTXSID9027609
Nikkaji Number:J223.909D
Wikipedia:Sorbitan_monolaurate
NCI Thesaurus Code:C75653
RXCUI:1363055
ChEMBL ID:CHEMBL3706389

Synonyms:sorbitan monolaurate;Span 20

Suppliers and Price of Sorbitan monolaurate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
6-Dodecanoate-1,4-anhydro-D-glucitol
500mg
$ 165.00

American Custom Chemicals Corporation
1,4-ANHYDRO-6-DODECANOATE-D-GLUCITOL 95.00%
5MG
$ 499.49

Total 8 raw suppliers

Chemical Property of Sorbitan monolaurate

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Boiling Point:516.121°C at 760 mmHg
Flash Point:176.947°C
PSA：96.22000
Density:1.123g/cm³
LogP:1.93200
XLogP3:3.7
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:14
Exact Mass:346.23553880
Heavy Atom Count:24
Complexity:336

Purity/Quality:

99% ^*data from raw suppliers

6-Dodecanoate-1,4-anhydro-D-glucitol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Chemical Classes:Other Uses -> Emulsifiers/Surfactants
Canonical SMILES:CCCCCCCCCCCC(=O)OCC(C1C(C(CO1)O)O)O
Isomeric SMILES:CCCCCCCCCCCC(=O)OC[C@H]([C@@H]1[C@@H]([C@H](CO1)O)O)O
Uses 6-Dodecanoate-1,4-anhydro-D-glucitol is used in the synthetic preparation of nonionic surfactant.

Technology Process of Sorbitan monolaurate

There total 3 articles about Sorbitan 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: 23.0%

: 143-07-7
lauric acid

: 7726-97-8,10334-28-8,20662-31-1,22554-76-3,22554-77-4,22554-79-6,27299-12-3,28218-56-6,32742-35-1,40026-08-2,51196-40-8,51607-77-3,53648-56-9,96243-58-2,124379-08-4,124379-13-1
1,4-anhydro-D-glucitol

: 120200-78-4,16287-68-6,5959-89-7
Span 20

Guidance literature:: With lipase; In hexane; tert-butyl alcohol; at 64 ℃; Enzymatic reaction;
DOI:10.1039/c5gc02131f

Reference yield:

: 50-70-4
D-sorbitol

: 120200-78-4,16287-68-6,5959-89-7
Span 20

Guidance literature:: Multi-step reaction with 2 steps

1: sulfuric acid; water / 74 h / 104 °C

2: lipase / tert-butyl alcohol; hexane / 64 °C / Enzymatic reaction

With sulfuric acid; water; lipase; In hexane; tert-butyl alcohol;
DOI:10.1039/c5gc02131f