Sorbitan monostearate

Base Information

• Chemical Name: Sorbitan monostearate
• CAS No.: 5093-91-4
• Deprecated CAS: 56940-43-3,58052-16-7,64772-18-5,76011-53-5,76169-00-1,1051378-63-2,107461-71-2,1629855-82-8,2245272-62-0,368449-23-4,1051378-63-2,107461-71-2,1629855-82-8,2245272-62-0,368449-23-4,58052-16-7,64772-18-5,76011-53-5,76169-00-1
• Molecular Formula: C₂₄H₄₆O₆
• Molecular Weight: 430.626
• European Community (EC) Number: 215-664-9,616-298-6
• UNII: NVZ4I0H58X
• ChEMBL ID: CHEMBL3186117
• DSSTox Substance ID: DTXSID70872695
• Metabolomics Workbench ID: 44105
• NCI Thesaurus Code: C75656
• RXCUI: 1363057
• Wikidata: Q907898
• Wikipedia: Sorbitan_monostearate
• Mol file: 5093-91-4.mol

Synonyms:sorbitan monostearate;sorbitan monostearate, (1,4)-isomer;Span 60

Chemical Property of Sorbitan monostearate

Chemical Property:

• Boiling Point: 579.0±45.0 °C(Predicted)
• PKA: 13.17±0.20(Predicted)
• PSA: 96.22000
• Density: 1.056±0.06 g/cm3(Predicted)
• LogP: 4.27260
• XLogP3: 6.9
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 20
• Exact Mass: 430.32943918
• Heavy Atom Count: 30
• Complexity: 417

Purity/Quality:

99.0%min ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCCCCCCCCC(=O)OCC(C1C(C(CO1)O)O)O
• Isomeric SMILES: CCCCCCCCCCCCCCCCCC(=O)OC[C@H]([C@@H]1[C@@H]([C@H](CO1)O)O)O
• Recent NIPH Clinical Trials: The evaluation of usefulness of peppermint oil solution as an antispasmodic drug for esophagogastroduodenoscopy.

Technology Process of Sorbitan monostearate

There total 1 articles about Sorbitan monostearate 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:

→ sorbitan monostearate (5093-91-4,96094-21-2)

Guidance literature:

Reference yield:

Cetomacrogol 1000 + Tetradecanoic acid 1-methylethyl ester (110-27-0,1405-98-7) + sorbitan monostearate (5093-91-4,96094-21-2) → 1-Hexadecanol (36653-82-4,124-29-8)

Guidance literature:

In paraffin oil;

Reference yield:

α,ω-di(2-propoxyethanol)polydimethylsiloxane + DL-panthenyl ethyl ether (667-84-5) + isophorone diisocyanate (4098-71-9,101701-80-8,129212-17-5,149579-36-2,194936-84-0,26602-93-7,53895-32-2,66708-07-4,70936-97-9,74091-63-7,74520-92-6,102771-74-4,50974-99-7,52985-93-0) + sorbitan monostearate (5093-91-4,96094-21-2) → sugar ester panthenol-silicone/urethane copolymer

Guidance literature:

α,ω-di(2-propoxyethanol)polydimethylsiloxane; isophorone diisocyanate; zinc stearate; In 2-methylundecane; at 95 ℃; for 3h; Heating / reflux;

sorbitan monostearate; In 2-methylundecane; at 95 ℃; for 5h;

DL-panthenyl ethyl ether; With ethanol; more than 3 stages;

Downstream raw materials:

1-Hexadecanol

Refernces

• 1、 -. "Encapsulation of microparticles in teardrop shaped polymer capsules of cellular size". . . Retrieved 2008/06/13.
• 2、 -. "Self-emulsifiable dermatologic cream". . . Retrieved 2008/06/13.