Dodecyl 5-oxo-L-prolinate

Base Information

• Chemical Name: Dodecyl 5-oxo-L-prolinate
• CAS No.: 22794-26-9
• Molecular Formula: C17H31 N O3
• Molecular Weight: 297.438
• European Community (EC) Number: 245-224-1,278-210-9
• UNII: 29C5O2BJYA
• DSSTox Substance ID: DTXSID201018272
• Nikkaji Number: J179.411F
• Wikidata: Q27254410
• Mol file: 22794-26-9.mol

Synonyms:Dodecyl 5-oxo-L-prolinate;L-Proline, 5-oxo-, dodecyl ester;lauryl PCA;lauryl pidolate

Chemical Property of Dodecyl 5-oxo-L-prolinate

Chemical Property:

• Vapor Pressure: 7.28E-08mmHg at 25°C
• Boiling Point: 437.8°C at 760 mmHg
• PKA: 14?+-.0.40(Predicted)
• Flash Point: 218.6°C
• PSA: 55.40000
• Density: 0.99g/cm³
• LogP: 4.05790
• XLogP3: 5.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 13
• Exact Mass: 297.23039385
• Heavy Atom Count: 21
• Complexity: 304

Purity/Quality:

99.9% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCCCOC(=O)C1CCC(=O)N1
• Isomeric SMILES: CCCCCCCCCCCCOC(=O)[C@@H]1CCC(=O)N1
• Uses: dodecyl 5-oxo-L-prolinate is an emulsifier that has good affinity with skin lipids. It can increase a product’s moisturizing action by decreasing transepidermal water loss. dodecyl 5-oxo-L-prolinate is a lipophilic moisturizer with a delayed and remnant effect. Also used as a thickener or viscosity-control agent, it is derived from natural raw materials.

Technology Process of Dodecyl 5-oxo-L-prolinate

There total 2 articles about Dodecyl 5-oxo-L-prolinate 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: 54.0%

1-dodecyl alcohol (112-53-8) + L-Pyroglutamic acid (98-79-3) → pyroglutamic acid n-dodecyl ester (22794-26-9)

Guidance literature:

With toluene-4-sulfonic acid;

DOI:10.1016/0040-4039(96)01828-X

Reference yield:

→ pyroglutamic acid n-dodecyl ester (22794-26-9)

Guidance literature:

upstream raw materials:

1-dodecyl alcohol

L-Pyroglutamic acid

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