Lauryl laurate

Base Information

• Chemical Name: Lauryl laurate
• CAS No.: 13945-76-1
• Molecular Formula: C24H48 O2
• Molecular Weight: 368.644
• Hs Code.: 2915900090
• European Community (EC) Number: 237-725-9
• NSC Number: 404384
• UNII: GPW77G0937
• DSSTox Substance ID: DTXSID6065684
• Nikkaji Number: J115.179G
• Wikidata: Q27279226
• RXCUI: 1426922
• Metabolomics Workbench ID: 3676
• Mol file: 13945-76-1.mol

Synonyms:Lauryl laurate;dodecyl dodecanoate;13945-76-1;Dodecanoic acid, dodecyl ester;Dodecyl laurate;Lauric acid, dodecyl ester;dodecanyl dodecanoate;UNII-GPW77G0937;GPW77G0937;WE(12:0/12:0);EINECS 237-725-9;NSC 404384;NSC-404384;AI3-18181;cis-EpoxysuccinicAcid;LAURYL LAURATE [INCI];SCHEMBL432184;DTXSID6065684;CHEBI:141061;LMFA07010031;NSC404384;AS-80296;FT-0697019;F87107;Q27279226

Chemical Property of Lauryl laurate

Chemical Property:

• Vapor Pressure: 4.52E-07mmHg at 25°C
• Melting Point: 27 °C
• Boiling Point: 414.2°Cat760mmHg
• Flash Point: 209.9°C
• PSA: 26.30000
• Density: 0.86g/cm³
• LogP: 8.37140
• Storage Temp.: 2-8°C
• XLogP3: 10.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 22
• Exact Mass: 368.365430770
• Heavy Atom Count: 26
• Complexity: 275

Purity/Quality:

99.9% ^*data from raw suppliers

LaurylLaurate ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CCCCCCCCCCCCOC(=O)CCCCCCCCCCC
• Uses: Lauryl Laurate is a fugitive wax and is used in the creation of biomimetic self-healing materials with interpenetrating microvascular networks based on fugitive inks and epoxy systems.

Technology Process of Lauryl laurate

There total 34 articles about Lauryl laurate 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: 99.0%

1-dodecyl alcohol (112-53-8) → dodecyl laurate (13945-76-1)

Guidance literature:

With N-Bromosuccinimide; L-proline; In water; at 20 ℃; for 3h;

DOI:10.1080/00397911.2010.521966

Reference yield: 99.0%

lauric acid (143-07-7) + 1-dodecyl alcohol (112-53-8) → dodecyl laurate (13945-76-1)

Guidance literature:

polyaniline sulfate; at 70 ℃; for 24h;

Reference yield: 98.0%

1-dodecyl alcohol (112-53-8) + methyl n-dodecanoate (111-82-0) → dodecyl laurate (13945-76-1)

Guidance literature:

With high p-toluenesulfonate content diphenylamine and terephthalaldehyde resin; In neat (no solvent); at 110 ℃; for 24h;

DOI:10.1080/00304948.2016.1127103

upstream raw materials:

lauric acid

1-dodecyl alcohol

n-dodecanoyl chloride

dimethyl amine

Downstream raw materials:

lauric acid

1-dodecyl alcohol

dodecane

Refernces

• 1、 Liu, Yun,Chen, Dawei,Yan, Yunjun. "Effect of ionic liquids, organic solvents and supercritical CO2 pretreatment on the conformation and catalytic properties of Candida rugosa lipase". . p. 123 - 127. Retrieved 2013.
• 2、 Basheer, Sobhi,Nakajima, Mitsutoshi,Cogan, Uri. "Sugar ester-modified lipase for the esterification of fatty acids and long-chain alcohols". . p. 1475 - 1479. Retrieved 1996.
• 3、 Y?ld?r?m, Ayhan,K?raylar, Kaan. "Efficient greener methodology for the preparation of bio-based phase change materials from lipids". . p. 407 - 413. Retrieved 2020.
• 4、 Kulkarni,Sawant. "Kinetics of the formation of symmetrical wax esters from the corresponding alcohols with the use of hydrobromic acid and hydrogen peroxide". . p. 719 - 723. Retrieved 2001.
• 5、 Toyao, Takashi,Ting, Kah Wei,Siddiki, S. M. A. Hakim,Touchy, Abeda S.,Onodera, Wataru,Maeno, Zen,Ariga-Miwa, Hiroko,Kanda, Yasuharu,Asakura, Kiyotaka,Shimizu, Ken-ichi. "Mechanistic study of the selective hydrogenation of carboxylic acid derivatives over supported rhenium catalysts". . p. 5413 - 5424. Retrieved 2019/10/29.