Benzyl laurate

Base Information

• Chemical Name: Benzyl laurate
• CAS No.: 140-25-0
• Molecular Formula: C19H30 O2
• Molecular Weight: 290.446
• Hs Code.: 2915900090
• European Community (EC) Number: 205-405-8
• NSC Number: 404342
• UNII: HSB3L16SHO
• DSSTox Substance ID: DTXSID7059692
• Nikkaji Number: J34.812K
• Wikidata: Q27280071
• Mol file: 140-25-0.mol

Synonyms:Benzyl laurate;Benzyl dodecanoate;140-25-0;Dodecanoic acid, phenylmethyl ester;Lauric acid, benzyl ester;DODECANOIC ACID, BENZYL ESTER;Lauric Acid Benzyl Ester;Dodecanoic acid,phenylmethyl ester;Phenylmethyl dodecanoate;EINECS 205-405-8;UNII-HSB3L16SHO;HSB3L16SHO;NSC 404342;BRN 2280321;AI3-17966;NSC-404342;4-06-00-02267 (Beilstein Handbook Reference);BENZYLLAURATE;dodecanoic acid benzyl ester;BENZYL LAURATE [INCI];SCHEMBL296362;WLN: 11VO1R;DTXSID7059692;MFCD00026558;NSC404342;AKOS024332341;HY-W129181;BS-49105;LS-63492;CS-0187318;FT-0760024;L0107;D91246;Q27280071

Chemical Property of Benzyl laurate

Chemical Property:

• Vapor Pressure: 7.75E-06mmHg at 25°C
• Melting Point: 9.5 °C
• Refractive Index: 1.4810 to 1.4830
• Boiling Point: 375.5 °C at 760 mmHg
• Flash Point: 109 °C
• PSA: 26.30000
• Density: 0.945 g/cm³
• LogP: 5.65070
• XLogP3: 6.8
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 13
• Exact Mass: 290.224580195
• Heavy Atom Count: 21
• Complexity: 244

Purity/Quality:

98%,99%, ^*data from raw suppliers

Benzyl Laurate >98.0%(GC) ^*data from reagent suppliers

Safty Information:

• Statements: 36/37/38
• Safety Statements: 26-36/37/39

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CCCCCCCCCCCC(=O)OCC1=CC=CC=C1
• Uses: benzyl laurate is an emollient ester that is easily emulsified and leaves the skin feeling silky. It is non-toxic, non-irritating, nonviscous, and non-oily. It also reduces the oiliness of mineral oil and solubilizes sunscreen actives.

Technology Process of Benzyl laurate

There total 17 articles about Benzyl 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%

3-(1-oxododecyl)oxazolidin-2-one (128276-02-8) + benzyl alcohol (100-51-6,185532-71-2) → dimethylenecyclourethane (497-25-6) + benzyl dodecanoate (140-25-0)

Guidance literature:

With samarium diiodide; In tetrahydrofuran; at 20 ℃; for 168h;

DOI:10.1055/s-2008-1072587

Reference yield: 99.0%

(4S)-3-(dodecanoyl)-4-benzyl-2-oxazolidinone (198649-20-6) + benzyl alcohol (100-51-6,185532-71-2) → benzyl dodecanoate (140-25-0) + (S)-4-Benzyl-2-oxazolidinone (90719-32-7)

Guidance literature:

With samarium diiodide; In tetrahydrofuran; at 20 ℃; for 168h;

DOI:10.1055/s-2008-1072587

Reference yield: 99.0%

(S)-N-dodecanoyl-4-isopropyloxazolidinone (153428-19-4) + benzyl alcohol (100-51-6,185532-71-2) → benzyl dodecanoate (140-25-0) + (4S)-4-isopropyl-1,3-oxazolidin-2-one (17016-83-0)

Guidance literature:

With samarium diiodide; In tetrahydrofuran; at 20 ℃; for 16h;

DOI:10.1055/s-2008-1072587

upstream raw materials:

Sodium laurate

benzyl chloride

lauric acid

benzyl alcohol

Downstream raw materials:

((dodecyloxy)methyl)benzene

lauric acid

1-methyl-3-(phenylmethyl)-benzene

1-methyl-4-(phenylmethyl)benzene

Refernces

• 1、 Ho, Wen-Yueh,Lin, Wesley,Lin, Yi-Jyun,Luo, Shun-Yuan,Pantawane, Amit,Su, Po-Fang,Thul, Mayur,Tseng, Shao-An,Wu, Hsin-Ru. "Tunable aryl imidazolium ionic liquids (TAIILs) as environmentally benign catalysts for the esterification of fatty acids to biodiesel fuel". . . Retrieved 2020/12/02.
• 2、 -. "IN VIVO IMMOBILIZATION OF PROTEINS". Paragraph 0110. . Retrieved 2020/11/03.