Boric acid, tridodecyl ester

Base Information

• Chemical Name: Boric acid, tridodecyl ester
• CAS No.: 2467-15-4
• Molecular Formula: C36H75 B O3
• Molecular Weight: 566.801
• Hs Code.: 2920909090
• European Community (EC) Number: 219-582-4
• NSC Number: 785
• UNII: N3A3W3S7VW
• DSSTox Substance ID: DTXSID80179405
• Nikkaji Number: J42.799C
• Wikidata: Q83049939
• Mol file: 2467-15-4.mol

Synonyms:Tridodecyl borate;2467-15-4;Dodecyl borate;Lauryl borate;BORIC ACID, TRIDODECYL ESTER;Tri-n-dodecyl borate;Boric acid (H3BO3), tridodecyl ester;Dodecyl borate, (C12H25O)3 B;NSC 785;EINECS 219-582-4;BRN 1716459;N3A3W3S7VW;Boric acid (H3BO3), O,O,O-tridodecyl ester;NSC-785;4-01-00-01850 (Beilstein Handbook Reference);Boric acid tridodecyl ester;UNII-N3A3W3S7VW;SCHEMBL50779;NSC785;C36H75BO3;DTXSID80179405;Dodecyl borate, (C12H25O)3B;C36-H75-B-O3;DODECYL BORATE (C12H25O)3B;LS-45036;Boric acid (H3BO3), tridodecyl ester (8CI)

Chemical Property of Boric acid, tridodecyl ester

Chemical Property:

• Vapor Pressure: 3.55E-10mmHg at 25°C
• Refractive Index: 1.4470 (20℃)
• Boiling Point: 514.2°C at 760 mmHg
• Flash Point: 238.1°C
• PSA: 27.69000
• Density: 0.853g/cm³
• LogP: 12.78380
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 36
• Exact Mass: 566.5809264
• Heavy Atom Count: 40
• Complexity: 373

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: B(OCCCCCCCCCCCC)(OCCCCCCCCCCCC)OCCCCCCCCCCCC

Technology Process of Boric acid, tridodecyl ester

There total 3 articles about Boric acid, tridodecyl ester 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:

1-dodecyl alcohol (112-53-8) + boric acid (11113-50-1,14635-83-7) → tris(dodecyloxy)borane (2467-15-4)

Guidance literature:

In toluene; at 130 ℃; Dean-Stark;

Reference yield:

1-dodecyl alcohol (112-53-8) → tris(dodecyloxy)borane (2467-15-4)

Guidance literature:

With boric acid; toluene; unter Entfernen des entstehenden Wassers;

DOI:10.1021/ie50566a023

Reference yield:

→ tris(dodecyloxy)borane (2467-15-4)

Guidance literature:

BH3*S(CH3)2, CH3(CH2)10CH2OH;

DOI:10.1021/jo00407a051

upstream raw materials:

1-dodecyl alcohol

boric acid

Downstream raw materials:

sodium dodecyl-sulfate

n-dodecyl sulfate

1-dodecyl alcohol

boric acid

Refernces

• 1、 Gunes, Deniz,Sirkecioglu, Okan,Bicak, Niyazi. "Aliphatic thioethers by s-alkylation of thiols via trialkyl borates". body text. p. 1685 - 1690. Retrieved 2010/09/17.