Tripentyl borate

Base Information

• Chemical Name: Tripentyl borate
• CAS No.: 621-78-3
• Molecular Formula: C15H33 B O3
• Molecular Weight: 272.236
• Hs Code.: 2920909090
• European Community (EC) Number: 210-706-2
• NSC Number: 780
• UNII: XW9Q7KC9DH
• DSSTox Substance ID: DTXSID9060738
• Nikkaji Number: J42.797G
• Wikidata: Q81989179
• Mol file: 621-78-3.mol

Synonyms:Tripentyl borate;tri-n-Amylborate;Triamyl borate;621-78-3;Tri-n-amyl borate;Tri-n-pentyl borate;Boric acid (H3BO3), tripentyl ester;Boric acid, tri-n-amyl ester;Tripentyl borate ((C5H11O)3B);Pentyl borate, (C5H11O)3B;(tri-n-Pentoxy)borane;BORIC ACID, TRI-n-PENTYL ESTER;Pentyl borate;NSC 780;Boric acid, tripentyl ester;EINECS 210-706-2;XW9Q7KC9DH;BRN 1706686;AI3-51862;NSC780;Pentyl borate, (C5H11O)3 B;NSC-780;Tripentyl=borate;UNII-XW9Q7KC9DH;boric acid tripentyl ester;Pentyl borate (6CI,7CI);SCHEMBL171017;WLN: 5OBO5&O5;DTXSID9060738;C15H33BO3;MFCD00027261;AKOS024333427;LS-45044;FT-0632606

Chemical Property of Tripentyl borate

Chemical Property:

• Vapor Pressure: 0.00882mmHg at 25°C
• Melting Point: 180°C (dec.)
• Refractive Index: 1.4200
• Boiling Point: 63°C 0mm
• Flash Point: 83°C
• PSA: 27.69000
• Density: 0.858g/cm³
• LogP: 4.59170
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 15
• Exact Mass: 272.2522751
• Heavy Atom Count: 19
• Complexity: 139

Purity/Quality:

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

TRIPENTYL BORATE Aldrich ^*data from reagent suppliers

Safty Information:

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

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: B(OCCCCC)(OCCCCC)OCCCCC

Technology Process of Tripentyl borate

There total 3 articles about Tripentyl borate 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:

triamyl arsenite (15606-93-6) + boron trifluoride diethyl etherate (109-63-7) → tri-n-amylborate (621-78-3) + arsenic(III) fluoride (7784-35-2)

Guidance literature:

In neat (no solvent); byproducts: (C2H5)2O; heating equimolar mixt. of BF3*(C2H5)2O and (C5H11O)3As;;

Reference yield:

pentan-1-ol (71-41-0) → tri-n-amylborate (621-78-3)

Guidance literature:

With boric acid;

DOI:10.1021/ja01228a024

Reference yield:

→ tri-n-amylborate (621-78-3)

Guidance literature:

Diboran, Tetrahydropyran;

upstream raw materials:

pentan-1-ol

triamyl arsenite

boron trifluoride diethyl etherate

Downstream raw materials:

Borsaeure-pentylester-dichlorid

pentan-1-ol

Refernces