Diphosphoric acid, tetrabutyl ester

Base Information

Chemical Name:Diphosphoric acid, tetrabutyl ester
CAS No.:1474-75-5
Molecular Formula:C16H36 O7 P2
Molecular Weight:402.405
Hs Code.:
NSC Number:70159
UNII:WB3SBT7MYX
DSSTox Substance ID:DTXSID2074534
Nikkaji Number:J1.549.952D
Wikidata:Q82002849
Mol file:1474-75-5.mol

Synonyms:Diphosphoric acid, tetrabutyl ester;Butyl pyrophosphate;1474-75-5;dibutyl dibutoxyphosphoryl phosphate;Tetrabutyl pyrophosphate;Pyrophosphoric acid, Tetrabutyl ester;WB3SBT7MYX;NSC 70159;BRN 1716363;Diphosphoric acid,tetrabutyl ester (9CI);NSC70159;NSC-70159;4-01-00-01533 (Beilstein Handbook Reference);Tetrabutylpyrophosphat;Tetrabutyl diphosphate;tetrabutylpyrophosphate;UNII-WB3SBT7MYX;SCHEMBL379134;DTXSID2074534;Diphosphoric acid tetrabutyl ester;LS-136498;P,P,P',P'-TETRABUTYL (DIPHOSPHATE);DIPHOSPHORIC ACID, P,P,P',P'-TETRABUTYL ESTER

Suppliers and Price of Diphosphoric acid, tetrabutyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 10 raw suppliers

Chemical Property of Diphosphoric acid, tetrabutyl ester

Chemical Property:

Vapor Pressure:5.26E-06mmHg at 25°C
Boiling Point:392.2°C at 760 mmHg
Flash Point:204.5°C
Density:1.079g/cm³
XLogP3:4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:18
Exact Mass:402.19362748
Heavy Atom Count:25
Complexity:340

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Chemical Classes:Pesticides -> Organophosphate Insecticides
Canonical SMILES:CCCCOP(=O)(OCCCC)OP(=O)(OCCCC)OCCCC

Technology Process of Diphosphoric acid, tetrabutyl ester

There total 3 articles about Diphosphoric acid, tetrabutyl 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: 51.0%

: 71-36-3
butan-1-ol

: 126-73-8
phosphoric acid tributyl ester

: 1474-75-5
n-butyl pyrophosphate

Guidance literature:: With tetraethylammonium iodide; water; In acetonitrile; at 55 ℃; electrosynthesis;
DOI:10.1007/BF00863576

Reference yield: 50.0%

: 2244-27-1
sodium dibutyl phosphite

: 1809-19-4
dibutyl hydrogen phosphite

: 54305-86-1
diphosphorous acid tetrabutyl ester

: 1474-75-5
n-butyl pyrophosphate

: 682-23-5
O,O'-dibutyl-phosphoric O,O'-dibutyl-phosphorous anhydride

: 16298-74-1
sodium salt of dibutyl phosphate

Guidance literature:: With sodium perchlorate; In acetonitrile; Product distribution; Ambient temperature; object of study - electrochemical oxidation at platinum electrode;

Reference yield:

: 109-47-7
dibutyl hydrogen phosphite

: 102-85-2
tri-n-butyl phosphite

: 54305-86-1
diphosphorous acid tetrabutyl ester

: 1474-75-5
n-butyl pyrophosphate

: 682-23-5
O,O'-dibutyl-phosphoric O,O'-dibutyl-phosphorous anhydride

Guidance literature:: With sodium perchlorate; In acetonitrile; Title compound not separated from byproducts; electrochemical oxidation, 2.4 A h; Pt anode, Ni cathode; Ag/AgNO₃ reference electrode;