≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Product Application：
Tetrapropylammonium tetrafluoroborate (Pr4NBF4 or TPABF4) can be used as:An electrolyte in the determination of phenolic compounds from grape seed extracts by capillary electrophoretic method. A supporting electrolyte in the electrochemical hydrogenation of dimethylformamide (DMF) to trimethylamine (TMA).
| Pubchem Sid | 504751843 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504751843 |
| Canonical Smiles | [B-](F)(F)(F)F.CCC[N+](CCC)(CCC)CCC |
| IUPAC Name | tetrapropylazanium;tetrafluoroborate |
| InChIKey | ADADJCUTHQJPCB-UHFFFAOYSA-N |
| INCHI | 1S/C12H28N.BF4/c1-5-9-13(10-6-2,11-7-3)12-8-4;2-1(3,4)5/h5-12H2,1-4H3;/q+1;-1 |
| Isomeric SMILES | [B-](F)(F)(F)F.CCC[N+](CCC)(CCC)CCC |
| WGK Germany | 3 |
| RTECS | BS8420000 |
| PubChem CID | 9558 |
| Molecular Weight | 273.16 |
| Beilstein | 3637590 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic nitrogen compounds |
| Class | Organonitrogen compounds |
| Subclass | Quaternary ammonium salts |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Tetraalkylammonium salts |
| Alternative Parents | Organic metalloid salts Organopnictogen compounds Hydrocarbon derivatives Amines |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Tetraalkylammonium salt - Organic metalloid salt - Organopnictogen compound - Hydrocarbon derivative - Organic salt - Amine - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as tetraalkylammonium salts. These are organonitrogen compounds containing a quaternary ammonium substituted with four alkyl chains. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
 I2226178 | Certificate of Analysis | Jul 10, 2025 | T169686 |
| I2226179 | Certificate of Analysis | Jul 10, 2025 | T169686 |
| K2113399 | Certificate of Analysis | Aug 22, 2024 | T169686 |
| K2115409 | Certificate of Analysis | Aug 22, 2024 | T169686 |
| K2115419 | Certificate of Analysis | Aug 22, 2024 | T169686 |
| Melt Point(°C) | 245-247 °C |
|---|---|
| Molecular Weight | 273.160 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 8 |
| Exact Mass | 273.225 Da |
| Monoisotopic Mass | 273.225 Da |
| Topological Polar Surface Area | 0.000 Ų |
| Heavy Atom Count | 18 |
| Formal Charge | 0 |
| Complexity | 99.300 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 2 |
