Sodium tetrafluoroborate, >98%
$55.50 – $211.50Price range: $55.50 through $211.50
Product Code: KI-0025-HPCAS NO: 13755-29-8
- Chemical Formula: BF4Na
- Synonyms: Na BF4, sodium fluoroborate
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Category: Metal Salts
SUM Formula: BF4Na
Molecular Weight: 109.79
Purity: >98%
- SUM Formula: BF4Na
- Molecular Weight: 109.79
Sodium tetrafluoroborate, CAS: 13755-29-8
Key Application:
Electrolytes and Energy Storage
- Serves as a precursor for synthesizing tetrafluoroborateโbased salts used in nonโaqueous electrolytes.
- Supports development of ionicโliquid and moltenโsalt electrolyte systems for highโvoltage batteries and electrochemical devices.
- Utilized in research on fluoroborateโstabilized electrolyte additives that enhance conductivity and thermal stability.
Catalysis and Organic Synthesis
- Functions as a fluoroborate source in the preparation of BFโโป salts of organometallic and organic cations.
- Applied in phaseโtransfer and Lewisโacidโmediated transformations where BFโโป provides a weakly coordinating counterion.
- Enables synthesis of ionic liquids, quaternary ammonium salts, and pyridinium/imidazolium derivatives.
Materials Science and Inorganic Chemistry
- Used in the formation of metal tetrafluoroborates for coordination chemistry, thinโfilm precursors, and advanced materials research.
- Supports development of fluoroborateโbased ceramics, glasses, and specialty inorganic materials requiring controlled fluorine incorporation.
Analytical Chemistry
- Employed as a reagent for generating BFโโป complexes in spectroscopic and electroanalytical studies.
- Useful for calibrating or validating methods involving fluoroborate detection or counterion exchange.
Industrial and Process Chemistry
- Acts as a fluorinating agent or fluorine donor in selected inorganic synthesis routes.
- Utilized in salt metathesis processes to introduce the BFโโป anion into target compounds with high purity.
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Demirci, S., Suner, S. S., Yildiz, M., & Sahiner, N. (2022). Polymeric ionic liquid forms of PEI microgels as catalysts for hydrogen production via sodium borohydride methanolysis. Journal of Molecular Liquids, 360, 119562.
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