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TCI

CAS 14104-20-2

Silver Tetrafluoroborate TCI S0446

Silver Tetrafluoroborate TCI S0446

Chemical Identity

Other names
AgBF4
CAS No.
14104-20-2
PubChem
CID 159722·SID 87575928
Formula
AgBF4
Molecular weight
194.68 g/mol
Purity
>98.0%(T)
Reference databases
ChemSpider·ECHA·Wikipedia
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
silver tetrafluoroborate
SMILES
[B-](F)(F)(F)F.[Ag+]
InChIKey
CCAVYRRHZLAMDJ-UHFFFAOYSA-N
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Silver Tetrafluoroborate (AgBF₄) is a chemical compound widely used in laboratory settings for catalytic reactions and C-H activation processes. As a key reagent in inorganic chemistry and catalysis, it plays a crucial role in accelerating chemical reactions without being consumed in the final product. This compound is particularly valuable in applications where metal-based catalysts are required to facilitate complex transformations. Its utility spans across multiple research areas, making it an essential component in modern chemical experimentation.

The stability and controlled reactivity of Silver Tetrafluoroborate make it a preferred choice for researchers. Its ionic structure allows the silver ion (Ag⁺) to act as a reactive center, enabling efficient activation of carbon-hydrogen bonds. The compound is soluble in various organic solvents such as ethyl acetate and dimethyl sulfoxide (DMSO), which enhances its versatility in different experimental setups. These properties ensure consistent performance, making it a reliable material for both academic and industrial research.

In Indonesian laboratories, Silver Tetrafluoroborate is extensively used in both fundamental and applied chemical research. It is commonly found in educational institutions and research centers where it supports a wide range of chemical investigations. Its ability to interact with diverse organic substrates makes it ideal for applications requiring precise control over reaction pathways. This compound is a staple in the chemical toolkit of Indonesian researchers due to its effectiveness and reliability.

TCI brochures (PDF)

  • C-H Activation Reactions: Silver Tetrafluoroborate is ideal for C-H activation due to its ability to facilitate selective bond cleavage in organic substrates.
  • Catalytic Organic Synthesis: The compound serves as an efficient catalyst in various organic transformations, enhancing reaction rates without being consumed.
  • Inorganic Chemistry Research: Its role in metal-based catalysis makes it a valuable tool for exploring inorganic reaction mechanisms and pathways.
  • Solvent Compatibility Studies: The solubility of Silver Tetrafluoroborate in organic solvents allows it to be used in investigations of solvent effects on reaction outcomes.
  • Green Chemistry Applications: Its stability and controlled reactivity make it suitable for developing sustainable and environmentally friendly chemical processes.

From the TCI brochure

  • Step 2 reagent in the Corey-Nicolaou macrolactonization scheme

Brand TCI
CAS number 14104-20-2
Molecular formula —
Purity —
Category Chemistry > Catalysis and Inorganic Chemistry > C-H Activation [Catalysis]
Pack sizes Available in various quantities as per standard laboratory supply options
Physical form Solid powder
Storage Store in a cool, dry place away from moisture and direct sunlight

Silver Tetrafluoroborate should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to moisture, which can affect its performance. The compound is generally non-hazardous under normal conditions but should be handled with care to avoid direct contact with skin or inhalation of dust. In laboratory settings, it is important to ensure proper ventilation when working with this material. Always follow standard safety protocols when handling chemical substances to ensure a safe working environment.

References cited in the TCI brochure

  1. Nadia O. Ilchenko. Mild Silver‐Mediated Geminal Difluorination of Styrenes Using an Air‐ and Moisture‐Stable Fluoroiodane Reagent Angewandte Chemie International Edition, 2014. doi:10.1002/anie.201408812