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TCI

CAS 26042-64-8

Silver Hexafluoroantimonate(V) TCI S0463

Silver Hexafluoroantimonate(V) TCI S0463

Chemical Identity

Other names
AgSbF6
CAS No.
26042-64-8
PubChem
CID 16687962·SID 87575944
Formula
AgF6Sb
Molecular weight
343.619 g/mol
Purity
>97.0%(T)
Reference databases
ChemSpider·ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
silver hexafluoroantimony(1-)
SMILES
F[Sb-](F)(F)(F)(F)F.[Ag+]
InChIKey
GSXFODUDOAXUBF-UHFFFAOYSA-H
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Silver Hexafluoroantimonate(V) is a chemical compound widely used in laboratory settings for catalytic reactions and C-H activation processes. As a key reagent in inorganic chemistry, it plays a crucial role in facilitating chemical transformations without altering the core structure of the target molecules. Its application spans across various research fields, particularly in organic chemistry, where it is employed to enhance reaction efficiency and selectivity. This compound is especially valuable in experiments requiring precise control over reaction pathways and minimal side reactions.

The compound's strong catalytic properties and stability under specific conditions make it a preferred choice for researchers. It exhibits a complex molecular structure that enables strong interactions with target molecules, promoting efficient activation of carbon-hydrogen bonds. Its stability during reactions minimizes degradation or unwanted side reactions, ensuring consistent and reliable results. These characteristics make it an essential tool in modern chemical research, particularly in catalysis and organic synthesis.

In Indonesian laboratories, Silver Hexafluoroantimonate(V) is commonly used in chemical research, especially in catalytic and organic reaction studies. It is a key component in experiments aimed at improving reaction efficiency and selectivity. Its reliability and performance have made it a popular choice among researchers in both academic and industrial settings, contributing to the advancement of chemical sciences in the region.

TCI brochures (PDF)

  • C-H Activation Reactions: This compound is ideal for C-H activation due to its strong catalytic properties and ability to interact effectively with target molecules.
  • Organic Synthesis Processes: It is widely used in organic synthesis to enhance reaction efficiency and control reaction pathways with minimal side reactions.
  • Catalytic Research Studies: Its stability and catalytic activity make it a preferred choice for studies involving complex catalytic mechanisms and reaction conditions.
  • Industrial Chemical Processes: It is applied in industrial settings where efficient and selective catalytic reactions are required for large-scale chemical production.
  • Analytical Chemistry Applications: Its unique properties allow it to be used in analytical methods where precise and consistent results are essential.

From the TCI brochure

  • Co-catalyst in oxidative annulation and olefination of anilides (cat. AgSbF6)

Brand TCI
CAS number 26042-64-8
Molecular formula —
Purity —
Category Chemistry > Catalysis and Inorganic Chemistry > C-H Activation [Catalysis]
Pack sizes —
Physical form —
Storage Store in a cool, dry place away from moisture and direct sunlight

Silver Hexafluoroantimonate(V) should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to keep the compound in a sealed container to avoid exposure to moisture and air, which could affect its performance. Suitable storage conditions include a controlled temperature range, typically between 15°C and 25°C, to ensure long-term stability. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure that the compound is stored away from incompatible materials to prevent any potential chemical reactions. Proper labeling and storage practices are essential to maintain the integrity and safety of the compound in the laboratory setting.

References cited in the TCI brochure

  1. Yu Shibata. Catalytic [2+2+1] Cross‐Cyclotrimerization of Silylacetylenes and Two Alkynyl Esters To Produce Substituted Silylfulvenes Angewandte Chemie International Edition, 2011. doi:10.1002/anie.201105517
  2. Yuki Hoshino. Oxidative Annulation of Anilides with Internal Alkynes Using an (Electron‐Deficient η5‐Cyclopentadienyl)Rhodium(III) Catalyst Under Ambient Conditions Advanced Synthesis & Catalysis, 2014. doi:10.1002/adsc.201300884
  3. Yuji Takahama. Oxidative Olefination of Anilides with Unactivated Alkenes Catalyzed by an (Electron‐Deficient η5‐Cyclopentadienyl)Rhodium(III) Complex Under Ambient Conditions Chemistry – A European Journal, 2015. doi:10.1002/chem.201501232