Nickel(II) p-Toluenesulfonate Hexahydrate TCI T0276

Chemical Identity

CAS No.: 6944-05-4
PubChem: CID 13577672·SID 87576254
Formula: C14H14NiO6S2
Molecular weight: 401.1 g/mol
Purity: >98.0%(T)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: bis(4-methylbenzenesulfonate);nickel(2+)
SMILES: CC1=CC=C(C=C1)S(=O)(=O)[O-].CC1=CC=C(C=C1)S(=O)(=O)[O-].[Ni+2]
InChIKey: IDYLMOYUCOPIRT-UHFFFAOYSA-L

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Nickel(II) p-Toluenesulfonate Hexahydrate is a chemical compound widely used in catalytic reactions and C-H activation processes within laboratory settings. As a key reagent in inorganic and organic chemistry, it plays a vital role in facilitating complex chemical transformations. Its unique structure allows for effective interaction with various organic substrates, making it a valuable component in synthetic pathways. This compound is commonly utilized in research focused on the development of new catalytic systems and the exploration of reaction mechanisms. Its versatility and reactivity make it an essential tool for chemists working in both academic and industrial environments.

The compound is known for its stability under controlled conditions, which ensures reliable performance in laboratory experiments. It exhibits good solubility in organic solvents such as ethyl acetate and acetone, which simplifies its handling and application in solution-based reactions. Its crystalline structure also aids in identification and purification processes, enhancing its usability in analytical and preparative applications. These properties collectively contribute to its popularity among researchers seeking efficient and effective catalytic agents.

In Indonesian laboratories, Nickel(II) p-Toluenesulfonate Hexahydrate is frequently used in studies related to C-H activation and catalytic substitution reactions. Its application spans across various research fields, including organic synthesis and catalysis. The compound is particularly favored for its ability to support the synthesis of complex molecules, making it an essential reagent in modern chemical research. Its availability and performance make it a preferred choice for both academic and industrial chemical processes.

TCI brochures (PDF)

C-H Bond Activation Reaction 2025-06-20 · p. 6
Transition Metal Catalysts 2026-04-10 · p. 12

Related TCI products

C-H Activation Studies – This compound is ideal for investigating C-H bond activation due to its ability to facilitate selective transformations in organic substrates.
Catalytic Substitution Reactions – Its catalytic properties make it suitable for promoting substitution reactions in synthetic pathways.
Oxidation Reactions – It is commonly used in oxidation processes where controlled redox conditions are required for efficient reaction outcomes.
Organic Synthesis – Its reactivity and solubility make it a preferred reagent in the synthesis of complex organic molecules.
Crystal Structure Analysis – The compound’s clear crystalline form aids in spectroscopic and structural analysis techniques used in laboratory research.

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Brand – TCI
CAS Number – 6944-05-4
Category – Chemistry > Catalysis and Inorganic Chemistry > C-H Activation [Catalysis]
Pack Sizes – Available in various quantities to suit different laboratory needs
Physical Form – Crystalline solid
Storage Note – Requires protection from moisture and oxidation

Nickel(II) p-Toluenesulfonate Hexahydrate should be stored in a cool, dry place away from moisture and strong oxidizing agents. It is recommended to keep the compound in airtight containers to prevent exposure to humidity, which can lead to degradation. Laboratory personnel should handle the material with care, using appropriate personal protective equipment such as gloves and safety goggles. Due to its sensitivity to oxidation, it should be stored in a controlled environment to maintain its chemical integrity. Regular monitoring of storage conditions is essential to ensure the compound remains suitable for use in experimental procedures. Proper labeling and storage practices help minimize risks and ensure safe handling in laboratory settings.

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