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Triphenylsulfonium chloride
[CAS# 4270-70-6]

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Identification
Classification Organic raw materials >> Aryl compounds
Name Triphenylsulfonium chloride
Molecular Structure CAS # 4270-70-6, Triphenylsulfonium chloride
Molecular Formula C18H15ClS
Molecular Weight 298.83
CAS Registry Number 4270-70-6
EC Number 224-259-6
SMILES C1=CC=C(C=C1)[S+](C2=CC=CC=C2)C3=CC=CC=C3.[Cl-]
Safety Data
Hazard Symbols symbol   GHS07 Warning    Details
Hazard Statements H315-H319-H335    Details
Precautionary Statements P261-P264-P264+P265-P271-P280-P302+P352-P304+P340-P305+P351+P338-P319-P321-P332+P317-P337+P317-P362+P364-P403+P233-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Eye irritationEye Irrit.2H319
Skin irritationSkin Irrit.2H315
Specific target organ toxicity - single exposureSTOT SE3H335
SDS Available
up Discovory and Applicatios
Triphenylsulfonium chloride is a chemical compound widely recognized for its utility in the field of organic chemistry, particularly in photochemistry and as a photoinitiator in polymerization processes. This compound, denoted as Ph₃SCl, features a sulfonium ion where three phenyl groups are attached to a sulfur atom, with a chloride ion as the counterion.

The discovery of triphenylsulfonium chloride dates back to the mid-20th century, with its synthesis involving the reaction of triphenylsulfonium salts with various halogenating agents. The introduction of triphenylsulfonium chloride into the chemical literature provided a new tool for researchers exploring photochemical reactions and polymerization techniques. Its distinctive structure, featuring a sulfonium center surrounded by phenyl groups, imparts unique properties to the compound that are valuable in various chemical processes.

In practical applications, triphenylsulfonium chloride is primarily used as a photoinitiator in polymer chemistry. Photoinitiators are substances that initiate polymerization reactions upon exposure to light. Triphenylsulfonium chloride, upon irradiation with ultraviolet (UV) light, generates reactive species that can start the polymerization of monomers, leading to the formation of polymers. This property is particularly useful in the production of photoresists and coatings, where precise control over the polymerization process is required.

Additionally, triphenylsulfonium chloride finds application in the field of photochemistry as a reagent for generating sulfur-based radicals. These radicals can participate in various chemical reactions, making triphenylsulfonium chloride a valuable compound for studying reaction mechanisms and developing new synthetic pathways. The compound's ability to generate reactive intermediates under UV light conditions is exploited in the synthesis of complex organic molecules and materials.

Another notable application of triphenylsulfonium chloride is in the production of advanced materials such as electronic and optical devices. Its role as a photoinitiator is crucial in the development of materials with specific properties, including those used in high-resolution printing and microfabrication technologies.

Overall, triphenylsulfonium chloride has established itself as an important compound in both academic research and industrial applications. Its unique properties as a photoinitiator and radical generator make it a versatile tool in the synthesis of organic compounds and materials, contributing to advancements in various fields of chemistry and materials science.
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