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Catalog Number:
31288
CAS Number:
7403-46-5
2-Chloro-1-methylpyridinium p-toluenesulfonate
Purity:
≥ 98% (HPLC)
Documents
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Product Information

2-Chloro-1-methylpyridinium p-toluenesulfonate is a versatile chemical compound widely utilized in organic synthesis and various industrial applications. This compound serves as an effective reagent for the chlorination of aromatic compounds, making it invaluable in the development of pharmaceuticals and agrochemicals. Its unique structure allows for selective reactions, enhancing the efficiency of synthetic pathways. Researchers appreciate its stability and solubility in polar solvents, which facilitates its use in diverse chemical reactions, including nucleophilic substitutions and coupling reactions.

Moreover, 2-Chloro-1-methylpyridinium p-toluenesulfonate is recognized for its role in facilitating the formation of complex organic molecules, thereby streamlining the synthesis process in laboratories. Its application extends to the production of dyes and pigments, where it contributes to the development of vibrant colors with excellent fastness properties. With its ability to enhance reaction rates and yields, this compound is a preferred choice for professionals seeking reliable and efficient solutions in their chemical processes.

CAS Number
7403-46-5
Purity
≥ 98% (HPLC)
Molecular Formula
C7H7O3S·C6H7ClN
Molecular Weight
299.77
MDL Number
MFCD00011985
PubChem ID
10990220
Melting Point
121-126 ?C
Appearance
White to off-white crystalline powder
Conditions
Store at ≤ -4 °C
General Information
CAS Number
7403-46-5
Purity
≥ 98% (HPLC)
Molecular Formula
C7H7O3S·C6H7ClN
Molecular Weight
299.77
MDL Number
MFCD00011985
PubChem ID
10990220
Melting Point
121-126 ?C
Appearance
White to off-white crystalline powder
Conditions
Store at ≤ -4 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-Chloro-1-methylpyridinium p-toluenesulfonate is widely utilized in research focused on:

  • Synthesis of Quaternary Ammonium Compounds: This chemical serves as an effective reagent in the synthesis of various quaternary ammonium compounds, which are important in pharmaceuticals and surfactants.
  • Organic Synthesis: It is commonly used in organic synthesis reactions, particularly in the formation of carbon-nitrogen bonds, making it valuable for researchers developing new organic molecules.
  • Electrophilic Aromatic Substitution: The compound acts as an electrophile in aromatic substitution reactions, facilitating the introduction of functional groups into aromatic systems, which is crucial in the development of dyes and agrochemicals.
  • Biological Research: It is employed in studies related to enzyme inhibition and receptor binding, providing insights into drug design and development in the pharmaceutical industry.
  • Polymer Chemistry: This chemical is used in the modification of polymers, enhancing their properties for applications in coatings, adhesives, and materials science.

Citations