1-Methyl-1H-benzimidazol-3-ium Trifluoromethanesulfonate TCI M3384

Chemical Identity

Other names: N-MeBIT
CAS No.: 361447-89-4
PubChem: CID 164186535·SID 468592437
Formula: C9H9F3N2O3S
Molecular weight: 282.24 g/mol
Purity: >98.0%(HPLC)(T)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 3-methyl-1H-benzimidazol-3-ium;trifluoromethanesulfonate
SMILES: C[N+]1=CNC2=CC=CC=C21.C(F)(F)(F)S(=O)(=O)[O-]
InChIKey: SLCPRHIKNIDSJJ-UHFFFAOYSA-N

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1-Methyl-1H-benzimidazol-3-ium Trifluoromethanesulfonate is a chemical compound widely used in laboratory settings for its unique chemical properties and versatility in various biochemical applications. This compound is particularly valuable in nucleic acid chemistry, where it plays a crucial role in DNA and RNA modification processes. Its ability to participate in ionization reactions makes it an essential reagent for molecular biology experiments. As a key component in chemical synthesis, it supports the development of new compounds and the refinement of existing ones.

The compound’s polar nature and high reactivity make it a preferred choice for researchers seeking reliable and efficient chemical reactions. Its stability under controlled laboratory conditions ensures consistent results, which is vital in scientific research. The compound’s ability to interact with a wide range of substrates and reagents enhances its applicability in diverse chemical processes. Additionally, its solubility in organic solvents simplifies its handling and use in various experimental setups.

In Indonesian laboratories, this compound is commonly used in research focused on nucleic acid chemistry. It is often employed in the preparation of modified nucleotides and in the study of molecular interactions. Its stability and reactivity make it a go-to choice for scientists working in biochemistry and chemical biology. The compound’s role in supporting precise and reproducible experiments is critical in maintaining the integrity of scientific research.

TCI brochures (PDF)

Coupling Activators for Oligonucleotide Synthesis 2025-06-30 · p. 1
Oligonucleotide Synthesis Reagents 2025-07-24 · p. 1
Nucleosides, Nucleotides, Nucleic Acids and Related Reagents 2026-03-23 · p. 15

Related TCI products

Nucleic Acid Modification: This compound is ideal for modifying DNA and RNA molecules, enabling the study of genetic material in various biological processes.
Ionization Reactions: Its ability to act as an ionizing agent makes it suitable for chemical reactions requiring active ionization, enhancing reaction efficiency.
Molecular Biology Research: It supports research in molecular biology by facilitating the synthesis and analysis of nucleic acid structures.
Chemical Synthesis: The compound is used in the synthesis of complex organic molecules, contributing to the development of new chemical compounds.
Biochemical Assays: Its reactivity and stability make it a valuable reagent in biochemical assays that require precise chemical interactions.

Brand	TCI
CAS number	361447-89-4
Molecular formula	—
Purity	—
Category	Chemistry > Chemical Biology > Nucleic Acid Chemistry
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid or powder, depending on the specific product variant
Storage	Store in a cool, dry place away from moisture and direct sunlight

This compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a sealed container to prevent exposure to moisture and air. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid contact with incompatible substances to ensure safe laboratory practices. Proper ventilation is essential when working with this compound to minimize exposure risks. Always follow standard laboratory safety protocols to ensure a secure working environment.

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