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TCI

CAS 16427-44-4

2-Methoxyethyl Methanesulfonate TCI M1446

2-Methoxyethyl Methanesulfonate TCI M1446

Chemical Identity

CAS No.
16427-44-4
PubChem
CID 146293·SID 87573391
Formula
C4H10O4S
Molecular weight
154.19 g/mol
Purity
>97.0%(GC)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
2-methoxyethyl methanesulfonate
SMILES
COCCOS(=O)(=O)C
InChIKey
BCKAHDGFNHDQST-UHFFFAOYSA-N
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2-Methoxyethyl Methanesulfonate is a chemical compound widely used as a building block in organic synthesis. It serves as a versatile reagent in laboratory settings, particularly in reactions where methanesulfonate groups are required for substitution or functionalization. Its role in the laboratory is critical for the development of complex molecules, especially in esterification and substitution reactions. This compound is commonly employed in synthetic pathways to introduce specific functional groups into target molecules, making it an essential tool for chemists working on molecular design and modification.

The compound is known for its reactivity and solubility in organic solvents, which makes it a preferred choice for a variety of chemical processes. Its ability to participate in multiple reaction types, such as nucleophilic substitution and esterification, enhances its utility in synthetic chemistry. Additionally, its stability under controlled conditions allows for predictable outcomes in laboratory experiments. These properties make it a reliable and efficient reagent for researchers aiming to achieve high yields and purity in their chemical syntheses.

In Indonesian laboratories, 2-Methoxyethyl Methanesulfonate is extensively used in organic chemistry research. It plays a key role in the synthesis of new compounds, modification of existing molecules, and the development of chemical materials. Its widespread application in both academic and industrial research settings highlights its importance in advancing chemical innovation and scientific discovery within the region.

  • Organic Synthesis: Ideal for creating complex molecules through esterification and substitution reactions.
  • Functional Group Modification: Used to introduce methanesulfonate groups into target compounds for further chemical transformations.
  • Esterification Reactions: Facilitates the formation of ester bonds, essential in the synthesis of various organic compounds.
  • Research and Development: Applied in the development of new chemical materials and pharmaceutical intermediates.
  • Analytical Chemistry: Serves as a reagent in analytical procedures requiring precise chemical interactions and reactions.

Brand TCI
CAS number 16427-44-4
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply formats
Physical form Liquid
Storage Store in a cool, dry place away from direct light and heat

This compound should be stored in a cool, dry place, away from direct light and heat to maintain its stability and reactivity. It is recommended to use sealed containers made of materials compatible with organic solvents to prevent contamination and evaporation. Due to its reactive nature, it should be handled with appropriate personal protective equipment, including gloves and safety goggles. Proper ventilation is essential when working with this compound to minimize exposure. It is important to avoid contact with incompatible substances and to follow standard laboratory safety protocols to ensure safe handling and use.

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