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TCI

CAS 2188151-68-8

Sodium Pyrimidine-2-sulfinate TCI O0541

Sodium Pyrimidine-2-sulfinate TCI O0541

Chemical Identity

CAS No.
2188151-68-8
Formula
C4H3N2NaO2S
Molecular weight
166.14 g/mol
Purity
>97.0%(T)(HPLC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
sodium pyrimidine-2-sulfinate
SMILES
C1=CN=C(N=C1)S(=O)[O-].[Na+]
InChIKey
YFKHXLGPONXLRC-UHFFFAOYSA-M
PubChem
CID 139269667
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Sodium Pyrimidine-2-sulfinate is a chemical compound widely used in laboratory settings as a building block for the synthesis of heterocyclic compounds. Its core structure is based on pyrimidine, modified with a sulfonate group, which enhances its reactivity in various chemical reactions. This compound plays a vital role in organic chemistry by enabling the formation of complex molecular structures necessary for advanced research. Its versatility makes it an essential tool for scientists working in diverse fields such as pharmacology and materials science.

The compound is valued for its chemical stability under controlled conditions and its solubility in polar solvents like water and acetone. These properties make it ideal for purification and separation processes in the laboratory. Sodium Pyrimidine-2-sulfinate is also highly reactive, allowing it to participate in substitution, condensation, and bond-forming reactions without significant degradation. Its ability to maintain chemical integrity during reactions ensures reliable results in experimental studies.

In Indonesian laboratories, Sodium Pyrimidine-2-sulfinate is commonly used in the development of bioactive compounds, drug synthesis, and the creation of novel organic materials. Its availability and chemical properties make it a preferred choice for researchers seeking to explore new synthetic pathways and molecular structures. This compound is a key component in many research projects aimed at advancing scientific knowledge and innovation.

  • Bioactive compound synthesis: Sodium Pyrimidine-2-sulfinate is ideal for creating compounds with biological activity due to its reactivity and structural versatility.
  • Drug development: Its ability to participate in various chemical reactions makes it useful in the synthesis of pharmaceutical compounds and medicinal agents.
  • Organic material synthesis: The compound is used to build complex molecular structures necessary for the development of advanced organic materials.
  • Heterocyclic compound research: Its pyrimidine core allows it to be a fundamental building block in the study of heterocyclic chemistry and related fields.
  • Analytical chemistry applications: Its solubility and reactivity make it suitable for use in analytical procedures requiring precise chemical interactions.

Brand TCI
CAS number 2188151-68-8
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes —
Physical form —
Storage Store in a cool, dry place away from moisture and oxidizing agents

Sodium Pyrimidine-2-sulfinate should be stored in a cool, dry environment to prevent moisture exposure and degradation. It is recommended to use airtight containers to minimize contact with air and potential oxidizing agents. Due to its sensitivity, it should be handled in a well-ventilated laboratory setting to ensure safety. Avoid prolonged exposure to light and maintain a controlled temperature to preserve its chemical integrity. Proper labeling and storage practices are essential to ensure safe handling and prevent contamination. Always follow standard laboratory safety protocols when working with this compound.

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