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Catalog Number:
12814
CAS Number:
5188-07-8
Solución de metanotiolato de sodio (15 % en peso en agua)
Purity:
14,5-16,5% en agua
Synonym(s):
Sal sódica de metilmercaptano
Hazmat
Documents
$18.53 /25G
Tamaño
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Product Information

Nucleófilo fuerte utilizado para la síntesis de sulfuros de metilarilo a partir de haloarenos.

Synonyms
Sal sódica de metilmercaptano
CAS Number
5188-07-8
Purity
14,5-16,5% en agua
Molecular Formula
CH3NaS
Molecular Weight
70.09
MDL Number
MFCD00174316
PubChem ID
4378561
Density
1.08
Appearance
Líquido transparente e incoloro
Conditions
Tienda en RT
General Information
Synonyms
Sal sódica de metilmercaptano
CAS Number
5188-07-8
Purity
14,5-16,5% en agua
Molecular Formula
CH3NaS
Molecular Weight
70.09
MDL Number
MFCD00174316
PubChem ID
4378561
Density
1.08
Appearance
Líquido transparente e incoloro
Conditions
Tienda en RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Sodium methanethiolate solution (15 wt % in water) is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a powerful nucleophile in various organic reactions, enabling the formation of carbon-sulfur bonds. It is particularly useful in synthesizing thiols and thioethers, which are essential in pharmaceuticals and agrochemicals.
  • Analytical Chemistry: It is employed in the detection and quantification of metal ions, as it forms stable complexes with heavy metals. This application is crucial in environmental monitoring and waste management.
  • Material Science: Sodium methanethiolate is used in the production of advanced materials, including polymers and coatings, enhancing their properties such as durability and resistance to corrosion.
  • Biochemistry: Researchers utilize this solution in biochemical assays to study enzyme activity and protein interactions, particularly in the context of sulfur-containing compounds.
  • Pharmaceutical Development: It plays a role in drug formulation and development, particularly in the synthesis of active pharmaceutical ingredients (APIs) that require thiol functionalities for their biological activity.

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