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Atomfair Methylethylenethiourea C4H8N2S
Description Methylethylenethiourea (CAS No. 13431-10-2) is a high-purity organic compound with the molecular formula C4H8N2S , widely utilized in chemical research and industrial applications. Known by its IUPAC name 1-methylimidazolidine-2-thione , this thiourea derivative exhibits excellent stability and reactivity, making it a valuable reagent in synthetic chemistry. Its crystalline form ensures consistent performance in reactions involving sulfur-containing intermediates. Suitable for laboratory and bulk-scale use, our Methylethylenethiourea is rigorously tested for purity, ensuring optimal results in your experiments. Store in a cool, dry place away from oxidizing agents to maintain integrity.
Description
Description
Methylethylenethiourea (CAS No. 13431-10-2) is a high-purity organic compound with the molecular formula C4H8N2S, widely utilized in chemical research and industrial applications. Known by its IUPAC name 1-methylimidazolidine-2-thione, this thiourea derivative exhibits excellent stability and reactivity, making it a valuable reagent in synthetic chemistry. Its crystalline form ensures consistent performance in reactions involving sulfur-containing intermediates. Suitable for laboratory and bulk-scale use, our Methylethylenethiourea is rigorously tested for purity, ensuring optimal results in your experiments. Store in a cool, dry place away from oxidizing agents to maintain integrity.
- CAS No: 13431-10-2
- Molecular Formula: C4H8N2S
- Molecular Weight: 116.19
- Exact Mass: 116.04081944
- Monoisotopic Mass: 116.04081944
- IUPAC Name: 1-methylimidazolidine-2-thione
- SMILES: CN1CCNC1=S
- Synonyms: 1-methylimidazolidine-2-thione, 13431-10-2, 1-Methyl-2-imidazolidinethione, 2-Imidazolidinethione, 1-methyl-, N-Methylethylenethiourea
Application
Methylethylenethiourea is primarily employed as an accelerator in rubber vulcanization processes, enhancing cross-linking efficiency. It also serves as a key intermediate in the synthesis of pharmaceuticals and agrochemicals due to its reactive thione group. Researchers utilize it in coordination chemistry to form complexes with transition metals for catalytic studies.
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