Determine the necessary mass, volume, or concentration for preparing a solution.
≥98% para flujos de trabajo cromatográficos y analíticos sensibles que requieren una interferencia mínima de la línea base.
Room temperature Envío Normal. Consulte el COA específico del lote para conocer las especificaciones exactas.
SDS, COA, ficha técnica y hoja de especificaciones disponibles para descargar. COA específico del lote accesible mediante búsqueda por número de lote.
Citado en 10 publicaciones revisadas por pares sobre cromatografía, síntesis orgánica y reacciones de acoplamiento cruzado.
Application
2-Imino-4-thiobiuret is used in the design and synthesis of guanylthiourea derivatives which are potential inhibitors of plasmodium falciparum dihydrofolate reductase enzyme. 2-Imino-4-thiobiuret is also used as a reagent in recyclization reactions of N-arylmaleimides with polynucleophilic compounds.
Documento completo sobre peligros, manipulación, almacenamiento y cumplimiento normativo.
<<<<<<< HEAD Descargar SDS → ======= Descargar SDS → >>>>>>> release248-p3Datos de calidad específicos del lote. Introduzca su número de lote para obtener el COA exacto.
Buscar COA →Resumen de referencia rápida de las especificaciones y aplicaciones del producto.
Ver ficha técnica →Atributos de calidad completos y criterios de aceptación para esta calidad.
Ver hoja de especificaciones →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic nitrogen compounds |
| Clase | Organonitrogen compounds |
| Subclass | Guanidines |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Guanidines |
| Alternative Parents | Propargyl-type 1,3-dipolar organic compounds Carboximidamides Organosulfur compounds Organopnictogen compounds Imines Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Guanidine - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Organopnictogen compound - Hydrocarbon derivative - Organosulfur compound - Imine - Aliphatic acyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as guanidines. These are compounds containing a guanidine moiety, with the general structure (R1R2N)(R3R4N)C=N-R5. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
| Certificate of Analysis | Oct 13, 2025 | A111256 | |
| Certificate of Analysis | Oct 13, 2025 | A111256 | |
| Certificate of Analysis | Oct 13, 2025 | A111256 | |
| Certificate of Analysis | Mar 04, 2025 | A111256 | |
| Certificate of Analysis | Mar 04, 2025 | A111256 | |
| Certificate of Analysis | Jun 20, 2024 | A111256 | |
| Certificate of Analysis | Jun 20, 2024 | A111256 | |
| Certificate of Analysis | May 07, 2022 | A111256 | |
| Certificate of Analysis | Dec 13, 2021 | A111256 | |
| Certificate of Analysis | Dec 13, 2021 | A111256 | |
| Certificate of Analysis | Dec 13, 2021 | A111256 | |
| Certificate of Analysis | Dec 13, 2021 | A111256 | |
| Certificate of Analysis | Dec 13, 2021 | A111256 | |
| Certificate of Analysis | Dec 13, 2021 | A111256 | |
| Certificate of Analysis | Dec 13, 2021 | A111256 |
| Solubilidad | Soluble in water (70g/L). |
|---|---|
| Punto de fusión (°C) | 160-164°C |
| Peso molecular | 118.160 g/mol |
| XLogP3 | -1.300 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 0 |
| Exact Mass | 118.031 Da |
| Monoisotopic Mass | 118.031 Da |
| Topological Polar Surface Area | 123.000 Ų |
| Heavy Atom Count | 7 |
| Formal Charge | 0 |
| Complexity | 102.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |