≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Product Application:
Reactant for:
Guanylation of amines
Synthesis of tantalum dimethylamido diamidato and guanidinato complexes for CVD of nitride thin films
Preparation of titanium amidinate guanidinate alkylamide complex precursors for HfO2 films
Ketene cycloadditions
Hydroamination of carbodiimides using group-2-element amides as precatalysts
Synthesis of cobalt amidinato derivative complexes for studies involving thermal stability, vapro pressure, vaporization rate and thermal decomposition properties.
| Pubchem Sid | 504763078 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504763078 |
| Sonrisas canónicas | CCN=C=NC(C)(C)C |
| InChIKey | AXTNYCDVWRSOCU-UHFFFAOYSA-N |
| INCHI | 1S/C7H14N2/c1-5-8-6-9-7(2,3)4/h5H2,1-4H3 |
| Isómeros SMILES | CCN=C=NC(C)(C)C |
| WGK Alemania | 3 |
| PubChem CID | 4594009 |
| Número ONU | 1993 |
| Grupo de embalaje | III |
| Peso molecular | 126.2 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic nitrogen compounds |
| Clase | Organonitrogen compounds |
| Subclass | Carbodiimides |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Carbodiimides |
| Alternative Parents | Propargyl-type 1,3-dipolar organic compounds Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carbodiimide - Hydrocarbon derivative - Aliphatic acyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as carbodiimides. These are organic compounds containing a functional group consisting of the formula RN=C=NR. |
| External Descriptors | Not available |
| Sensibilidad | Moisture sensitive |
|---|---|
| Índice de refracción | n20/D 1.432 (lit.) |
| Punto de inflamación (°F) | 93.2 °F |
| Punto de inflamación (°C) | 34 °C |
| Punto de ebullición (°C) | 137-139° C (lit.) |
| Peso molecular | 126.200 g/mol |
| XLogP3 | 2.400 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 2 |
| Exact Mass | 126.116 Da |
| Monoisotopic Mass | 126.116 Da |
| Topological Polar Surface Area | 24.700 Ų |
| Heavy Atom Count | 9 |
| Formal Charge | 0 |
| Complexity | 124.000 |
| 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 |
C2311657