≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Conservar a 2-8°C,Protegido de la luz,Cargado con argón Ships Hielo húmedo 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.
| Sonrisas canónicas | CN(C)C(N(C)C)N(C)C |
|---|---|
| IUPAC Name | N,N,N',N',N\",N\"-hexamethylmethanetriamine |
| InChIKey | MUMVIYLVHVCYGI-UHFFFAOYSA-N |
| INCHI | 1S/C7H19N3/c1-8(2)7(9(3)4)10(5)6/h7H,1-6H3 |
| Isómeros SMILES | CN(C)C(N(C)C)N(C)C |
| WGK Alemania | 3 |
| PubChem CID | 79831 |
| Número ONU | 2733 |
| Grupo de embalaje | II |
| Peso molecular | 145.25 |
| Beilstein | 1901160 |
| Reaxy-Rn | 1901162 |
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 acids and derivatives |
| Clase | Orthocarboxylic acid derivatives |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Orthocarboxylic acid derivatives |
| Alternative Parents | Ortho amides Organopnictogen compounds Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Orthocarboxylic acid derivative - Ortho amide - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aliphatic acyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as orthocarboxylic acid derivatives. These are organic compounds containing the orhtocarboxylic acid functional group, with the RC(X)(X)X (R=H, alkyl, aryl; X=OH, alkoxy, aryloxy, substituted amino, etc.). |
| 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 |
|---|---|---|---|
 J2424940 | Certificate of Analysis | Oct 18, 2024 | T162013 |
| J2424941 | Certificate of Analysis | Oct 18, 2024 | T162013 |
| J2424943 | Certificate of Analysis | Oct 18, 2024 | T162013 |
| J2424944 | Certificate of Analysis | Oct 18, 2024 | T162013 |
| Sensibilidad | Light Sensitive；Moisture Sensitive；Heat Sensitive |
|---|---|
| Índice de refracción | 1.44 |
| Punto de inflamación (°F) | 51.8 °F |
| Punto de inflamación (°C) | -15°C(lit.) |
| Punto de ebullición (°C) | 43 °C/12 mmHg |
| Peso molecular | 145.250 g/mol |
| XLogP3 | 0.600 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 3 |
| Exact Mass | 145.158 Da |
| Monoisotopic Mass | 145.158 Da |
| Topological Polar Surface Area | 9.700 Ų |
| Heavy Atom Count | 10 |
| Formal Charge | 0 |
| Complexity | 69.800 |
| 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 |
