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≥85% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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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.
N-dodecyl-1,3-propanediamine (N-lauryl-1,3-propanediamine, DA12) can be used to synthesize nonionic surfactants with ethylene oxide, propylene oxide, etc.;
it is used as an asphalt emulsifier;
as a mineral flotation agent,it has unique effects in the flotation of minerals such as phosphate ore;
it can also be used as a chain lubricant and applied in the lubricant additive industry;
in the pigment industry, it is commonly used as a pigment dispersant;
| Sonrisas canónicas | CCCCCCCCCCCCNCCCN |
|---|---|
| IUPAC Name | N'-dodecylpropane-1,3-diamine |
| InChIKey | XMMDVXFQGOEOKH-UHFFFAOYSA-N |
| INCHI | 1S/C15H34N2/c1-2-3-4-5-6-7-8-9-10-11-14-17-15-12-13-16/h17H,2-16H2,1H3 |
| Isómeros SMILES | CCCCCCCCCCCCNCCCN |
| Peso molecular | 242.45 |
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 | Amines |
| Intermediate Tree Nodes | Secondary amines |
| Direct Parent | Dialkylamines |
| Alternative Parents | Organopnictogen compounds Monoalkylamines Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Secondary aliphatic amine - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Primary aliphatic amine - Aliphatic acyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as dialkylamines. These are organic compounds containing a dialkylamine group, characterized by two alkyl groups bonded to the amino nitrogen. |
| 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 23, 2025 | L694679 | |
| Certificate of Analysis | Oct 23, 2025 | L694679 | |
| Certificate of Analysis | Oct 23, 2025 | L694679 | |
| Certificate of Analysis | Oct 15, 2025 | L694679 | |
| Certificate of Analysis | Oct 15, 2025 | L694679 | |
| Certificate of Analysis | Oct 15, 2025 | L694679 |
| Sensibilidad | light sensitive;Moisture sensitive |
|---|---|
| Punto de ebullición (°C) | 326°C at 760 mmHg |
| Punto de fusión (°C) | 24.5-25.5 °C |
| Peso molecular | 242.440 g/mol |
| XLogP3 | 4.800 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 14 |
| Exact Mass | 242.272 Da |
| Monoisotopic Mass | 242.272 Da |
| Topological Polar Surface Area | 38.100 Ų |
| Heavy Atom Count | 17 |
| Formal Charge | 0 |
| Complexity | 126.000 |
| 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 |