Determine the necessary mass, volume, or concentration for preparing a solution.
average Mn ~60,000 by GPC, average Mw ~750,000 by LS, 50 wt. % in H2O for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature,Argon charged 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 2254 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
This product is an aqueous solution of a branched polyethyleneimine polymer with a very high cationic charge density. This high charge density makes it a highly effective adhesion promoter, flocculant, and dispersing agent. It is offered as a clear-to-slightly-turbid viscous liquid containing 50% solids.
This polymer is infinitely soluble in water and can be easily diluted to working concentrations with water and most polar solvents. Due to the cationic nature of this product, it is recommended for use in nonionic and cationic formulations. The addition of Lupasol® P to anionic or highly acidic formulations can result in incompatibility. This product may be used as an adhesion promoter additive in compatible coating, ink, and adhesive systems to improve the adhesion to difficult substrates, such as paper, plastic, and metal.
This product is most commonly used in water-based primer formulations as a primer to improve the adhesion of coatings, inks, and adhesives. For example, in flexible packaging applications, it is applied to foils or low-surface energy films directly before applying adhesives to improve bonding between dissimilar materials.
Considerable improvement in the adhesion of UV-curable coatings and paints can be also obtained by using this product as a primer, where the increased adhesion helps mitigate the lateral shrinkage that occurs during curing.
In textile applications, cotton treated with this product is much more receptive to inks and flame retardants. This product is also very effective at chelating divalent heavy metals for water treatment applications, making them easier to remove by ultrafiltration. This chelation is reversible, and the heavy metals can then be recovered by electrodeposition.
Features & Benefits
Miscible with water in all proportions
Ames negative
Exhibits no detectable ethylenimine importunity
Forms insoluble matrix to fix and immobilize enzymes
Maximizes bonding using ionic, hydrogen, and Van der Waals forces
Compatibilizes and promotes adhesion between dissimilar substrates
Applications
Flexible packaging films
UV-curable coatings and inks
Textiles
Water treatment
Application
Detergents, adhesives, water treatment, printing inks, dyes, cosmetics, and paper industry, adhesion promoter, lamination primer, fixative agent, flocculant, cationic dispersant, stability enhancer, surface activator, chelating agent, scavenger for aldehydes and oxides. Protein precipitant.
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 | Organoheterocyclic compounds |
| Classe | Aziridines |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Aziridines |
| Alternative Parents | Dialkylamines Azacyclic compounds Organopnictogen compounds Hydrocarbon derivatives |
| Molecular Framework | Aliphatic heteromonocyclic compounds |
| Substituents | Azacycle - Secondary amine - Secondary aliphatic amine - Aziridine - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Amine - Aliphatic heteromonocyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as aziridines. These are organic compounds containing a saturated three-member heterocycle with one amino group and two methylene groups. |
| External Descriptors | azacycloalkane - saturated organic heteromonocyclic parent - aziridines |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Data | Oggetto |
|---|---|---|---|
| Certificate of Analysis | Mar 25, 2025 | P434396 | |
| Certificate of Analysis | Mar 25, 2025 | P434396 | |
| Certificate of Analysis | Jan 07, 2025 | P434396 | |
| Certificate of Analysis | Jan 07, 2025 | P434396 | |
| Certificate of Analysis | Jan 07, 2025 | P434396 | |
| Certificate of Analysis | Jan 07, 2025 | P434396 | |
| Certificate of Analysis | Jan 07, 2025 | P434396 | |
| Certificate of Analysis | Jan 07, 2025 | P434396 | |
| Certificate of Analysis | Jan 07, 2025 | P434396 | |
| Certificate of Analysis | Jan 07, 2025 | P434396 | |
| Certificate of Analysis | Jan 07, 2025 | P434396 | |
| Certificate of Analysis | Jan 07, 2025 | P434396 | |
| Certificate of Analysis | Jul 07, 2023 | P434396 | |
| Certificate of Analysis | Jul 07, 2023 | P434396 | |
| Certificate of Analysis | Jun 26, 2023 | P434396 | |
| Certificate of Analysis | Jun 26, 2023 | P434396 | |
| Certificate of Analysis | Mar 14, 2023 | P434396 | |
| Certificate of Analysis | Mar 14, 2023 | P434396 | |
| Certificate of Analysis | Mar 14, 2023 | P434396 |
| Sensibilità | Carbon dioxide Sensitive |
|---|---|
| Indice di rifrazione | 1.5290 |
| Punto di ebollizione (°C) | 100 °C |
| Punto di fusione (°C) | -10 °C |
| Peso molecolare | 43.070 g/mol |
| XLogP3 | -0.400 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 0 |
| Exact Mass | 43.0422 Da |
| Monoisotopic Mass | 43.0422 Da |
| Topological Polar Surface Area | 21.900 Ų |
| Heavy Atom Count | 3 |
| Formal Charge | 0 |
| Complexity | 10.300 |
| 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 |