≥90% 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 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Bis(hexamethylene)triamine (Bis-HEA, BHMT, BHMTA) is an aliphatic polyamine. It is a spermidine analog and has been reported to lack the enhancing effect on mitochondrial Ca(2+) accumulation but shows inhibitory effect on the Ca(2+) and Pi-induced mitochondrial permeability transition. Its ability in inhibiting shale swelling and dispersion in water-based drilling fluid has been investigated.
Application
Bis(hexamethylene)triamine is the suitable reagent used in the synthesis of xylylated dimer of polyamine and as a solvent to coat amphiphilic polymer on CdSe/ZnS quantum dots (QDs) for enhanced water solubilization.
It may be used in the following studies:
• Synthesis of bis(hexamethylene) triacetamide (BHTA) by acetylation.
• As a precursors for the ZnO outgrowths on TiO2 nanofibers.
• As organic bifunctional guest molecules for {W36} polyoxotungstate host compounds to form 1D chains of directly connected {W36} cluster units.
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 |
| Classe | 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 |
| Description | 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 |
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Article |
|---|---|---|---|
 G2623308 | Certificate of Analysis | May 27, 2026 | B661868 |
| G2623312 | Certificate of Analysis | May 27, 2026 | B661868 |
| J2515274 | Certificate of Analysis | Sep 30, 2025 | B661868 |
| J2524754 | Certificate of Analysis | Sep 30, 2025 | B661868 |
| C2412185 | Certificate of Analysis | Mar 18, 2024 | B661868 |
| C2412186 | Certificate of Analysis | Mar 18, 2024 | B661868 |
| C2412187 | Certificate of Analysis | Mar 18, 2024 | B661868 |
| C2412188 | Certificate of Analysis | Mar 18, 2024 | B661868 |
| Solubilité | Soluble in methanol |
|---|---|
| Sensibilité | Moisture sensitive |
| Indice de réfraction | 1.49 |
| Point d'éclair (°F) | 235.4 °F |
| Point d'éclair (°C) | 113 °C |
| Point d'ébullition (°C) | 164°C/4mmHg(lit.) |
| Point de fusion (°C) | 35 °C |
| Poids moléculaire | 215.380 g/mol |
| XLogP3 | 0.800 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 12 |
| Exact Mass | 215.236 Da |
| Monoisotopic Mass | 215.236 Da |
| Topological Polar Surface Area | 64.099 Ų |
| Heavy Atom Count | 15 |
| Formal Charge | 0 |
| Complexity | 95.000 |
| 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 |
