≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships 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.
Description
4,4′-Trimethylenebis(1-methylpiperidine) has been used in the synthesis of:di-, tri- and tetracationic monomeric and homodimeric monomethine cyanine dyes for nucleic acid detectionstructure directing agents containing 4,4′-trimethylenebis(1-methylpiperidine)piperidine-based dicationic ionic liquidsReactant for synthesis of cyanine dyes for nucleic acid detection
| Sonrisas canónicas | CN1CCC(CC1)CCCC2CCN(CC2)C |
|---|---|
| IUPAC Name | 1-methyl-4-[3-(1-methylpiperidin-4-yl)propyl]piperidine |
| InChIKey | JWOTWWORMYMZCR-UHFFFAOYSA-N |
| INCHI | 1S/C15H30N2/c1-16-10-6-14(7-11-16)4-3-5-15-8-12-17(2)13-9-15/h14-15H,3-13H2,1-2H3 |
| Isómeros SMILES | CN1CCC(CC1)CCCC2CCN(CC2)C |
| PubChem CID | 116563 |
| Peso molecular | 238.41 |
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 |
| Clase | Piperidines |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Piperidines |
| Alternative Parents | Trialkylamines Azacyclic compounds Organopnictogen compounds Hydrocarbon derivatives |
| Molecular Framework | Aliphatic heteromonocyclic compounds |
| Substituents | Piperidine - Tertiary aliphatic amine - Tertiary amine - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Amine - Aliphatic heteromonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as piperidines. These are compounds containing a piperidine ring, which is a saturated aliphatic six-member ring with one nitrogen atom and five carbon atoms. |
| External Descriptors | Not available |
| Índice de refracción | n20/D 1.482 (lit.) |
|---|---|
| Punto de inflamación (°F) | 235.4 °F - closed cup |
| Punto de inflamación (°C) | 113 °C - closed cup |
| Punto de ebullición (°C) | 215℃/50mmHg (lit.) |
| Punto de fusión (°C) | 13℃ (lit.) |
| Peso molecular | 238.410 g/mol |
| XLogP3 | 3.400 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 4 |
| Exact Mass | 238.241 Da |
| Monoisotopic Mass | 238.241 Da |
| Topological Polar Surface Area | 6.500 Ų |
| Heavy Atom Count | 17 |
| Formal Charge | 0 |
| Complexity | 179.000 |
| 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 |
