Determine the necessary mass, volume, or concentration for preparing a solution.
≥97%(GC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature,Argon charged,Desiccated,Cool 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 7 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
4,4′-Trimethylenedipyridine undergoes Willgerodt-Kindler reaction by on pot- polycondensation with dialdehydes in the presence of sulphur to form polythioamides.
| Pubchem Sid | 488186338 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488186338 |
| Canonical Smiles | C1CNCCC1CCCC2CCNCC2 |
| IUPAC Name | 4-(3-piperidin-4-ylpropyl)piperidine |
| InChIKey | OXEZLYIDQPBCBB-UHFFFAOYSA-N |
| INCHI | 1S/C13H26N2/c1(2-12-4-8-14-9-5-12)3-13-6-10-15-11-7-13/h12-15H,1-11H2 |
| Isomeric SMILES | C1CNCCC1CCCC2CCNCC2 |
| WGK Germany | 3 |
| Molecular Weight | 210.37 |
| Reaxy-Rn | 2521 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2521&ln= |
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 |
| Class | Piperidines |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Piperidines |
| Alternative Parents | Dialkylamines Azacyclic compounds Organopnictogen compounds Hydrocarbon derivatives |
| Molecular Framework | Aliphatic heteromonocyclic compounds |
| Substituents | Piperidine - Azacycle - Secondary amine - Secondary aliphatic amine - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Amine - Aliphatic heteromonocyclic compound |
| Description | 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 |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Apr 02, 2026 | D154524 | |
| Certificate of Analysis | Apr 02, 2026 | D154524 | |
| Certificate of Analysis | Apr 02, 2026 | D154524 | |
| Certificate of Analysis | Apr 27, 2025 | D154524 | |
| Certificate of Analysis | Apr 27, 2025 | D154524 | |
| Certificate of Analysis | Apr 27, 2025 | D154524 | |
| Certificate of Analysis | Apr 22, 2024 | D154524 | |
| Certificate of Analysis | Jan 13, 2023 | D154524 | |
| Certificate of Analysis | Jan 13, 2023 | D154524 | |
| Certificate of Analysis | Jan 13, 2023 | D154524 | |
| Certificate of Analysis | Jan 13, 2023 | D154524 | |
| Certificate of Analysis | Jan 13, 2023 | D154524 | |
| Certificate of Analysis | Jan 13, 2023 | D154524 | |
| Certificate of Analysis | Jan 13, 2023 | D154524 | |
| Certificate of Analysis | Jan 21, 2022 | D154524 |
| Solubility | Soluble in water |
|---|---|
| Sensitivity | Hygroscopic |
| Specific Rotation[α] | >110℃(230°F) |
| Boil Point(°C) | 327℃ |
| Melt Point(°C) | 65-68℃ |
| Molecular Weight | 210.360 g/mol |
| XLogP3 | 2.500 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 4 |
| Exact Mass | 210.21 Da |
| Monoisotopic Mass | 210.21 Da |
| Topological Polar Surface Area | 24.100 Ų |
| Heavy Atom Count | 15 |
| Formal Charge | 0 |
| Complexity | 140.000 |
| 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 |
| 1. Zhang Yu, Zheng Jianzhi, Li Xijuan, Wu Ying, Zhang Ke. (2023) Stoichiometric Imbalance-promoted Step-growth Polymerization Based on Self-accelerating Three-component Reaction. CHEMICAL RESEARCH IN CHINESE UNIVERSITIES, 39 (5): (822-828). [PMID:] [10.1007/s40242-023-3173-3] |
| 2. Hongyan Zhang, Shuang Dong, Sheng Zhang, Yufen Li, Ji Li, Yinghui Dai, Dongkai Wang. (2020) pH-responsive lipid polymer hybrid nanoparticles (LPHNs) based on poly (β-amino ester) as a promising candidate to resist breast cancers. JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY, [PMID:] [10.1016/j.jddst.2020.102102] |
| 3. Mingxing Yin, Yuling Bao, Xueqin Gao, Yupei Wu, Yu Sun, Xinyuan Zhao, Hongzhe Xu, Zhiping Zhang, Songwei Tan. (2017) Redox/pH dual-sensitive hybrid micelles for targeting delivery and overcoming multidrug resistance of cancer. Journal of Materials Chemistry B, 5 (16): (2964-2978). [PMID:32263989] [10.1039/C6TB03282F] |
| 4. Haijun Zhao, Qian Li, Zehui Hong. (2016) Paclitaxel-Loaded Mixed Micelles Enhance Ovarian Cancer Therapy through Extracellular pH-Triggered PEG Detachment and Endosomal Escape. MOLECULAR PHARMACEUTICS, [PMID:27266442] [10.1021/acs.molpharmaceut.6b00164] |
| 5. Jing Guo, Rui Liu, Chunhui Shen, Shanjun Gao. (2025) Anion Exchange Membranes of Alkaline Resistance Based on Acrylonitrile-Styrene Copolymer with N-Spirocyclic Ammonium. ENERGY & FUELS, [PMID:] [10.1021/acs.energyfuels.4c06302] |
| 6. Xing Liu, Ting Zhang, Lei Zhou, Ming Li, Rongxing He. (2024) Dual-Emissive γ-[Cu4I8]4– Enables Luminescent Thermochromism in an Organic–Inorganic Hybrid Copper(I) Halide. INORGANIC CHEMISTRY, [PMID:38511502] [10.1021/acs.inorgchem.3c04141] |
| 7. Yanchao Zhang, Jingyi Wu, Song Wang, Junjian Yu, Yiman Gu, Yan Wang, Jian Gao, Chang Sun, Zhanyu Li, Yijia Lei, Na Li, Jialin Zhao, Zhe Wang. (2024) Poly(p-terphenyl-piperidine-bromoacetophenone) anion exchange membranes with pendant N-spirocyclic cations: Cations synergistic build efficient ion transport networks. JOURNAL OF MEMBRANE SCIENCE, [PMID:] [10.1016/j.memsci.2024.123134] |