≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Argon charged Ships Wet ice 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Product Application：
Reactant for synthesis of: CB1 cannabinoid receptor ligands Hydrazones Tetrahydronaphthalene derivatives affecting proliferation and nitric oxide production in LPS activated RAW 264.7 macrophages Phosphorus(V) hydrazines 1-Aminopiperidine can be used as a reactant to prepare N-1-piperidinylformamide by reacting with ethyl formate. It is also reacted with aluminum hydride and gallium hydride to form corresponding hydrazides. In the pharmaceutical industry, aminopiperidine is utilized as a building block to synthesize various bioactive molecules.
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 | Piperidines |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Piperidines |
| Alternative Parents | Azacyclic compounds Alkylhydrazines Organopnictogen compounds Hydrocarbon derivatives |
| Molecular Framework | Aliphatic heteromonocyclic compounds |
| Substituents | Piperidine - Alkylhydrazine - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Hydrazine derivative - Aliphatic heteromonocyclic compound |
| Descrizione | 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 | Data | Oggetto |
|---|---|---|---|
 H2628131 | Certificate of Analysis | Aug 15, 2026 | A113934 |
| H2628132 | Certificate of Analysis | Aug 15, 2026 | A113934 |
| F2604245 | Certificate of Analysis | May 23, 2026 | A113934 |
| F2604247 | Certificate of Analysis | May 23, 2026 | A113934 |
| K2517297 | Certificate of Analysis | Nov 08, 2025 | A113934 |
| K2517298 | Certificate of Analysis | Nov 08, 2025 | A113934 |
| H2511195 | Certificate of Analysis | Jul 18, 2025 | A113934 |
| A2408202 | Certificate of Analysis | Nov 25, 2023 | A113934 |
| A2408203 | Certificate of Analysis | Nov 25, 2023 | A113934 |
| A2408204 | Certificate of Analysis | Nov 25, 2023 | A113934 |
| A2408205 | Certificate of Analysis | Nov 25, 2023 | A113934 |
| A2408223 | Certificate of Analysis | Nov 25, 2023 | A113934 |
| A2408224 | Certificate of Analysis | Nov 25, 2023 | A113934 |
| Sensibilità | Air Sensitive；heat sensitive |
|---|---|
| Indice di rifrazione | 1.475-1.477 |
| Punto di infiammabilità (°F) | 96.8 °F |
| Punto di infiammabilità (°C) | 36 °C |
| Punto di ebollizione (°C) | 145-147°C |
| Peso molecolare | 100.160 g/mol |
| XLogP3 | -0.300 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 0 |
| Exact Mass | 100.1 Da |
| Monoisotopic Mass | 100.1 Da |
| Topological Polar Surface Area | 29.300 Ų |
| Heavy Atom Count | 7 |
| Formal Charge | 0 |
| Complexity | 48.000 |
| 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 |
