≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Reactant for synthesis of: ? Pim-1 inhibitors1 ? Vasotocin1b receptor antagonists2 ? CXCR4 antagonists as anti-HIV agents3 ? Amide CCR5 antagonist4 ? PSSRI-based inhibitors of S. aureus multidrug efflux pumps5 ? Human GnRH receptor antagonists6
| Pubchem Sid | 488193375 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488193375 |
| Canonical Smiles | CC(C)(C)OC(=O)N1CCCC(C1)CO |
| IUPAC Name | tert-butyl 3-(hydroxymethyl)piperidine-1-carboxylate |
| InChIKey | OJCLHERKFHHUTB-UHFFFAOYSA-N |
| INCHI | 1S/C11H21NO3/c1-11(2,3)15-10(14)12-6-4-5-9(7-12)8-13/h9,13H,4-8H2,1-3H3 |
| Isomeric SMILES | CC(C)(C)OC(=O)N1CCCC(C1)CO |
| WGK Germany | 3 |
| Molecular Weight | 215.29 |
| Reaxy-Rn | 5850868 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=5850868&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 | Piperidinecarboxylic acids and derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Piperidinecarboxylic acids |
| Alternative Parents | Carbamate esters Organic carbonic acids and derivatives Azacyclic compounds Primary alcohols Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic heteromonocyclic compounds |
| Substituents | Piperidinecarboxylic acid - Carbamic acid ester - Carbonic acid derivative - Azacycle - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Organonitrogen compound - Carbonyl group - Alcohol - Aliphatic heteromonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as piperidinecarboxylic acids. These are compounds containing a piperidine ring which bears a carboxylic acid group. |
| 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 |
|---|---|---|---|
 C1827047 | Certificate of Analysis | Oct 14, 2025 | B121553 |
| C1827046 | Certificate of Analysis | Oct 14, 2025 | B121553 |
| C1319030 | Certificate of Analysis | Nov 07, 2024 | B121553 |
| C2313471 | Certificate of Analysis | Mar 21, 2023 | B121553 |
| C2313472 | Certificate of Analysis | Mar 21, 2023 | B121553 |
| C2313470 | Certificate of Analysis | Mar 20, 2023 | B121553 |
| Solubility | Soluble in Methanol,Dimethylformamide |
|---|---|
| Melt Point(°C) | 77-81°C |
| Molecular Weight | 215.290 g/mol |
| XLogP3 | 1.200 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 3 |
| Exact Mass | 215.152 Da |
| Monoisotopic Mass | 215.152 Da |
| Topological Polar Surface Area | 49.800 Ų |
| Heavy Atom Count | 15 |
| Formal Charge | 0 |
| Complexity | 222.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
