Determine the necessary mass, volume, or concentration for preparing a solution.
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Description
For a synthetic protocol using NMP initiators, contributed by Prof. Karen Wooley, please visit ourtechnology spotlight.TEMPO (2,2,6,6-Tetramethyl-1-piperidinyloxy) was used for trapping the styrenyl radical generated from benzoyl peroxide during nitroxide-mediated radical polymerization of styrene. TEMPO-mediated oxidation was employed for the carboxylation of water-resistant nanofibrillated cellulose (NFC) films.Stable nitroxide radical useful in controlling living polymerizations
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 Organopnictogen compounds Organonitrogen compounds Organic oxygen compounds Hydrocarbon derivatives |
| Molecular Framework | Aliphatic heteromonocyclic compounds |
| Substituents | Piperidine - Azacycle - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - 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 | piperidines - aminoxyls |
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Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Data | Oggetto |
|---|---|---|---|
| Certificate of Analysis | Nov 12, 2026 | T478495 | |
| Certificate of Analysis | Nov 12, 2026 | T478495 | |
| Certificate of Analysis | Sep 20, 2026 | T478495 | |
| Certificate of Analysis | Sep 20, 2026 | T478495 | |
| Certificate of Analysis | Jul 16, 2026 | T478495 | |
| Certificate of Analysis | Jul 16, 2026 | T478495 | |
| Certificate of Analysis | May 06, 2026 | T478495 | |
| Certificate of Analysis | May 06, 2026 | T478495 | |
| Certificate of Analysis | Jan 22, 2026 | T478495 | |
| Certificate of Analysis | Jan 22, 2026 | T478495 | |
| Certificate of Analysis | Oct 28, 2025 | T478495 | |
| Certificate of Analysis | Oct 28, 2025 | T478495 | |
| Certificate of Analysis | Jul 02, 2025 | T478495 | |
| Certificate of Analysis | Jul 02, 2025 | T478495 | |
| Certificate of Analysis | Feb 07, 2025 | T478495 | |
| Certificate of Analysis | Feb 07, 2025 | T478495 | |
| Certificate of Analysis | Jul 05, 2023 | T478495 | |
| Certificate of Analysis | Jul 05, 2023 | T478495 | |
| Certificate of Analysis | Jul 05, 2023 | T478495 | |
| Certificate of Analysis | Jul 05, 2023 | T478495 | |
| Certificate of Analysis | Jun 29, 2023 | T478495 |
| Punto di infiammabilità (°F) | 152.6 °F |
|---|---|
| Punto di infiammabilità (°C) | 67℃ |
| Punto di ebollizione (°C) | 193°C |
| Punto di fusione (°C) | 39°C |
| Peso molecolare | 156.250 g/mol |
| XLogP3 | 1.400 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 0 |
| Exact Mass | 156.139 Da |
| Monoisotopic Mass | 156.139 Da |
| Topological Polar Surface Area | 4.200 Ų |
| Heavy Atom Count | 11 |
| Formal Charge | 0 |
| Complexity | 136.000 |
| 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 |
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