≥96% 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
2-Methyl-1-pyrroline, a monocyclic imine, is a pyrroline derivative. It is a five-membered heterocyclic compound having various biological and pharmacological applications. It is formed during the Rh(I) complexes (containing N,N-donor ligands and N,P-donor ligand) immobilized on glassy carbon electrode surfaces catalyzed intramolecular hydroamination of 4-pentyn-1-amine. It reacts with with 2-oxopropanal to afford acetyl-1-pyrroline (AP).
| Pubchem Sid | 488184474 |
|---|---|
| Sonrisas canónicas | CC1=NCCC1 |
| IUPAC Name | 5-methyl-3,4-dihydro-2H-pyrrole |
| InChIKey | CTSZPNIMMLSKDV-UHFFFAOYSA-N |
| INCHI | 1S/C5H9N/c1-5-3-2-4-6-5/h2-4H2,1H3 |
| Isómeros SMILES | CC1=NCCC1 |
| WGK Alemania | 3 |
| Peso molecular | 83.1 |
| Reaxy-Rn | 103485 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=103485&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 |
| Clase | Pyrrolines |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Pyrrolines |
| Alternative Parents | Ketimines Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Organopnictogen compounds Hydrocarbon derivatives |
| Molecular Framework | Aliphatic heteromonocyclic compounds |
| Substituents | Pyrroline - Ketimine - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Imine - Aliphatic heteromonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as pyrrolines. These are compounds containing a pyrroline ring, which is a five-member unsaturated aliphatic ring with one nitrogen atom and four carbon atoms. |
| External Descriptors | imine - pyrroline |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 D2321513 | Certificate of Analysis | Feb 04, 2026 | M187405 |
| D2321520 | Certificate of Analysis | Feb 04, 2026 | M187405 |
| D2321525 | Certificate of Analysis | Feb 04, 2026 | M187405 |
| K1907120 | Certificate of Analysis | Jun 16, 2025 | M187405 |
| C2208407 | Certificate of Analysis | Dec 06, 2024 | M187405 |
| C2208410 | Certificate of Analysis | Dec 06, 2024 | M187405 |
| C2208416 | Certificate of Analysis | Dec 06, 2024 | M187405 |
| Solubilidad | Soluble in water. |
|---|---|
| Índice de refracción | 1.444 |
| Punto de inflamación (°F) | 20 °F |
| Punto de inflamación (°C) | 10 °C |
| Punto de ebullición (°C) | 104-105 °C |
| Peso molecular | 83.130 g/mol |
| XLogP3 | 0.000 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 0 |
| Exact Mass | 83.0735 Da |
| Monoisotopic Mass | 83.0735 Da |
| Topological Polar Surface Area | 12.400 Ų |
| Heavy Atom Count | 6 |
| Formal Charge | 0 |
| Complexity | 74.000 |
| 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. Lihong Ding, Xiuliang Sun, Chongpin Huang, Jianwei Li, Biaohua Chen. (2024) Structure–reactivity relationships in the ionic-liquid-catalyzed oxidation of cumene: Cation effects. JOURNAL OF MOLECULAR LIQUIDS, [PMID:] [10.1016/j.molliq.2024.124563] |
