≥96% 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 4 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
application：
N-Allylmethylamine is used in the production of N-allyl-alfa,alfa-dichloro-N-methylacetamide. It is used as a functional monomer to coordinate with Cd(II)/Zn(II) ions to get the poly methyl methacrylate -butyl methacrylate - N-allylmethylamine (PMBA) films, which is useful as building blocks to fabricate a photo-catalytic cell.
| Pubchem Sid | 504754381 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504754381 |
| Canonical Smiles | CNCC=C |
| IUPAC Name | N-methylprop-2-en-1-amine |
| InChIKey | IOXXVNYDGIXMIP-UHFFFAOYSA-N |
| INCHI | 1S/C4H9N/c1-3-4-5-2/h3,5H,1,4H2,2H3 |
| Isomeric SMILES | CNCC=C |
| WGK Germany | 3 |
| RTECS | UC6632500 |
| UN Number | 3286 |
| Packing Group | II |
| Molecular Weight | 71.12 |
| Beilstein | 1098387 |
| Reaxy-Rn | 1098387 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1098387&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 | Organic nitrogen compounds |
| Class | Organonitrogen compounds |
| Subclass | Amines |
| Intermediate Tree Nodes | Secondary amines |
| Direct Parent | Dialkylamines |
| Alternative Parents | Organopnictogen compounds Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Secondary aliphatic amine - Organopnictogen compound - Hydrocarbon derivative - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as dialkylamines. These are organic compounds containing a dialkylamine group, characterized by two alkyl groups bonded to the amino nitrogen. |
| 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 |
|---|---|---|---|
 J2215131 | Certificate of Analysis | May 08, 2026 | I136680 |
| I2201659 | Certificate of Analysis | Mar 09, 2026 | I136680 |
| I2201664 | Certificate of Analysis | Mar 09, 2026 | I136680 |
| I2201662 | Certificate of Analysis | Mar 09, 2026 | I136680 |
| E2411019 | Certificate of Analysis | Feb 04, 2026 | I136680 |
| E1822043 | Certificate of Analysis | Aug 15, 2025 | I136680 |
| I2511677 | Certificate of Analysis | Jul 07, 2025 | I136680 |
| I2511678 | Certificate of Analysis | Jul 07, 2025 | I136680 |
| I2511681 | Certificate of Analysis | Jul 07, 2025 | I136680 |
| I2522650 | Certificate of Analysis | Jul 07, 2025 | I136680 |
| D2602008 | Certificate of Analysis | Jul 07, 2025 | I136680 |
| C2522090 | Certificate of Analysis | Apr 01, 2025 | I136680 |
| E2529450 | Certificate of Analysis | Jul 13, 2024 | I136680 |
| F2510839 | Certificate of Analysis | Jul 13, 2024 | I136680 |
| H1519048 | Certificate of Analysis | Apr 13, 2023 | I136680 |
| I2201663 | Certificate of Analysis | Jul 22, 2022 | I136680 |
| E1822042 | Certificate of Analysis | Jan 19, 2022 | I136680 |
| Sensitivity | CO2 sensitive；Air sensitive；Heat sensitive |
|---|---|
| Refractive Index | 1.41 |
| Flash Point(°F) | -18.4 °F |
| Flash Point(°C) | -28 °C |
| Melt Point(°C) | 66℃ |
| Molecular Weight | 71.120 g/mol |
| XLogP3 | 0.400 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 2 |
| Exact Mass | 71.0735 Da |
| Monoisotopic Mass | 71.0735 Da |
| Topological Polar Surface Area | 12.000 Ų |
| Heavy Atom Count | 5 |
| Formal Charge | 0 |
| Complexity | 24.800 |
| 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. Ting-ting Bai, Ming-yan Cong, Yu-xiang Jia, Ke-ke Ma, Meng Wang. (2020) Preparation of self-crosslinking anion exchange membrane with acid block performance from side-chain type polysulfone. JOURNAL OF MEMBRANE SCIENCE, [PMID:] [10.1016/j.memsci.2020.117831] |
| 2. Jiye Teng, Tao Zhang, Hongbo Zhao, Peiling Zhang, Zhengzhe Wu, Zhiwei Chang, Ming Li, Chenjie Zhu. (2025) Dual-functionalization of lignin towards superior reinforcement for styrene-butadiene rubber. INDUSTRIAL CROPS AND PRODUCTS, [PMID:] [10.1016/j.indcrop.2025.120500] |
| 3. Xiuqin Fang, Chang Wang, Hong-Hui Shu, Sheng-Li Han, Cheng-Mei Liu. (2024) Improving the removal rate of bisphenol A and Cu2+ from water using P/N coexisting β-cyclodextrin-based adsorbents by enhancing adsorbents-pollutants interactions. CARBOHYDRATE POLYMERS, [PMID:39174082] [10.1016/j.carbpol.2024.122437] |
| 4. Nianming Jiao, Zhang Jiang, Yuan Yao, Long Liu, Yanqiang Zhang. (2025) Multicyclopropyl-functionalized hypergolic ionic liquids with enhanced energetic performance. JOURNAL OF MOLECULAR LIQUIDS, [PMID:] [10.1016/j.molliq.2025.128777] |
