Determine the necessary mass, volume, or concentration for preparing a solution.
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C 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 6 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
2-Aminoimidazole is a potent antimicrobial agent that effectively targets drug-resistant Mycobacterium tuberculosis by disrupting the proton motive force and blocking the electron transport chain, potentiates the action of beta-lactam antibiotics against Mycobacterium tuberculosis by decreasing the secretion of beta-lactamases and increasing the permeability of cell membranes, activates drug-resistant bacteria and improves therapeutic efficacy.
| Pubchem Sid | 488186057 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488186057 |
| Sonrisas canónicas | C1=CN=C(N1)N |
| IUPAC Name | 1H-imidazol-2-amine |
| InChIKey | DEPDDPLQZYCHOH-UHFFFAOYSA-N |
| INCHI | 1S/C3H5N3/c4-3-5-1-2-6-3/h1-2H,(H3,4,5,6) |
| Isómeros SMILES | C1=CN=C(N1)N |
| Peso molecular | 83.1 |
| Reaxy-Rn | 105870 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=105870&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 | Azoles |
| Subclass | Imidazoles |
| Intermediate Tree Nodes | Substituted imidazoles |
| Direct Parent | Aminoimidazoles |
| Alternative Parents | Heteroaromatic compounds Azacyclic compounds Primary amines Organopnictogen compounds Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | Aminoimidazole - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Amine - Aromatic heteromonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as aminoimidazoles. These are organic compounds containing an amino group linked to an imidazole ring. |
| External Descriptors | Not available |
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Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
| Certificate of Analysis | Mar 04, 2026 | H186542 | |
| Certificate of Analysis | Mar 04, 2026 | H186542 | |
| Certificate of Analysis | Mar 04, 2026 | H186542 | |
| Certificate of Analysis | Jan 19, 2026 | H186542 | |
| Certificate of Analysis | Jan 19, 2026 | H186542 | |
| Certificate of Analysis | Sep 23, 2025 | H186542 | |
| Certificate of Analysis | Sep 23, 2025 | H186542 | |
| Certificate of Analysis | Sep 23, 2025 | H186542 | |
| Certificate of Analysis | Dec 05, 2023 | H186542 | |
| Certificate of Analysis | Dec 05, 2023 | H186542 | |
| Certificate of Analysis | Dec 05, 2023 | H186542 | |
| Certificate of Analysis | Jul 17, 2023 | H186542 | |
| Certificate of Analysis | Jul 17, 2023 | H186542 | |
| Certificate of Analysis | Jul 17, 2023 | H186542 | |
| Certificate of Analysis | Jul 17, 2023 | H186542 | |
| Certificate of Analysis | Jul 17, 2023 | H186542 | |
| Certificate of Analysis | Jul 17, 2023 | H186542 | |
| Certificate of Analysis | Jul 17, 2023 | H186542 | |
| Certificate of Analysis | Mar 06, 2023 | H186542 | |
| Certificate of Analysis | Mar 06, 2023 | H186542 |
| Peso molecular | 83.090 g/mol |
|---|---|
| XLogP3 | -0.300 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 0 |
| Exact Mass | 83.0483 Da |
| Monoisotopic Mass | 83.0483 Da |
| Topological Polar Surface Area | 54.700 Ų |
| Heavy Atom Count | 6 |
| Formal Charge | 0 |
| Complexity | 45.300 |
| 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. Futing Yang, Wenjie Yu, Qiying Yu, Xiyu Liu, Chunping Liu, Chong Lu, Xinghua Liao, Yi Liu, Na Peng. (2023) Mitochondria-Targeted Nanosystem with Reactive Oxygen Species-Controlled Release of CO to Enhance Photodynamic Therapy of PCN-224 by Sensitizing Ferroptosis. Small, 19 (16): (2206124). [PMID:36693788] [10.1002/smll.202206124] |
| 2. Huan Xu, Mingyue Yang, Yijing Du, Tian Gao, Yi Liu, Liwei Xiong, Na Peng. (2022) Self-assembly of micelles with pH/ROS dual-responsiveness and mitochondrial targeting for potential anti-tumor applications. NEW JOURNAL OF CHEMISTRY, 46 (44): (21235-21244). [PMID:] [10.1039/D2NJ03244A] |
| 3. Wu Zou, Fuchun Gong, Tingting Gu, Zhong Cao, Jiaoyun Xia. (2018) An efficient strategy for sensing pyrophosphate based on nitrogen-rich quantum dots combined with graphene oxide. MICROCHEMICAL JOURNAL, [PMID:] [10.1016/j.microc.2018.06.004] |
| 4. Yujie Guo, Lingfei Li, Maofeng Zhang, Shihao Xu, Changlong Jiang. (2025) A Self-Assembly MOF-on-MOF Heterostructure-Driven Fluorescence Sensor for Aerogel-Based Visualization Detection of Flavomycin. Small, [PMID:39924837] [10.1002/smll.202410911] |
| 5. Xue Chen, Yong Xiang, Xiaojing Zhang, Guanlin Li, Sihan Ai, Daoyong Yu, Baosheng Ge. (2024) Synthesis of a Zn(II)-2-aminoimidazole Framework as an Efficient Carbonic Anhydrase Mimic. LANGMUIR, [PMID:39226467] [10.1021/acs.langmuir.4c02563] |
| 6. Yong Xiang, Xue Chen, Liang Zhang, Yu Chen, Xiaowei Peng, Zhongzhen Cai, Qiping Gao, Daoyong Yu, Lu Zhang, Baosheng Ge. (2026) Engineering Carbonic Anhydrase Mimics via Metal Ion Doping: Tailoring the Structure and Catalytic Properties of a 2-Aminoimidazole-Based MOF. LANGMUIR, [PMID:] [10.1021/acs.langmuir.5c06793] |