≥98% 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 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
It may be used in the preparation of following compounds: . Tetragonal nickel(II) complexes, NiL4X2 (X = Cl-, Br-, I-, SCN-, SeCN-, NO3-, ClO4-, PF6- or NiL4XClO4 (X = Cl-, Br-, I-, SCN-); . 1-Dodecyl-2-isopropylimidazole; . Bromidotetrakis(2-isopropyl-1H-imidazole-[κN3)copper(II) bromide.
| Pubchem Sid | 488187742 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488187742 |
| Sonrisas canónicas | CC(C)C1=NC=CN1 |
| IUPAC Name | 2-propan-2-yl-1H-imidazole |
| InChIKey | FUOZJYASZOSONT-UHFFFAOYSA-N |
| INCHI | 1S/C6H10N2/c1-5(2)6-7-3-4-8-6/h3-5H,1-2H3,(H,7,8) |
| Isómeros SMILES | CC(C)C1=NC=CN1 |
| WGK Alemania | 3 |
| Peso molecular | 110.16 |
| Reaxy-Rn | 107804 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=107804&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 | Not available |
| Direct Parent | Imidazoles |
| Alternative Parents | Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | Heteroaromatic compound - Imidazole - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteromonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as imidazoles. These are compounds containing an imidazole ring, which is an aromatic five-member ring with two nitrogen atoms at positions 1 and 3, and three carbon atoms. |
| External Descriptors | Not available |
| Punto de ebullición (°C) | 256-260 °C(lit.) |
|---|---|
| Punto de fusión (°C) | 129-131°C(lit.) |
| Peso molecular | 110.160 g/mol |
| XLogP3 | 1.200 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 1 |
| Exact Mass | 110.084 Da |
| Monoisotopic Mass | 110.084 Da |
| Topological Polar Surface Area | 28.700 Ų |
| Heavy Atom Count | 8 |
| Formal Charge | 0 |
| Complexity | 70.900 |
| 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. Zhen-Yu Chen, Yu Chen, Hai-Xia Zhang, Jian Zhang. (2022) Synthesis of chiral boron imidazolate frameworks with second-order nonlinear optics. JOURNAL OF SOLID STATE CHEMISTRY, [PMID:] [10.1016/j.jssc.2022.123001] |
| 2. Haolan Gou, Yingying Zhao, Yanglong Zhou, Wei Wei, Xiaoma Fei, Xiaojie Li, Xiaoya Liu. (2021) Effects of different imidazole accelerators on curing behavior and cross-linked network of epoxy resin/phenolic resin/benzoxazine ternary system. POLYMERS FOR ADVANCED TECHNOLOGIES, 33 (2): (610-626). [PMID:] [10.1002/pat.5543] |
B2217078