Determine the necessary mass, volume, or concentration for preparing a solution.
This is a demo store. No orders will be fulfilled.
| SKU | Size | Availability |
Price | Qty |
|---|---|---|---|---|
|
M708368-10ml
|
10ml |
1
|
$39.90
|
|
|
M708368-50ml
|
50ml |
1
|
$99.90
|
|
| Synonyms | 2-Methylbut-2-ene | Amylene | Pentene |
|---|---|
| Specifications & Purity | ≥99% |
| Storage Temp | Store at 2-8°C |
| Shipped In |
Wet ice This product requires cold chain shipping. Ground and other economy services are not available. |
| Product Description |
2-Methyl-2-butene is a trisubstituted olefin. It acts as guest and forms stable solid host-guest complexes with self-assembled benzophenone bis-urea macrocycles.The impact of active chlorine on photo-oxidation of 2-methyl-2-butene was studied.Photosensitized oxidation of 2-methyl-2-butene adsorbed on internal framework of Na-ZSM-5 zeolite was studied. Gas-phase reaction of 2-methyl-2-butene with ozone has been investigated. Kinetics of liquid-phase alkylation of 3-methylthiophene with 2-methyl-2-butene on supported phosphoric acid has been reported.2-methyl-2-butene undergoes ultraviolet irradiation, leading to the formation of trimethylene oxides.
|
Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Hydrocarbons |
| Class | Unsaturated hydrocarbons |
| Subclass | Branched unsaturated hydrocarbons |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Branched unsaturated hydrocarbons |
| Alternative Parents | Unsaturated aliphatic hydrocarbons Alkenes |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Branched unsaturated hydrocarbon - Unsaturated aliphatic hydrocarbon - Olefin - Alkene - Acyclic olefin - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as branched unsaturated hydrocarbons. These are hydrocarbons that contains one or more unsaturated carbon atoms, and an aliphatic branch. |
| External Descriptors | alkene |
|
|
|
| IUPAC Name | 2-methylbut-2-ene |
|---|---|
| INCHI | InChI=1S/C5H10/c1-4-5(2)3/h4H,1-3H3 |
| InChIKey | BKOOMYPCSUNDGP-UHFFFAOYSA-N |
| Smiles | CC=C(C)C |
| Isomeric SMILES | CC=C(C)C |
| WGK Germany | 3 |
| UN Number | 2460 |
| Packing Group | II |
| Molecular Weight | 70.13 |
| Beilstein | 1361353 |
| Reaxy-Rn | 1361353 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1361353&ln= |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Oct 23, 2024 | M708368 | |
| Certificate of Analysis | Oct 23, 2024 | M708368 | |
| Certificate of Analysis | Oct 23, 2024 | M708368 | |
| Certificate of Analysis | Oct 23, 2024 | M708368 | |
| Certificate of Analysis | Aug 07, 2024 | M708368 | |
| Certificate of Analysis | Aug 07, 2024 | M708368 | |
| Certificate of Analysis | Aug 07, 2024 | M708368 |
| Solubility | Miscible with alcohol, benzene, ligroin, ethylene oxide and ether. Immiscible with water |
|---|---|
| Sensitivity | Hygroscopic;Heat sensitive |
| Refractive Index | 1.3874 |
| Flash Point(°F) | -4 °F |
| Flash Point(°C) | -20℃ |
| Boil Point(°C) | 38.4°C |
| Melt Point(°C) | -133.77°C |
| Molecular Weight | 70.130 g/mol |
| XLogP3 | 2.300 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 0 |
| Exact Mass | 70.0783 Da |
| Monoisotopic Mass | 70.0783 Da |
| Topological Polar Surface Area | 0.000 Ų |
| Heavy Atom Count | 5 |
| Formal Charge | 0 |
| Complexity | 38.000 |
| 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. Ziping Li, Jia-ao Wang, Si Ma, Zhenwei Zhang, Yongfeng Zhi, Fuchun Zhang, Hong Xia, Graeme Henkelman, Xiaoming Liu. (2022) 2D covalent organic frameworks for photosynthesis of α-trifluoromethylated ketones from aromatic alkenes. APPLIED CATALYSIS B-ENVIRONMENTAL, 310 (121335). |
| 2. Du Jianzeng, Li Yonghong, Miao Zhenyu. (2019) Difunctional Adsorbents Ni/ZnO–HZSM-5 on Adsorption Desulfurization and Aromatization of Olefin Reaction. TRANSACTIONS OF TIANJIN UNIVERSITY, 25 (2): (143-151). |
| 3. Tingting Huang, Qingyi Peng, Wenjin Shi, Jundong Xu, Yu Fan. (2018) An anionic surfactant-assisted equilibrium adsorption method to prepare highly dispersed Fe-promoted Ni/Al2O3 catalysts for highly selective mercaptan removal. APPLIED CATALYSIS B-ENVIRONMENTAL, 230 (154). |
| 4. Zixuan Yu, Xiaohui Liu, Xiaoxiang Xu, Wenquan Tao, Zhuo Li, Boyu Li. (2025) Enhanced selectivity and stability for CO2 capture through amine-functionalized COFs-based mixed matrix membranes. SEPARATION AND PURIFICATION TECHNOLOGY, 361 (131274). |