≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C Ships Wet ice,FedEx DG Service 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.
2,3-Dimethyl-2-butene undergoes hydrolysis to form hydroxyl radical
2,3-Dimethyl-2-butene was used in the preparation of thexyl NHC-borane (diMe-Imd-BH2thexyl)
| Canonical Smiles | CC(=C(C)C)C |
|---|---|
| IUPAC Name | 2,3-dimethylbut-2-ene |
| InChIKey | WGLLSSPDPJPLOR-UHFFFAOYSA-N |
| INCHI | 1S/C6H12/c1-5(2)6(3)4/h1-4H3 |
| Isomeric SMILES | CC(=C(C)C)C |
| WGK Germany | 3 |
| Molecular Weight | 84.16 |
| Beilstein | 1218 |
| Reaxy-Rn | 1340496 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1340496&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 | 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 | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
 F2611187 | Certificate of Analysis | Jun 24, 2026 | D107648 |
| C2202284 | Certificate of Analysis | Sep 16, 2025 | D107648 |
| C2202553 | Certificate of Analysis | Sep 16, 2025 | D107648 |
| E1803099 | Certificate of Analysis | Jun 12, 2025 | D107648 |
| E1803100 | Certificate of Analysis | Jun 10, 2025 | D107648 |
| B2518049 | Certificate of Analysis | Feb 28, 2025 | D107648 |
| B2626013 | Certificate of Analysis | Feb 28, 2025 | D107648 |
| G2515040 | Certificate of Analysis | Feb 28, 2025 | D107648 |
| B2301590 | Certificate of Analysis | Nov 11, 2024 | D107648 |
| J2524378 | Certificate of Analysis | Jul 23, 2024 | D107648 |
| C1826082 | Certificate of Analysis | Aug 07, 2023 | D107648 |
| F1523054 | Certificate of Analysis | May 09, 2023 | D107648 |
| C2202246 | Certificate of Analysis | Dec 21, 2021 | D107648 |
| Solubility | Insoluble in water; Soluble in Ether,Acetone,Chloroform,Ethanol |
|---|---|
| Sensitivity | Air Sensitive,Heat Sensitive |
| Refractive Index | 1.412 |
| Flash Point(°F) | 17.6 °F |
| Flash Point(°C) | -16℃ |
| Boil Point(°C) | 73°C |
| Melt Point(°C) | -75°C |
| Molecular Weight | 84.160 g/mol |
| XLogP3 | 2.900 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 0 |
| Exact Mass | 84.0939 Da |
| Monoisotopic Mass | 84.0939 Da |
| Topological Polar Surface Area | 0.000 Ų |
| Heavy Atom Count | 6 |
| Formal Charge | 0 |
| Complexity | 50.100 |
| 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. Li-Zhi Huang, Xiang Zhan, Weiguo Chen, Changye Li, Liandong Zhu, Yitao Dai, Jia Deng. (2024) Catalytic dechlorination of carbon tetrachloride to combustible hydrocarbons by Pd-Fe hydroxides through atomic hydrogen attack and direct electron transfer. SEPARATION AND PURIFICATION TECHNOLOGY, [PMID:] [10.1016/j.seppur.2024.127449] |
