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2-Methyl-2-butene - ≥99%, high purity , CAS No.513-35-9

    Grade & Purity:
  • ≥99%
In stock
Item Number
M708368
Grouped product items
SKU Size
Availability
Price Qty
M708368-10ml
10ml
1
$39.90
M708368-50ml
50ml
1
$99.90

Basic Description

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.


Application:
2-Methyl-2-butene may be employed as precursor for peroxyacetyl nitrate for the calibration purposes.

Taxonomic Classification

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

Names and Identifiers

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=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

7 results found

Lot Number Certificate Type Date Item
L2411244 Certificate of Analysis Oct 23, 2024 M708368
J2429515 Certificate of Analysis Oct 23, 2024 M708368
J2429519 Certificate of Analysis Oct 23, 2024 M708368
J2429520 Certificate of Analysis Oct 23, 2024 M708368
H2414391 Certificate of Analysis Aug 07, 2024 M708368
H2414392 Certificate of Analysis Aug 07, 2024 M708368
H2414415 Certificate of Analysis Aug 07, 2024 M708368

Chemical and Physical Properties

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

Citations of This Product

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). 

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