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About This Item
Linear Formula:
(CH3)2CHCH2CH3
CAS Number:
UNSPSC Code:
12191502
EC Index Number:
201-142-8
MDL number:
Assay:
≥95% (GC)
Bp:
28 °C/1013 hPa
Vapor pressure:
800 hPa ( 20 °C)
vapor pressure
800 hPa ( 20 °C)
Quality Level
assay
≥95% (GC)
form
liquid
color
APHA: ≤30
bp
28 °C/1013 hPa
mp
-160 °C
transition temp
flash point -57 °C
solubility
0.048 g/L
density
0.62 g/cm3 at 20 °C
shipped in
ambient
storage temp.
room temp
SMILES string
C(CC)(C)C
InChI
1S/C5H12/c1-4-5(2)3/h5H,4H2,1-3H3
InChI key
QWTDNUCVQCZILF-UHFFFAOYSA-N
General description
EMPARTA solvents are designed for routine chemical synthesis, drying, purification, and critical labware cleaning in quality control environments. Engineered for precision, they deliver consistently reproducible results essential for rigorous validation and documentation.
Exceptional Quality Standards: These solvents meet or exceed ACS specifications, providing assurance of high quality that is crucial for accurate testing and analysis in quality control.
Consistent Reproducibility: Designed for precision, the solvents ensure that results can be reliably reproduced, which is vital for maintaining compliance and integrity in quality control processes.
Versatile Applications: Suitable for a variety of QC tasks, including analytical testing, method validation, and testing USP/NF monographs, these solvents support a comprehensive approach to quality assurance in laboratory settings.
Exceptional Quality Standards: These solvents meet or exceed ACS specifications, providing assurance of high quality that is crucial for accurate testing and analysis in quality control.
Consistent Reproducibility: Designed for precision, the solvents ensure that results can be reliably reproduced, which is vital for maintaining compliance and integrity in quality control processes.
Versatile Applications: Suitable for a variety of QC tasks, including analytical testing, method validation, and testing USP/NF monographs, these solvents support a comprehensive approach to quality assurance in laboratory settings.
Application
2-Methylbutane can be used as a reactant to synthesize:
It can also be used as a weakly polar solvent to study the intramolecular charge transfer (ICT) effect and the solvatochromic behavior of the pyrene substituted 1,3,4-oxadiazole derivatives.
- Isoprene by two-stage dehydrogenation process using chromia-alumina catalyst.
- Alkyl aromatic compounds via silver-catalyzed selective C(sp3)–H benzylation reaction in the presence of N-triftosylhydrazones as carbene precursor.
It can also be used as a weakly polar solvent to study the intramolecular charge transfer (ICT) effect and the solvatochromic behavior of the pyrene substituted 1,3,4-oxadiazole derivatives.
Packaging
M-Bottle for Solvents
As a global leader in lab reagents, we are constantly looking for new ways to optimize the safety of our products. The newly developed 4L solvent bottle design features advanced sealing technology that eliminates leaks to make the handling of solvents safer and more convenient than ever before.
See all the new features here!
As a global leader in lab reagents, we are constantly looking for new ways to optimize the safety of our products. The newly developed 4L solvent bottle design features advanced sealing technology that eliminates leaks to make the handling of solvents safer and more convenient than ever before.
See all the new features here!
Analysis Note
Assay (GC): 95% min
Color (APHA): 30 max
Form: Clear liquid
Infrared Spectrum: Conforms to standard
Color (APHA): 30 max
Form: Clear liquid
Infrared Spectrum: Conforms to standard
signalword
Danger
hcodes
Hazard Classifications
Aquatic Chronic 2 - Asp. Tox. 1 - Flam. Liq. 1 - STOT SE 3
target_organs
Central nervous system
supp_hazards
Storage Class
3 - Flammable liquids
wgk
WGK 2
flash_point_f
-59.8 °F - closed cup
flash_point_c
-51 °C - closed cup
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Power-efficient synthesis of isoprene via two-stage dehydrogenation of isopentane
Karimov OK, et al.
World Applied Sciences Journal , 24(3) (2013)
Synthesis, characterization and photophysical properties of a new class of pyrene substituted 1, 3, 4-oxadiazole derivatives
Najare Mahesh S, et al.
Optical Materials, 88 (2019)
Site-selective C-H benzylation of alkanes with N-triftosylhydrazones leading to alkyl aromatics
Liu Zhaohong, et al.
Chem, 6(8) (2020)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| MX0760-1 | 04061839429819 |



