Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Linear Formula:
CH3CH2C(CH3)2OH
CAS Number:
Molecular Weight:
88.15
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
200-908-9
MDL number:
Beilstein/REAXYS Number:
1361351
Assay:
≥99%
Bp:
102 °C (lit.)
Vapor pressure:
12 mmHg ( 20 °C)
Product Name
2-Methyl-2-butanol, ReagentPlus®, ≥99%
vapor density
3 (vs air)
Quality Level
vapor pressure
12 mmHg ( 20 °C)
product line
ReagentPlus®
assay
≥99%
form
liquid
autoignition temp.
819 °F
expl. lim.
9 %
dilution
(for general lab use)
refractive index
n20/D 1.405 (lit.)
bp
102 °C (lit.)
mp
−12 °C (lit.)
density
0.805 g/mL at 25 °C (lit.)
functional group
hydroxyl
SMILES string
CCC(C)(C)O
InChI
1S/C5H12O/c1-4-5(2,3)6/h6H,4H2,1-3H3
InChI key
MSXVEPNJUHWQHW-UHFFFAOYSA-N
General description
2-Methyl-2-butanol is a sterically hindered alcohol.
Application
2-Methyl-2-butanol may be used as a solvent in the following processes:
It may also be used in the preparation of 2-chloro-2-methylbutane by reacting with concentrated hydrochloric acid.
- Palladium (II)-catalyzed ortho-C–H olefination of phenylacetic acids.
- Rhodium-catalyzed direct C-H functionalization at the C7 position of N-pivaloylindoles.
It may also be used in the preparation of 2-chloro-2-methylbutane by reacting with concentrated hydrochloric acid.
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
Still not finding the right product?
Explore all of our products under 2-Methyl-2-butanol
signalword
Danger
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Eye Dam. 1 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Central nervous system, Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 1
flash_point_f
68.9 °F - closed cup
flash_point_c
20.5 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
?-tert-alkylation of ketones: 2-tert-pentylcyclopentanone
Organic Syntheses, 62, 95-95 (1984)
Rhodium?Catalyzed Regioselective C7?Functionalization of N?Pivaloylindoles.
Xu L, et al.
Angewandte Chemie (International Edition in English), 55(1), 321-325 (2016)
Ternary and Binary LLE Measurements for Solvent (4-Methyl-2-pentanone and 2-Methyl-2-butanol)+ Furfural+ Water between 298 and 401K.
Ma?nnisto? M, et al.
Journal of Chemical and Engineering Data, 61(2), 903-911 (2016)


