Skip to Content
Merck
All Photos(1)

Key Documents

B85927

Sigma-Aldrich

tert-Butanol

TEBOL® 99, ≥99.3%

Synonym(s):

2-Methyl-2-propanol, tert-Butyl alcohol, Trimethyl carbinol

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
(CH3)3COH
CAS Number:
Molecular Weight:
74.12
Beilstein:
906698
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.21

vapor density

2.5 (vs air)

Quality Level

vapor pressure

31 mmHg ( 20 °C)
44 mmHg ( 26 °C)

Assay

≥99.3%

form

solid or liquid

autoignition temp.

896 °F

expl. lim.

8 %

manufacturer/tradename

TEBOL® 99

impurities

≤0.15% (water)

refractive index

n20/D 1.387 (lit.)

pH

7 (20 °C)

bp

83 °C (lit.)

mp

23-26 °C (lit.)

density

0.775 g/mL at 25 °C (lit.)

SMILES string

CC(C)(C)O

InChI

1S/C4H10O/c1-4(2,3)5/h5H,1-3H3

InChI key

DKGAVHZHDRPRBM-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

tert-Butanol (tert-butyl alcohol, TBA) is a monohydric alcohol. It is commonly used as a solvent in chemistry and a denaturant for ethanol. TBA is an ingredient in paint removers, an octane booster for gasoline, and an oxygenate gasoline additive. It is also an intermediate material in the synthesis of other chemical compounds like methyl tert-butyl ether, tert-butyl hydroperoxide, ethyl tert-butyl ether.

Application

tert-Butanol is used as:
  • A cosolvent with water (tert-Butanol/Water binary system) in the production of poly-ε-caprolactone (PCL) nanoparticles.
  • A solvent in the synthesis of ZnO nanoparticles (Zinc oxide nanoparticles) from zinc acetylacetonate hydrate.

Features and Benefits

tert-Butanol has:,Low vaporization latent

Legal Information

TEBOL is a registered trademark of Lyondell Chemical Properties, LP

Pictograms

FlameExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Inhalation - Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3

Target Organs

Central nervous system, Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

59.0 °F - closed cup

Flash Point(C)

15 °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.

Visit the Document Library

Jaime Salazar et al.
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 81(1), 82-90 (2012-01-12)
Nanosizing is a non-specific approach to improve the oral bioavailability of poorly soluble drugs. The decreased particle size of these compounds results in an increase in surface area. The outcome is an increased rate of dissolution, which can lead to
Arnau Bassegoda et al.
Applied microbiology and biotechnology, 97(19), 8559-8568 (2013-01-22)
Rhodococci are highly adaptable bacteria, capable to degrade or transform a large number of organic compounds, including recalcitrant or toxic products. However, little information is available on the lipases of the genus Rhodococcus, except for LipR, the first lipase isolated
Ee Ling Yong et al.
Water research, 46(6), 1990-1998 (2012-02-14)
Ozonation is widely employed in water treatment to purify water. The R(ct) concept, which is defined as the ratio of OH exposure to ozone exposure, has been commonly used to quantify the OH concentration generating from ozone decomposition and model
Virginie Colombel et al.
The Journal of organic chemistry, 77(6), 2966-2970 (2012-03-07)
Efficient Csp(3)-Csp(3) Suzuki couplings have been developed with both potassium cyclopropyl- and alkoxymethyltrifluoroborates. Moderate to good yields have been achieved in the cross-coupling of potassium cyclopropyltrifluoroborate with benzyl chlorides possessing electron-donating or electron-withdrawing substituents. Benzyl chloride was also successfully cross-coupled
Kohsaku Kawakami
Journal of pharmaceutical sciences, 104(1), 276-279 (2014-11-11)
In our previous study, initiation time of crystallization was shown to be basically expressed as a function of only the reduced temperature, which was a ratio of storage and glass transition temperatures. This conclusion was obtained using quenched glasses with

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service