B85927
tert-Butanol
TEBOL® 99, ≥99.3%
Synonym(s):
2-Methyl-2-propanol, tert-Butyl alcohol, Trimethyl carbinol
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About This Item
Linear Formula:
(CH3)3COH
CAS Number:
Molecular Weight:
74.12
UNSPSC Code:
41116107
NACRES:
NA.21
PubChem Substance ID:
EC Number:
200-889-7
Beilstein/REAXYS Number:
906698
MDL number:
Assay:
≥99.3%
Vapor pressure:
31 mmHg ( 20 °C), 44 mmHg ( 26 °C)
SMILES string
CC(C)(C)O
InChI key
DKGAVHZHDRPRBM-UHFFFAOYSA-N
InChI
1S/C4H10O/c1-4(2,3)5/h5H,1-3H3
vapor density
2.5 (vs air)
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)
Quality Level
pH
7 (20 °C)
density
0.775 g/mL at 25 °C (lit.)
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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
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Inhalation - Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3
target_organs
Central nervous system, Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 1
flash_point_f
59.0 °F - closed cup
flash_point_c
15 °C - closed cup
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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
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
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
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
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