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Merck

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:
75-65-0
Molecular Weight:
74.12
UNSPSC Code:
41116107
NACRES:
NA.21
PubChem Substance ID:
329773135
EC Number:
200-889-7
Beilstein/REAXYS Number:
906698
MDL number:
MFCD00004464
assay:
≥99.3%
bp:
83 °C (lit.)
vapor pressure:
31 mmHg ( 20 °C)
44 mmHg ( 26 °C)

Product Name

tert-Butanol, TEBOL® 99, ≥99.3%

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)

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.)

Quality Level

100

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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

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.

Legal Information

TEBOL is a registered trademark of Lyondell Chemical Properties, LP

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

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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Certificates of Analysis (COA)

Lot/Batch Number
SHBS1796
SHBQ4699
BCCK3567
BCCH8313
BCCG7752

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Jaime Salazar et al.
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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
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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
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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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Bioresource technology, 116, 259-265 (2012-05-01)
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