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Sigma-Aldrich

tert-Butanol

≥99% (GC)

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
Beilstein:
906698
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.21

vapor density

2.5 (vs air)

vapor pressure

31 mmHg ( 20 °C)
44 mmHg ( 26 °C)

Assay

≥99% (GC)

form

liquid

autoignition temp.

896 °F

expl. lim.

8 %

impurities

≤0.001% free acid (as C3H7COOH)
≤0.001% non-volatile matter
≤0.1% water (Karl Fischer)

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

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General description

tert-Butanol is a tertiary alcohol. Aqueous potassium peroxodisulfate undergoes photolysis in the presence of tert-butanol on irradiation with 254nm light at 20°C to afford hydrogen sulfate.

Application

tert-Butanol may be employed for the preparation of carbohydrate fatty acid esters. It may be employed as a reaction medium during the production of fatty acid methyl ester (FAME) from waste cooking palm oil (WCPO) by lipase-catalyzed reaction.

It can be used for the butylation of p-cresol in the presence of 12-tungstophosphoric acid supported on zirconia catalyst. 2-tert-Butyl-p-cresol (TBC), 2,6-di-tert-butyl-p-cresol (DTBC) and tert-butyl-p-tolyl ether (ether) are formed as butylation reaction products.

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)

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Catalytic studies of lipase on FAME production from waste cooking palm oil in a tert-butanol system.
Halim SFA and Kamaruddin AH.
Process. Biochem., 43(12), 1436-1439 (2008)
Sebastian Björklund et al.
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There is a current clinical need for the development of bone void fillers and bioactive bone graft substitutes. The use of mesenchymal stem cells (MSCs) that are seeded into 3D scaffolds and induce bone generation in the event of MSCs
The photolysis of potassium peroxodisulphate in aqueous solution in the presence of tert-butanol: a simple actinometer for 254nm radiation.
Mark G, et al.
Journal of Photochemistry and Photobiology A: Chemistry, 55(2), 157-160 (1990)
Mojtaba Yegane Badi et al.
Journal of environmental health science & engineering, 17(2), 685-700 (2020-02-08)
The present study aimed to model and optimize the dimethyl phthalate (DMP) degradation from aqueous solution using UVC/ Na2S2O8/Fe2+ system based on the response surface methodology (RSM). A high removal efficiency (97%) and TOC reduction (64.2%) were obtained under optimum

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