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Tert-Butyl Alcohol (TBA)

  • Product Name: Tert-Butyl Alcohol (TBA)
  • CAS: 75-65-0
  • Purity:
  • Appearance: clear colourless liquid after melting

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  • Molecular Formula:C4H10O
  • Molecular Weight:74.1228
  • Appearance/Colour:clear colourless liquid after melting 
  • Melting Point:23-26 °C(lit.) 
  • Refractive Index:n20/D 1.399(lit.)  
  • Boiling Point:84.603 °C at 760 mmHg 
  • Flash Point:11.667 °C 
  • PSA:20.23000 
  • Density:0.805 g/cm3 
  • LogP:0.77720 

tert-Butyl alcohol(Cas 75-65-0) Usage

General Description

Tert-butyl alcohol, also known as 2-methylpropan-2-ol, is a colorless organic compound with a strong, sweet odor. It is commonly used as a solvent and as a raw material in the production of other chemicals, such as tert-butyl acetate and tert-butyl chloride. Tert-butyl alcohol is flammable and can be harmful if inhaled, ingested, or absorbed through the skin. It is also known to cause irritation to the eyes, skin, and respiratory system. Tert-butyl alcohol is considered to have low acute toxicity, but prolonged exposure can lead to adverse health effects. As a result, proper handling and safety precautions should be taken when working with this chemical.

InChI:InChI=1/C4H10O/c1-4(2,3)5/h5H,1-3H3

75-65-0 Relevant articles

Electrocatalytic features of a heme protein attached to polymer-functionalized magnetic nanoparticles

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Direct electron-transfer and electrocata...

Correlation of the product E/Z framework geometry and O/O vs O/N regioselectivity in the dialkylation of hyponitrite

Arulsamy, Navamoney,Bohle, D. Scott,Imonigie, Jerome A.,Sagan, Elizabeth S.

, p. 5539 - 5549 (2000)

The products from the alkylation of silv...

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Walling,Heaton

, p. 38,44 (1965)

-

Homolytic reactivity of ligated boranes toward alkyl, alkoxyl, and peroxyl radicals

Lucarini, Marco,Pedulli, Gian Franco,Valgimigli, Luca

, p. 1161 - 1164 (1996)

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Kinetics of Oxidation of Hydrazine and of t-Butylhydrazine using Tris(dimethylglyoximato)nickelate(IV) in the Presence of Added Cu(2+) (aq)

Acharya, Sridhara,Neogi, Gautam,Panda, Rama Krushna,Ramaswamy, Dorai

, p. 1477 - 1484 (1984)

The kinetics of the oxidation of hydrazi...

Temperature dependence of the rate and activation parameters for tert-butyl chloride solvolysis: Monte Carlo simulation of confidence intervals

Sung, Dae Dong,Kim, Jong-Youl,Lee, Ikchoon,Chung, Sung Sik,Park, Kwon Ha

, p. 378 - 382 (2004)

The solvolysis rate constants (kobs) of ...

Decomposition of tert-butyl hydroperoxide into tert-butyl alcohol and O2 catalyzed by birnessite-type manganese oxides: Kinetics and activity

Qi, Lin,Qi, Xingyi,Wang, Lili,Feng, Lili,Lu, Shupei

, p. 6 - 9 (2014)

Birnessite-type manganese oxides (M-OL-1...

Possible Role of Non-hydrogen-bonded Units in the Chemistry of Liquid Water

Pay, Nicholas G. M.,Symons, Martyn C. R.

, p. 2417 - 2422 (1993)

Pure liquid water is thought to contain ...

A search for mode-selective chemistry: The unimolecular dissociation of t-butyl hydroperoxide induced by vibrational overtone excitation

Chandler, David W.,Farneth, William E.,Zare, Richard N.

, p. 4447 - 4458 (1982)

The use of optoacoustic spectroscopy per...

Homolytic cleavage of the O-Cu(II) bond: XAFS and EPR spectroscopy evidence for one electron reduction of Cu(II) to Cu(i)

Yi, Hong,Zhang, Guanghui,Xin, Jie,Deng, Yi,Miller, Jeffrey T.,Kropf, Arthur J.,Bunel, Emilio E.,Qi, Xiaotian,Lan, Yu,Lee, Jyh-Fu,Lei, Aiwen

, p. 6914 - 6917 (2016)

The investigation into the active copper...

Enhanced catalytic performance of porphyrin cobalt(II) in the solvent-free oxidation of cycloalkanes (C5~C8) with molecular oxygen promoted by porphyrin zinc(II)

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Dual-metalloporphyrins catalytic system ...

CHANGE IN THE REACTIVITY OF DI-tert-BUTYL PEROXIDE DURING HOMOLYSIS WITH AN INCREASE IN THE DEGREE OF CONVERSION AND PRESSURE

Zhulin, V. M.,Khueidzha, I.,Koreshkov, Yu. D.

, p. 643 - 649 (1992)

It was found that the differential react...

Characterization of co-metabolic biodegradation of methyl: Tert -butyl ether by a Acinetobacter sp. strain

Li, Shanshan,Wang, Dan,Du, Dan,Qian, Keke,Yan, Wei

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Co-metabolic bioremediation is a promisi...

Partial Oxidation of Olefins: Conversion of Isobutene to tert-Butyl Alcohol on Oxygen-Covered Rh(111)

Xu, Xueping,Friend, C. M.

, p. 10753 - 10759 (1991)

The selective oxidation reactions of iso...

Kinetics of a Hydrolysis Reaction in an Oil/Water Microemulsion System Near the Critical Point

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We have constructed the pseudoternary ph...

Effect of Temperature on the Specific Heat of Activation for the Solvolysis of Tert-butyl Chloride and Tert-pentyl Chloride in Water

Adams, Paul A.,Sheppard, John G.

, p. 2114 - 2123 (1980)

Precise first-order rate constants for t...

Effect of Fluorination of the meso-Phenyl Groups on Selective Tetraphenylporphyrinatometal(III)-catalysed Reactions of Isobutane with Molecular Oxygen

Ellis, Jr., Paul E.,Lyons, James E.

, p. 1189 - 1190 (1989)

A series of tetrakis(pentafluorophenyl)p...

Solvent Ionizing Power. Comparisons of Solvolyses of 1-Adamantyl Chlorides, Bromides, Iodides and Tosylates in Protic Solvents

Bentley, William T.,Carter, Gillian E.,Roberts, Karl

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Solvolytic rate constants for 1-adamanty...

Autocatalysis in oxidation reactions of verdazyl radicals with hydroperoxides

Buzulukov

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The reaction of 2,4,6-triphenyl- and 2,3...

New evaluation scheme for two-dimensional isotope analysis to decipher biodegradation processes: Application to groundwater contamination by MTBE

Zwank, Luc,Berg, Michael,Elsner, Martin,Schmidt, Torsten C.,Schwarzenbach, Rene P.,Haderlein, Stefan B.

, p. 1018 - 1029 (2005)

Compound-specific analysis of stable car...

Control of electrochemical and ferryloxy formation kinetics of cyt P450s in polyion films by heme iron spin state and secondary structure

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, p. 16215 - 16224 (2009)

Voltammetry of cytochrome P450 (cyt P450...

Selective Functionalization of Hydrocarbons Using a ppm Bioinspired Molecular Tweezer via Proton-Coupled Electron Transfer

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An expanded porphyrin-biscopper hexaphyr...

Low-Level Quantification oftert-Butyl Nitrite in a Pharmaceutical Intermediate

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supporting information, p. 2415 - 2424 (2021/11/01)

A sensitive, reliable, and reproducible ...

Efficient oxidation of cycloalkanes with simultaneously increased conversion and selectivity using O2 catalyzed by metalloporphyrins and boosted by Zn(AcO)2: A practical strategy to inhibit the formation of aliphatic diacids

Shen, Hai-Min,Wang, Xiong,Ning, Lei,Guo, A-Bing,Deng, Jin-Hui,She, Yuan-Bin

, (2020/11/20)

The direct sources of aliphatic acids in...

Fast Addition of s-Block Organometallic Reagents to CO2-Derived Cyclic Carbonates at Room Temperature, Under Air, and in 2-Methyltetrahydrofuran

Elorriaga, David,de la Cruz-Martínez, Felipe,Rodríguez-álvarez, María Jesús,Lara-Sánchez, Agustín,Castro-Osma, José Antonio,García-álvarez, Joaquín

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Fast addition of highly polar organometa...

75-65-0 Process route

1,1-dimethylethyl-1-phenylethyl peroxide
28047-94-1

1,1-dimethylethyl-1-phenylethyl peroxide

1-Phenylethanol
98-85-1,13323-81-4

1-Phenylethanol

benzaldehyde
100-52-7

benzaldehyde

acetophenone
98-86-2

acetophenone

acetone
67-64-1

acetone

<i>tert</i>-butyl alcohol
75-65-0

tert-butyl alcohol

Conditions
Conditions Yield
In chlorobenzene; at 129.2 ℃; Product distribution; Rate constant; also with styrene, dimethylaniline, and 2,6-di-tert-butyl-p-cresol (radical traps);
78.8%
3.12%
1.1%
26.2%
49.4%
t-butyl phenylperacetate
3377-89-7

t-butyl phenylperacetate

benzyl bromide
100-39-0

benzyl bromide

acetone
67-64-1

acetone

benzeneacetic acid methyl ester
101-41-7

benzeneacetic acid methyl ester

<i>tert</i>-butyl alcohol
75-65-0

tert-butyl alcohol

Conditions
Conditions Yield
With toluene-p-sulfonyl bromide; In benzene; at 70 ℃; for 40h; Further byproducts given;
139.7 mg
51.6 mg
20.5 mg
4.0 mg

75-65-0 Upstream products

  • 186581-53-3
    186581-53-3

    diazomethane

  • 67-63-0
    67-63-0

    isopropyl alcohol

  • 67-56-1
    67-56-1

    methanol

  • 507-20-0
    507-20-0

    tertiary butyl chloride

75-65-0 Downstream products

  • 7580-85-0
    7580-85-0

    tert-butyl glycidyl ether

  • 80783-53-5
    80783-53-5

    3-(tert-butoxy)propan-1-ol

  • 1191-99-7
    1191-99-7

    2,3-dihydro-2H-furan

  • 1689-77-6
    1689-77-6

    2,5-di-tert-butylthiophene

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