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tert-Butyl hydroperoxide

CAS No.
75-91-2
Chemical Name:
tert-Butyl hydroperoxide
Synonyms
TBHP;T-Hydro;T-BUTYL HYDROPEROXIDE;Trigonox;tert-Butyl hydrogen peroxide;2-Hydroperoxy-2-methylpropane;butylhydroperoxide;tert-Butyl hydroperoxide Solution;tertiary-;Butylhydroperoxid
CBNumber:
CB3854248
Molecular Formula:
C4H10O2
Molecular Weight:
90.12
MDL Number:
MFCD00002130
MOL File:
75-91-2.mol
MSDS File:
SDS
Last updated:2024-12-18 14:08:52

tert-Butyl hydroperoxide Properties

Melting point -2.8 °C
Boiling point 37 °C (15 mmHg)
Density 0.937 g/mL at 20 °C
vapor pressure 62 mmHg at 45 °C
refractive index n20/D 1.403
Flash point 85 °F
storage temp. 2-8°C
form Liquid
pka pK1: 12.80 (25°C)
color Clear colorless
Water Solubility Miscible
Merck 14,1570
BRN 1098280
Exposure limits No exposure limit is set. On the basis of its irritant properties a ceiling limit of 1.2 mg/m3 (0.3 ppm) is recommended.
Stability Stable, but may explode if heated under confinement. Decomposition may be accelerated by traces of metals, molecular sieve or other contaminants. Incompatible with reducing agents, combustible material, acids.
InChIKey CIHOLLKRGTVIJN-UHFFFAOYSA-N
LogP 1.230 (est)
Indirect Additives used in Food Contact Substances TERT-BUTYL HYDROPEROXIDE
FDA 21 CFR 175.105; 176.170
CAS DataBase Reference 75-91-2(CAS DataBase Reference)
FDA UNII 955VYL842B
NIST Chemistry Reference Tert-butyl hydroperoxide(75-91-2)
EPA Substance Registry System tert-Butyl hydroperoxide (75-91-2)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictogramsGHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
GHS02,GHS05,GHS06,GHS07,GHS08,GHS09
Signal word  Danger
Hazard statements  H311-H330-H371-H372-H373-H226-H242-H302-H311+H331-H314-H317-H341-H411-H304-H336-H410-H300-H310-H318
Precautionary statements  P220-P261-P273-P280-P305+P351+P338-P310-P210-P234-P301+P310-P303+P361+P353-P304+P340+P310-P331-P403+P233-P201-P202-P233-P240-P241+P242+P243-P260-P264-P270-P271-P272-P284-P301+P330+P331+P310-P303+P361+P353+P310+P363-P301+P310a-P304+P340-P320-P405-P410-P501a
Hazard Codes  O,C,N,T
Risk Statements  7-10-20/21/22-34-65-52/53-43-67-53-68-51/53-23-21/22
Safety Statements  14-3/7-61-45-36/37/39-24-17-16-14A-26-62-47-43
RIDADR  UN 3109 5.2
WGK Germany  3
RTECS  EQ4900000
3-21
Autoignition Temperature Self-accelerating decomposition at 88 to 93 °C
TSCA  Yes
HazardClass  5.2
PackingGroup  II
HS Code  29094990
Hazardous Substances Data 75-91-2(Hazardous Substances Data)
Toxicity LD50 oral (rat) 406 mg/kg
LD50 skin (rabbit) 460 mg/kg
LC50 inhal (rat) 500 ppm (4 h)
NFPA 704
4
4 4
OX

tert-Butyl hydroperoxide price More Price(32)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemical B3153 tert-Butyl Hydroperoxide (70% in Water) 75-91-2 100g $30 2024-03-01 Buy
Alfa Aesar A13926 tert-Butyl hydroperoxide 70% aq. soln. 75-91-2 100ml $33.2 2024-03-01 Buy
Alfa Aesar A13926 tert-Butyl hydroperoxide 70% aq. soln. 75-91-2 500ml $67 2024-03-01 Buy
Sigma-Aldrich 458139 Luperox? TBH70X, tert-Butyl hydroperoxide solution 70 wt. % in H2O 75-91-2 25ml $45.8 2024-03-01 Buy
Sigma-Aldrich 458139 Luperox? TBH70X, tert-Butyl hydroperoxide solution 70 wt. % in H2O 75-91-2 100ml $51.6 2024-03-01 Buy
Product number Packaging Price Buy
B3153 100g $30 Buy
A13926 100ml $33.2 Buy
A13926 500ml $67 Buy
458139 25ml $45.8 Buy
458139 100ml $51.6 Buy

tert-Butyl hydroperoxide Chemical Properties,Uses,Production

Chemical Properties

tert-Butyl hydroperoxide (TBHP) is a water-white liquid commonly commercially available as a 70% solution in water; 80% solutions are also available. It is used to initiate polymerization reactions and in organic syntheses to introduce peroxy groups into the molecule.

Uses

TBHP is an intermediate in the production of propylene oxide and t-butyl alcohol from isobutane and propylene. It is primarily used as an initiator and finishing catalyst in the solution and emulsion polymerization methods for polystyrene and polyacrylates. Other uses are for the polymerization of vinyl chloride and vinyl acetate and as an oxidation and sulfonation catalyst in bleaching and deodorizing operations. It is a strong oxidant and reacts violently with combustible and reducing materials, and metallic and sulfur compounds.

Uses

tert-Butyl hydroperoxide is used as an initiator for radical polymerization and in various oxidation process such as sharpless epoxidation. It is involved in osmium catalyzed vicinal hydroxylation of olefins under alkaline conditions. Furthermore, it is used in catalytic asymmetric oxidation of sulfides to sulfoxides using binaphthol as a chiral auxiliary and in the oxidation of dibenzothiophenes. It plays an important role for the introduction of peroxy groups in organic synthesis.

Production Methods

TBHP is produced by the liquid-phase reaction of isobutane and molecular oxygen or by mixing equimolar amounts of t-butyl alcohol and 30–50% hydrogen peroxide. TBHP can also be prepared from t-butyl alcohol and 30% hydrogen peroxide in the presence of sulfuric acid or by oxidation of tert-butylmagnesium chloride. The manufacturing process of TBHP is in a closed system.

Description

Tert-butyl hydroperoxide is an alkyl hydroperoxide in which the alkyl group is tert-butyl. It is widely used in a variety of oxidation processes. It has a role as an antibacterial agent and an oxidising agent.tert-Butyl hydroperoxide molecular weight

General Description

Watery odorless colorless liquid. Floats and mixes slowly with water.

Reactivity Profile

Most alkyl monohydroperoxides are liquid. The explosivity of the lower members (e.g., methyl hydroperoxide, or possibly, traces of the dialkyl peroxides) decreasing with increasing chain length and branching [Bretherick 2nd ed. 1979 p. 10]. Though relatively stable, explosions have been caused by distillation to dryness [Milas, JACS 1946, 68, 205] or attempted distillation at atmospheric pressure [Castrantas 1965 p. 15].

Health Hazard

tert-Butyl hydroperoxide is a strong irritant.Floyd and Stockinger (1958) observed thatdirect cutaneous application in rats did notcause immediate discomfort, but the delayedaction was severe. The symptoms were erythemaand edema within 2–3 days. Exposureto 500 mg in 24 hours produced asevere effect on rabbit skin, while a rinse of150 mg/min was severe to eyes.
It is moderately toxic; the effects aresomewhat similar to those of MEK peroxide.Symptoms from oral administration in ratswere weakness, shivering, and prostration.
LD50 value, intraperitoneal (rats): 87 mg/kg
LD50 value, oral (rats): 406 mg/kg.

Flammability and Explosibility

tert-Butyl hydroperoxide is a flammable liquid and a highly reactive oxidizing agent. Pure TBHP is shock sensitive and may explode on heating. Carbon dioxide or dry chemical extinguishers should be used for fires involving tert-butyl hydroperoxide.

Mechanism of action

The general mechanism of transition metal-catalyzed oxidative Mannich reactions of N, N-dialkyl anilines with tert-butyl hydroperoxide (TBHP) as the oxidant consists of a rate-determining single electron transfer (SET) that is uniform from 4-methoxy- to 4-cyano-N, N-dimethylanilines. The tert-butylperoxy radical is the major oxidant in the rate-determining SET step that is followed by competing backward SET and irreversible heterolytic cleavage of the carbon–hydrogen bond at the α-position to nitrogen. A second SET completes the conversion of N, N-dimethylaniline to an iminium ion that is subsequently trapped by the nucleophilic solvent or the oxidant prior to the formation of the Mannich adduct[1].
Tert-butyl hydroperoxide could induce oxidative stress in liver mitochondria at low concentrations. The damaging effect of low concentrations of tBHP in the course of pyruvate oxidation in isolated liver mitochondria is caused by the opening of the nonspecific Ca2+-dependent cyclosporin A-sensitive pore in the inner mitochondrial membrane[2].

Safety Profile

Moderately toxic by ingestion and inhalation. A severe skin and eye irritant. Mutation data reported. At highest dosage levels, symptoms noted were severe depression, incoordmation, and cyanosis. Death was due to respiratory arrest. Very dangerous fire hazard when exposed to heat or flame, or by spontaneous chemical reaction such as with reducing materials. Moderately explosive; may explode during distillation. Violent reaction with traces of acid. Concentrated solutions may ignite spontaneously on contact with molecular sieve. Mixtures with transition metal salts may react vigorously and release oxygen. Forms an unstable solution with 1,2-dichloroethane. To fight fire, use alcohol foam, CO2, dry chemical. When heated to decomposition it emits acrid smoke and fumes.

Carcinogenicity

A study performed to evaluate the carcinogenicity of TBHP found it was not carcinogenic when applied to the skin of mice at 16.6% of the peroxide 6 times a week for 45 weeks. However, if its application was preceded by 0.05 mg of 4-nitroquinoline-1-oxide as a 0.25% solution in benzene applied 20 times over 7 weeks followed by TBHP (16.6% in benzene), then malignant skin tumors appeared between days 390 and 405 of the experiment . This supports the theory that peroxides are not complete carcinogens, but may act as promoters . The effects of TBHP on promotable and nonpromotable mouse epidermal cell culture lines were reported by Muehlematter et al. .

storage

tert-butyl hydroperoxide should be stored in the dark at room temperature (do not refrigerate) separately from oxidizable compounds, flammable substances, and acids. Reactions involving this substance should be carried out behind a safety shield.

Toxicity evaluation

TBHP accelerates oxidation of glutathione and decreases the metabolism of sodium hexobarbital in rat livers and is a strong oxidation agent.

Incompatibilities

tert-Butyl hydroperoxide and concentrated aqueous solutions of TBHP react violently with traces of acid and the salts of certain metals, including, in particular, manganese, iron, and cobalt. Mixing anhydrous tert-butyl hydroperoxide with organic and readily oxidized substances can cause ignition and explosion. TBHP can initiate polymerization of certain olefins.

Waste Disposal

Excess tert-butyl hydroperoxide and waste material containing this substance should be placed in an appropriate container, clearly labeled, and handled according to your institution's waste disposal guidelines.

References

[1] Maxim O, et al. Mechanistic Investigation of Oxidative Mannich Reaction with tert-Butyl Hydroperoxide. The Role of Transition Metal Salt. Journal of the American Chemical Society, 2013; 135: 1549–1557.
[2] Fedotcheva N, et al. Mechanism of induction of oxidative stress in liver mitochondria by low concentrations of tert-butyl hydroperoxide. Biochemistry (Moscow), 2013; 78: 75–79.

75-64-9
75-91-2
Synthesis of tert-Butyl hydroperoxide from tert-Butylamine
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Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Tert-Butyl Hydroperoxide pictures 2024-12-11 Tert-Butyl Hydroperoxide
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US $80.00-150.00 / L 1000L 0.7 5000 Metric Ton/Metric Tons per Year Wuxi High Mountain Hi-tech Development Co.,Ltd.
tert-Butyl hydroperoxide pictures 2024-11-01 tert-Butyl hydroperoxide
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US $10.00 / KG 1KG 99% 10 mt Hebei Weibang Biotechnology Co., Ltd
T-Butyl Hydro Peroxide pictures 2024-10-11 T-Butyl Hydro Peroxide
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US $10.00 / kg 1kg 98% 10 ton Hebei Chuanghai Biotechnology Co,.LTD
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