Di-tert-butyl peroxide is a stable organic peroxide used primarily as a radical initiator in polymerization reactions and organic synthesis, due to its controlled decomposition at high temperatures which releases free radicals.
With the chemical formula C8H18O2, Di-tert-butyl peroxide is a colorless to faintly yellow liquid that is insoluble in water but soluble in organic solvents, making it versatile in various industrial applications.
Di-tert-butyl peroxide is employed in polymer chemistry for the production of Low Density Polyethylene (LDPE), as well as in cross-linking agents for silicones and rubber, due to its efficiency as a radical initiator and its role in polymerization processes.
CAS Number: 110-05-4
EC Number: 203-733-6
Chemical Formula: C8H18O2
Molar Mass: 146.23 g/mol
Synonyms: Peroxide, bis(1,1-dimethylethyl), tert-Butyl peroxide, Bis(tert-butyl) peroxide, Cadox TBP, DTBP, Trigonox B, (tert-C4H9O)2, Cadox, Di-tert-butyl peroxyde, Di-tert-butylperoxid, Perossido di butile terziario, Peroxyde de butyle tertiaire, t-Butyl peroxide, Bis(1,1-dimethylethyl) peroxide, Di-t-butyl peroxide, Di-tertiary-butyl peroxide, t-butyl peroxide bis(1,1-di-methylethyl)peroxide, Peroxide, tert-butyl-, Interox DTB, Kayabutyl D, NSC 673, Perbutyl D, Peroxide, bis-tert-butyl-, 2-(tert-Butylperoxy)-2-methylpropane, tert-Butyl peroxide, Di-tert-butyl peroxide, 110-05-4, Di-t-butyl peroxide, t-Butyl peroxide, Cadox, Peroxide, bis(1,1-dimethylethyl), Trigonox B, Cadox TBP, Kayabutyl D, Perbutyl D, Interox DTB, Bis(tert-butyl) peroxide, Di-tert-butylperoxid, Peroxyde de butyle tertiaire, Di-tert-butyl peroxyde, Di-tert-Butyl hydroperoxide, di-tert-butylperoxide, Perossido di butile terziario, NSC 673, Bis(1,1-dimethylethyl) peroxide, Di-tertiary-butyl peroxide, M7ZJ88F4R1, DTXSID2024955, NSC-673, (Tributyl)peroxide, DTXCID704955, Bis(t-butyl)peroxide, 2,2'-dioxybis(2-methylpropane), CAS-110-05-4, UNII-M7ZJ88F4R1, t-butylperoxide, tBuOOtBu, Di-t-butylperoxide, di-tertbutylperoxide, ditert.butylperoxide, MFCD00008803, di-tertbutyl peroxide, ditert-butyl peroxide, di-tert.butyl peroxide, di-tertiarybutylperoxide, ditertiary butylperoxide, ditertiarybutyl peroxide, Peroxide, tert-butyl-, di(tert.-butyl)peroxide, di(tert.butyl) peroxide, di-tert.-butyl peroxide, di-tertiary butylperoxide, (tert-C4H9O)2, di-tertiary butyl peroxide, DTBP [MI], Peroxide, bis-tert-butyl-, EC 203-733-6, SCHEMBL14861, NSC673, CHEMBL1558599, (CH3)3CO-OC(CH3)3, 2-tert-butyldioxy-2-methylpropane, Tox21_201461, Tox21_300099, AKOS015902599, NCGC00091801-01, NCGC00091801-02, NCGC00091801-03, NCGC00254065-01, NCGC00259012-01, tert-Butyl peroxide (Luperox DI), 97%, Luperox(R) DI, tert-Butyl peroxide, 98%, D3411, NS00006093, BIS(1,1-DIMETHYLETHYL)PEROXIDE [HSDB], A802134, Q413043, t-butyl peroxide bis(1,1-di-methylethyl)peroxide, J-002365, J-520402, WLN: 1X1 & 1 & OOX1 & 1 & 1, F0001-0215, di-tert-butyl peroxide, tert-butyl peroxide, di-t-butyl peroxide, cadox, peroxide, bis 1,1-dimethylethyl, dtbp, trigonox b, t-butyl peroxide, cadox tbp, kayabutyl d, Peroxide, bis(1,1-dimethylethyl), tert-Butyl peroxide, Bis(tert-butyl) peroxide, Cadox TBP, DTBP, Trigonox B, (tert-C4H9O)2, Cadox, Di-tert-butyl peroxyde, Di-tert-butylperoxid, Perossido di butile terziario, Peroxyde de butyle tertiaire, t-Butyl peroxide, Bis(1,1-dimethylethyl) peroxide, Di-t-butyl peroxide, Di-tertiary-butyl peroxide, t-butyl peroxide bis(1,1-di-methylethyl)peroxide, Peroxide, tert-butyl-, Interox DTB, Kayabutyl D, NSC 673, Perbutyl D, Peroxide, bis-tert-butyl-, di-tert-butyl peroxide,tert-butyl peroxide,di-t-butyl peroxide,cadox,peroxide, bis 1,1-dimethylethyl,dtbp,trigonox b,t-butyl peroxide,cadox tbp,kayabutyl d, Bis(1,1-dimethylethyl)peroxide, Bis(t-butyl)peroxide, Bis(tert-butyl) peroxide, Cadox, Cadox TBP, DTBP, Di-t-butyl peroxide, Di-tert-Butyl hydroperoxide, Trigonox B, t-Butyl peroxide, tert-Butyl peroxide, UN3107, tert-Butyl peroxide , Luperox(R) DI, tert-Butyl peroxide, (tert-C4H9O)2, (tributyl)peroxide, 2-(tert-Butylperoxy)-2-methylpropane, Aztec di-t-butyl peroxoide, bis(1,1-dimethylethyl)-peroxid, bis(t-butyl)peroxide, Bis(tert-butyl) peroxide, bis(tert-butyl)peroxide, DTBP, 2-(tert-Butylperoxy)-2-methylpropane, TERT-BUTYL PEROXIDE, DI-T-BUTYL PEROXIDE, Trigonox b, (tributyl)peroxide, bis(tert-butyl)peroxide, DI-TERTIARY-BUTYL PEROXIDE, Cadox, cadoxtbp,
Di-tert-butyl peroxide is a volatile, slightly yellow transparent liquid, which is an alkyl hydrogen organic peroxide.
Di-tert-butyl peroxide is an efficient initiator (30% active ingredient in odorless mineral spirits) to produce low-density polyethylene (LDPE) and (meth)acrylates.
Di-tert-butyl peroxide is also known as DTBP, peroxide bis(1,1-dimethylethyl) and tert-Butyl peroxide.
Di-tert-butyl peroxide is a transparant liquid which has C8H18O2 as chemical formula.
Di-tert-butyl peroxide is typically produced by the oxidation of tert-butanol with hydrogen peroxide and sodium citrate.
Di-tert-butyl peroxide has been shown to be highly resistant to degradation, even at high pH values.
Di-tert-butyl peroxide has also been shown to induce neuronal death in vivo, which may be due to its ability to produce hydroxyl radicals and other reactive oxygen species.
Di-tert-butyl peroxide can be used for wastewater treatment because it reacts with organic matter and produces less sludge than chlorine.
Di-tert-butyl peroxide is also known as DTBP, peroxide bis(1,1-dimethylethyl) and tert-Butyl peroxide.
Di-tert-butyl peroxide is a transparant liquid which has C8H18O2 as chemical formula.
Di-tert-butyl peroxide is an organic compound used in polymer chemistry and organic synthesis as a radical initiator.
Di-tert-butyl peroxide is a clear, water-white or yellow liquid.
Di-tert-butyl peroxide is insoluble in water.
Di-tert-butyl peroxide is faintly yellow clear liquid.
Di-tert-butyl peroxide is insoluble in water.
In most cases a combination of Di-tert-butyl peroxide with other peroxides is used to ensure a broad reactivity range.
Di-tert-butyl peroxide is a reactive oxygen species that has been used as an oxidant in organic synthesis.
Di-tert-butyl peroxide is a highly efficient initiator for the production of low density polyethylene (LDPE).
Di-tert-butyl peroxide is an initiator for the (co-)polymerization of ethylene and (meth)acrylates.
Furthermore, Di-tert-butyl peroxide contributes to the production of polymers and various materials, acting as a cross-linker in the synthesis of polyolefins.
Di-tert-butyl peroxide is an organic compound consisting of a peroxide group bonded to two tert-butyl groups.
Di-tert-butyl peroxide is insoluble in water.
Di-tert-butyl peroxide is one of the most stable organic peroxides, due to the tert-butyl groups being bulky.
Di-tert-butyl peroxide is a colorless liquid.
Di-tert-butyl peroxide is a clear colorless liquid.
Di-tert-butyl peroxide is a clear, water-white liquid.
Di-tert-butyl peroxide has a specific gravity of 0.79, which is lighter than water, and Di-tert-butyl peroxide will float on the surface.
Di-tert-butyl peroxide is nonpolar and insoluble in water.
Di-tert-butyl peroxide is a stable organic peroxide that releases free radicals upon decomposition at elevated temperatures.
With the chemical formula C8H18O2, Di-tert-butyl peroxide serves as an organic peroxide compound.
Di-tert-butyl peroxide finds extensive applications in both research and industry.
Di-tert-butyl peroxide plays a crucial role as an initiator in polymerization reactions and acts as a catalyst for organic synthesis.
Di-tert-butyl peroxide is commonly used as a radical initiator in polymerization reactions and exhibits solubility in organic solvents but not in water.
Di-tert-butyl peroxide is an efficient initiator for the production of Low Density Polyethylene (LDPE).
Di-tert-butyl peroxide is used both for tubular and autoclave processes.
Di-tert-butyl peroxide also has the ability to react with chemicals in a variety of ways, including transfer reactions, such as the addition of alcohols or esters.
The mechanisms of these reactions are still being studied.
Di-tert-butyl peroxide is a transparant liquid which has C8H18O2 as chemical formula.
Di-tert-butyl peroxide is a colorless, volatile liquid characterized by its sweet odor.
Di-tert-butyl peroxideplays a crucial role as an initiator in polymerization reactions and acts as a catalyst for organic synthesis.
Furthermore, Di-tert-butyl peroxide contributes to the production of polymers and various materials, acting as a cross-linker in the synthesis of polyolefins.
Di-tert-butyl peroxide is a strong oxidizer and may ignite organic materials or explode if shocked or in contact with reducing agents.
In addition to being an oxidizer, Di-tert-butyl peroxide is highly flammable.
Di-tert-butyl peroxide has a boiling point of 231°F (110°C) and a flash point of 65°F (18°C).
The NFPA 704 designation is health 3, flammability 2, and reactivity 4.
The prefix “oxy” for oxidizer is placed in the white section at the bottom of the 704 diamond.
Di-tert-butyl peroxide is a clear colorless liquid.
Di-tert-butyl peroxide is a colorless, volatile liquid characterized by its sweet odor.
With the chemical formula C8H18O2, Di-tert-butyl peroxide serves as an organic peroxide compound.
Di-tert-butyl peroxide finds extensive applications in both research and industry.
Applications of Di-Tert-Butyl Peroxide:
Di-tert-butyl peroxide finds application in alkylating reactions, facilitating α-functionalization of α-amino carbonyl compounds.
Di-tert-butyl peroxide is used in formulation or re-packing, at industrial sites and in manufacturing.
In practice, combinations of two or more peroxides with diverging activities are used to reduce the residual monomer content in the final polymer and to increase reactor efficiency.
Di-tert-butyl peroxide is an efficient initiator (30% active ingredient in odorless mineral spirits) for the production of Low Density Polyethylene (LDPE).
Di-tert-butyl peroxide is used for both tubular and autoclave processes.
Release to the environment of Di-tert-butyl peroxide can occur from industrial use: formulation of mixtures and formulation in materials.
Di-tert-butyl peroxide also plays a role in methylation reactions, acting as a direct aromatic methylation agent when combined with a palladium catalyst.
The shelf life of Di-tert-butyl peroxide is 3 months.
Di-tert-butyl peroxide is used as an initiator for the (co)polymerization of ethylene, styrene, acrylates and methacrylates.
In most cases a combination with other peroxides is used to ensure a broad reactivity range.
Di-tert-butyl peroxide may also be used for the polymerization and copolymerization of styrene in the temperature range of 95-185°C.
Di-tert-butyl peroxide is used as ignition accelerator for diesel fuels.
Di-tert-butyl peroxide is used as a cross-linking agent (rubber and resins).
Di-tert-butyl peroxide is used as initiator for the production of Low Density Polyethylene (LDPE).
Further Di-tert-butyl peroxide finds its application in the polymerization and copolymerization of styrene, olefins and acrylic resins and as modification agent of polypropylene degradation.
The reaction mechanism involves both radical and non-radical pathways, with reductive elimination playing a crucial role in forming important C-C bonds.
Di-tert-butyl peroxide is used as a polymerization catalyst for acrylonitrile polymers and resins (including olefins, styrene, styrenated alkyds, and silicones).
Di-tert-butyl peroxide is used as curing agent for styrenated alkyds and silicone rubbers.
Being thermally unstable substance, Di-tert-butyl peroxide may undergo self-accelerating decomposition.
Di-tert-butyl peroxide is used for tubular and autoclave processes.
Di-tert-butyl peroxide can be used for the market segments: polymer production, polymer crosslinking and acrylics production with their different applications/functions.
Di-tert-butyl peroxide is an efficient initiator for the production of Low Density Polyethylene (LDPE).
Di-tert-butyl peroxide is used both for tubular and autoclave processes.
Di-tert-butyl peroxide is used as a crosslinking agent for unsaturated polyesters and silicone rubbers, also as a polymerization initiator.
Di-tert-butyl peroxide is used as an initiator for high-temperature, high-pressure polymerizations of ethylene and halogenated ethylene.
Di-tert-butyl peroxide is used in the synthesis of polyketones.
Di-tert-butyl peroxide is used as a finishing catalyst for polystyrene.
Di-tert-butyl peroxide is used both for tubular and autoclave processes.
In most cases a combination of Di-tert-butyl peroxide with other peroxides is used to ensure a broad reactivity range.
Di-tert-butyl peroxide is used for both tubular and autoclave processes.
Di-tert-butyl peroxide is widely used as a crosslinking agent for unsaturated polyester and silicone rubber, a polymerization initiator for monomers, a polypropylene modifier, a rubber vulcanizing agent, etc.
Di-tert-butyl peroxide is used in the following products: polymers.
This substance is used for the manufacture of: plastic products and chemicals.
Release to the environment of Di-tert-butyl peroxide can occur from industrial use: as processing aid and as processing aid.
Release to the environment of Di-tert-butyl peroxide can occur from industrial use: manufacturing of the substance.
Di-tert-butyl peroxide is used as initiator for the production of Low Density Polyethylene (LDPE).
The decomposition reaction proceeds via the generation of methyl radicals.
Di-tert-butyl peroxide is mainly used as initiator for polymerization reaction (such as elimination of monomer after polymerization of PVC and polyacrylic lotion).
Further Di-tert-butyl peroxide finds its application in the polymerization and copolymerization of styrene, olefins and acrylic resins and as modification agent of polypropylene degradation.
Di-tert-butyl peroxide is used for synthesis.
Di-tert-butyl peroxide can be used for the market segments: polymer production, polymer crosslinking and acrylics production with their different applications/functions.
The decomposition reaction proceeds via the generation of methyl radicals.
In most cases a combination with other peroxides is used to ensure a broad reactivity range.
Di-tert-butyl peroxide is used both for tubular and autoclave processes.
In most cases a combination with other peroxides is used to ensure a broad reactivity range.
Di-tert-butyl peroxide can be used for the market segments: polymer production, polymer crosslinking and acrylics production with their different applications/functions.
In most cases, combinations with other peroxides are used to ensure a wide reaction range.
Di-tert-butyl peroxide is used as a cross-linking agent (rubber and resins).
Di-tert-butyl peroxide can also be widely used as a raw material for synthesizing other organic peroxides.
The peroxide bond undergoes homolysis at temperatures above 100°C.
Hence Di-tert-butyl peroxide is commonly used as a radical initiator in organic synthesis and polymer chemistry.
Di-tert-butyl peroxide can in principle be used in engines where oxygen is limited, since the molecule supplies both the oxidizer and the fuel.
Di-tert-butyl peroxide has been used as a radical initiator to induce free radical polymerization.
Di-tert-butyl peroxide has also been used as a cetane enhancer in a study to determine the phase behavior of carboxylate-based extended surfactant reverse micellar microemulsions with ethanol and vegetable oil/diesel blends.
Di-tert-butyl peroxide is widely used as crosslinking agent of unsaturated polyester and silicone rubber, polymerization initiator of monomer, polypropylene modifier, rubber curing agent
Di-tert-butyl peroxide is used in tube and autoclave processes.
Applications of Di-tert-butyl peroxide in organic synthesis:
Alkylating reactions:
Di-tert-butyl peroxide is a compound that finds application in alkylating reactions, specifically in the α-alkylation of α-amino carbonyl compounds using simple alkanes.
This reaction is noteworthy as Di-tert-butyl peroxide proceeds through the cleavage of dual sp (3) C-H bonds, providing a facile pathway for the α-functionalization of α-amino ketones and α-amino esters.
The use of Di-tert-butyl peroxide as a promoter allows for the radical pathway to be involved in this transformation.
The radical mechanism involves the generation of alkyl radicals from the simple alkanes, which then react with the α-amino carbonyl compounds to form the desired α-alkylated products.
This method demonstrates the versatility and utility of Di-tert-butyl peroxide in the field of alkylating reactions, particularly in the context of α-functionalization.
Di-tert-butyl peroxide provides a convenient and efficient route for the introduction of alkyl groups onto α-amino ketones and α-amino esters, expanding the synthetic possibilities for these important classes of compounds.
Functions of Di-Tert-Butyl Peroxide:
Di-tert-butyl peroxide is used as a modifier of drying oil, adding this product can significantly improve the drying properties of castor oil, whale oil, tung oil, soybean oil and linseed oil.
Adding to other plastics can improve Di-tert-butyl peroxide's gloss and chemical resistance.
As a crosslinking agent, Di-tert-butyl peroxide can be used in silicone rubber, synthetic and natural rubber, polyethylene, EVA and EPT, etc.
As a polymerization initiator, Di-tert-butyl peroxide can be used for polystyrene and polyethylene.
Though many 1,1-bis-peroxides have been reported, few have been purified because of the higher explosion hazards compared with the monofunctional peroxides.
Di-tert-butyl peroxide is unlikely that this derivative would be particularly unstable compared to other peroxides in it's class, Bretherick 1979v.
Experimental Properties of Di-Tert-Butyl Peroxide:
Di-tert-butyl peroxide is an organic peroxide with the chemical formula (CH3)3COOOH.
Di-tert-butyl peroxide is a colorless to yellow liquid with a characteristic odor.
Di-tert-butyl peroxide is soluble in organic solvents such as ethers, hydrocarbons, and halogenated solvents, but Di-tert-butyl peroxide is insoluble in water.
One of the notable characteristics of Di-tert-butyl peroxide is its stability at room temperature.
However, when exposed to elevated temperatures, Di-tert-butyl peroxide undergoes slow decomposition, releasing free radicals.
This property makes Di-tert-butyl peroxide useful as a radical initiator in various chemical reactions.
Di-tert-butyl peroxide exhibits stability in the presence of moisture and most acids.
Di-tert-butyl peroxide can maintain its integrity under these conditions without decomposition.
However, it is important to note that Di-tert-butyl peroxide decomposes in the presence of strong bases.
In summary, Di-tert-butyl peroxide is a versatile organic peroxide used primarily as a radical initiator in polymerization reactions.
Di-tert-butyl peroxide is stable at room temperature, soluble in organic solvents, but insoluble in water.
Di-tert-butyl peroxide’s-controlled decomposition at high temperatures releases free radicals, making Di-tert-butyl peroxide valuable in a wide range of industrial applications.
Chemical Properties:
Di-tert-butyl peroxide consists of a peroxide group bonded to two tert-butyl groups.
Since the tert-butyl groups are bulky, Di-tert-butyl peroxide is one of the most stable organic peroxides.
Reactions of Di-Tert-Butyl Peroxide:
The peroxide bond undergoes homolysis at temperatures above 100°C.
For this reason Di-tert-butyl peroxide is commonly used as a radical initiator in organic synthesis and polymer chemistry.
The decomposition reaction proceeds via the generation of methyl radicals.
(CH3)3COOC(CH3)3 → 2 (CH3)3CO•(CH3)3CO• → (CH3)2CO + CH•3
2 CH•3 → C2H6
Di-tert-butyl peroxide can in principle be used in engines where oxygen is limited, since the molecule supplies both the oxidizer and the fuel.
Methylation Reaction:
Di-tert-butyl peroxide has been widely used in the methylation reaction as a direct aromatic methylation process with palladium (PdCl2) catalyst.
In a study, the mechanism of methylation reactions using Di-tert-butyl peroxide has been elucidated through energy calculations based on M06 density functional theory.
The research specifically focuses on the introduction of methyl radicals to the ortho position of the commonly used substrate, 2-phenylpyridine, via Di-tert-butyl peroxide.
By identifying the key intermediates and transition states in the reaction sequence, the reaction mechanism is explained.
Different possibilities regarding the coordination site between the substrate and the catalyst as well as subsequent mechanisms are discussed in detail.
The main mechanistic events include:
(a) oxidative or solvolysis of the peroxide O-O bond,
(b) C-H bond activation,
(c) C-C bond activation, and
(d) reductive elimination leading to the transfer of the methyl group onto the aromatic ring.
Both radical and non-radical pathways are considered. In the non-radical pathway, the lowest energy path involves C-H bond activation prior to peroxide coordination to palladium, followed by O-O bond cleavage and C-C bond activation.
Intermediate species generated through reductive elimination play a crucial role in forming important C-C bonds between the methyl and aromatic carbon.
In the non-radical pathway, the energy barrier for C-C bond activation is higher and identified as the rate-limiting step of the reaction.
However, in the radical pathway, the activation energy for C-C bond cleavage is lower than that for peroxide O-O bond cleavage.
Di-tert-butyl peroxide is found that a combination of both radical and non-radical pathways, involving the formation of a palladium methyl intermediate, is the most favorable route.
The predicted mechanism is consistent with experimental observations of the PdCl2-catalyzed methylation reaction using tert-butyl peroxide on 2-phenylpyridine.
Handling And Storage of Di-Tert-Butyl Peroxide:
Precautions for safe handling:
Advice on protection against fire and explosion:
Take precautionary measures against static discharge.
Hygiene measures:
Change contaminated clothing.
Wash hands after working with substance.
Conditions for safe storage, including any incompatibilities:
Storage conditions:
Tightly closed.
Storage stability:
Recommended storage temperature:
2 - 8 °C
Stability And Reactivity of Di-Tert-Butyl Peroxide:
Reactivity:
The explosive instability of the lower dialkyl peroxides (e.g., dimethyl peroxide) and 1,1-bis-peroxides decreases rapidly with increasing chain length and degree of branching, the di-tert-alkyl derivatives being amongst the most stable class of peroxides.
Chemical stability:
Di-tert-butyl peroxide is chemically stable under standard ambient conditions (room temperature).
Incompatible materials:
No data available
First Aid Measures of Di-Tert-Butyl Peroxide:
General advice:
Show this material safety data sheet to the doctor in attendance.
If inhaled:
After inhalation:
Fresh air.
Call in physician.
In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.
Consult a physician.
In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Call in ophthalmologist.
Remove contact lenses.
If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
Indication of any immediate medical attention and special treatment needed:
No data available
Fire Fighting Measures of Di-Tert-Butyl Peroxide:
Suitable extinguishing media:
Carbon dioxide (CO2)
Foam
Dry powder
Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
Further information:
Remove container from danger zone and cool with water.
Prevent fire extinguishing water from contaminating surface water or the ground water system.
Accidental Release Measures of Di-Tert-Butyl Peroxide:
Environmental precautions:
Do not let product enter drains.
Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up carefully with liquid-absorbent material.
Dispose of properly.
Clean up affected area.
Exposure Controls/Personal Protection of Di-Tert-Butyl Peroxide:
Personal protective equipment:
Eye/face protection:
Use equipment for eye protection.
Safety glasses
Skin protection:
Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0,4 mm
Break through time: 480 min
Splash contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 30 min
Body Protection:
Flame retardant antistatic protective clothing.
Respiratory protection:
Recommended Filter type: Respirator.
Control of environmental exposure:
Do not let product enter drains.
Identifiers of Di-Tert-Butyl Peroxide:
Chemical formula: C8H18O2
Molar mass: 146.230 g·mol−1
Density: 0.796 g/cm3
Melting point: −40 °C (−40 °F; 233 K)
Boiling point: 109 to 111 °C (228 to 232 °F; 382 to 384 K)
CAS Number: 110-05-4
Molecular Weight: 146.23
Beilstein: 1735581
EC Number: 203-733-6
MDL number: MFCD00008803
Physical state: clear, liquid
CAS number: 110-05-4
EC index number: 617-001-00-2
EC number: 203-733-6
Hill Formula: C₈H₁₈O₂
Molar Mass: 146.23 g/mol
HS Code: 2909 60 90
Density: 0.80 g/cm3 (20 °C)
Flash point: 6 °C
Ignition temperature: 182 °C
Melting Point: -40 °C
Vapor pressure: 53 hPa (20 °C)
Solubility: 0.063 g/l
CBNumber:CB8852799
Molecular Formula:C8H18O2
Molecular Weight:146.23
Properties of Di-Tert-Butyl Peroxide:
Color: colorless
Odor: very faint
Melting point/freezing point:
Melting point/range: < -29 °C -
Initial boiling point and boiling range: 109 - 110 °C - lit.
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits:
Upper explosion limit: > 99 %(V)
Flash point: 6 °C at ca.1.013 hPa - closed cup
Autoignition temperature: No data available
Decomposition temperature: No data available
pH: No data available
Viscosity:
Viscosity, kinematic: No data available
Viscosity, dynamic: 7,5 mPa.s at 20 °C
Water solubility: 0,171 g/l at 20 °C
Partition coefficient: n-octanol/water:
log Pow: 3,2 at 22 °C
Vapor pressure: 53 hPa at 20 °C
Density: 0,796 g/mL at 25 °C - lit.
Relative density: No data available
Relative vapor density: No data available
Particle characteristics: No data available
Explosive properties: No data available
Oxidizing properties: none
Other safety information: No data available
Molecular Weight: 146.23 g/mol
XLogP3-AA: 2.1
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 2
Rotatable Bond Count: 3
Exact Mass: 146.130679813 g/mol
Monoisotopic Mass: 146.130679813 g/mol
Topological Polar Surface Area: 18.5Ų
Heavy Atom Count: 10
Complexity: 80.8
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
color: Clear
Odor: distinctive odor
Water Solubility: immiscible
Merck: 14,3461
BRN: 1735581
Stability: May decompose explosively if heated,
subjected to shock, or treated with reducing agents.
InChIKey: LSXWFXONGKSEMY-UHFFFAOYSA-N
LogP: 3.2 at 22℃
CAS DataBase Reference 110-05-4(CAS DataBase Reference)
Indirect Additives used in Food Contact Substances: TERT-BUTYL PEROXIDE
FDA 21 CFR: 176.170; 177.2600