
Shandong Do Sender Chemicals Co.,Ltd.
- Organic Peroxide
- Hydroperoxides
- Ketone Peroxides
- Alkyl Peroxides
- Acyl Peroxides
- Ester Peroxides
- …
- Organic Peroxide
- Hydroperoxides
- Ketone Peroxides
- Alkyl Peroxides
- Acyl Peroxides
- Ester Peroxides
Shandong Do Sender Chemicals Co.,Ltd.
- Organic Peroxide
- Hydroperoxides
- Ketone Peroxides
- Alkyl Peroxides
- Acyl Peroxides
- Ester Peroxides
- …
- Organic Peroxide
- Hydroperoxides
- Ketone Peroxides
- Alkyl Peroxides
- Acyl Peroxides
- Ester Peroxides

Perodox® D - 2,2-Di(tert-butylperoxy) butane
CAS: 2167-23-9
A high-purity organic peroxide used as a free radical initiator in polymerization and crosslinking applications
Product Overview
Perodox® D,2,2-Di(tert-butylperoxy)butane is an organic peroxide compound with the molecular formula C₁₂H₂₆O₄ and a molecular weight of 234.33 g/mol. It is typically handled as a solution in mineral oil or other suitable solvents for safety reasons, with common commercial grades available as 50% solutions.
This compound belongs to the class of organic peroxides, which are characterized by the presence of an oxygen-oxygen single bond (peroxy functional group). Organic peroxides like 2,2-Di(tert-butylperoxy)butane are widely employed as initiators for free radical polymerization and as crosslinking agents for polymers and elastomers.
The compound appears as a clear, colorless to pale yellow liquid with a characteristic odor. It has a density of 0.88 g/mL at 25°C and is immiscible with water. Its boiling point is approximately 296.66°C, and it has a flash point of 118°F (47.78°C).
CAS Number: 2167-23-9
Molecular Formula: C₁₂H₂₆O₄
Molecular Weight: 234.33 g/mol
EINECS Number: 218-507-2
Common Synonyms: Perodox D, Trigonox D,Lupersol 220,Perhexa 22,Chaloxyd P 1200AL
Applications
2,2-Di(tert-butylperoxy)butane serves as a efficient free-radical initiator in various industrial processes, particularly in polymer chemistry. Its decomposition characteristics make it suitable for applications requiring specific temperature ranges and reaction kinetics
Polymerization Initiator
This compound is extensively used as a free radical initiator for the polymerization of monomers such as ethylene, styrene, vinyl chloride, and acrylates. The decomposition temperature and half-life of 2,2-Di(tert-butylperoxy)butane make it suitable for both high-pressure and solution polymerization processes
Crosslinking Agent for Polymers and Elastomers
In the rubber and plastics industry, 2,2-Di(tert-butylperoxy)butane is employed to crosslink polyethylene, ethylene-propylene-diene monomer (EPDM), silicone rubber, and other elastomers. Crosslinking enhances the thermal stability, chemical resistance, and mechanical properties of these materials
Curing Agent for Thermoset Resins
The compound is used in the curing of unsaturated polyester resins and vinyl ester resins, which are widely used in fiber-reinforced plastics, coatings, and composite materials
Organic Synthesis
2,2-Di(tert-butylperoxy)butane serves as a radical source in various organic transformations, including radical addition reactions and oxidations
Product Technical Specifications
Comprehensive technical specifications and performance characteristics of Perodox® D
Property
Assay (as 100% active): ≥ 95.0%
Appearance: Clear, colorless to pale yellow liquid
Active oxygen content: ≈ 6.83%
Density at 25°C: 0.88 g/mL
Refractive index (n20/D): 1.445
Flash point: 118°F (48°C)
Water solubility: Immiscible
Vapor pressure at 25°C: 50 Pa
SADT (Self-accelerating decomposition temperature): ≥ 80°C UN Recommendations
Safety & Storage
Proper handling and storage procedures for Perodox® D
2,2-Di(tert-butylperoxy)butane is classified as an organic peroxide and possesses significant hazards.
It may cause fire or explosion if mishandled, is harmful if swallowed, and causes serious eye irritation
Hazard Identification
Oxidizing (O) - May cause or intensify fire; oxidizer
Irritant (Xi) - Causes skin and eye irritation
Specific target organ toxicity (single exposure)
Risk Phrases
R8 - Contact with combustible material may cause fire
R41 - Risk of serious damage to eyes
R7 - May cause fire
R36/38 - Irritating to eyes and skin
R10 - Flammable
R37/38 - Irritating to respiratory system and skin
R65 - Harmful: May cause lung damage if swallowed
Safe Handling Procedures
When handling 2,2-Di(tert-butylperoxy)butane, implement the following safety measures
Personal Protective Equipment (PPE): Wear suitable protective clothing, gloves, and eye/face protection. Use chemical safety goggles and face shield if splash risk exists. Impermeable gloves and protective clothing are recommended.
Engineering Controls: Use only in well-ventilated areas, preferably with local exhaust ventilation. Avoid all sources of ignition (heat, sparks, open flames).
Handling Precautions: Do not grind or subject to friction or impact. Avoid contact with incompatible materials. Keep away from heat, sparks, and open flames.
Storage Conditions
Proper storage is critical for maintaining stability and ensuring safety:
Temperature: Store in a refrigerator at approximately 4°C in a dedicated flammables area
Container: Keep in original container, tightly closed
Segregation: Store away from incompatible materials (acids, bases, strong oxidizing agents, powdered metals, strong reducing agents)
Ventilation: Ensure adequate ventilation in storage area
Light: Protect from direct sunlight
Incompatible Materials
2,2-Di(tert-butylperoxy)butane is incompatible with:
Acids and bases (may catalyze decomposition)
Strong oxidizing agents
Strong reducing agents (may cause violent reaction)
Powdered metals (may catalyze decomposition)
Combustible materials
Transport Information
UN Number: UN 3103
Hazard Class: 5.2 (Organic peroxide)
Packing Group: II
Transport Emergency Card: According to ADR/RID/ADNR/IMDG/IATA/ICAO
Frequently Asked Questions
Common questions about Perodox® D and its applications
What is the CAS number for 2,2-Di(tert-butylperoxy)butane?
What is the molecular formula of 2,2-Di(tert-butylperoxy)butane?
What is the molecular weight of 2,2-Di(tert-butylperoxy)butane?
What is the structure of 2,2-Di(tert-butylperoxy)butane?
What is the IUPAC name for this compound?
What is the typical physical form of 2,2-Di(tert-butylperoxy)butane as supplied?
What are some common trade names for 2,2-Di(tert-butylperoxy)butane?
Is 2,2-Di(tert-butylperoxy)butane the same as DTBPB?
What is the primary industrial use of 2,2-Di(tert-butylperoxy)butane?
How is 2,2-Di(tert-butylperoxy)butane used in the plastics industry?
Can this peroxide be used for curing resins?
Is 2,2-Di(tert-butylperoxy)butane used in organic synthesis?
What makes this peroxide suitable as a polymerization initiator?
What is the density of 2,2-Di(tert-butylperoxy)butane?
What is the boiling point of 2,2-Di(tert-butylperoxy)butane?
What is the flash point of 2,2-Di(tert-butylperoxy)butane?
Is 2,2-Di(tert-butylperoxy)butane soluble in water?
What is the active oxygen content of this peroxide?
What is the self-accelerating decomposition temperature (SADT) for this peroxide?
What is the half-life of 2,2-Di(tert-butylperoxy)butane at 120°C?
What is the half-life of 2,2-Di(tert-butylperoxy)butane at 140°C?
What are the major hazards associated with 2,2-Di(tert-butylperoxy)butane?
What personal protective equipment (PPE) is recommended when handling this peroxide?
Is 2,2-Di(tert-butylperoxy)butane flammable?
What should you do in case of skin contact with this chemical?
What should you do in case of eye contact?
What are the first aid measures for inhalation?
Does this peroxide require any special ventilation?
How should 2,2-Di(tert-butylperoxy)butane be stored safely?
What materials are incompatible with 2,2-Di(tert-butylperoxy)butane?
What is the shelf life of this organic peroxide?
What are the stability concerns for this compound?
What is the UN number for transporting 2,2-Di(tert-butylperoxy)butane?
What is the hazard class for transport according to international regulations?
What is the Packing Group for transport?
How is this substance classified under GHS (Globally Harmonized System)?
How does 2,2-Di(tert-butylperoxy)butane compare to other dialkyl peroxides like dicumyl peroxide?
When should I choose 2,2-Di(tert-butylperoxy)butane over other initiators like benzoyl peroxide?
What factors should be considered when selecting this peroxide for a process?
How should waste or spillage of 2,2-Di(tert-butylperoxy)butane be disposed of?
What is the environmental impact of this peroxide?
What does a decrease in the activity of my peroxide solution indicate?
Why is it crucial to avoid contamination of this peroxide?
Can I mix 2,2-Di(tert-butylperoxy)butane with other additives?
How can I determine the concentration/activity of the peroxide upon receipt?
Where can I buy 2,2-Di(tert-butylperoxy)butane?
What information should I expect to receive from the supplier?
Can this peroxide be shipped internationally?
What is the mechanism of free radical generation for this peroxide?
How does the concentration of peroxide affect the polymerization rate and molecular weight?
Can the decomposition kinetics be modeled for process design?
What are the main decomposition products of 2,2-Di(tert-butylperoxy)butane?
Organic Peroxides - Perodox®
Hydroperoxides
Ketone Peroxides
Alkyl Peroxides
Acyl Peroxides
Perodox® 187
Ester Peroxides
Perodox® 23
Perodox® EHP
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Perodox® 125
Perodox® 121
Perodox® 42
Perodox® 117
Perodox® F
Perodox® 133
Perodox® 131
Perodox® BPIC
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