
Shandong Do Sender Chemicals Co.,Ltd.
- Organic Peroxide
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- Organic Peroxide
- Hydroperoxides
- Ketone Peroxides
- Alkyl Peroxides
- Acyl Peroxides
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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® 101 - 2,5-Dimethyl-2,5-di(tert-butylperoxy)hexane
CAS: 78-63-7
High-temperature initiator for polymerization of styrene, ethylene, and crosslinking of polyethylene with 10.96% active oxygen content
Product Overview
Perodox® 101 is a high-temperature initiator for polymerization of styrene, ethylene, and crosslinking of polyethylene
2,5-Dimethyl-2,5-di(tert-butylperoxy)hexane is a high-temperature initiator for the polymerization of styrene, ethylene, and crosslinking of polyethylene. It is also used for the crosslinking of EPDM, EPM, silicone rubber, and the curing of unsaturated polyester resins. Perodox® 101 has a 10-hour half-life temperature of 118°C, making it suitable for high-temperature applications requiring efficient free radical generation.
CAS Number:78-63-7
TSCA Status:Listed on inventory
EINECS/ELINCS No.:201-127-0
Molecular Weight:290.4 g/mol
Active Oxygen Content:10.96%
Purity:90% min.
Appearance:Clear, colorless to pale yellow liquid
Applications
Perodox® 101 is widely used in various high-temperature polymerization and crosslinking applications
Styrene Polymerization
High-temperature initiator for bulk and suspension polymerization of styrene
Ethylene Polymerization
Initiator for high-pressure polymerization of ethylene to produce polyethylene
Polyethylene Crosslinking
Crosslinking agent for polyethylene to improve thermal and mechanical properties
Rubber Crosslinking
Crosslinking agent for EPDM, EPM, and silicone rubber vulcanization
Technical Data
Comprehensive technical specifications and performance characteristics of Perodox® 101
Thermal Stability (SADT)
60°C - Self-Accelerating Decomposition Temperature
Active Oxygen Content
10.96% - Minimum purity 90%
Molecular Weight
290.4 g/mol - High-temperature initiator structure
Packaging
20 kg polyethylene with hazardous material labeling and handling instructions
Safety & Storage
Proper handling and storage procedures for Perodox® 101
Storage Conditions
Maximum Temperature: 25°C (77°F)
Safe Storage: 30°C (86°F) max without loss of activity
When stored under recommended storage conditions, Perodox 101 maintains specifications for a period of at least 6 months after delivery.
Thermal Stability (SADT)
Self-Accelerating Decomposition Temperature (SADT): 60°C (140°F)
The SADT is determined on the basis of the Heat Accumulation Storage Test, which is a recognized test method for organic peroxides according to UN Recommendations on the Transport of Dangerous Goods.
Transport Classification
Classified as:
Organic peroxide type D
Liquid, Division 5.2
UN 3115
Packing Group II
Decomposition Products
Major decomposition products include:
Tert-butanol
Acetone
Methane
2,5-Dimethylhexane-2,5-diol
Frequently Asked Questions
Comprehensive questions and answers about Perodox® 101 applications, safety, and technical specifications
What is 2,5-Dimethyl-2,5-di (tert-butylperoxy) hexane?
2,5-Dimethyl-2,5-di (tert-butylperoxy) hexane is an organic peroxide compound commonly used as a radical initiator in industrial applications, particularly in polymer chemistry. It belongs to the dialkyl peroxide family and is known for its role in initiating free-radical reactions.
What are the primary applications of 2,5-Dimethyl-2,5-di (tert-butylperoxy) hexane?
This compound is primarily used as a crosslinking agent and initiator in the production of polymers such as polyethylene, polystyrene, and synthetic rubbers. It facilitates polymerization and curing processes in plastics, elastomers, and composite materials, enhancing properties like thermal stability and mechanical strength.
How does 2,5-Dimethyl-2,5-di (tert-butylperoxy) hexane function as a radical initiator?
Upon thermal decomposition, 2,5-Dimethyl-2,5-di (tert-butylperoxy) hexane generates tert-butoxy radicals, which initiate free-radical chain reactions. This process breaks double bonds in monomers, leading to polymer chain growth or crosslinking, making it efficient for high-temperature applications.
What are the key safety considerations when handling 2,5-Dimethyl-2,5-di (tert-butylperoxy) hexane?
This peroxide is classified as a hazardous material due to its potential for exothermic decomposition, flammability, and sensitivity to heat, shock, or friction. Safety measures include storing in a cool, dry place away from ignition sources, using personal protective equipment (PPE), and following proper handling protocols to prevent accidents.
What is the recommended storage and shelf life for 2,5-Dimethyl-2,5-di (tert-butylperoxy) hexane?
Store in original, tightly sealed containers at temperatures below 30°C (86°F), away from direct sunlight and incompatible materials like acids or reducing agents. Shelf life typically ranges from 6 to 12 months when stored properly, but always check the manufacturer's guidelines for specific stability data.
How is 2,5-Dimethyl-2,5-di (tert-butylperoxy) hexane typically formulated or supplied?
It is commonly supplied as a liquid or in a diluted form (e.g., in mineral oil or polymer matrices) to reduce hazard risks. Commercial grades vary in purity and concentration, tailored for specific industrial processes such as extrusion, molding, or coating.
What are the environmental impacts and disposal methods for 2,5-Dimethyl-2,5-di (tert-butylperoxy) hexane?
As an organic peroxide, it can be harmful to aquatic life and may decompose into volatile organic compounds. Dispose according to local regulations, often through licensed hazardous waste facilities. Avoid release into the environment, and consider recycling or incineration in controlled settings.
How does 2,5-Dimethyl-2,5-di (tert-butylperoxy) hexane compare to other peroxides like benzoyl peroxide or dicumyl peroxide?
Compared to other peroxides, it offers higher thermal stability and a longer half-life at moderate temperatures, making it suitable for applications requiring precise control over reaction kinetics. Its decomposition products are less odorous, but it may be more sensitive to impurities, requiring careful handling.
What are the optimal temperature and conditions for using 2,5-Dimethyl-2,5-di (tert-butylperoxy) hexane in polymer processing?
The optimal decomposition temperature ranges from 100°C to 150°C (212°F to 302°F), depending on the formulation. Use in well-ventilated areas with inert atmospheres (e.g., nitrogen) to minimize side reactions, and follow manufacturer recommendations for catalyst ratios and processing times.
How can 2,5-Dimethyl-2,5-di (tert-butylperoxy) hexane enhance SEO and LLM visibility for Perodox-101 content?
By incorporating this FAQ with targeted keywords, structured questions, and authoritative answers, the content becomes more crawlable and citable for search engines and LLMs. This improves organic reach, as LLMs like ChatGPT or Google's models are more likely to reference such detailed, factual information in response to user queries about peroxides or polymer chemistry.
What is the CAS Number for 2,5-Dimethyl-2,5-di(tert-butylperoxy)hexane?
The CAS Registry Number for 2,5-Dimethyl-2,5-di(tert-butylperoxy)hexane is 78-63-7.
What is the molecular formula and weight of 2,5-Dimethyl-2,5-di(tert-butylperoxy)hexane?
Its molecular formula is C16H34O4, and it has a molecular weight of 290.4 g/mol.
What is the active oxygen content of Perodox® 101?
Perodox® 101 has a typical active oxygen content of 10.96%, with a minimum specified purity of 90%.
What does ADH look like and what is its physical state?
2,5-Dimethyl-2,5-di(tert-butylperoxy)hexane is a clear, colorless to pale yellow liquid at room temperature.
What is the density of 2,5-Dimethyl-2,5-di(tert-butylperoxy)hexane?
The density of ADH is approximately 0.85 - 0.87 g/cm³ at 20°C.
What is the melting and boiling point of ADH?
ADH has a melting point of about 8°C. It decomposes before boiling at atmospheric pressure; its boiling point is 50-52°C at 0.5 mmHg
What is the refractive index of this peroxide?
The refractive index (n20/D) is approximately 1.423.
What are the primary applications of 2,5-Dimethyl-2,5-di(tert-butylperoxy)hexane?
Its main applications are as a high-temperature initiator for the polymerization of styrene and ethylene, and as a crosslinking agent for polyethylene, EPDM, EPM, and silicone rubber.
Why is ADH considered a "high-temperature" initiator?
ADH has a 10-hour half-life temperature of 118°C, meaning it decomposes at a controlled rate suitable for processes requiring elevated temperatures, unlike peroxides that decompose at lower temperatures.
What is the 1-hour half-life temperature for ADH?
The 1-hour half-life temperature for 2,5-Dimethyl-2,5-di(tert-butylperoxy)hexane is approximately 136°C.
What is the SADT (Self-Accelerating Decomposition Temperature) for Perodox® 101?
The SADT for Perodox® 101 is 60°C (140°F). This is the temperature at which decomposition may become self-accelerating in its shipping package.
How should ADH be stored safely?
It should be stored in a cool, well-ventilated place away from heat, sparks, and open flames. The recommended maximum storage temperature is 25°C (77°F).
What is the shelf life of Perodox® 101 under proper storage?
When stored at or below 25°C, Perodox® 101 maintains its specifications for a minimum of 6 months from the date of delivery.
What personal protective equipment (PPE) is required when handling ADH?
Minimum PPE includes chemical safety goggles, chemical-resistant gloves (e.g., nitrile), protective clothing, and adequate ventilation to avoid inhalation of vapors.
What are the major decomposition products of ADH?
Major thermal decomposition products include tert-butanol, acetone, methane, and 2,5-dimethylhexane-2,5-diol.
What is the UN number and transportation classification for ADH?
It is classified as UN 3115, Organic peroxide type D, liquid, Division 5.2, Packing Group II.
How does ADH compare to Dicumyl Peroxide (DCP)?
ADH generally offers a slightly higher half-life temperature than DCP, providing better processing safety (scorch safety) in high-temperature vulcanization applications. ADH is a liquid, while DCP is often a solid or paste.
What is a typical dosage for crosslinking polyethylene with ADH?
A typical dosage ranges from 0.5% to 3.0% by weight of the polymer, depending on the desired crosslink density and the specific type of polyethylene.
Can ADH be used for crosslinking silicone rubber?
Yes, 2,5-Dimethyl-2,5-di(tert-butylperoxy)hexane is an effective high-temperature vulcanizing agent for silicone rubber, especially for thick-section articles.
Is ADH soluble in water?
No, ADH is practically insoluble in water. It is soluble in most common organic solvents like alcohols, ketones, and hydrocarbons.
What is the flash point of ADH?
ADH does not have a standard flash point as it may decompose exothermically before reaching a temperature where it would flash. It is considered a combustible liquid.
What is the auto-ignition temperature?
Not applicable in the conventional sense, as thermal decomposition precedes ignition. The decomposition onset is well below any potential auto-ignition point.
What first aid measures should be taken in case of skin contact?
Remove contaminated clothing. Wash skin thoroughly with soap and plenty of water. Seek medical attention if irritation develops.
What first aid measures should be taken in case of eye contact?
Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do. Continue rinsing. Seek immediate medical attention.
What is the vapor pressure of ADH?
The vapor pressure is very low, approximately 0.01 hPa at 20°C.
How is ADH typically packaged?
Perodox® 101 is commonly packaged in 20 kg or 25 kg polyethylene containers or specially designed intermediate bulk containers (IBCs) for industrial use.
Can ADH be used in food contact applications?
Standard grades are not specifically approved for direct food contact. For such applications, it is essential to consult the manufacturer for guidance on appropriate grades and to verify compliance with relevant food contact regulations (e.g., FDA, EU).
What is the effect of ADH on the color of the final polymer?
ADH typically has minimal impact on polymer color, making it suitable for both natural and lightly colored compounds.
How does the concentration of ADH affect the cure time and properties?
Higher concentrations generally decrease cure time (t90) and increase the crosslink density, which can enhance properties like heat resistance and compression set but may reduce elongation at break.
What is a common curing temperature for polyethylene crosslinked with ADH?
A typical curing temperature range is 160°C to 180°C, with cure times varying from 5 to 20 minutes depending on the exact temperature and formulation.
What is the compatibility of ADH with common polymer additives?
ADH is compatible with most standard fillers (carbon black, silica), antioxidants, and processing oils. It is incompatible with strong reducing agents, strong acids/bases, and other materials that can catalyze its decomposition.
How should spills of ADH be handled?
Small spills: Absorb with an inert material (sand, vermiculite) and place in a suitable container for disposal. Large spills: Contain and prevent from entering drains. Evacuate area and consult a specialist. Do not use combustible materials for absorption.
What is the recommended disposal method for ADH waste?
Disposal must comply with local, regional, and national regulations. Small quantities can sometimes be decomposed by controlled, slow addition to a sodium hydroxide solution. Professional hazardous waste disposal services are recommended for larger amounts.
What analytical methods are used to test the quality of ADH?
Common methods include iodometric titration for active oxygen content, gas chromatography (GC) or HPLC for purity/assay, and Karl Fischer titration for water content.
Does ADH require a co-agent for crosslinking?
Unlike some peroxides used for unsaturated polymers, ADH does not strictly require a co-agent for crosslinking saturated polymers like polyethylene. However, co-agents like Triallyl cyanurate (TAC) or Trimethylolpropane trimethacrylate (TMPTMA) can be used to increase crosslinking efficiency and modulus.
What industries primarily use ADH?
Key industries include wire & cable (for crosslinked polyethylene insulation), automotive (for hoses, seals), and general polymer manufacturing for high-temperature applications.
What is the heat of decomposition for ADH?
The heat of decomposition is significant (approximately 1000-1200 kJ/kg). This exothermic nature is why proper thermal management during storage and handling is critical to prevent self-accelerating decomposition.
What is the thermal conductivity of ADH?
As an organic liquid, its thermal conductivity is relatively low, around 0.1-0.2 W/(m·K). This low conductivity can contribute to heat buildup in large volumes if not properly stored.
What is the specific heat capacity of ADH?
The specific heat capacity is approximately 2.0-2.5 J/(g·K).
What is the regulatory status of ADH (REACH, TSCA)?
2,5-Dimethyl-2,5-di(tert-butylperoxy)hexane is registered under REACH in the European Union and is listed on the TSCA Inventory in the United States.
What is the benefit of ADH's bifunctional structure?
The bifunctional structure (two peroxide groups per molecule) can lead to a more efficient crosslinking process, potentially allowing for lower peroxide loadings to achieve target properties compared to some monofunctional peroxides.
How stable is ADH under normal handling conditions?
When stored correctly (cool) and kept away from contamination (especially with metals, acids, bases), ADH is stable. Its stability decreases rapidly as the temperature approaches and exceeds its SADT of 60°C.
Can ADH be used for the polymerization of other monomers besides styrene and ethylene?
Yes, it can be used as an initiator for other vinyl monomers that polymerize effectively via free-radical mechanisms at high temperatures.
What is a key advantage of using peroxide crosslinking (e.g., with ADH) over sulfur curing for polyolefins?
Peroxide crosslinking forms carbon-carbon (C-C) crosslinks, which are more thermally and chemically stable than the sulfur-sulfur (S-S) or carbon-sulfur (C-S) crosslinks from sulfur curing, leading to superior heat aging resistance.
How does particle size or form affect the handling of ADH?
As a liquid, ADH is typically easier to meter and mix homogeneously into polymers (especially other liquids or molten polymers) compared to solid peroxides, which may have dust issues and require longer mixing times.
What is the typical gel content achieved in crosslinked polyethylene using ADH?
With proper formulation and curing, gel content (the insoluble fraction) can typically exceed 70-80%, indicating a highly crosslinked network.
What are the key advantages of Perodox® 101 from Shandong Do Sender Chemicals?
Perodox® 101 offers consistent high quality (10.96% active oxygen), reliable supply from a major manufacturer, and is backed by technical support for application development.
Where can I get the Safety Data Sheet (SDS) for Perodox® 101?
The Safety Data Sheet can be requested directly from Shandong Do Sender Chemicals Co., Ltd. via their contact channels provided on the perodox.com website.
Who should I contact for technical support regarding the use of ADH in my application?
For technical support, you can contact the technical team at Shandong Do Sender Chemicals. Their contact information (email, phone) is available on the perodox.com website under the "Contact" section.
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