2,2-Azobisisobutyronitrile is a white crystalline powder that is soluble in organic solvents like methanol, ethanol, and acetone, water.
2,2-Azobisisobutyronitrile is commonly used as a polymerization initiator in various industrial processes, including the produc rubber, and acrylic fibers.
2,2-Azobisisobutyronitrile appears as a white powder that is soluble in alcohols and common organic solvents but remains ins.
CAS Number: 78-67-1
Molecular Formula: C8H12N4
Molecular Weight: 164.21
EINECS Number: 201-132-3
Synonyms: 78-67-1, 2,2'-Azobis(2-methylpropionitrile), Azobisisobutyronitrile, AIBN, 2,2'-Azobisisobutyronitrile, Genitron, 2,2'-AZOBIS(ISOBUTYRONITRILE), Aivn, Azdh, Vazo, Azobisisobutylonitrile, Porofor N, 2,2'-Azodiisobutyronitrile, Pianofor an, Porophor N, Aceto AZIB, Azobis(isobutyronitrile), Porofor 57, Chkhz 57, VAZO 64, (E)-Azobis(isobutyronitrile), 34241-39-9, Propanenitrile, 2,2'-azobis[2-methyl-, 2,2-Azodiisobutyronitrile, AZODIISOBUTYRONITRILE, 2,2'-Dimethyl-2,2'-azodipropiononitrile, Azodiisobutyrodinitrile, azo-bisisobutyronitrile, 2,2'-Azobis(2-methylpropanenitrile), azo-bis-isobutyronitrile, 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile, alpha,alpha'-Azodiisobutyronitrile, 2,2'-Dicyano-2,2'-azopropane, NSC 1496, alpha,alpha-azoisobutyronitrile, Propionitrile, 2,2'-azobis(2-methyl-, 2,2'-Dimethyl-2,2'-azodipropiononitrile, Propanenitrile, 2,2'-azobis(2-methyl-, Azodi(isobutyronitrile), FZ6PX8U5YB, Azobis(2-methylpropionitrile), 2,2'-Azodi(isobutyronitrile), (E)-2,2'-(diazene-1,2-diyl)bis(2-methylpropanenitrile), 2,2'-azobis(2-cyanopropane), 2,2'-Azobis[isobutyronitrile], DTXSID1026457, NSC-1496, NSC-68042, 2,2'-(E)-diazene-1,2-diylbis(2-methylpropanenitrile), 2,2'-Azobis-(2-methylpropanitrile), Propionitrile, 2,2'-azobis[2-methyl-, Azobis[isobutyronitrile], .alpha.,.alpha.'-Azodi(isobutyronitrile), .alpha.,.alpha.'-Azobis(isobutylonitrile), 2,2'-azodipropionitrile, 2,2'-Azobis(2-methylpropionitrile), 98%, 2-[(E)-2-(1-cyano-1-methylethyl)diazen-1-yl]-2-methylpropanenitrile, Propanenitrile, 2'-azobis[2-methyl-, Propanenitrile, 2'-azobis[2-methyl-, 2,2'-Azobis[2-methylpropionitrile], WLN: NCX1&1&NUNX1&1&CN, 2,2'-azobis-(2-methylpropionitrile), 2,2'-azobis-[2-methylpropionitrile], CAS-78-67-1, .alpha.,.alpha.'-Azobis(isobutyronitrile), .alpha.,.alpha.'-Azobis[isobutyronitrile], CCRIS 4287, HSDB 5220, .alpha.,.alpha.'-Azodisobutyric acid dinitrile), EINECS 201-132-3, UNII-FZ6PX8U5YB, 2,2'-Azobis (2-methylpropionitrile), AI3-28716, alpha,alpha'-Azodiisobutyric acid dinitrile, alpha,alpha-Azobisisobutyronitrile, Genitron AZDN, 2,2-Azobis(2-Methylpropionitrile), Genitron AZDN-FF, 2,2'-Azobis(2-methylpropanitrile), MFCD00013808, ADZN, azo-diisobutyronitrile, azo bisisobutyronitrile, azobis isobutyronitrile, azobis-isobutylonitrile, azobis-isobutyronitrile, azobisiso butyronitrile, azobisiso-butylonitrile, azobisiso-butyronitrile, azobisisobutyro nitrile, azobisisobutyro-nitrile, PERKADOX AIBN, PEROXAN AZDN, azo-di-isobutyronitrile, Vazo-64, azo(bisisobutyronitrile), azo-bisiso-butyronitrile, azobis-iso-butylonitrile, azobis-iso-butyronitrile, a,a'-azoisobutyronitrile, azo-bis-iso-butyronitrile, azo-bis-isobutyro-nitrile, azobis(iso-butyronitrile), Azobis (isobutyronitrile), POROFOR-57, SCHEMBL120, SCHEMBL122, VAZO CATALYST 64, 2,2'azobisisobutyronitrile, azo-bis-(isobutyronitrile), 2,2'-azobisisobutyronitril, EC 201-132-3, trans-Azo-2-cyanoisopropane, 2.2'-Azobisisobutyronitrile, 2,2'-azodi-isobutyronitrile, 2,2-azodi(isobutyronitrile), 2,2'-azo bisisobutyronitrile, 2,2'-azobis isobutyronitrile, 2,2'-azobis(2cyanopropane), 2,2'-azobis-isobutyronitrile, 2,2'-azobisiso-butyronitrile, 2,2'-azobisisobutyro-nitrile, a,a'-azobis(isobutyronitrile), azobis (2-methylpropionitrile), 2,2'-azo-bis-isobutyronitrile, 2,2'-azobis isobutyro-nitrile, 2,2'azobis-(isobutyronitrile), 2.2'-azobis(isobutyronitrile), alpha,alpha-azoisobutyro-nitrile, SCHEMBL6522063, 2-(1-cyano-1-methyl-ethyl)azo-2-methyl-propanenitrile, azobis (2-methyl-propionitrile), CHEMBL1886625, 2,2'-azo-bis(isobutyronitrile), 2,2'-Azobis (isobutyronitrile), 2,2'-azobis-(isobutyronitrile), alpha,alpha' azodiisobutyronitrile, DTXSID70859108, NSC1496, CHEBI:189360, OZAIFHULBGXAKX-VAWYXSNFSA-N, 2,2'azobis(2-methylproponitrile), alpha,alpha'-azobisisobutyronitrile, 2,2'azobis(2-methylpropionitrile), alpha, alpha'-azodiisobutyronitrile, 2,2' azobis(2-methylproponitrile), 2,2'-azobis(2-methylpropinitrile), 2-[2-(1-cyano-1-methylethyl)diazen-1-yl]-2-methylpropanenitrile, alpha, alpha'-azobisisobutyronitrile, alpha,alpha'-azobis isobutyronitrile, alpha,alpha'-azobis-isobutyronitrile, alpha,alpha-azo bis isobutyronitrile, AMY25782, BCP09376, NSC68042, Tox21_202084, Tox21_303177, 2,2'-azobis(2-methylpropannitrile), AB8084, alpha,alpha'-azo-bis-isobutyronitrile, alpha,alpha'-azobis(isobutyronitrile), STL299672, (E)-(NCC(CH3)2)2N2, 2,2'-azobis(2-methylproprionitrile), Alpha,alpha'-azo-di-iso-butyronitrile, N,N'-Bis(2-cyano-2-propyl)diazene, 2,2'-azo-bis(2-methylpropionitrile), 2,2'-azobis(2'-methylpropionitrile), 2,2'-azobis(2-methyl-propionitrile), A,A'-AZOISOBUTYRONITRILE,AIBN,ALPHA,ALPHA'-AZOBISISOBUTYRONITRILE,ALPHA,ALPHA-AZOBISISOBUTYRONITRILE,ALPHA,ALPHA'-AZO-DI-ISO-BUTYRONITRILE,ALPHA,ALPHA'-AZOISOBUTYRONITRILE,2,2'-dicyano-2,2'-azopropane,2,2'-Dimethyl-2,2'-azodipropionitrile
2,2-Azobisisobutyronitrile is a chemical compound that is primarily used as a radical initiator in polymer chemistry.
This white powder is soluble in alcohols and common organic solvents but is insoluble in water.
2,2-Azobisisobutyronitrile is often used as a foamer in plastics and rubber and as a radical initiator.
2,2-Azobisisobutyronitrile's soluble in a wide variety of organic solvents, including alcohol-based solvents.
Insoluble in water and denser than water. Moderately toxic by ingestion.
Readily ignited by sparks or flames and burns intensely and persistently.
2,2-Azobisisobutyronitrile toxic oxides of nitrogen produced during combustion.
2,2-Azobisisobutyronitrile is used as a catalyst, in vinyl polymerizations and a blowing agent for plastics.
2,2-Azobisisobutyronitrile is an organic compound with the formula [(CH3)2C(CN)]2N2.
2,2-Azobisisobutyronitrile is an organic compound with the formula [(CH3)2C(CN)]2N2.
This white powder is soluble in alcohols and common organic solvents but is insoluble in water.
2,2-Azobisisobutyronitrile is often used as a foamer in plastics and rubber and as a radical initiator.
As an azo initiator, radicals resulting from 2,2-Azobisisobutyronitrile have multiple benefits over common organic peroxides.
2,2-Azobisisobutyronitrile with methanol (by 1:12) and air-dry in a ventilated dark overnight, then place in a vacuum oven with phosphorus pentoxide as a desiccant, vacuum degree 1.013 * 105Pa, under reduced pressure, and dry to 24h.Refined 2,2'-Azobis(2-methylpropionitrile) needs to be put in the colored jar, sealed and kept in cold dark place.
2,2-Azobisisobutyronitrile with a reflux condenser , heat in a water bath to near boiling, quickly add 5gAIBN, shak to make it be completely dissolved (boiling time not too long, if too long, severe decomposition ), filter hot solution rapidly ( the funnel and filter flask using for filter must be warmed) and cool the filtrate to give white crystals, dry in a vacuum desiccator, a melting point of 102℃, store the product in a brown bottle, cryopreservation.
2,2-Azobisisobutyronitrile is insoluble in water and denser than water.
2,2-Azobisisobutyronitrile is readily ignited by sparks or flames.
2,2-Azobisisobutyronitrile is burns intensely and persistently.
2,2-Azobisisobutyronitrile is used as a catalyst, in vinyl polymerizations and a blowing agent for plastics.
2,2-Azobisisobutyronitrile, with the formula [(CH3)2C(CN)]2N2, is an organic compound that appears as a white powder.
2,2-Azobisisobutyronitrile is soluble in alcohols and common organic solvents but insoluble in water.
2,2-Azobisisobutyronitrile is commonly used as a foaming agent in plastics and rubber and as a radical initiator.
As an azo initiator, 2,2-Azobisisobutyronitrile has several advantages over common organic peroxides.
For example, 2,2-Azobisisobutyronitrile does not produce oxygen-containing byproducts or excessive yellowing.
Additionally, 2,2-Azobisisobutyronitrile causes less crosslinking, making it frequently used in the production of adhesives, acrylic fibers, detergents, and similar products.
2,2-Azobisisobutyronitrile is a chemical compound that has become increasingly popular in various industries.
2,2-Azobisisobutyronitrile is known by many names, including AIBN, Azobis, and V-azo.
2,2-Azobisisobutyronitrile's chemical formula is C8H12N4, and its CAS number is 78-67-1.
Appearance-wise, 2,2-Azobisisobutyronitrile is a white crystalline powder that is soluble in organic solvents such as ethanol, methanol, and chloroform, but not in water.
2,2-Azobisisobutyronitrile has a melting point of 104-106°C and a density of 1.02-1.03 g/mL.
2,2-Azobisisobutyronitrile has become quite essential in various industries such as polymer production, pharmaceuticals, and cosmetics.
2,2-Azobisisobutyronitrile is used as a polymerization initiator in the production of plastics, resins, and rubbers.
2,2-Azobisisobutyronitrile is also known for its use in radical reactions and organic synthesis.
In the medical industry, 2,2-Azobisisobutyronitrile is used to produce bone cements and in dental applications.
2,2-Azobisisobutyronitrile is also used in the cosmetics industry as a polymerization initiator for hair dyes.
When it comes to packaging, 2,2-Azobisisobutyronitrile should be stored in a cool, dry place in tightly sealed containers to prevent contamination.
During transportation, 2,2-Azobisisobutyronitrile should be kept away from heat, sources of ignition, moisture, and direct sunlight.
The manufacture of 2,2-Azobisisobutyronitrile begins with the reaction of sodium nitrite and isobutyronitrile.
The resultant solution is then cooled to the optimal temperature range of 0-5℃.
After filtration, the solid product is then washed with anhydrous ethanol and dried to obtain the final product.
In conclusion, 2,2-Azobisisobutyronitrile is an important chemical compound that has various uses in different industries.
2,2-Azobisisobutyronitrile is easily accessible and can be synthesized using simple procedures.
However, 2,2-Azobisisobutyronitrile should be handled with care due to its flammability and toxicity.
2,2-Azobisisobutyronitrile is important to follow all guidelines and regulations while handling and storing 2,2-Azobisisobutyronitrile.
2,2-Azobisisobutyronitrile is the most well-known azo initiator, which is easy and safe to use as a catalyst for free radical polymerization in the operating temperature range of 45-90 ºC, which is the main criterion for controlling polymerization reactions (Initiator for (co)polymerization of styrene, vinyl chloride, vinylidene chloride , acrylonitrile, acrylates and methacrylates.).
2,2-Azobisisobutyronitrile have low molecular mass.
And freedom from side reactions, 2,2-Azobisisobutyronitrile is more efficient and economical for controlled polymerizations at low concentrations.
The presence of additives does not affect 2,2-Azobisisobutyronitrile's rate of decomposition into free radicals.
2,2-Azobisisobutyronitrile does not cause oxidative degradation and discoloration, generally associated with peroxides.
This allows even transparent polymers to maintain their physical properties.
2,2-Azobisisobutyronitrile is an organic compound with the formula [(CH3)2C(CN)]2N2.
This white powder is soluble in alcohols and common organic solvents but is insoluble in water.
2,2-Azobisisobutyronitrile is maily used as polymerization initiator of monomer such as chloroethylene,vinyl acetate,acrylonitrile,etc.
2,2-Azobisisobutyronitrile is also used as blowing agent for PVC, polyalkene,polyurethane, polyvinyl alcohol, acrylonitrile/butadiene copolymer, chloroethylene copolymer, acrylonitrile/ butadiene/styrene copolymer, polyisocyanate, polyvinyl acetate, polyamide and polyester, etc.
Moreover, 2,2-Azobisisobutyronitrile is also used in other organic synthesis.
2,2-Azobisisobutyronitrile is used as polymerization initiator of monomers such as polyvinyl chlorida, polyvinyl alcohol,polystyrene and polyacrylonitrila.
2,2-Azobisisobutyronitrile is used as initiator for polymerization of vinyl chlorida acrylonitrila and other monomers, and also as foaming agent for rubber and plastics.
2,2-Azobisisobutyronitrile can also be used as vulcanizing agent, pesticide and intermediate of organic synthesis.
2,2-Azobisisobutyronitrile is used as blowing agent (elastomers and plastics), catalyst (vinyl polymerizations), curing agent (unsaturated polyester resins), and fumigant (when heated)
2,2-Azobisisobutyronitrile is used as a catalyst, in vinyl polymerizations and a blowing agent for plastics.
2,2-Azobisisobutyronitrile is used as an initiator in the polymerization of monomers such as vinyl chloride, vinyl acetate and acrylonitrile, and the amount thereof is 04% to 0.2%.
2,2-Azobisisobutyronitrile is also can be used as polyvinyl chloride, polyurethane, polyvinyl alcohol, acrylonitrile and butadiene copolymer rubber, plastic foaming agent.
As an azo initiator, radicals resulting from AIBN have multiple benefits over common organic peroxides.
For example, they do not have oxygenated byproducts or much yellow discoloration.
Additionally, they do not cause too much grafting and therefore are often used when making adhesives, acrylic fibers, detergents, etc.
2,2-Azobisisobutyronitrile is an organic compound with the formula [(CH3)2C(CN)]2N2.
This white powder is soluble in alcohols and common organic solvents but is insoluble in water.
2,2-Azobisisobutyronitrile is often used as a foamer in plastics and rubber and as a radical initiator.
These radicals formed by the decomposition of AIBN can initiate free-radical polymerizations and other radical-induced reactions.
For instance, a mixture of styrene and maleic anhydride in toluene will react if heated, forming the copolymer upon addition of AIBN.
Another example of a radical reaction that can be initiated by AIBN is the anti-Markovnikov hydrohalogenation of alkenes.
2,2-Azobisisobutyronitrile has also been used as the radical initiator for Wohl–Ziegler bromination.
2,2-Azobisisobutyronitrile-derived 2-cyano-2-propyl radical abstracts the hydrogen from tributyltin hydride.
The resulting tributyltin radical can be used for removal of a bromine atom.
2,2-Azobisisobutyronitrile-derived radicals abstract a hydrogen from HBr to give a bromine radical, which can add to alkenes.
This type of hydrohalogenation of an alkene proceeds with anti-Markovnikov selectivity.
Because 2,2-Azobisisobutyronitrile readily gives off free radicals, it is often used as a radical initiator.
This happens at temperatures above 40 °C, but in experiments is more commonly done at temperatures between 66 °C and 72 °C.
This decomposition has a ΔG‡ of 131 kJ/mol and results in two 2-cyano-2-propyl (carbon) radicals and a molecule of nitrogen gas.
The release of nitrogen gas pushes this decomposition forward due to the increase in entropy.
Melting point: 102-104 °C (dec.)(lit.)
Boiling point: 281.68°C (rough estimate)
Density: 1.11
vapor pressure: 0.81Pa at 24.85℃
refractive inde: n20/D1.495
Flash point: 4℃
storage temp.: 2-8°C
solubility: Chloroform (Slightly), Methanol (Slightly)
form: Solid
color: Crystals from EtOH
Odor: odorless
Water Solubility: Insoluble
Merck: 13,920
BRN: 1708400
Stability: Stability Flammable solid. Shock sensitive. Thermally unstable. May be explosive in combination with acetone or heptane. Incompatible with oxidizing agents.
InChIKey: OZAIFHULBGXAKX-VAWYXSNFSA-N
LogP: 1.1 at 25℃
White columnar crystals or white crystalline powder.
Insoluble in water, soluble in methanol, ethanol, acetone, ether, petroleum ether and aniline and other organic solvents.
2,2-Azobisisobutyronitrile is used as an initiator for the polymerization of vinyl chloride, vinyl acetate, acrylonitrile and other monomers, as well as a foaming agent for rubber and plastics, the dosage is 10% ~ 20%.
2,2-Azobisisobutyronitrile can also be used as a curing agent, pesticide and organic synthesis intermediates.
2,2-Azobisisobutyronitrile is used as polyvinyl chloride, polyvinyl alcohol, polystyrene, polymerization initiator of monomer such as polyacrylonitrile organic synthesis intermediate.
2,2-Azobisisobutyronitrile is used as initiator for high molecular polymer.
2,2-Azobisisobutyronitrile is used as initiator for polymerization or copolymerization of vinyl acetate and acrylate.
2,2-Azobisisobutyronitrile may also be used as a blowing agent.
2,2-Azobisisobutyronitrile is mainly used as vinyl chloride, vinyl acetate, acrylonitrile monomer polymerization initiator.
2,2-Azobisisobutyronitrile can also be used as a foaming agent of polyvinyl chloride, polyolefin, Polyurethane, polyvinyl alcohol, vinyl chloride and butadiene copolymer, vinyl chloride copolymer, acrylonitrile and butadiene and styrene copolymer, polyisocyanate, polyvinyl acetate, polyamide and polyester.
In addition, 2,2-Azobisisobutyronitrile can be used for other organic synthesis.
2,2-Azobisisobutyronitrile is used in polymerization of monomers like vinyl chloride, vinyl acetate, ethylene, styrene, methyl methacrylate, etc.
2,2-Azobisisobutyronitrile is used as chemical blowing agent for section rigid PVC foams when the processing temperature range is 100-120 ºC.
2,2-Azobisisobutyronitrile is used as initiator in manufacture of nytron fibre.
2,2-Azobisisobutyronitrile is used for initiating of process of chlorination of dichloroethane.
2,2-Azobisisobutyronitrile is used in silicone foam and rubber foam applications
2,2-Azobisisobutyronitrile is used in the manufacture of acrylic sheet, bangles, tubes, rods etc.
2,2-Azobisisobutyronitrile is used as a low temperature blowing agent for making cellular plastics.
2,2-Azobisisobutyronitrile is used in the manufacture of acrylic resins.
2,2-Azobisisobutyronitrile is used in water treatment.
2,2'-Azobis(2-methylpropionitrile) is a particularly excellent free radical initiator , nitrogen will be released by the decomposition when it is heated to about 70 ° C and free radicals (CH3) 2CCN is generated which is affected by cyano radical , more stable.
2,2-Azobisisobutyronitrile can react with other organic substrates, and then generates a new radical in annihilation of itself , causing chain reaction of free radicals (see radical reaction).
At the same time, it can also be two coupled molecules, generating highly toxic tetramethoxysilane succinonitrile (TMSN).
2,2-Azobisisobutyronitrile melts when heated to 100~107 ° C and dramaticly decomposes, releases nitrogen and several organic nitrile compound toxic to humans, and may cause an explosion, fire.
Slowly decomposes at room temperature, and it should be stored at 10 ° C or less.
2,2-Azobisisobutyronitrile metabolizes into hydrocyanic acid in the blood, liver, brain and other tissues of animals.
2,2-Azobisisobutyronitrile the temperature of condensation reaction above is 55~60 ℃, reaction time is 5h, and then cool down to 25~30 ℃ ,time is 2h.
2,2-Azobisisobutyronitrile when to be cooled to below 10 ℃,begin to flow chlorine and carry out the reaction at below 20 ℃.
Ratio of material: HCN: acetone: hydrazine = 1L:1.5036kg:0.415kg.
Acetone cyanide alcohol and hydrazine hydrate react, and then the use of chlorine oxidation or amino nitrile with sodium hypochlorite oxidation.
Self-decomposition or self-ignition may be triggered by heat, chemical reaction, friction or impact.
Self-accelerating decomposition may occur if the specific control temperature is not maintained.
These materials are particularly sensitive to temperature rises. 2,2'-Azobis(2-methylpropionitrile) is an azo compound.
2,2-Azobisisobutyronitriles can detonate.
This applies in particular to organic azides that have been sensitized by the addition of metal salts or strong acids.
Toxic gases are formed by mixing materials of this class with acids, aldehydes, amides, carbamates, cyanides, inorganic fluorides, halogenated organics, isocyanates, ketones, metals, nitrides, peroxides, phenols, epoxides, acyl halides, and strong oxidizing or reducing agents.
Flammable gases are formed by mixing materials in this group with alkali metals.
Explosive combination can occur with strong oxidizing agents, metal salts, peroxides, and sulfides.
If this chemical gets into the eyes, remove anycontact lenses at once and irrigate immediately for at least15 min, occasionally lifting upper and lower lids.
2,2-Azobisisobutyronitrile contacts theskin, remove contaminated clothing and wash immediatelywith soap and water.
2,2-Azobisisobutyronitrile has been inhaled, remove from exposure,begin rescue breathing (using universal precautions, including resuscitation mask) if breathing has stopped and CPR ifheart action has stopped.
Transfer promptly to a medicalfacility.
2,2-Azobisisobutyronitrile has been swallowed, get medical attention.
Give large quantities of water and inducevomiting.
Allarea employees should be trained regularly in emergencymeasures for cyanide poisoning and in CPR.
2,2-Azobisisobutyronitrile a cyanide antidote kit should be kept in the immediate work area and mustbe rapidly available.
Kit ingredients should be replaced every1°2 years to ensure freshness.
Persons trained in the use ofthis kit, oxygen use, and CPR must be quickly available.
Flammable; dust may form explosive mixture with air.
2,2-Azobisisobutyronitrile unstable and easily oxidized material; keep away from oxidizers, strong acids.
Warming causes production of 2,2-Azobisisobutyronitrile and cyanide fumes.
Keep away from acetone and other ketones, alcohols, lithium, aluminum, aldehydes, and hydrocarbons, such as heptane.
This applies in particular to organic azides that have been sensitized by the addition of metal salts or strong acids.
Toxic gases are formed by mixing materials of this class with acids, aldehydes, amides, carbamates, cyanides, inorganic fluorides, halogenated organics, isocyanates, ketones, metals, nitrides, peroxides, phenols, epoxides, acyl halides, and strong oxidizing or reducing agents.
Flammable gases are formed by mixing materials in this group with alkali metals.
Explosive combination can occur with strong oxidizing agents, metal salts, peroxides, and sulfides.
2,2-Azobisisobutyronitrile is sensitive to prolonged exposure to heat.
2,2-Azobisisobutyronitrile is incompatible with strong oxidizing agents.
Uses Of 2,2-Azobisisobutyronitrile:
2,2-Azobisisobutyronitrile is used as an initiator in polymer radical polymerization because its molecules can easily undergo split reactions and form molecules with high activation energy.
2,2-Azobisisobutyronitrile is the most commonly used azo initiator.
Its characteristic is that the decomposition reaction is relatively stable, only one kind of free radical is generated, and basically no induced decomposition occurs, so it is often used in the kinetics research of free radical polymerization.
2,2-Azobisisobutyronitrile is an azo-compound and is widely used as a free radical initiator.
2,2-Azobisisobutyronitrile has labile carbon-nitrogen covalent bond which undergoes homolytic scission under thermal, chemical or photochemical conditions producing free radicals.
They are useful in many reactions like halogenation, polymerisation of vinyl monomers, grafting reactions, curing of rubbers and unsaturated polymers and cross-linking of polyolefins.
2,2-Azobisisobutyronitrile can be used as an initiator in the synthesis of highly cross-linked Poly(divinylbenzene) (PDVB) polymers.
It also can be used as an initiator in the polymerization process of 2-hydroxyethyl methacrylate (HEMA).
The polymerization initiator for Vinyl chloride, vinyl acetate, acrylonitrile and blowing agent for rubber, plastic , in an amount of 10% to 20%.
2,2-Azobisisobutyronitrile can also be used as curing agents, pesticides and organic synthesis intermediates.
2,2-Azobisisobutyronitrile is a highly toxic substance, mice are orally LD5017.2~25mg/kg, the organic cyanide released by the decomposition when it is heated has a greater poison on the human body .
2,2-Azobisisobutyronitrile is widely used in free radical polymerization to initiate the polymerization process.
When heated or decomposed, it generates free radicals that can initiate the polymerization of various monomers, such as styrene, acrylates, and methacrylates.
2,2-Azobisisobutyronitrile is used in the production of polymers and copolymers for various applications, including coatings, adhesives, and plastics.
2,2-Azobisisobutyronitrile is also used in other organic synthesis reactions where radical initiation is required.
2,2-Azobisisobutyronitrile is maily used as polymerization initiator of monomer such as chloroethylene,vinyl acetate,acrylonitrile,etc.
2,2-Azobisisobutyronitrile is also used as blowing agentfor PVC,polyalkene,polyurethane,polyvinyl alcohol,acrylonitrile/butadiene copolymer,chloroethylene copolymer,acrylonitrile/ butadiene/styrene copolymer,polyisocyanate,polyvinyl acetate,polyamide and polyester,etc.
Moreover, 2,2-Azobisisobutyronitrile is also used in other organic synthesis.
Azobisisobutyronitrile can be used as an initiator in the preparation of: Polystyrene by soap-free emulsion polymerization.
Molecularly imprinted polymer(MIP) using 1-vinyl imidazole, MIP can be used to quantify acid violet 19 dye in river water samples.
2,2-Azobisisobutyronitrile is a well-known azo initiator used as a catalyst for free radical polymerization.
2,2-Azobisisobutyronitrile is used polymerization of monomers such as vinyl chloride, vinyl acetate, ethylene, styrene, and methyl methacrylate.
Chemical foaming agent for rigid PVC foams at processing temperatures of 100-120 ºC.
2,2-Azobisisobutyronitrile is widely used to initiate free radical polymerization reactions for various monomers, including styrene, acrylates, and methacrylates.
This is fundamental in producing a wide range of plastics, coatings, and adhesives.
2,2-Azobisisobutyronitrile is employed in the synthesis of copolymers that combine different monomers to achieve specific properties, such as flexibility, strength, or thermal stability.
2,2-Azobisisobutyronitrile can also be used to produce block copolymers, which have distinct polymer segments with different physical and chemical properties.
2,2-Azobisisobutyronitrile serves as a source of free radicals in various organic synthesis reactions, allowing the formation of complex organic compounds.
It can be utilized in the functionalization of existing polymers, enabling the introduction of new functional groups to modify properties.
2,2-Azobisisobutyronitrile is commonly used in academic and industrial research settings for studying polymerization mechanisms and developing new polymer materials.
2,2-Azobisisobutyronitrile is used to produce crosslinked polymer networks, which enhance the material's mechanical strength, chemical resistance, and thermal stability.
While not its primary use, 2,2-Azobisisobutyronitrile can also be employed as a photoinitiator in UV-curable systems when combined with other compounds.
Storage Of 2,2-Azobisisobutyronitrile:
Color Code—Red Stripe: Flammability Hazard:
Donot store in the same area as other flammable materials.
Priorto working with this chemical should be trained on itsproper handling and storage.
2,2-Azobisisobutyronitrile must bestored to avoid contact with acetone, lithium, aluminumhydride, and water, since violent reactions occur.
2,2-Azobisisobutyronitrile is self-reactive and will explode at elevated temperatures.
2,2-Azobisisobutyronitrile should be stored under nitrogen, dry ice, or ice.
Sources of ignition, such as smoking and open flames, areprohibited where 2,2-Azobisisobutyronitrile is used, handled, or stored in amanner that could create a potential fire or explosion hazard.
Safety Profile Of 2,2-Azobisisobutyronitrile:
Poison by intraperitoneal route.
Moderately toxic by ingestion.
2,2-Azobisisobutyronitrile violent exothermic decomposition when heated.
Solution in acetone may decompose explosively.
Explodes when heated with heptane.
When heated to decomposition it emits toxic fumes of NO, and CN-.
2,2-Azobisisobutyronitrile is safer to use than benzoyl peroxide (another radical initiator) because the risk of explosion is far less.
However, 2,2-Azobisisobutyronitrile is still considered as an explosive compound, decomposing above 65 °C.
A respirator dust mask, protective gloves and safety glasses are recommended.
Pyrolysis of 2,2-Azobisisobutyronitrile without a trap for the formed 2-cyanopropyl radicals results in the formation of tetramethyl succinonitrile, which is highly toxic.