- Melting point:102-104 °C (dec.)(lit.)
- Boiling point:281.68°C (rough estimate)
- Density 1.11
- refractive index n20/D1.495
- Flash point:4℃
- storage temp. 2-8°C
- color Crystals from EtOH
- 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.
- CAS DataBase Reference78-67-1(CAS DataBase Reference)
- NIST Chemistry Reference2,2'-Azo-bis-isobutyronitrile(78-67-1)
- EPA Substance Registry SystemAzobis(isobutyronitrile) (78-67-1)
- Hazard Codes E,Xn,F,Xi
- Risk Statements 2-11-20/22-52/53-67-65-48/20-38-63-66-36
- Safety Statements 39-41-47-61-62-36/37-16-26
- RIDADR UN 3234 4.1
- WGK Germany 2
- RTECS UG0800000
- F 4.4
- HazardClass 4.1
- PackingGroup II
- HS Code 29269090
- Hazardous Substances Data78-67-1(Hazardous Substances Data)
- ToxicityLDLo orl-rat: 670 mg/kg 34ZIAG 0,117,69
Azobisisobutyronitrile (abbreviated AIBN) 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. It is often used as a foamer in plastics and rubber and as a radical initiator. It'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. Burns intensely and persistently. Toxic oxides of nitrogen produced during combustion. Used as a catalyst, in vinyl polymerizations and a blowing agent for plastics.
Azobisisobutyronitrile (AIBN) is an azo-compound and is widely used as a free radical initiator. This compound 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. AIBN 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).
- Recrystallization1, recrystallize twice a chemically pure 2,2'-Azobis(2-methylpropionitrile) 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, add 50ml 95% alcohol into 150ml Erlenmeyer flask equipped 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.
- Temperature of initiator2,2'-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. It 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).
AIBN 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. Away from fire, heat source. poisonous. Metabolizes into hydrocyanic acid in the blood, liver, brain and other tissues of animals.
The above information is edited by the Chemicalbook of Tian Ye.
- Chemical propertiesWhite columnar crystals or white crystalline powder. Insoluble in water, soluble in methanol, ethanol, acetone, ether, petroleum ether and aniline and other organic solvents.
- UsesThe polymerization initiator for Vinyl chloride, vinyl acetate, acrylonitrile and blowing agent for rubber, plastic , in an amount of 10% to 20%.
This product can also be used as curing agents, pesticides and organic synthesis intermediates.
This product 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 .
- Production methodAcetone, hydrazine hydrate and sodium cyanide as raw materials:
The temperature of condensation reaction above is 55~60 ℃, reaction time is 5h, and then cool down to 25~30 ℃ ,time is 2h. 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.
- categoryFlammable solids
- Toxicity gradingMiddle toxic
- Acute toxicityOral-rat LDL0: 670 mg/kg; Oral-Mouse LD50: 700 mg/kg
- Explosive hazardous characteristicsExplosive when mixed with oxidants ; easily oxidized, unstable and intense heat decomposition, explosive when heated with heptane, acetone
- Flammability hazard characteristicsFlammable in case of fire, high temperature, oxidant ; decomposition and generating combustible gas in case of thermal ; combustion produces toxic fumes of nitrogen oxides
- Storage characteristicsTreasury ventilation low-temperature drying; and separated from oxidants
- Extinguishing agentWater, dry sand, carbon dioxide, foam, 1211 fire extinguishing agent
- Chemical Propertieswhite solid
- Chemical PropertiesAzobisisobutylonitrile is a white crystalline compound.
- UsesUsed as an initiator in the synthesis of highly cross-linked Poly(divinylbenzene) (PDVB) polymers. 1 Used as an initiator in the polymerization process of 2-hydroxyethyl methacrylate (HEMA). 2
- General DescriptionInsoluble in water and denser than water. Moderately toxic by ingestion. Readily ignited by sparks or flames. Burns intensely and persistently. Toxic oxides of nitrogen produced during combustion. Used as a catalyst, in vinyl polymerizations and a blowing agent for plastics.
- Air & Water ReactionsDust may form an explosive mixture in air. Insoluble in water.
- Reactivity ProfileSelf-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. Azo, diazo, azido compounds 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.
- HazardToxic by ingestion.
- Safety ProfilePoison by intraperitoneal route. Moderately toxic by ingestion. Easily oxidized, unstable. 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-. See also NITRILES. A free-radcal generator.
- Potential ExposureAzobisisobutylonitrile is both a nitrile and azo compound. Used as a polymerization initiator, free radical generator (or initiator); as a catalyst in vinyl polymerizations; as a blowing agent for elastomers and plastics.
- ShippingUN3234 Self-reactive solid type C, temperature controlled materials, Hazard Class: 4.1; Labels: 4.1- Flammable solid, Technical Name Required.
- IncompatibilitiesFlammable; dust may form explosive mixture with air. Unstable and easily oxidized material; keep away from oxidizers, strong acids. Keep at temperature not ≧30° C (this may vary by manufacturer). Risk of explosion from heat, shock, friction. Warming causes production of tetramethylsuccinonitrile and cyanide fumes. Keep away from acetone and other ketones, alcohols, lithium, aluminum, aldehydes, and hydrocarbons, such as heptane. Azo compounds 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. This chemical is sensitive to prolonged exposure to heat. This chemical is incompatible with strong oxidizing agents.
- Raw materialsAcetoneChlorineHydrazinium hydroxideSodium cyanideSodium hypochloriteAcetone cyanohydrin BUTYRONITRILE
- Preparation Products4-(PYRROLIDIN-1-YLMETHYL)BENZENEBORONIC ACID, PINACOL ESTER 97%1-[4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)BENZYL]PYRROLIDINE4-(2-CYANOETHYLAMINOCARBONYL)PHENYLBORONIC ACID2,1,3-Benzothiadiazole-5-carbaldehyde3-(2-CYANOETHYLAMINOCARBONYL)PHENYLBORONIC ACID4-(PIPERIDINE-1-CARBONYL)PHENYLBORONIC ACID2,1,3-Benzothiadiazol-5-ylmethanol3-(PIPERIDINOMETHYL)BENZALDEHYDE4-(1,2,3-THIADIAZOL-4-YL)BENZYLAMINE HYDROCHLORIDE3-PHENOXYPHENYLACETONITRILE2,6-Dichlorobenzaldehyde5-Dibenzosuberenone2-Chlorobenzyl chloride4-(1,2,3-THIADIAZOL-4-YL)BENZALDEHYDE3-QUINOLIN-2-YLPROPANOIC ACIDDichloroacetyl chlorideDicofol4-Benzofurazancarboxaldehyde2-(DIPHENYLPHOSPHINO)ETHYLTRIETHOXYSILANE5-(BROMOMETHYL)-2,1,3-BENZOTHIADIAZOLE11b,21-Dihydroxy-2'-methyl-5'bH-pregna-1,4-dieno[17,16-d]oxazole-3,20-dione 21-acetateDideoxyinosinegraft copolymer PAA-G-PIPA microsphere2-(Bromomethyl)benzoic acid2-TRIFLUOROMETHYLQUINOLINE-7-CARBOXYLIC ACID4-[4-(BROMOMETHYL)PHENYL]-1,2,3-THIADIAZOLE3-CHLORO-4-((CYCLOPROPYLAMINO)METHYL)BENZALDEHYDEMETHYL ALPHA-BROMO-2-CHLOROPHENYLACETATEMaleic acid-allyl alcohol copolymer11-Bromoundecanoic acid1-(3-CHLORO-4-((CYCLOPROPYLAMINO)METHYL)PHENYL)ETHANONE2,4-Dichlorobenzyl chloridesuper absorbent resin synthesized by microwave cation ion radiation3，7-dichloro-8-dichloro methyl quinolineMETHYL 4-(BROMOMETHYL)-3-METHOXYBENZOATEdimethylacrolyl phenoxy propanestyrene copolymer optical plastics2-Nitroacetophenoneamphoteric super absorbent resin synthesized by microwave radiation2-Nitrobenzyl bromide
- BISMUTH TRIBROMOPHENATE Propionitrile Di-tert-Butyl azodicarboxylate 4,4'-Azobis(4-cyanovaleric acid) 4,4'-Azobis(4-cyano-1-pentanol) 2,2'-AZOBIS(4-METHOXY-2,4-DIMETHYLVALERONITRILE) 1,1'-Azobis(cyanocyclohexane) 2,2'-Azodi(2-methylbutyronitrile) 2,2'-Azobis(2-methylpropionitrile) N,N-Dimethylformamide Dimethyl sulfoxide Dimethyl fumarate Dimethyl sulfide Dimethyl ether Diisopropyl azodicarboxylate ETHANE Azobis (2-methylpropionitrile) 2,2'-Azobis(2,4-dimethyl)valeronitrile
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