755745
2,2′-azobis(2-metilpropionitrile)
recrystallized from methanol, 99%
Sinonimo/i:
α,α′-azoisobutirronitrile, AIBN, Azobisisobutirronitrile, Iniziatore di radicali liberi
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About This Item
Formula condensata:
(CH3)2C(CN)N=NC(CH3)2CN
Numero CAS:
Peso molecolare:
164.21
Beilstein:
1708400
Numero CE:
Numero MDL:
Codice UNSPSC:
12162002
ID PubChem:
NACRES:
NA.23
Prodotti consigliati
Livello qualitativo
Saggio
99%
Stato
crystals
Punto di fusione
102-104 °C (dec.) (lit.)
103-107 °C
Temperatura di conservazione
−20°C
Stringa SMILE
CC(C)(\N=N\C(C)(C)C#N)C#N
InChI
1S/C8H12N4/c1-7(2,5-9)11-12-8(3,4)6-10/h1-4H3/b12-11+
OZAIFHULBGXAKX-VAWYXSNFSA-N
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Descrizione generale
This AIBN was recrystallized and is ready for use as a polymerization initiator.
Applicazioni
- Porous Acid-Base Hybrid Polymers for Enhanced NH3 Uptake: This study discusses the use of 2,2′-Azobis(2-methylpropionitrile) in the synthesis of acid-base hybrid polymers, highlighting its role in enhancing ammonia uptake through cooperative hydrogen bonds (X Luo, Y Liu, et al., 2023).
- Extraction of Fluoroquinolones from Milk: The development of molecularly imprinted polymers using 2,2′-Azobis(2-methylpropionitrile) as an initiator for the extraction of antibiotics from milk showcases its application in food safety and pharmaceutical analysis (E Megias-Pérez, et al., 2023).
- Thermo-responsive Copolymer Visible Light Catalyst: Highlighting the use of 2,2′-Azobis(2-methylpropionitrile) in the synthesis of thermo-responsive copolymers, this study explores its applications in catalysis and material science, particularly in photoreactive polymers (S Wu, et al., 2024).
Avvertenze
Danger
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Self-react. C
Rischi supp
Codice della classe di stoccaggio
4.1A - Other explosive hazardous materials
Classe di pericolosità dell'acqua (WGK)
WGK 2
Punto d’infiammabilità (°F)
122.0 °F
Punto d’infiammabilità (°C)
50 °C
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In the presence of a catalytic amount of radical initiator AIBN, primary amines are oxidatively coupled to imines and tertiary amines are cyanated to α-aminonitriles. These "metal-free" aerobic oxidative coupling reactions may find applications in a wide range of "green"
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We have developed new urethane acrylate-based root canal sealers using polycarbonate (PC) as polyol and 2,2-azobis(2-methyl)butyronitrile (AMBN) as a thermal initiator. The purpose of this study was to compare the properties among a group of seven sealers: (1) polybutyleneadipate (PBA)
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