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Key Documents
755745
2,2′-Azobis(2-methylpropionitrile)
recrystallized from methanol, 99%
Synonim(y):
α,α′-Azoisobutyronitrile, AIBN, Azobisisobutyronitrile, Free radical initiator
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About This Item
Wzór liniowy:
(CH3)2C(CN)N=NC(CH3)2CN
Numer CAS:
Masa cząsteczkowa:
164.21
Beilstein:
1708400
Numer WE:
Numer MDL:
Kod UNSPSC:
12162002
Identyfikator substancji w PubChem:
NACRES:
NA.23
Polecane produkty
Poziom jakości
Próba
99%
Postać
crystals
mp
102-104 °C (dec.) (lit.)
103-107 °C
temp. przechowywania
−20°C
ciąg SMILES
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+
Klucz InChI
OZAIFHULBGXAKX-VAWYXSNFSA-N
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Opis ogólny
This AIBN was recrystallized and is ready for use as a polymerization initiator.
Zastosowanie
- 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).
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Hasło ostrzegawcze
Danger
Zwroty wskazujące rodzaj zagrożenia
Zwroty wskazujące środki ostrożności
Klasyfikacja zagrożeń
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Self-react. C
Zagrożenia dodatkowe
Kod klasy składowania
4.1A - Other explosive hazardous materials
Klasa zagrożenia wodnego (WGK)
WGK 2
Temperatura zapłonu (°F)
122.0 °F
Temperatura zapłonu (°C)
50 °C
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Organic letters, 14(22), 5692-5695 (2012-10-31)
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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