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2 2 azobisisobutyronitrile

Manufactured by Fujifilm
Sourced in Japan

2,2'-azobisisobutyronitrile is a chemical compound commonly used as an initiator in various polymerization reactions. It functions by decomposing to generate free radicals, which then initiate the polymerization process. The core function of this product is to serve as a polymerization initiator.

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13 protocols using 2 2 azobisisobutyronitrile

1

Fabrication of Flexible Electrochemical Devices

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VBE, BA, and octyl acylate (OA) were purchased
from Tokyo Chemical Industry Co., Ltd. (Japan). Methanol, N,N-dimethylformamide (DMF), methyl ethyl
ketone (MEK), and 2,2′-azobis(isobutyronitrile) (AIBN) were
purchased from FUJIFILM Wako Pure Chemical Corporation (Japan). NALOACTY
CL-120, used as an emulsifier, was purchased from SANYO Chemical Industries,
Ltd. (Japan). HXNBR (Therban XT 8889; CN: 33.8 mol %, COOH: 3.8 mol
%, and residual double bond content: 3.5 mol %) was obtained from
LANXESS (USA). NBR samples (Nipol DN302 with 27.5% AN, DN2850 with
28.0% AN, and DN3350 with 33.0% AN) were obtained from ZEON Corporation
(Japan). PET3811 obtained from Lintec Corporation (Japan) was used
as a releasable film. As a finger contact prevention film for the
electrode, a PET film (Diafoil, Mitsubishi Chemical Corporation, Japan)
was used.
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2

Synthesis and Characterization of PEG-PAA-PS Copolymer

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Poly(ethylene glycol) 4-cyano-4-(phenylcarbonothioylthio)pentanoate (PEG macro-CTA, average molecular weight = 2.00 × 103 g/mol) from Aldrich (Tokyo, Japan) was used without further purification. 2.2′-Azobis(isobutyronitrile) (AIBN, >98%) from Wako pure chemical (Osaka, Japan) was recrystallized from methanol. Acrylic acid (AA, >99.0%), N, N-dimethylformamide (DMF, >99.5%), and 1,4-dioxane (>99.0%) from Tokyo Industry (Tokyo, Japan) were dried over 4 Å molecular sieves and distilled under reduced pressure. Styrene was washed with an aqueous alkaline solution and distilled from calcium hydride under reduced pressure. PEG-PAA-PS was synthesized (Figure 2) using RAFT polymerization as previously reported [25 (link)]. Na2CO3, BaCl2·2H2O, and methotrexate were purchased from Thermo Scientific (Waltham, MA, USA). A 0.1 M tris buffer (solution of pH 7.4, EMD millipore corp.) was used as release media. Dulbecco’s modified Eagle’s medium (DMEM) and Dulbecco’s phosphate-buffered saline (DPBS) were obtained from Life Technologies (Grand Island, NY, USA). Alamar Blue, lactate dehydrogenase (LDH) assay kit and every other materials not otherwise specified were purchased from Thermo Scientific.
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3

Synthesis and Purification of Methacrylate Monomers

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Methacrylic acid (MAA), N,N’-methylenebisacrylamide (MBAA), ethylene glycol dimethacrylate (EGDMA), 2,2′-azobisisobutyronitrile (AIBN), and acetonitrile were obtained from FUJIFILM Wako Pure Chemical Co. (Osaka, Japan). Diethylene glycol dimethacrylate (DEGDMA), triethylene glycol dimethacrylate (TEGDMA), and tetraethylene glycol dimethacrylate (TETEGDMA) were obtained from Tokyo Chemical Industry Co., Ltd. (Tokyo, Japan). All of the reagents were of the best grade available. The cross-linkers were purified with active basic aluminum oxide 60 (Sigma-Aldrich Co. LLC., St. Louis, MO, USA) to remove polymerization inhibitors.
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4

Synthesis of Fluorescent Copolymers

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N-Isopropylacrylamide (NIPAAm) was kindly provided by KJ Chemicals (Tokyo, Japan) and purified by recrystallization from n-hexane. N,N-Dimethylacrylamide (DMAAm) and 2,2′-Azobisisobutyronitrile (AIBN) were obtained from Wako Pure Chemical Industry (Osaka, Japan) and purified by distillation and recrystallization, respectively. 4-Cyano-4-(phenylcarbonothioylthio)pentanoic acid and fluorescein-5-maleimide were obtained from Sigma-Aldrich (St. Louis, MO, USA). l-Phenylalanine and l-tyrosine were purchased from Peptide Institute (Tokyo, Japan). N,N′-Dicyclohexylcarbodiimide (DCC) was purchased from Kanto Chemicals (Tokyo, Japan). N-Hydroxysuccinimide (NHS) was obtained from Merck Japan (Tokyo, Japan). Water was purified using a PURELAB FLEX (Organo, Tokyo, Japan).
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5

Synthesis and Characterization of Ionic Liquid Monomers

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All chemical reagents, except for ionic liquid imidazolium cations, were purchased from Wako Pure Chemical Industries, Ltd. (Wako) (Tokyo, Japan) and Tokyo Chemical Industry Co., Ltd. (TCI) (Tokyo, Japan). 2,2′-Azobis(isobutyronitrile) (AIBN, Wako) was purified by recrystallization from ethanol before use, and the other reagents were employed as received. MAImC1 and [{CH2=C(CH3)COO(CH2)2}C3H3N2(C8H17)]+ (MAImC8) were prepared as iodide salt (MAImC1-I) and bromide salt (MAImC8-Br), respectively, according to the procedures described below.
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6

Fluorescent Hydrogel Synthesis and Characterization

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N-isopropylmethacrylamide (NIPMAAm), 4-(2-acrylamidoethylcarbamoyl)-3-fluorophenylboronic acid (AmECFPBA), N-hydroxyethylacrylamide (NHEAAm), N,N′-methylenebisacrylamide (MBAAm), 2,2′-Azobis(2,4-dimethylvaleronitrile) (V-65), 2,2′-azobisisobutyronitrile (AIBN), FITC (fluorescein isothiocyanate)-labeled bovine insulin and all organic solvents (ethanol, methanol, hexane, dimethyl sulfoxide (DMSO)) were all purchased from Wako Pure Chemical Industries (Tokyo, Japan). Acryloxyethyl thiocarbamoyl rhodamine B was purchased from Polyscience, Inc. (Warrington, USA). NIPMAAm was recrystallized in hexane and then dried in vacuo overnight before use.
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7

Fabrication of Fluorinated Polymer Nanocomposites

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The
material 2-(perfluorooctyl)ethyl
acrylate (FAC8) was provided by Daikin Industries Co.,
Ltd. and was distilled under vacuum before polymerization. The material
2,2′-azobis(isobutyronitrile) (AIBN, Wako) was recrystallized
from methanol. Dopamine hydrochloride (Sigma-Aldrich) and acryloyl
chloride (Wako) were used as received. Triethylamine (Wako) and methanol
(MeOH, Wako) were distilled before use. Hexafluoroisopropanol (HFIP)
and dichloropentafluoropropanes (HCFC-225s, a mixture of 225ca, CF3CF2CHCl2, and 225cb, CCl2FCF2CHClF) were obtained from Wako Pure Chemical Industries
and Asahi Glass Co., respectively. Halloysite nanotubes (HNTs) with
external diameter of 30–70 nm and length of 1–3 μm
were purchased from Sigma-Aldrich.
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8

Synthesis of Advanced Polymer Materials

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Triethyl silyl chloride, N,N-dimethylformamide (super-dehydrated), NaHCO3, tetrabutylammonium fluoride, tetrahydrofuran solution (~1 mol/L), acetic acid, and BaTiO3 were purchased from FUJIFILM Wako Pure Chemical Co.(Osaka, Japan)., and they were used as received. Imidazole was purchased from Tokyo Chemical Industry Co., Ltd (Tokyo, Japan)., and it was used as received. 1,2-Dichloroethane (super-dehydrated) was purchased from Kanto Chemical Co., Inc., and it was used as received. 2-Ethylhexyl methacrylate was purchased from FUJIFILM Wako Pure Chemical Co., and it was passed through an A2O3 column before use to remove the radical inhibitor. 2-Cyano-2-propyl dodecyl trithiocarbonate was purchased from Sigma-Aldrich Co., and it was used as received. 2,2′-Azobisisobutyronitrile was purchased from FUJIFILM Wako Pure Chemical Co., and it was recrystallized from methanol before use. 1 was provided by NOF CORPORATION (Hyogo, Japan).
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9

Synthesis of Functional Polymers from MMA and St

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Methyl methacrylate (MMA, ≥99.0%), styrene (St, ≥99.0%), anhydrous 1,4-dioxane (≥99.0%), boron tribromide (BBr3, ≥99.5%), 2,2-azobis(isobutyronitrile) (AIBN, ≥98.0%), tetrahydrofuran (THF/GR), dichloromethane (GR), and methanol (GR) were purchased from Wako Pure Chemical Industries, Ltd. Technical grade 3,4-dimethoxystyrene (99%) and 2-cyano-2-propyldodecyltrithiocarbonate (CPDTTC, 97%) were purchased from Sigma-Aldrich, USA. The inhibitor in St was removed by alumina column chromatography followed by drying with molecular sieves 3/4 Å overnight. AIBN was recrystallized from methanol and dried in vacuo before use. All other reagents were used as received.
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10

Synthesis and Characterization of Tartaric Acid Derivatives

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l-Tartaric, d-tartaric,
and meso-tartaric acids were purchased from Nacalai
Tesque. 3-Buten-1-ol, Sc(OTf)3, ethylene bis(thioglycolate)
(EBTG), 1,2-ethanedithiol (ED), d,l-dithiothreitol
(DTT), 1,4-butanedithiol (BD), and 2,2′-azobis(isobutyronitrile)
(AIBN) were obtained from Wako Pure Chemical Industries.
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