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11590

Sigma-Aldrich

4,4′-Azobis(4-cyanovaleric acid)

≥98.0% (T)

Sinonimo/i:

4,4′-Azobis(4-cyanopentanoic acid), ABCVA, ACVA

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About This Item

Formula condensata:
HOCOCH2CH2C(CH3)(CN)N=NC(CH3)(CN)CH2CH2COOH
Numero CAS:
2638-94-0
Peso molecolare:
280.28
Beilstein:
1729856
Numero CE:
220-135-0
Numero MDL:
MFCD00002799
Codice UNSPSC:
12352100
ID PubChem:
57646934
NACRES:
NA.22

Livello qualitativo

200

Saggio

≥98.0% (T)

Stato

solid

Impurezze

≤1% water

Punto di fusione

118-125 °C (dec.) (lit.)

Gruppo funzionale

azo
carboxylic acid
nitrile

Temperatura di conservazione

2-8°C

Stringa SMILE

CC(CCC(O)=O)(\N=N\C(C)(CCC(O)=O)C#N)C#N

InChI

1S/C12H16N4O4/c1-11(7-13,5-3-9(17)18)15-16-12(2,8-14)6-4-10(19)20/h3-6H2,1-2H3,(H,17,18)(H,19,20)/b16-15+
VFXXTYGQYWRHJP-FOCLMDBBSA-N

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Categorie correlate

Applicazioni

4,4′-Azobis(4-cyanovaleric acid) has been used in the preparation of polystyrene particles by polymerizing styrene in ethyl alcohol.

Azioni biochim/fisiol

4,4′-azobis(4-cyanovaleric acid) is an azo-initiator that induces lipid peroxidation of sunflower oil.

Pittogrammi

Flame
GHS02

Avvertenze

Danger

Indicazioni di pericolo

H242

Classi di pericolo

Self-react. D

Codice della classe di stoccaggio

5.2 - Organic peroxides and self-reacting hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

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Certificati d'analisi (COA)

Lot/Batch Number
BCCM7457
BCCL6698
BCCJ6327
BCCH2949
BCCD8612

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Ray Chang et al.
Polymers, 10(10) (2019-04-10)
Temperature stimulus, easy modulation in comparison to other environmental stimuli, makes thermo-responsive nanocarriers popular in the applications of controlled drug release for cancer therapy. In this study, photosensitive sodium copper chlorophyllin (SCC) was incorporated into thermo-responsive polymeric nanogels consisted of
B Pekiner et al.
Biochemistry and molecular biology international, 33(6), 1159-1167 (1994-08-01)
Haemolysis induced by a free radical initiator (4,4'azobis-(4-cyanovaleric acid) has been studied with transfusion blood. Azobis cyanovaleric acid caused an increase in haemolysis. The effect of alpha- and gamma-tocopherol, 2,2,5,7,8 pentamethyl-6-chromanol and 2,2,7,8 tetramethyl-6-chromanol on the red blood cell haemolysis
Eric D Nelson et al.
Journal of pharmaceutical sciences, 95(7), 1527-1539 (2006-05-26)
AIBN and ACVA oxidative forced degradation models are examined for two drug molecules whose predominant oxidation chemistries arise from different reaction mechanisms (i.e., free radical vs. nucleophilic). Stress was conducted under a variety of initiator concentrations, and under ambient and
Dragana D Cetojević-Simin et al.
Journal of medicinal food, 13(2), 452-459 (2010-02-23)
In this study we investigated antioxidative and antiproliferative activity of different horsetail (Equisetum arvense L.) extracts. The antioxidative activity was measured by the electron spin resonance (ESR) spectroscopy-spin trapping method. The influence of different horsetail extracts during lipid peroxidation of
J A Tripp et al.
Journal of combinatorial chemistry, 3(2), 216-223 (2001-04-13)
Polyethylene encased porous poly(chloromethylstyrene-co-divinylbenzene) disks have been prepared by polymerization in a cylindrical glass mold and cut to a disk format. Following attachment of a free radical azo initiator 4,4'-azobis(4-cyanovaleric acid) to available functionalities at the surface of the pores
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