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V-65, Azo Initiator

Wako 1st Grade
Specification Assay :
95.0+% (After Drying)(Titration)
Manufacturer :
FUJIFILM Wako Pure Chemical Corporation
Storage Condition :
FREEZE -20 C
CAS RN® :
4419-11-8
Molecular Formula :
C14H24N4
Molecular Weight :
248.37
GHS :
  • Structural Formula
  • Label
  • Packing
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LB-V65-50GS
50 G
List Price
80.00 USD

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Spectral Data
Certificate of Analysis
Calibration Certificate

Applications

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Plastics manufacturing
Photocurable


When compared with AIBN, the 10-hour half-life temperature of this oil-soluble azo polymerization initiator is 10 ℃ or lower than AIBN.
This product can be used for a wide range of applications, from versatile polymers to cosmetics-related use.

  • Oil-soluble azo initiator having a low decomposition temperature
  • Soluble in various organic solvents
  • Employed in various polymerizations for general purposes
  • 10 Hour half-life decomposition temperature; 51℃
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Comparison of V-65 and V-65B

Kinetic parameters & half-life

Frequent factor LnA ∆Ea Half-life (min)
30°C 50°C 70°C
V-65 34.18 28.97 (kcal/mol) 13,408 680 49
V-65B 34.41 29.11 (kcal/mol) 13,434 672 48

Changes of half-life near 50°C

Temperature (°C) 49.7 49.8 49.9 50.0 50.1 50.2
V-65 710 700 690 680 671 662
V-65B 701 691 681 672 662 653

Solubilities

(w/w at 20℃)
Solvent V-65B V-65
Acetone 69.7 50.0
Benzene 63.2 66.0
Cyclohexane 17.6 -
Dichloroethane 56.9 -
Dioxane 58.7 56.0
DMF 60.8 50.0
DMSO 26.0 -
Ethanol 24.0 -
Ethylether 58.3 -
Isopropanol 20.3 -
Methanol 44.5 14.3
n-Hexane 10.0 4.0
THF 66.0 -
Toluene 150.0 72.0

References

  1. Matsumoto, A., Kuwata, H., Kimura, S., Matsumoto, H., Ochi, K., Moro-Oka, Y., Watanabe, A., Yamada, H., Ishii H., Miyazawa, T., Chen, S., Baba, T., Yoshida, H., Nakamura, T., Inoue, H., Ogawa, Y., Tanaka, M., Miyahara, Y., and Suganami, T.: Hollow fiber-combined glucose-responsive gel technology as an in vivo electronics-free insulin delivery system. Commun Biol., 3(1), 313 (2020). PMID: 32555343
  2. Akimoto, J., Tamate, R., Okazawa, S., Akimoto, A. M., Onoda, M., Yoshida, R., and Ito, Y.: Reactivity Control of Polymer Functional Groups by Altering the Structure of Thermoresponsive Triblock Copolymers. ACS Omega., 4(15), 16344-16351 (2019). PMID: 31616812
  3. Guo, Y., van Ravensteijn, B. G. P., and Kegel, W.K.: Dimple Colloids with Tunable Cavity Size and Surface Functionalities. Macromolecules. 52(11), 4287-4294 (2019). PMID: 31231140
  4. Baghirov, H., Snipstad, S., Sulheim, E., Berg, S., Hansen, R., Thorsen, F., Mørch, Y., Davies, C. L., and Åslund, A. K. O.: Ultrasound-mediated delivery and distribution of polymeric nanoparticles in the normal brain parenchyma of a metastatic brain tumour model. PLoS One, 13(1), e0191102, (2018). PMID: 29338016
  5. Yang, S. B., Yoo, S. H., Lee, J. S., Kim, J. W., and Yeum, J. H.: Surface Properties of a Novel Poly(vinyl alcohol) Film Prepared by Heterogeneous Saponification of Poly(vinyl acetate) Film. Polymers (Basel), 9(10), 493 (2017). PMID: 30965796
  6. Onoda, M., Ueki, T., Tamate, R., Shibayama, M., and Yoshida, R.: Amoeba-like self-oscillating polymeric fluids with autonomous sol-gel transition. Nat Commun.13, 8, 15862 (2017). PMID: 28703123
  7. Maoka, T., Nishino, A., Yasui, H., Yamano, Y., and Wada, A.: Anti-Oxidative Activity of Mytiloxanthin, a Metabolite of Fucoxanthin in Shellfish and Tunicates. Mar Drugs. 14(5), 93 (2016). PMID: 27187417
  8. Carrasco, S., Benito-Peña, E., Walt, D. R., and Moreno-Bondi, M. C.: Fiber-optic array using molecularly imprinted microspheres for antibiotic analysis. Chem Sci., 6(5), 3139-3147 (2015). PMID: 29142687
  9. Takahashi, Y., Ichimori, K., Okano, M., and Goto, H.: Novel antioxidant capacity assay for lipophilic compounds using electron paramagnetic resonance spectroscopy. J Clin Biochem Nutr. 56(2):105-10 (2015). PMID: 25759515
  10. Verma, A., and Murray, G. M.: A path to soluble molecularly imprinted polymers. J Funct Biomater. 3(1), 1-22 (2011). PMID: 24956512
  11. Kusumoto, C., Kinugawa, T., Morikawa, H., Teraoka, M., Nishida, T., Murawaki, Y., Yamada, K., and Matsura, T.: Protection by Exogenously Added Coenzyme Q(9) against Free Radical-Induced Injuries in Human Liver Cells. J Clin Biochem Nutr. 46(3), 244-51 (2010). PMID: 20490320

Overview / Applications

Outline When compared with AIBN, the 10-hour half-life temperature of this oil-soluble azo polymerization initiator is 10 ºC or lower than AIBN.
This product can be used for a wide range of applications, from versatile polymers to cosmetics-related use.

Property

Appearance white, crystalline powder
Specificity 10-hour half life temperature: 51 ºC (Toluene)
Solubility water: insoluble.
benzene, acetone, ether, N,N-Dimethylformamide, toluene, methanol: soluble.
Melting Point 45-70 °C

Manufacturer Information

Alias

  • 2,2'-Azobis(2,4-dimethylvaleronitrile)

Author : [WKUS] Naomi Tsurutani

For research use or further manufacturing use only. Not for use in diagnostic procedures.

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