Date published: 2025-12-1

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1,6-Hexanediol diacrylate (CAS 13048-33-4)

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CAS Number:
13048-33-4
Purity:
≥80%
Molecular Weight:
226.27
Molecular Formula:
C12H18O4
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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1,6-Hexanediol diacrylate emerges as a multifaceted acrylate monomer, finding wide-ranging utilization across diverse applications. It proves instrumental in the synthesis of polymer materials, contributing to the formulation of coatings, adhesives, and sealants. This compound′s versatility makes it a cornerstone in various industries, where its properties play a pivotal role in creating functional and durable products.


1,6-Hexanediol diacrylate (CAS 13048-33-4) References

  1. Solid phase synthesis of hydrophobic peptides on 1,6-hexanediol diacrylate cross-linked polystyrene resin.  |  Varkey, JT. and Pillai, VN. 1999. J Pept Sci. 5: 577-81. PMID: 10628657
  2. Solid-phase synthesis of a modified 13-residue seminalplasmin fragment on 1,6-hexanediol diacrylate-crosslinked polystyrene support.  |  Arunan, C., et al. 2000. Peptides. 21: 773-7. PMID: 10958996
  3. Extended mechanistic aspects on photoinitiated polymerization of 1,6-hexanediol diacrylate by hexaarylbisimidazoles and heterocyclic mercapto compounds.  |  Berdzinski, S., et al. 2014. Photochem Photobiol Sci. 13: 789-98. PMID: 24671230
  4. Phosphonate-functionalized poly(β-amino ester) macromers as potential biomaterials.  |  Akyol, E., et al. 2018. J Biomed Mater Res A. 106: 1390-1399. PMID: 29318781
  5. Allergic contact dermatitis caused by 1,6-hexanediol diacrylate in a hospital wristband.  |  van Amerongen, CCA., et al. 2019. Contact Dermatitis. 81: 446-449. PMID: 31392731
  6. The polymerization kinetics, oxidation-responsiveness, and in vitro anticancer efficacy of poly(ester-thioether)s.  |  Cheng, F., et al. 2019. J Mater Chem B. 7: 1005-1016. PMID: 32255105
  7. Self-detachable UV-curable polymers for open-access microfluidic platforms.  |  Tahk, D., et al. 2020. Lab Chip. 20: 4215-4224. PMID: 33170919
  8. Development of 3D Slurry Printing Technology with Submersion-Light Apparatus in Dental Application.  |  Jiang, CP., et al. 2021. Materials (Basel). 14: PMID: 34947467
  9. Anisotropic frontal polymerization in a model resin-copper composite.  |  Gao, Y., et al. 2022. Chaos. 32: 013109. PMID: 35105137
  10. The photooxidative sensitization of bis(p-substituted diphenyl)iodonium salts in the radical polymerization of acrylates.  |  Balcerak, A. and Kabatc, J. 2019. RSC Adv. 9: 28490-28499. PMID: 35529669
  11. Molecular Dynamics Study on Behavior of Resist Molecules in UV-Nanoimprint Lithography Filling Process.  |  Iwata, J. and Ando, T. 2022. Nanomaterials (Basel). 12: PMID: 35893522
  12. Synthesis of thioredoxin partial sequences on 1,6-hexanediol diacrylate (HDODA)-cross-linked polystyrene resin.  |  Varkey, JT. and Pillai, VN. 1998. J Pept Res. 51: 49-54. PMID: 9495591

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

1,6-Hexanediol diacrylate, 100 g

sc-223110
100 g
$50.00

1,6-Hexanediol diacrylate, 500 g

sc-223110A
500 g
$118.00