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Hexanediol diacrylate

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Identification
Molecular formula
C12H18O4
CAS number
13048-33-4
IUPAC name
6-prop-2-enoyloxyhexyl prop-2-enoate
State
State

Liquid at room temperature.

Melting point (Celsius)
-25.00
Melting point (Kelvin)
248.15
Boiling point (Celsius)
282.00
Boiling point (Kelvin)
555.15
General information
Molecular weight
226.27g/mol
Molar mass
226.2650g/mol
Density
1.0420g/cm3
Appearence

Hexanediol diacrylate is a colorless to pale yellow liquid. It may exhibit a slight characteristic odor.

Comment on solubility

Solubility of 6-prop-2-enoyloxyhexyl prop-2-enoate

The solubility of 6-prop-2-enoyloxyhexyl prop-2-enoate (C12H18O4) can be influenced by a variety of factors due to its organic nature and molecular structure. Here are some key aspects to consider:

  • Polarity: This compound features a combination of hydrophobic hydrocarbon chains and polar functional groups, suggesting that it may exhibit moderate solubility in organic solvents.
  • Solvent Compatibility: It is likely to dissolve well in polar aprotic solvents (e.g., acetone, ethyl acetate) and could have limited solubility in water due to the presence of hydrophobic segments.
  • Temperature Effects: As with many organic compounds, solubility can increase with temperature. Thus, heating the solvent may enhance the solubility of this compound.
  • Concentration: Higher concentrations of solute may lead to saturation in a given solvent, beyond which solubility is significantly reduced.

In summary, while specific solubility data for 6-prop-2-enoyloxyhexyl prop-2-enoate is not readily available, understanding its structure and the nature of the solvents can provide insight into its solubility characteristics. As with many organic compounds, experimentation may offer the most accurate conclusions regarding its behavior in different solvent systems.

Interesting facts

Interesting Facts about 6-Prop-2-enoyloxyhexyl Prop-2-enoate

6-Prop-2-enoyloxyhexyl prop-2-enoate is a fascinating compound that belongs to a class known as acrylates. These compounds are recognized for their versatile applications in various fields, particularly in materials science and polymer chemistry.

Key Characteristics

  • Versatility: This compound can be utilized in producing polymers that can be applied in coatings, adhesives, and sealants.
  • Reactivity: Thanks to the presence of double bonds, it readily participates in polymerization reactions, paving the way for the creation of complex polymeric structures.
  • Customizability: By modifying the chemical structure, scientists can tailor the properties of the resulting polymers, such as flexibility, durability, and thermal stability.

Applications

Because of its properties, 6-prop-2-enoyloxyhexyl prop-2-enoate is employed in various innovative applications:

  • Coatings: Used in protective and decorative coatings due to its ability to form durable films.
  • Adhesives: Serves as a bonding agent in various industrial applications.
  • 3D Printing: Plays a crucial role in the formulation of resins for 3D printing technologies, allowing for creative and complex designs.

In the Laboratory

In laboratory settings, this compound can also be examined for its potential in creating new polymers with enhanced properties. Scientists often explore:

  • Methods to optimize polymerization processes
  • How varying the concentration of this compound affects the physical properties of the polymer
  • The interactions between this compound and different monomers to synthesize copolymers

As the field of polymer science continues to evolve, compounds like 6-prop-2-enoyloxyhexyl prop-2-enoate are at the forefront of exciting research, offering endless possibilities for innovation!

Synonyms
13048-33-4
1,6-HEXANEDIOL DIACRYLATE
Hexamethylene diacrylate
NK Ester A HD
Hexaneglycol diarcylate
CCRIS 4823
1,6-Hexanediol di-2-propenoate
HSDB 6109
UNII-FY751V5MMY
EINECS 235-921-9
FY751V5MMY
BRN 1870540
DTXSID9025401
LAROMER HDDA
KAYARAD KS-HDDA
KS-HDDA
NEW FRONTIER HDDA
NK ESTER A-HD-N
A-HD-N
ACTILANE 425
hexamethylenediol diacrylate
SARTOMER SR-238
PHOTOMER 4017F
2-Propenoic acid, 1,1'-(1,6-hexanediyl) ester
C-6DA
hexamethyleneglycol diacrylate
GENOMER 1223
HEXANEGLYCOL DIACRYLATE
AGISYN 2816
LIGHT ESTER 1.6HX-A
M-200 (ACRYLATE)
DTXCID705401
EM-221TF
SR-238NS
1,6-hexamethylenediol diacrylate
LIGHT ACRYLATE 1,6HX-A
LIGHT ACRYLATE SR-238F
1,6HX-A
SR-238F
1,6-HEXANEDIYL DIACRYLATE
EC 235-921-9
1.6HX
HEXANEDIOL DIACRYLATE (HDDA)
EM-221
SM-626
SR-238
SR-2389
HEXAMETHYLENE DIACRYLATE, 1,6-
1,6-HEXANEDIOL DIACRYLATE [HSDB]
M 200
V-230
1,6hexanediol diacrylate
Kayard HDDA
1,6-hexenediol diacrylate
1,6Hexamethylene diacrylate
1,6Hexanediol di2propenoate
1,6HDDA
1,6-HDDA
1,6HXA
propenoic acid, 1,6-hexanediol ester
2Propenoic acid, 1,6hexanediyl ester
2Propenoic acid, 1,1'(1,6hexanediyl) ester
fihbhsqysyvzqe-uhfffaoysa-n
Hexane-1,6-diyl diacrylate
Kayarad HDDA
1,6-Hexamethylene diacrylate
Sartomer 238
Hexamethylene glycol diacrylate
HDODA
Viscoat 230
Hexamethylene acrylate
Photomer 4017
Setalux UV 2243
Sartomer SR 238
Acrylic acid, hexamethylene ester
2-Propenoic acid, 1,6-hexanediyl ester
HDDA
6-prop-2-enoyloxyhexyl prop-2-enoate
SR 238
NK Ester A-HD
C 716
hexane-1,6-diyl bisacrylate
MFCD00008631
Hexane-1,6-diyl diacrylate (stabilized with MEHQ)
CAS-13048-33-4
Hexanediol diacrylate(9 cp(25 degrees c))
hexamethylenediacrylate
1,6-Bis(acryloyloxy)hexane
1,6-Hexanediol Diacrylate (stabilized with 100 ppm MEHQ) (>85%)
1,6-hexandiol diacrylate
1,6 hexanediol diacrylate
SCHEMBL33725
1,6-Bis(acryloyloxy)hexane (stabilized with MEHQ)
1,6-Hexanediol diacrylate (stabilized with MEHQ)
CHEMBL1530684
6-(Acryloyloxy)hexyl acrylate #
1,6-Hexanediol diacrylate, 90%
Tox21_201349
Tox21_303168
AKOS015904309
NCGC00091257-01
NCGC00091257-02
NCGC00091257-03
NCGC00091257-04
NCGC00257183-01
NCGC00258901-01
AS-75465
DB-254921
B2936
CS-0158045
NS00007428
1,6-Hexanediol diacrylate, technical grade, 80%
1,6-Bis(acryloyloxy)hexane, (stabilized with MEHQ)
Q1276266
1,6-Hexamethylene diacrylate (1,6-Hexanediol diacrylate), visc.5-8 cps