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3,4-Epoxycyclohexylmethyl 3,4-epoxycyclohexanecarboxylate
[CAS# 2386-87-0]

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Identification
Classification Chemical reagent >> Organic reagent >> Ester >> Butyl ester compound
Name 3,4-Epoxycyclohexylmethyl 3,4-epoxycyclohexanecarboxylate
Synonyms 7-Oxabicyclo[4.1.0]hept-3-ylmethyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate
Molecular Structure CAS # 2386-87-0, 3,4-Epoxycyclohexylmethyl 3,4-epoxycyclohexanecarboxylate, 7-Oxabicyclo[4.1.0]hept-3-ylmethyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate
Molecular Formula C14H20O4
Molecular Weight 252.31
CAS Registry Number 2386-87-0
EC Number 219-207-4
SMILES C1CC2C(O2)CC1COC(=O)C3CCC4C(C3)O4
Properties
Density 1.2±0.1 g/cm3, Calc.*, 1.17 g/cm3
Index of Refraction 1.539, Calc.*, 1.498
Boiling Point 363.4±17.0 ºC (760 mmHg), Calc.*
Flash Point 160.5±21.0 ºC, Calc.*, 245 ºF
* Calculated using Advanced Chemistry Development (ACD/Labs) Software.
Safety Data
Hazard Symbols symbol   GHS07 Warning    Details
Hazard Statements H317-H412    Details
Precautionary Statements P261-P272-P273-P280-P302+P352-P321-P333+P317-P362+P364-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Skin sensitizationSkin Sens.1H317
Chronic hazardous to the aquatic environmentAquatic Chronic3H412
Skin sensitizationSkin Sens.1BH317
Specific target organ toxicity - repeated exposureSTOT RE2H373
Germ cell mutagenicityMuta.2H341
Eye irritationEye Irrit.2H319
Skin irritationSkin Irrit.2H315
Specific target organ toxicity - single exposureSTOT SE3H335
Acute toxicityAcute Tox.4H302
SDS Available
up Discovory and Applicatios
3,4-Epoxycyclohexylmethyl 3,4-epoxycyclohexanecarboxylate is a distinctive chemical compound recognized for its role in the synthesis of advanced polymers and resins. This substance plays a crucial role in polymer chemistry and material science, with applications spanning from high-performance coatings to specialty adhesives.

The discovery of 3,4-epoxycyclohexylmethyl 3,4-epoxycyclohexanecarboxylate emerged from research aimed at developing new epoxy resins with enhanced properties. The compound is a member of the epoxy resin family, characterized by the presence of epoxy groups in its structure. These groups are reactive and can participate in crosslinking reactions, which are central to the formation of durable and resilient polymer networks.

The synthesis of 3,4-epoxycyclohexylmethyl 3,4-epoxycyclohexanecarboxylate involves the reaction of 3,4-epoxycyclohexylmethyl alcohol with 3,4-epoxycyclohexanecarboxylic acid. The resulting product features two epoxy groups that are critical for its function as a resin. The unique structure of this compound includes a cyclohexyl ring with epoxy substituents, which imparts distinctive properties to the resulting polymers.

One of the primary applications of 3,4-epoxycyclohexylmethyl 3,4-epoxycyclohexanecarboxylate is in the formulation of epoxy resins used for high-performance coatings. These coatings are valued for their excellent adhesion, chemical resistance, and mechanical strength. The compound's ability to form strong crosslinked networks makes it ideal for applications requiring durable and resistant coatings. These properties are particularly beneficial in industrial settings where materials are exposed to harsh environments and mechanical stresses.

In addition to coatings, 3,4-epoxycyclohexylmethyl 3,4-epoxycyclohexanecarboxylate is used in the production of specialty adhesives. The epoxy resins derived from this compound exhibit superior bonding strength and resistance to various environmental factors, including moisture and temperature fluctuations. This makes them suitable for use in applications ranging from construction to automotive industries, where reliable adhesive performance is essential.

The compound also finds applications in the manufacture of composite materials. Epoxy resins incorporating 3,4-epoxycyclohexylmethyl 3,4-epoxycyclohexanecarboxylate are used to create composites with enhanced mechanical properties and stability. These composites are employed in aerospace, automotive, and sporting goods industries, where the combination of strength and light weight is crucial.

Furthermore, 3,4-epoxycyclohexylmethyl 3,4-epoxycyclohexanecarboxylate contributes to the development of advanced electronic materials. Epoxy resins are widely used in the electronics industry for encapsulating electronic components and ensuring their protection from environmental damage. The unique properties of this compound help in producing resins that offer high dielectric strength and thermal stability, essential for reliable electronic performance.

Despite its advantages, handling 3,4-epoxycyclohexylmethyl 3,4-epoxycyclohexanecarboxylate requires caution. The epoxy groups in the compound are highly reactive and can cause skin and respiratory irritation. Proper safety measures should be implemented during its use and processing to mitigate potential health risks.

In conclusion, 3,4-epoxycyclohexylmethyl 3,4-epoxycyclohexanecarboxylate is an important chemical substance with diverse applications in polymer chemistry and material science. Its role in enhancing the properties of epoxy resins has significant implications for various industries, from coatings and adhesives to composites and electronics.

References

2024. Tri-band electrochromic smart window for energy savings in buildings. *Nature Sustainability*, 7(5).
DOI: 10.1038/s41893-024-01349-z

2022. NIR spectroscopy for reaction monitoring and reaction mixture identification of cycloaliphatic epoxides. *Journal of Polymer Research*, 29(5).
DOI: 10.1007/s10965-022-03038-x

2017. Preparation and characterization of UV-curable urethane acrylate oligomers modified with cycloaliphatic epoxide resin. *Journal of Coatings Technology and Research*, 14(6).
DOI: 10.1007/s11998-017-9994-6
Market Analysis Reports
List of Reports Available for 3,4-Epoxycyclohexylmethyl 3,4-epoxycyclohexanecarboxylate
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