| Identification | More | [Name]
Cyclohexyl acrylate | [CAS]
3066-71-5 | [Synonyms]
ACRYLIC ACID CYCLOHEXYL ESTER
CYCLOHEXYL ACRYLATE
2-propenoicacid,cyclohexylester
2-Propenoicacidcyclohexylester
sartomersr220
sr220
Cyclohexyl prop-2-enoate
Cyclohexyl acrylate, 98+%, stab. with 100ppm 4-methoxyphenol
Cyclohexyl Acrylate (stabilized with MEHQ)
Cyclohexyl acrylate, 98+%
Acrylic acid cyclohexyl
Propenoic acid cyclohexyl ester | [EINECS(EC#)]
221-319-3 | [Molecular Formula]
C9H14O2 | [MDL Number]
MFCD00046349 | [Molecular Weight]
154.21 | [MOL File]
3066-71-5.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xi,N | [Risk Statements ]
R37/38:Irritating to respiratory system and skin .
R51/53:Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S61:Avoid release to the environment. Refer to special instructions safety data sheet . | [RIDADR ]
3082 | [RTECS ]
AS7350000 | [TSCA ]
Yes | [HazardClass ]
9 | [PackingGroup ]
III | [HS Code ]
29161290 |
| Hazard Information | Back Directory | [Uses]
Cyclohexyl acrylate is commonly used in industrial and scientific laboratory research. Examples include phase behaviour studies of binary and ternary mixtures of poly(cyclohexyl acrylate) and poly(cyclohexyl methacrylate) in supercritical CO2[1]. As well as kinetic modelling studies of the ester exchange reaction between cyclohexyl acrylate and n-butanol[2], and so on. | [Synthesis]
Cyclohexyl acrylate is prepared by the reaction of acrylic acid methyl ester and cyclohexanol.
| [References]
[1] BYUN H S. Phase behavior on the binary and ternary mixtures of poly(cyclohexyl acrylate) and poly(cyclohexyl methacrylate) in supercritical CO2[J]. Journal of Applied Polymer Science, 2004. DOI:10.1002/app.21010.
[2] BASUDEB SAHA; Michael S. Transesterification of cyclohexyl acrylate with n-butanol and 2-ethylhexanol: acid-treated clay, ion exchange resins and tetrabutyl titanate as catalysts[J]. Reactive & Functional Polymers, 1999. DOI:10.1016/S1381-5148(98)00004-2.
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