- Isobornyl acrylate
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- $2.00
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2026-09-20
- CAS:5888-33-5
- Min. Order: 1kg
- Purity: 99%
- Supply Ability: 5000mt
- Isobornyl Acrylate
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- $16.00
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2026-09-17
- CAS:5888-33-5
- Min. Order: 1000kg
- Purity: ≥99.2%
- Supply Ability: 120 tons
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| Product Name: | Isobornyl acrylate | | Synonyms: | 1,7,7-trimethylbicyclo(2.2.1)hept-2-ylester,exo-2-propenoicaci;1,7,7-trimethylbicyclo[2.2.1]hept-2-ylester,exo-2-propenoicaci;1,7,7-trimethylbicyclo[2.2.1]hept-2-ylester,exo-2-Propenoicacid;al-co-cureiba;ebecryliboa;exo-isobornylacrylate;Isobornyl acrylate, stabilized with 100ppm 4-methoxyphenol;EM70DN | | CAS: | 5888-33-5 | | MF: | C13H20O2 | | MW: | 208.3 | | EINECS: | 227-561-6 | | Product Categories: | | | Mol File: | 5888-33-5.mol |  |
| | Isobornyl acrylate Chemical Properties |
| Melting point | <-35°C | | Boiling point | 119-121 °C15 mm Hg(lit.) | | density | 0.986 g/mL at 25 °C(lit.) | | vapor pressure | 1.3Pa at 20℃ | | refractive index | n20/D 1.476(lit.) | | Fp | 207 °F | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | solubility | Chloroform (Slightly), Methanol (Slightly) | | form | clear liquid | | color | Colorless to Almost colorless | | Optical Rotation | 0.41° (C=1.00 g/100ml, ETOH) | | Water Solubility | Difficult to mix in water. | | FreezingPoint | 5 | | Sensitive | Light Sensitive | | BRN | 2254825 | | Stability: | Light sensitive | | Cosmetics Ingredients Functions | NAIL SCULPTING | | InChI | 1S/C13H20O2/c1-5-11(14)15-10-8-9-6-7-13(10,4)12(9,2)3/h5,9-10H,1,6-8H2,2-4H3/t9-,10-,13+/m0/s1 | | InChIKey | PSGCQDPCAWOCSH-BREBYQMCSA-N | | SMILES | [H][C@]12CC[C@@](C)([C@@H](C1)OC(=O)C=C)C2(C)C | | LogP | 4.52 at 20℃ | | CAS DataBase Reference | 5888-33-5(CAS DataBase Reference) | | EPA Substance Registry System | Isobornyl acrylate (5888-33-5) |
| Hazard Codes | Xn,N,Xi | | Risk Statements | 20/22-36/37/38-51/53 | | Safety Statements | 26-36-61-28 | | RIDADR | UN 3082 9 / PGIII | | WGK Germany | 2 | | RTECS | UD3940000 | | TSCA | TSCA listed | | HazardClass | 9 | | PackingGroup | III | | HS Code | 29161290 | | Storage Class | 10 - Combustible liquids | | Hazard Classifications | Aquatic Acute 1
Aquatic Chronic 1
Eye Irrit. 2
Skin Irrit. 2
Skin Sens. 1A
STOT SE 3 | | Toxicity | LD50 oral in rat: 4890mg/kg |
| | Isobornyl acrylate Usage And Synthesis |
| Description | Isobornyl acrylate can be used to prepare block copolymers with n-butyl acrylate by atom transfer radical polymerization (ATRP)1. It is a photo-polymerizable monomer that is employed in micro-fluidic devices because of desirable properties, such as inertness, transparency, and resolution2.
| | Sources |
- https://www.sigmaaldrich.com/catalog/product/aldrich/392103?lang=en®ion=US
- López-García, M. D. C., D. J. Beebe, and W. C. Crone. Characterization of poly(isobornyl acrylate) as a construction material for microfluidic applications. Journal of Applied Polymer Science. 2007:1894–1902.
| | Uses |
Isobornyl acrylate (IBA) is used as UVcuring EBcuring adhesive, it can also be used to prepare block copolymers with n-butyl acrylate by atom transfer radical polymerization (ATRP).
| | Application | Isobornyl acrylate can be used as a co-monomer with other acrylic monomers in the preparation of pressure-sensitive adhesives (PSAs) for optical applications. It is also used in the development of high-performance and stable polymer gate dielectrics for organic thin-film transistors (OTFTs). Furthermore, it can also used in the preparation of UV-curable waterborne polyurethane (WPU) by copolymerization. | | Hazard | Moderately toxic by ingestion. Low toxicity by skin contact. A moderate skin and mild eye
irritant. | | Flammability and Explosibility | Non flammable | | Synthesis | Isobornyl acrylate is prepared by reacting (-)- borneol,triethylamine with acryloyl chloride in anhydrous THF.Dissolve (-)- borneol (1.00 g, 6.48 mmol, 1 equiv) and triethylamine (0.98 g, 9.72 mmol, 1.5 equiv) in anhydrous THF (20 mL) in a 100 mL round-bottom flask. Add acryloyl chloride (0.88 g, 9.72 mmol, 1.5 equiv) dropwise to the reaction mixture at 0 °C. Allow the reaction to stir at room temperature overnight. Filter the reaction solution. Concentrate the reaction solution on the rotary evaporator. Wash the mixture with water (20 mL). Extract the mixture with dichloromethane (3x20 mL). Dry the combined organic phases over anhydrous sodium sulfate. Filter and concentrate the residue. Purify the crude product further by silica gel column chromatography (petroleum ether/ethyl acetate = 4:1) to obtain isobornyl acrylate.
Fig Synthetic method of Isobornyl acrylate | | Toxics Screening Level | The Initial Threshold Screening Level (ITSL) is 14 μg/m3 annual average. |
| | Isobornyl acrylate Preparation Products And Raw materials |
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