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Isobornyl acrylate

Isobornyl acrylate Suppliers list
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Products Intro: Product Name:Isobornyl acrylate;IBOA;
CAS:5888-33-5
Purity:99.00% Package:25kg/drum;200kg/drum Remarks:pharmaceutical intermediates
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Products Intro: Product Name:IBOA
CAS:5888-33-5
Purity:0.99 Package:25kg/drum;200kg/drum Remarks:coating
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Products Intro: Product Name:Isobornyl acrylate;IBOA;
CAS:5888-33-5
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Products Intro: Product Name:Isobornyl acrylate
CAS:5888-33-5
Purity:98.0% Package:200kg
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Products Intro: Product Name:Isobornylacrylate
CAS:5888-33-5
Purity:0.99 Package:25KG

Isobornyl acrylate manufacturers

  • Isobornyl Acrylate
  • Isobornyl Acrylate pictures
  • $16.00/ kg
  • 2025-10-17
  • CAS:5888-33-5
  • Min. Order: 1000kg
  • Purity: ≥99.2%
  • Supply Ability: 120 tons

Related articles

Isobornyl acrylate Basic information
Description Sources
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;IBXA;Isobornyl acrylate, stabilized with 100ppm 4-methoxyphenol
CAS:5888-33-5
MF:C13H20O2
MW:208.3
EINECS:227-561-6
Product Categories:
Mol File:5888-33-5.mol
Isobornyl acrylate Structure
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 Rotation0.41° (C=1.00 g/100ml, ETOH)
Water Solubility Difficult to mix in water.
FreezingPoint 5
Sensitive Light Sensitive
BRN 2254825
Stability:Light sensitive
InChIKeyPSGCQDPCAWOCSH-BREBYQMCSA-N
LogP4.52 at 20℃
CAS DataBase Reference5888-33-5(CAS DataBase Reference)
EPA Substance Registry SystemIsobornyl acrylate (5888-33-5)
Safety Information
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 Yes
HazardClass 9
PackingGroup III
HS Code 29161290
ToxicityLD50 oral in rat: 4890mg/kg
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
Isobornyl acrylate Usage And Synthesis
DescriptionIsobornyl 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
  1. https://www.sigmaaldrich.com/catalog/product/aldrich/392103?lang=en&region=US
  2. 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).
ApplicationIsobornyl 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.
HazardModerately toxic by ingestion. Low toxicity by skin contact. A moderate skin and mild eye irritant.
Flammability and ExplosibilityNon flammable
SynthesisIsobornyl 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.
Synthetic method of Isobornyl acrylate Fig Synthetic method of Isobornyl acrylate
Toxics Screening LevelThe Initial Threshold Screening Level (ITSL) is 14 μg/m3 annual average.
Isobornyl acrylate Preparation Products And Raw materials
Tag:Isobornyl acrylate(5888-33-5) Related Product Information
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