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Isobornyl acrylate

Isobornyl acrylate Suppliers list
Company Name: Anhui Royal Chemical Co., Ltd.
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Email: marketing@royal-chem.com
Products Intro: Product Name:Isobornyl acrylate;IBOA;
CAS:5888-33-5
Purity:99.00% Package:25kg/drum;200kg/drum Remarks:pharmaceutical intermediates
Company Name: Yancheng Green Chemicals Co.,Ltd
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Products Intro: Product Name:IBOA
CAS:5888-33-5
Purity:0.99 Package:25kg/drum;200kg/drum Remarks:coating
Company Name: Gansu Jinyuantai New Material Co., Ltd.
Tel: +86-025-86618065 +86-13914714331
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Products Intro: Product Name:ISOBORNYL ACRYLATE/IBOA
CAS:5888-33-5
Purity:99 Package:200Kg/Drum;0USD
Company Name: Hubei Ipure Biology Co., Ltd
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Products Intro: Product Name:Isobornyl acrylate;IBOA;
CAS:5888-33-5
Purity:99% Package:180Kg/Drum;1USD
Company Name: Hebei Mojin Biotechnology Co., Ltd
Tel: +8613288715578
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Products Intro: Product Name:Isobornyl acrylate
CAS:5888-33-5
Purity:99% Package:25KG

Isobornyl acrylate manufacturers

  • Isobornyl acrylate
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  • $2.00 / 200kg
  • 2024-04-24
  • CAS:5888-33-5
  • Min. Order: 1kg
  • Purity: 99%
  • Supply Ability: 5000mt
  • Isobornyl acrylate
  • Isobornyl acrylate pictures
  • $100.00 / 1KG
  • 2023-12-24
  • CAS:5888-33-5
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: g-kg-tons, free sample is available
  • Isobornyl acrylate
  • Isobornyl acrylate pictures
  • $0.00 / 25KG
  • 2023-07-29
  • CAS:5888-33-5
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 50000KG/month

Related articles

Isobornyl acrylate Basic information
Description Uses 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;exo-isobornylacrylate;Isobornyl acrylate, stabilized with 100ppm 4-methoxyphenol;sr506(acrylate);ISOBORNYL ACRYLATE
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
Water Solubility Difficult to mix in water.
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.
UsesISOBORNYL ACRYLATE (cas# 5888-33-5) is a useful research chemical.
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.
UsesIsobornyl acrylate (IBA) can be used to prepare block copolymers with n-butyl acrylate by atom transfer radical polymerization (ATRP).
UsesIt is used as UVcuring EBcuring adhesive.
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
Isobornyl acrylate Preparation Products And Raw materials
Tag:Isobornyl acrylate(5888-33-5) Related Product Information
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