isobornyl acrylate
2-propenoic acid, (1S,4S)-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl ester
 
Notes:
None found
  • BOC Sciences
    • BOC Sciences
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      Product(s):
      5888-33-5 Isobornyl acrylate >93.0%(GC)
       
  • TCI AMERICA
    • TCI AMERICA
      Moving Your Chemistry Forward
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      Tokyo Chemical Industry Co., Ltd. (TCI) is a leading worldwide manufacturer of specialty organic chemicals founded in 1946. TCI provides organic laboratory chemicals as well as pharmaceutical, cosmetic and functional materials. More than 70 years of synthesis experience and multi-purpose plants enable TCI to offer more than 30,000 products as well as custom synthesis.
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      Product(s):
      I0638 isoBornyl Acrylate (stabilized with MEHQ) >90.0%(GC)
       
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CAS Number: 5888-33-5Picture of molecule3D/inchi
Other(deleted CASRN): 111821-21-7
ECHA EINECS - REACH Pre-Reg: 227-561-6
FDA UNII: IX0PRH184P
MDL: MFCD00080424
XlogP3: 3.90 (est)
Molecular Weight: 208.30080000
Formula: C13 H20 O2
NMR Predictor: Predict (works with chrome or firefox)
Category: film forming agents
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
Google Books: Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Google Patents: Search
US Patents: Search
EU Patents: Search
Pubchem Patents: Search
PubMed: Search
NCBI: Search
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Physical Properties:
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Specific Gravity: 0.98600 @  25.00 °C.
Boiling Point: 244.53 °C. @ 760.00 mm Hg (est)
Vapor Pressure: 0.030000 mmHg @ 25.00 °C. (est)
Flash Point: 207.00 °F. TCC ( 97.22 °C. )
logP (o/w): 4.029 (est)
Soluble in:
 water, 10.04 mg/L @ 25 °C (est)
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Organoleptic Properties:
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: film formers
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Suppliers:
BOC Sciences
For experimental / research use only.
Isobornyl acrylate >93.0%(GC)
Kowa Amerian Corporation
IBXA
Odor: characteristic
Use: IBXA is a mono-functional reactive diluent that polymerizes when exposed to sources of free radicals. The bicyclic structure of IBXA produces polymers of increased Tg, while its mono-functionality minimizes cross-linking to provide coatings and inks with good hardness, resiliency, flexibility and impact resistance. IBXA is recommended for coatings requiring flexibility, hardness & thermal resistance, maintaining high elongation in urethane acrylates, and screen inks and coating requiring increased adhesion to polyolefins.
Santa Cruz Biotechnology
For experimental / research use only.
isoBornyl Acrylate
Sigma-Aldrich: Aldrich
For experimental / research use only.
isoBornyl Acrylate technical grade
contains 200 ppm monomethyl ether hydroquinone as inhibitor
Silver Fern Chemical
IBOA: Isobornyl Acrylate
TCI AMERICA
For experimental / research use only.
isoBornyl Acrylate (stabilized with MEHQ) >90.0%(GC)
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Safety Information:
Preferred SDS: View
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
oral-rat LD50  4890 mg/kg
SKIN AND APPENDAGES (SKIN): HAIR: OTHER BEHAVIORAL: TREMOR LUNGS, THORAX, OR RESPIRATION: DYSPNEA
National Technical Information Service. Vol. OTS0536067

Dermal Toxicity:
skin-rabbit LD50 > 5000 mg/kg
National Technical Information Service. Vol. OTS0536067

Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: film forming agents
Recommendation for isobornyl acrylate usage levels up to:
 not for fragrance use.
 
Recommendation for isobornyl acrylate flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 5888-33-5
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 93013
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 2
 [(1S,4S)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] prop-2-enoate
Chemidplus: 0005888335
RTECS: UD3940000 for cas# 5888-33-5
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References:
 [(1S,4S)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] prop-2-enoate
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 5888-33-5
Pubchem (cid): 93013
Pubchem (sid): 135051195
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Other Information:
(IUPAC): Atomic Weights of the Elements 2011 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
HMDB (The Human Metabolome Database): Search
Export Tariff Code: 2916.12.5050
ChemSpider: View
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Potential Blenders and core components note
 
None Found
 
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Potential Uses:
None Found
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Occurrence (nature, food, other): note
 not found in nature
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Synonyms:
 acrylic acid isobornyl ester
 acrylic acid, isobornyl ester
2-propenoic acid, (1S,4S)-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl ester
2-propenoic acid, 1,7,7-trimethylbicyclo(2.2.1)hept-2-yl ester, exo-
 sartomer 506
(rel-1,7,7-trimethyl bicyclo(2.2.1)-2-propenoic acid hept-2-yl ester
exo-1,7,7-trimethyl bicyclo(2.2.1)hept-2-yl acrylate
[(1S,4S)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] prop-2-enoate
exo-1,7,7-trimethylbicyclo(2.2.1)hept-2-yl acrylate
(1S,4S)-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl acrylate
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Articles:
PubMed: Two decades of occupational (meth)acrylate patch test results and focus on isobornyl acrylate.
PubMed: Microscopic evaluation of polymeric film properties of anhydrous sunscreen compositions and their relation to absorption and water resistance.
PubMed: Pressure-sensitive adhesion system using acrylate block copolymers in response to photoirradiation and postbaking as the dual external stimuli for on-demand dismantling.
PubMed: Synthesis of cyclopentadienyl capped polyethylene and subsequent block copolymer formation via hetero Diels-Alder (HDA) chemistry.
PubMed: Mild and modular surface modification of cellulose via hetero Diels-Alder (HDA) cycloaddition.
PubMed: Star-Shaped Polyacrylates: Highly Functionalized Architectures via CuAAC Click Conjugation.
PubMed: Ultra-Fast RAFT-HDA Click Conjugation: An Efficient Route to High Molecular Weight Block Copolymers.
PubMed: Diffusion behavior of isobornyl acrylate into photopolymerized urethane acrylate films: influence of surface oxidation during curing.
PubMed: An accessible micro-capillary electrophoresis device using surface-tension-driven flow.
PubMed: Design and use of organic nanoparticles prepared from star-shaped polymers with reactive end groups.
PubMed: Evaluation of acrylate-based block copolymers prepared by atom transfer radical polymerization as matrices for paclitaxel delivery from coronary stents.
PubMed: An epidemic of occupational contact dermatitis from an acrylic glue.
PubMed: Dynamic hairspray analysis. II. Effect of polymer, hair type, and solvent composition.
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