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cyclohexyl methacrylate
methacrylic acid cyclohexyl ester

Supplier Sponsors

Name:cyclohexyl 2-methylprop-2-enoate
CAS Number: 101-43-9Picture of molecule3D/inchi
Other(deleted CASRN):2056117-96-3
ECHA EINECS - REACH Pre-Reg:202-943-5
Nikkaji Web:J68.537B
Beilstein Number:2045235
XlogP3-AA:2.90 (est)
Molecular Weight:168.23592000
Formula:C10 H16 O2
BioActivity Summary:listing
NMR Predictor:Predict (works with chrome, Edge 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
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Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
DG SANTE Food Contact Materials:methacrylic acid cyclohexyl ester
Physical Properties:
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Specific Gravity:0.96400 to 0.96800 @ 20.00 °C.
Pounds per Gallon - (est).: 8.031 to 8.064
Refractive Index:1.45600 to 1.46000 @ 20.00 °C.
Boiling Point: 210.00 °C. @ 760.00 mm Hg
Vapor Pressure:0.200000 mmHg @ 25.00 °C. (est)
Flash Point: 181.00 °F. TCC ( 82.78 °C. )
logP (o/w): 3.130
Soluble in:
 water, 133.1 mg/L @ 25 °C (est)
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
Cosmetic Information:
CosIng:cosmetic data
Cosmetic Uses: film formers
BOC Sciences
For experimental / research use only.
Cyclohexyl methacrylate 95%
Kowa Amerian Corporation
Odor: characteristic
Use: CHMA forms homopolymers and copolymers. Copolymers of DHMA can be prepared with acrylic acid and its salts, amides and esters, and with methacrylates, acrylonitrile, styrene, butadiene, unsaturated polyesters and drying oils, etc. CHMA is also a very useful feedstock for chemical syntheses, because it readily undergoes addition with a wide variety of organic and inorganic compounds.
Santa Cruz Biotechnology
For experimental / research use only.
Cyclohexyl Methacrylate
Sigma-Aldrich: Aldrich
For experimental / research use only.
Cyclohexyl Methacrylate ≥97%
contains ∼60 ppm monomethyl ether hydroquinone as inhibitor
For experimental / research use only.
Cyclohexyl Methacrylate (stabilized with MEHQ) >98.0%(GC)
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
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
Safety in Use Information:
film forming agents
Recommendation for cyclohexyl methacrylate usage levels up to:
 not for fragrance use.
Recommendation for cyclohexyl methacrylate flavor usage levels up to:
 not for flavor use.
Safety References:
EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA Substance Registry Services (TSCA):101-43-9
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :7561
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:1
cyclohexyl 2-methylprop-2-enoate
 cyclohexyl 2-methylprop-2-enoate
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):7561
Pubchem (sid):134970825
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
FDA Indirect Additives used in Food Contact Substances:View
HMDB (The Human Metabolome Database):Search
Export Tariff Code:2916.14.2050
Potential Blenders and core components note
None Found
Potential Uses:
None Found
Occurrence (nature, food, other):note
 not found in nature
 cyclohexyl 2-methylprop-2-enoate
 methacrylic acid cyclohexyl ester
 methacrylic acid, cyclohexyl ester (8CI)
2-methyl-2-propenoic acid cyclohexyl ester
2-propenoic acid, 2-methyl-, cyclohexyl ester


PubMed:Uniformly gold nanoparticles derived from P2VP-b-PCHMA block copolymer templates with different reduction methods.
PubMed:Conformal polymeric thin films by low-temperature rapid initiated chemical vapor deposition (iCVD) using tert-butyl peroxybenzoate as an initiator.
PubMed:Development of new bone cement utilizing low toxicity monomers.
PubMed:Final report of the safety assessment of methacrylate ester monomers used in nail enhancement products.
PubMed:SP-PLP-EPR study of chain-length-dependent termination in free-radical polymerization of n-dodecyl methacrylate, cyclohexyl methacrylate, and benzyl methacrylate: evidence of "composite" behavior.
PubMed:Carbohydrate/monomer complexes in aqueous polymerizations: methylated-beta-cyclodextrin mediated aqueous polymerization of hydrophobic methacrylic monomers.
PubMed:Improved blood compatibility of segmented polyurethane by polymeric additives having phospholipid polar group. II. Dispersion state of the polymeric additive and protein adsorption on the surface.
PubMed:Improved blood compatibility of segmented polyurethanes by polymeric additives having phospholipid polar groups. I. Molecular design of polymeric additives and their functions.
PubMed:Intermediate restoratives from n-hexyl vanillate-EBA-ZnO-glass composites.
None found
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