2231-91-6

Usage

Uses

Used in Cosmetic and Personal Care Products:
L-MENTHYL METHACRYLATE is used as a flavoring agent and fragrance for its refreshing minty scent and cooling effect on the skin.
Used in Dental Materials and Adhesives:
L-MENTHYL METHACRYLATE is used in the production of polymer resins for dental materials and adhesives, contributing to their properties and performance.
Used in Oral Care Products:
L-MENTHYL METHACRYLATE is used as an ingredient in oral care products for its cooling sensation and minty aroma, enhancing the user experience.
Used in Topical Products:
L-MENTHYL METHACRYLATE is used in topical products for its cooling effect and pleasant scent, providing a refreshing sensation to the skin.
Safety Precautions:
It is important to handle L-MENTHYL METHACRYLATE with caution, as it may cause irritation to the skin and eyes. It should be stored in a cool, well-ventilated area to ensure safety and stability.

Upstream product

• 2216-51-5 (-)-menthol 
• 920-46-7 Methacryloyl chloride 
• 760-93-0 methacryloyl anhydride 

Downstream Products

• 638209-26-4 (Dichlor-methyl-silyl)-isobuttersaeure-menthylester 
• 1430817-64-3 (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl (2S)-2-methyl-3-perfluorohexylpropanoate 
• 1430817-52-9 (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl (2R)-2-methyl-3-perfluorohexylpropanoate 
• 512776-88-4 (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl-2,3-dihydroxy-2-methyl-propanoate 
• 512776-89-5 (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl 2,2,4-trimethyl-1,3-dioxolane-4-carboxylate 
• 111832-28-1 2-Methyl-oxirane-2-carboxylic acid (1R,2R,5S)-2-isopropyl-5-methyl-cyclohexyl ester 
• 176774-74-6 (1S-endo)-2-methylbicyclo<2.2.1>hept-5-ene-2-carboxylic acid 
• 92007-58-4 (1S)-endo-2-methylbicyclo<2.2.1>hept-5-ene-2-carboxylic acid 
• 176774-73-5 [3S-(3α,3aβ,5α,6β,6aβ)]-hexahydro-6-iodo-3-methyl-3,5-methano-2H-cyclopenta[b]furan-2-one 

Relevant academic research and scientific papers

VCD study of synthetic chiral polymers: stereoregularity in poly-menthyl methacrilate

Menthyl metacrylate (MnMA) was polymerized both by free radical and anionic initiators in order to obtain polymers with low (poly-MnMA-rad) and high (poly-MnMA-an) isotactic content, respectively, and their VCD spectra were measured as CCl4 solutions between 1650-850 cm-1.Common growth of all VCD intensities, observed in the spectrum of poly-MnMA-an, indicate more and/or longer helical segments.The VCD spectra also revealed that the vibrations of the chain are most sensitive to changes in stereoregularity.

Multicatalytic Transformation of (Meth)acrylic Acids: a One-Pot Approach to Biobased Poly(meth)acrylates

Shifting from petrochemical feedstocks to renewable resources can address some of the environmental issues associated with petrochemical extraction and make plastics production sustainable. Therefore, there is a growing interest in selective methods for transforming abundant renewable feedstocks into monomers suitable for polymer production. Reported herein are one-pot catalytic systems, that are active, productive, and selective under mild conditions for the synthesis of copolymers from renewable materials. Each system allows for anhydride formation, alcohol acylation and/or acid esterification, as well as polymerization of the formed (meth)acrylates, providing direct access to a new library of unique poly(meth)acrylates.

PREPARATION OF (METH)ACRYLIC ACID ESTERS

The invention relates to a method for preparation of (meth)acrylic acid esters from (meth)acrylic acid anhydrides.

Process for making bicalutamide and intermediates thereof

Bicalutamide and/or its intermediates are made by the use of p-fluorobenzenesulfinic acid salt as a reagent.

Optically-active, amhiphilic, water-soluble free-radical addition copolymers and their use in the resolution of racemic mixtures

Optically-active, amphiphilic, free-radical addition copolymers having an optically-active hydrophobic portion and an ionic hydrophilic portion are effective resolving agents. This utility is based on a unique combination of properties, viz., water solubility, chirality and amphiphilicity, i.e., having a dual hydrophobic and hydrophilic nature.