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Methyl (R)-(+)-lactate CAS 17392-83-5

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  • Appearance: Colorless liquid 
  • Assay: 99. 0%min
  • Stock: In stock
  • Sample: Available

Basic Info of Methyl (R)-(+)-lactate

What is Methyl (R)-(+)-lactate?

Methyl (R)-(+)-lactate is methyl lactate with R configuration. It is derived from (R) – lactic acid. It is an enantiomer of (s) – methyl lactate.

Methyl (R)-(+)-lactate, also known as methyl lactate, is an organic compound with the molecular formula CH3CH(OH)CO2CH3. It is the methyl ester of lactic acid. Colorless liquid is the simplest chiral ester. As a natural derivative, it is easily obtained in the form of a single enantiomer.

The compound has mild properties, biodegradability and water solubility. It can be used as a multifunctional reagent for preparing cellulose acetate (CA) membrane. It can also be used as an intermediate in the production of a variety of compounds, polymers and derivatives. This product has been enhanced to “safer solvents and additives” methyl (r)-(+)-lactate.

Methyl (R)-(+)-lactate Uses

  1. Methyl (R) – (+) – lactate is the solvent of cellulose nitrate, cellulose acetate, cellulose acetylbutyrate and cellulose levulinate.
  2. Methyl (R) – (+) – lactate is used in the manufacture of varnishes and coatings. It has high tolerance to diluents, good defect resistance and whitening resistance.
  3. The synthesis of 1,2-propanediol from methyl lactate using macho catalyst has been commercialized.
  4. On the skin, methyl (R) – (+) – lactate will leave a refreshing and cool feeling. This ingredient has a pleasant and soothing mint flavor. Add it to your morning routine to wake up immediately. Like menthol, menthol lactate gently relieves itching and irritation.

Methyl (R) – (+) – lactate can be used as raw material for asymmetric preparation:

  • Neomethylmycin, a macrolide containing 12 membered macrolide, is used as a potent biological agent.
  • PM toxin A.

It can also be used as a chiral pool together with D – (-) – tartaric acid for the separation of monomers A and B through Trost rychnovsky alkyne rearrangement, Horner Wadsworth Emmons Olefination and stereoselective total synthesis of Corey Bakshi Shibata.

Reference

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