CAS 17392-83-5

(+)-Methyl lactate

Description:

(+)-Methyl lactate, with the CAS number 17392-83-5, is an organic compound classified as an ester derived from lactic acid. It is a colorless to pale yellow liquid with a characteristic sweet odor. This compound is known for its chiral nature, existing in two enantiomeric forms, with the (+) form being the naturally occurring one. (+)-Methyl lactate is soluble in water and organic solvents, making it versatile for various applications. It is commonly used as a solvent in the formulation of paints, coatings, and adhesives due to its low toxicity and biodegradability. Additionally, it serves as a flavoring agent and a potential feedstock in the production of biodegradable plastics. The compound exhibits good thermal stability and has a relatively low boiling point, which is advantageous in industrial processes. Its properties make it an attractive alternative to traditional solvents, aligning with the growing emphasis on sustainability and environmental safety in chemical manufacturing.

Formula: C₄H₈O₃

InChI: InChI=1S/C4H8O3/c1-3(5)4(6)7-2/h3,5H,1-2H3/t3-/m1/s1

InChI key: InChIKey=LPEKGGXMPWTOCB-GSVOUGTGSA-N

SMILES: C([C@@H](C)O)(OC)=O

Synonyms:

• (+)-2-Hydroxypropionic acid methyl ester
• (+)-Lactic acid methyl ester
• (+)-Methyl 2-hydroxypropionate
• (+)-Methyl lactate
• (2R)-2-Hydroxypropanoic acid methyl ester
• (2R)-Methyl 2-hydroxypropanate
• (R)-(+)-Lactic acid methyl ester
• (R)-(+)-Methyl Lactate
• (R)-2-Hydroxypropanoic acid methyl ester
• (R)-2-Hydroxypropionic acid methyl ester
• (R)-Methyl 2-hydroxypropanoate
• <span class="text-smallcaps">D</span>-Lactic acid methyl ester
• <span class="text-smallcaps">D</span>-Methyl lactate
• D-(+)-Lactic Acid Methyl Ester
• D-Methyl Lactate
• Methyl (R)-2-hydroxypropionate
• Methyl <span class="text-smallcaps">D</span>-lactate
• Methyl D-(+)-Lactate
• Propanoic acid, 2-hydroxy-, methyl ester, (2R)-
• Propanoic acid, 2-hydroxy-, methyl ester, (R)-
• methyl (2R)-2-hydroxypropanoate
• methyl (R)-2-hydroxypropanoate
• Methyl-(r)-lactate

Methyl D-(+)-Lactate

CAS: 17392-83-5

Formula: C₄H₈O₃

Purity: >98.0%(GC)

Color and Shape: Colorless to Almost colorless clear liquid

Molecular weight: 104.11

Ref: 3B-L0136

(R)-Methyl 2-hydroxypropanoate

CAS: 17392-83-5

Purity: 95.0%

Color and Shape: Liquid, Clear Liquid

Molecular weight: 104.1050033569336

Ref: 10-F219745

(R)-Methyl 2-hydroxypropanoate

CAS: 17392-83-5

(R)-Methyl 2-hydroxypropanoate, also known as D-lactic acid methyl ester, is a chiral ester compound widely used in biochemical experiments

Formula: C₄H₈O₃

Purity: 98.45%

Color and Shape: Solid

Molecular weight: 104.1

Ref: TM-TN9572

D-Methyl lactate

CAS: 17392-83-5

D-Methyl lactate

Purity: 98%

Molecular weight: 104.10g/mol

Ref: 54-OR72156

Methyl D-(+)-Lactate

Controlled Product

CAS: 17392-83-5

Formula: C₄H₈O₃

Color and Shape: Neat

Molecular weight: 104.1

Ref: TR-M315230

Methyl (R)-(+)-lactate

CAS: 17392-83-5

Formula: C₄H₈O₃

Purity: 98%

Color and Shape: Liquid

Molecular weight: 104.1045

Ref: IN-DA0032AW

D-Methyl lactate

CAS: 17392-83-5

D-Methyl lactate is a synthetic, broad-spectrum antibacterial agent that is synthesized by the ring-opening of l-glutamic acid methyl esters with methyl glycosides. It has been shown to have a greater effect on gram-positive bacteria than gram-negative bacteria. This drug also has stereoselective activity against Staphylococcus aureus and Escherichia coli, which may be related to its ability to inhibit the synthesis of dl-amino acids. D-Methyl lactate has also been shown to increase bacterial cell growth at low concentrations and inhibit bacterial growth at high concentrations. This may be due to its ability to induce dehydration in cells through the cleavage of fatty acids.

Formula: C₄H₈O₃

Purity: (¹H-Nmr) Min. 95 Area-%

Color and Shape: Colorless Clear Liquid

Molecular weight: 104.1 g/mol

Ref: 3D-FM14255