Production Method 1

4511-42-6

13076-17-0

13076-19-2

13076-19-2

4511-42-6

13076-17-0

Reaction Conditions

1.1 Catalysts: Stannous octanoate ;  24 h, 130 °C

Reference

Thermal Properties of Polylactides with Different Stereoisomers of Lactides Used as Comonomers

Feng, Lidong; et al, Macromolecules (Washington, Macromolecules (Washington, DC, United States) (2017), 50(16), 6064-6073, 50(16), 6064-6073

meso-Lactide Raw materials

• (3S,6S)-3,6-Dimethyl-1,4-dioxane-2,5-dione
• D-(+)-Lactide
• meso-Lactide

meso-Lactide Preparation Products

• (3S,6S)-3,6-Dimethyl-1,4-dioxane-2,5-dione (4511-42-6)
• D-(+)-Lactide (13076-17-0)
• meso-Lactide (13076-19-2)

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• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Dioxanes 1,4-dioxanes

• 95-96-5(DL-Lactide)
• 4511-42-6((3S,6S)-3,6-Dimethyl-1,4-dioxane-2,5-dione)
• 26780-50-7(Poly(D,L-lactide-co-glycolide), Resomer RG 858 S, Mw 190000-240000)
• 3853-80-3((+/-)-2-ACETOXYPROPIONIC ACID)
• 535-17-1(2-Acetoxypropanoic acid)
• 2098070-20-1(2-(3-(Pyridin-3-yl)-1H-pyrazol-1-yl)acetimidamide)
• 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)
• 1444113-98-7(N-(3-cyanothiolan-3-yl)-2-[(2,2,2-trifluoroethyl)sulfanyl]pyridine-4-carboxamide)
• 332062-08-5(Fmoc-S-3-amino-4,4-diphenyl-butyric acid)
• 1270529-38-8(1,2,3,4,5,6-Hexahydro-[2,3]bipyridinyl-6-ol)