Poly(L-lactide)(PLLA) - ester terminated， Viscosity 2.6~3.2dL/g (0.1% in CHCl3, 25 ℃), used for Biodegradable, biocompatible, and bioresorbable polymer composed of L-Lactide. This semi-crystalline material has been used in the fabrication of research medi

CAS: 33135-50-1 Cat. No.: P299052 Formule: -(C₆H₈O₄)n-

GRADE & PURITY ester terminated， Viscosity 2.6~3.2dL/g (0.1% in CHCl3, 25 ℃)

Synonyms

Poly(L-Lactic acid) | L-Lactide polymer | PLA | Resomer® L 210 S

Storage

Room temperature,Argon charged

Shipped In

Normal

Vue d’ensemble

Poly(L-lactide) (PLLA), a high-performance bio-based polymer, can be prepared from corn starch. Its properties include biodegradability, hydrophobicity, and excellent composting characteristics.

Specifications

Synonymes

Poly(L-Lactic acid) | L-Lactide polymer | PLA | Resomer® L 210 S

Spécifications et pureté

ester terminated， Viscosity 2.6~3.2dL/g (0.1% in CHCl3, 25 ℃)

Application

Biodegradable, biocompatible, and bioresorbable polymer composed of L-Lactide. This semi-crystalline material has been used in the fabrication of research medical devices and research tissue engineering solutions, such as orthopedic or soft tissue fixatio

Informations juridiques

RESOMER is a registered trademark of Evonik Rohm GmbH

Conditions de stockage de stockage

Room temperature,Argon charged

Expédié en

Normal

Noms et identifiants

Pubchem Sid

488180366

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488180366

Sourires canoniques

CC1C(=O)OC(C(=O)O1)C

IUPAC Name

3,6-dimethyl-1,4-dioxane-2,5-dione

InChIKey

JJTUDXZGHPGLLC-UHFFFAOYSA-N

INCHI

1S/C6H8O4/c1-3-5(7)10-4(2)6(8)9-3/h3-4H,1-2H3

Isomères SMILES

CC1C(=O)OC(C(=O)O1)C

CAS alternatif

26161-42-2

Reaxy-Rn

82121

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=82121&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Classe Dioxanes
      • Subclass 1,4-dioxanes

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: Dioxanes
• Subclass: 1,4-dioxanes
• Intermediate Tree Nodes: Not available
• Direct Parent: 1,4-dioxanes
• Alternative Parents: Dicarboxylic acids and derivatives Lactones Carboxylic acid esters Oxacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Dicarboxylic acid or derivatives - Para-dioxane - Lactone - Carboxylic acid ester - Oxacycle - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as 1,4-dioxanes. These are organic compounds containing 1,4-dioxane, an aliphatic six-member ring with two oxygen atoms in ring positions 1 and 4.
• External Descriptors: a small molecule

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Propriétés chimiques et physiques

• Sensibilité: Moisture sensitive
• Point de fusion (°C): 180 °C
• Poids moléculaire: 144.120 g/mol
• XLogP3: 0.600
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 0
• Exact Mass: 144.042 Da
• Monoisotopic Mass: 144.042 Da
• Topological Polar Surface Area: 52.600 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 155.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 2
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1