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Polycaprolactone - viscosity 0.40dL/g, high purity , CAS No.24980-41-4

    Grade & Purity:
  • viscosity 0.40dL/g
In stock
Item Number
P485966
Grouped product items
SKU Size
Availability
Price Qty
P485966-5g
5g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$457.90

Basic Description

Synonyms Hexanoic acid, 6-hydroxy-, lactone | 1219802-08-0 | e-Caprolactone--d6 | UNII-56RE988L1R | Hexanoic acid, 6-hydroxy-, .epsilon.-lactone | MFCD00084404 | Oxepan-2-one; Epsilon-Caprolactone | 1,6-Hexanolide | CHEBI:17915 | 2-Oxepanone | 6-Hydroxycaproic aci
Specifications & Purity viscosity 0.40dL/g
Storage Temp Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description

Description

Polycaprolactone (PCL) is a biodegradable, semicrystalline polyester for use in tissue engineering and drug delivery research applications. Due to the increased length of the aliphatic chain, polycaprolactone degrades significantly slower than other common biodegradable polymers, such as polylactide. PCL features a low melting point (55–60 °C), making it ideal for thermal processing and increasing its use in novel applications such as 3D bioprinting. In addition to its favorable thermal properties, PCL also features high solubility in organic solvent allowing for a multitude of other processing options. This product features low residual water, monomer, and catalyst (tin) making it an ideal choice for use in tissue engineering and 3D bioprinting research.Research applications of this material include:Tissue engineering scaffolds.3D Bioprinting.Drug delivery applications such as sustained release.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organoheterocyclic compounds
Class Lactones
Subclass Not available
Intermediate Tree Nodes Not available
Direct Parent Lactones
Alternative Parents Oxepanes  Carboxylic acid esters  Oxacyclic compounds  Monocarboxylic acids and derivatives  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular Framework Aliphatic heteromonocyclic compounds
Substituents Caprolactone - Oxepane - Lactone - Carboxylic acid ester - Oxacycle - Monocarboxylic acid or derivatives - 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 lactones. These are cyclic esters of hydroxy carboxylic acids, containing a 1-oxacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring.
External Descriptors a small molecule

Associated Targets(Human)

PON1 Tbio Serum paraoxonase/arylesterase 1 (96 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name oxepan-2-one
INCHI InChI=1S/C6H10O2/c7-6-4-2-1-3-5-8-6/h1-5H2
InChIKey PAPBSGBWRJIAAV-UHFFFAOYSA-N
Smiles C1CCC(=O)OCC1
Isomeric SMILES C1CCC(=O)OCC1
Reaxy-Rn 106919
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=106919&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Chemical and Physical Properties

Flash Point(°C) > 110°C
Melt Point(°C) 60°C
Molecular Weight 114.140 g/mol
XLogP3 0.000
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 2
Rotatable Bond Count 0
Exact Mass 114.068 Da
Monoisotopic Mass 114.068 Da
Topological Polar Surface Area 26.300 Ų
Heavy Atom Count 8
Formal Charge 0
Complexity 88.500
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Solution Calculators

Reviews

Customer Reviews

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