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Safety Information

189421

Sigma-Aldrich

Polycaprolactone diol

average Mn ~2,000

Synonym(s):

Polycaprolactone oxydiethylene ester, polycaprolactone

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About This Item

Linear Formula:
C4H8O3(C6H10O2)n
CAS Number:
36890-68-3
MDL number:
MFCD00084404
UNSPSC Code:
12162002
NACRES:
NA.23

form

solid (waxy)

Quality Level

100

mol wt

average Mn ~2,000

transition temp

softening point 50 °C

density

1.071 g/mL at 25 °C

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Application

Polycaprolactone diol (PCL-diol), along with polytetrahydrofuran diol (PTHF-diol) and ceric ammonium nitrate may be used to polymerize methyl methacrylate (MMA). The product may be used to prepare biocompatible poly(ester urethane)urea (PEUU) and as a precursor for polyurethane (PU) thermoplastic polymer.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H319

Hazard Classifications

Eye Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

189421-BULK:
189421-VAR:
189421-5G:
189421-500G:
189421-250G:

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Certificates of Analysis (COA)

Lot/Batch Number
WXBD6992V
WXBD6916V
WXBD6193V
WXBD5194V
WXBD4206V

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Polycaprolactone viscosity 0.40 dL/g 

Sigma-Aldrich

900825

Polycaprolactone

Fabrication of biodegradable elastomeric scaffolds with sub?micron morphologies.
Stankus J J, et al.
Journal of Biomedical Materials Research Part A, 70(4), 603-614 (2004)
Preparation, characterization and properties of polycaprolactone diol-functionalized multi-walled carbon nanotube/thermoplastic polyurethane composite.
Jing Q, et al.
Composites Part A: Applied Science and Manufacturing, 70, 8-15 (2015)
Ceric ion initiation of methyl methacrylate using polytetrahydrofuran diol and polycaprolactone diol.
Arslan H and Hazer B
European Polymer Journal, 35(8), 1451-1455 (1999)
Shih-Heng Chen et al.
International journal of molecular sciences, 20(7) (2019-04-04)
Peritendinous adhesion is a major complication after tendon injury and the subsequent repairs or reconstructions. The degree of adhesion can be reduced by the interposition of a membranous barrier between the traumatized tendon and the surrounding tissue. In the present

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