704067
ε-Caprolactone
97%
Synonym(s):
2-Oxepanone, 6-Caprolactone monomer, 6-Hexanolactone
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Empirical Formula (Hill Notation):
C6H10O2
CAS Number:
Molecular Weight:
114.14
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
EC Number:
207-938-1
Beilstein/REAXYS Number:
106919
MDL number:
vapor density
3.9 (vs air)
Quality Level
vapor pressure
0.01 mmHg ( 20 °C)
assay
97%
form
liquid
refractive index
n20/D 1.463 (lit.)
bp
97-98 °C/15 mmHg (lit.)
density
1.03 g/mL at 25 °C (lit.)
SMILES string
O=C1CCCCCO1
InChI
1S/C6H10O2/c7-6-4-2-1-3-5-8-6/h1-5H2
InChI key
PAPBSGBWRJIAAV-UHFFFAOYSA-N
General description
ε-caprolactone is a cyclic ester. Ring opening polymerization of ε-caprolactone initiated by, tributylin n butoxide, ethyl magnesium bromide, or samarium acetate or heteropolyacid, leads to the formation of poly caprolactone (PCL).
Application
ε-caprolactone is popularly used in the preparation of poly caprolactone (PCL).
Still not finding the right product?
Explore all of our products under ε-Caprolactone
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2
Storage Class
10 - Combustible liquids
wgk
WGK 1
flash_point_f
228.2 °F - closed cup
flash_point_c
109 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Related Content
Explore the design of cleavable comonomers for advanced deconstructable polymers and practical strategies to overcome synthesis challenges and their applications.
Ring-opening polymerization of e-caprolactone initiated by samarium acetate
Contreras JM, et al.
Journal of Polymer Research, 20 (2013)
Ring-opening polymerization of e-caprolactone initiated by heteropolyacid
Cheng G, et al.
Journal of Polymer Research, 17(6), 847-851 (2010)
Eliza Li Shan Fong et al.
Proceedings of the National Academy of Sciences of the United States of America, 110(16), 6500-6505 (2013-04-12)
The pronounced biological influence of the tumor microenvironment on cancer progression and metastasis has gained increased recognition over the past decade, yet most preclinical antineoplastic drug testing is still reliant on conventional 2D cell culture systems. Although monolayer cultures recapitulate
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 704067-500G | 04061838254214 |
| 704067-100G | 04061838254207 |