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Merck

704067

ε-Caprolactone

97%

Synonym(s):

2-Oxepanone, 6-Caprolactone monomer, 6-Hexanolactone

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About This Item

Empirical Formula (Hill Notation):
C6H10O2
CAS Number:
502-44-3
Molecular Weight:
114.14
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
329762090
EC Number:
207-938-1
Beilstein/REAXYS Number:
106919
MDL number:
MFCD00003267

Key Documents

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Product Name

ε-Caprolactone, 97%

SMILES string

O=C1CCCCCO1

InChI key

PAPBSGBWRJIAAV-UHFFFAOYSA-N

InChI

1S/C6H10O2/c7-6-4-2-1-3-5-8-6/h1-5H2

vapor density

3.9 (vs air)

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.)

Quality Level

200

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Application

ε-caprolactone is popularly used in the preparation of poly caprolactone (PCL).

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).

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H319

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

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Certificates of Analysis (COA)

Lot/Batch Number
MKCZ3720
MKCV8030
MKCT6636
MKCN3198
MKCJ7132

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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
Mark A Birch et al.
Tissue engineering. Part A, 19(17-18), 2087-2096 (2013-05-22)
Substrate topography influences cell adhesion, proliferation, and differentiation. In this study, poly (ε-caprolactone) (PCL) films with a well-defined honeycomb structure of porosity 3-4, 5-6, 10-11, or 15-16 μm were contrasted with flat surfaces for their ability to support primary rat
Ring-opening polymerization of e-caprolactone initiated by heteropolyacid
Cheng G, et al.
Journal of Polymer Research, 17(6), 847-851 (2010)
Rezvan Mobasseri et al.
Materials science & engineering. C, Materials for biological applications, 84, 80-89 (2018-03-10)
Long-term culture, passage and proliferation of human mesenchymal stem cells (hMSCs) cause loss of their stemness properties including self-renewal and multipotency. By optimizing the MSCs environment in vitro, maintaining the stemness state and better controlling the cell fate might be
Abegaz Tizazu Andrgie et al.
Macromolecular bioscience, 19(5), e1800409-e1800409 (2019-03-02)
Metastasis is a pathogenic spread of cancer cells from the primary site to surrounding tissues and distant organs, making it one of the primary challenges for effective cancer treatment and the major cause of cancer mortality. Heparin-based biomaterials exhibit significant
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