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Merck
CN

167363

ε-Caprolactone

99%

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
EC Number:
207-938-1
UNSPSC Code:
12352100
PubChem Substance ID:
24850206
Beilstein/REAXYS Number:
106919
MDL number:
MFCD00003267

Key Documents

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InChI key

PAPBSGBWRJIAAV-UHFFFAOYSA-N

InChI

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

SMILES string

O=C1CCCCCO1

vapor density

3.9 (vs air)

vapor pressure

0.01 mmHg ( 20 °C)

assay

99%

Gene Information

human ... CYP1A2(1544)

bp

97-98 °C/15 mmHg (lit.)

density

1.03 g/mL at 25 °C (lit.)

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signalword

Warning

hcodes

H319

pictograms

Exclamation mark
GHS07

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

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
07003CJ
U21325
13031ME
05023PT
19929TD

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Cindy Chung et al.
Biomaterials, 30(26), 4287-4296 (2009-05-26)
The potential of mesenchymal stem cells (MSCs) as a viable cell source for cartilage repair hinges on the development of engineered scaffolds that support adequate cartilage tissue formation. Evolving networks (hydrogels with mesh sizes that change over time due to

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