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ε-Caprolactone

Product Name
ε-Caprolactone
CAS No.
502-44-3
Chemical Name
ε-Caprolactone
Synonyms
CAPROLACTONE;2-OXEPANONE;oxepan-2-one;EPSILON-CAPROLACTONE;E-CAPROLACTONE;Oxepanone;6-HEXANOLACTONE;Polycaprolactone Polyol;6-CAPROLACTONE;6-Hydroxyhexan-6-olide
CBNumber
CB1362738
Molecular Formula
C6H10O2
Formula Weight
114.14
MOL File
502-44-3.mol
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ε-Caprolactone Property

Melting point:
-1 °C
Boiling point:
96-97.5 °C10 mm Hg(lit.)
Density 
1.03 g/mL at 25 °C(lit.)
vapor density 
3.9 (vs air)
vapor pressure 
0.01 mm Hg ( 20 °C)
refractive index 
n20/D 1.463(lit.)
Flash point:
229 °F
storage temp. 
Store below +30°C.
solubility 
Chloroform, Ethyl Acetate
form 
Liquid
color 
Clear colorless, yellowing on aging
explosive limit
1.2-9%(V)
Water Solubility 
>1000 MG/L (20 ºC)
BRN 
106919
InChIKey
PAPBSGBWRJIAAV-UHFFFAOYSA-N
LogP
0.32 at 20℃
CAS DataBase Reference
502-44-3(CAS DataBase Reference)
NIST Chemistry Reference
2-Oxepanone(502-44-3)
EPA Substance Registry System
2-Oxepanone (502-44-3)
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Safety

Hazard Codes 
Xi
Risk Statements 
37/38-41-36/38
Safety Statements 
26-39-37/39
WGK Germany 
2
RTECS 
MO8400000
Autoignition Temperature
204 °C
TSCA 
Yes
HS Code 
29322090
Hazardous Substances Data
502-44-3(Hazardous Substances Data)
Toxicity
LD50 orally in Rabbit: > 2000 mg/kg LD50 dermal Rabbit 5990 mg/kg
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H319Causes serious eye irritation

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P337+P313IF eye irritation persists: Get medical advice/attention.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
704067
Product name
ω-Caprolactone
Purity
97%
Packaging
100g
Price
$42.8
Updated
2024/03/01
Sigma-Aldrich
Product number
8.02801
Product name
ε-Caprolactone
Purity
for synthesis
Packaging
250ML
Price
$60.3
Updated
2024/03/01
Sigma-Aldrich
Product number
704067
Product name
ω-Caprolactone
Purity
97%
Packaging
500g
Price
$141
Updated
2024/03/01
TCI Chemical
Product number
C0702
Product name
epsilon-Caprolactone
Purity
>99.0%(GC)
Packaging
25mL
Price
$17
Updated
2024/03/01
TCI Chemical
Product number
C0702
Product name
epsilon-Caprolactone
Purity
>99.0%(GC)
Packaging
500mL
Price
$41
Updated
2024/03/01
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ε-Caprolactone Chemical Properties,Usage,Production

Chemical Properties

Clear colorless liquid, yellowing on ageing

Uses

Intermediate in adhesives, urethane coatings, and elastomers; solvent; diluent for epoxy resins; synthetic fibers; organic synthesis.

Uses

ε-Caprolactone is widely used as a monomer in the manufacturing of highly specialized polymers. It is mainly utilized as a precursor to caprolactam. It finds an application in the synthesis of polyglecaprone, which is used as a suture material in surgery.

Uses

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

Definition

ChEBI: A epsilon-lactone that is oxepane substituted by an oxo group at position 2.

Synthesis Reference(s)

Journal of the American Chemical Society, 80, p. 4079, 1958 DOI: 10.1021/ja01548a063
The Journal of Organic Chemistry, 61, p. 4560, 1996 DOI: 10.1021/jo952237x
Tetrahedron Letters, 17, p. 2455, 1976 DOI: 10.1016/0040-4039(76)90018-6

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).

Flammability and Explosibility

Not classified

ε-Caprolactone Preparation Products And Raw materials

Raw materials

Preparation Products

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ε-Caprolactone Suppliers

TOKYO CHEMICAL INDUSTRY CO., LTD.
Tel
03-36680489
Fax
03-3668-0520
Email
Sales-JP@TCIchemicals.com
Country
Japan
ProdList
28387
Advantage
80
TCI Japan
Tel
--
Fax
--
Email
@TCIchemicals.com
Country
Japan
ProdList
2741
Advantage
58
Daicel Corporation
Tel
--
Fax
--
Country
Japan
ProdList
31
Advantage
58
FUJIFILM Wako Pure Chemical Corporation
Tel
--
Fax
--
Email
ffwk-cservice@fujifilm.com
Country
Japan
ProdList
6222
Advantage
58
Nacalai Tesque, Inc.
Tel
--
Fax
--
Email
info-tech@nacalai.co.jp
Country
Japan
ProdList
6046
Advantage
75
Kanto Chemical Co., Inc.
Tel
--
Fax
--
Email
reag-info@gms.kanto.co.jp
Country
Japan
ProdList
6756
Advantage
74
Wako Pure Chemical Industries, Ltd.
Tel
--
Fax
--
Email
labchem-tec@wako-chem.co.jp
Country
Japan
ProdList
6819
Advantage
80
Junsei Chemical Co., Ltd.
Tel
--
Fax
--
Email
shiyaku@junsei.co.jp
Country
Japan
ProdList
3096
Advantage
46
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View Lastest Price from ε-Caprolactone manufacturers

Shandong Deshang Chemical Co., Ltd.
Product
ε-Caprolactone 502-44-3
Price
US $10.00-5.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
10 tons
Release date
2024-08-15
Hebei Weibang Biotechnology Co., Ltd
Product
6-Hexanalactone 502-44-3
Price
US $0.00-0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
500000kg
Release date
2024-10-30
Hebei Weibang Biotechnology Co., Ltd
Product
6-Hexanolactone 502-44-3
Price
US $10.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
10 mt
Release date
2024-10-25

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