ε-Caprolactone
Synonym(s):2-Oxepanone;ε-Caprolactone;gamma-Caprolactone;6-Hexanolactone;6-Caprolactone monomer
- CAS NO.:502-44-3
- Empirical Formula: C6H10O2
- Molecular Weight: 114.14
- MDL number: MFCD00003267
- EINECS: 207-938-1
- SAFETY DATA SHEET (SDS)
- Update Date: 2024-10-30 18:52:02
What is ε-Caprolactone?
Chemical properties
Clear colorless liquid, yellowing on ageing
The Uses of ε-Caprolactone
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.
The Uses of ε-Caprolactone
Intermediate in adhesives, urethane coatings, and elastomers; solvent; diluent for epoxy resins; synthetic fibers; organic synthesis.
The Uses of ε-Caprolactone
ε-caprolactone is popularly used in the preparation of poly caprolactone (PCL).
What are the applications of Application
ε-Caprolactone is a lactone building block used for the preparation of titanium alkoxides based on benzotriazole phenoxide ligands
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
Properties of ε-Caprolactone
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 | n |
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 |
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) |
Safety information for ε-Caprolactone
Signal word | Warning |
Pictogram(s) |
Exclamation Mark Irritant GHS07 |
GHS Hazard Statements |
H319:Serious eye damage/eye irritation |
Precautionary Statement Codes |
P264:Wash hands thoroughly after handling. P264:Wash skin thouroughly after handling. P280:Wear protective gloves/protective clothing/eye protection/face protection. P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing. P337+P313:IF eye irritation persists: Get medical advice/attention. |
Computed Descriptors for ε-Caprolactone
InChIKey | PAPBSGBWRJIAAV-UHFFFAOYSA-N |
New Products
4-Aminotetrahydropyran-4-carbonitrile Hydrochloride (R)-3-Aminobutanenitrile Hydrochloride 4-AMINO-TETRAHYDRO-PYRAN-4-CARBOXYLIC ACID HCL 4-(Dimethylamino)tetrahydro-2H-pyran-4-carbonitrile 3-((Dimethylamino)methyl)-5-methylhexan-2-one oxalate 1,4-Dioxa-8-azaspiro[4.5]decane 5-Bromo-2-nitropyridine Nimesulide BP Aceclofenac IP/BP/EP Diclofenac Sodium IP/BP/EP/USP Mefenamic Acid IP/BP/EP/USP Ornidazole IP Diclofenac Potassium SODIUM AAS SOLUTION ZINC AAS SOLUTION BUFFER SOLUTION PH 10.0(BORATE) GOOCH CRUCIBLE SINTERED AQUANIL 5 BERYLLIUM AAS SOLUTION 2-Bromo-1-(bromomethyl)-3-chloro-5-nitrobenzene 2-Bromo-3-nitroaniline N-(3-Hydroxypropyl)-N-methylacetamide 3-Bromo-6-chloropyridazine 4-ethyl-3-nitrobenzoic acidRelated products of tetrahydrofuran
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