1,3-dioxan-2-one

Base Information Edit

Chemical Name:1,3-dioxan-2-one
CAS No.:31852-84-3
Molecular Formula:C₄H₆O₃
Molecular Weight:102.09
Hs Code.:
Mol file:31852-84-3.mol

Synonyms:Carbonicacid, cyclic trimethylene ester, polymers (8CI); 1,3-Propanediol, cycliccarbonate, polymers (8CI); 1,3-Trimethylene carbonate homopolymer;Cyclotrimethylene carbonate homopolymer; Poly(trimethylene carbonate);Trimethylene carbonate homopolymer; Trimethylene carbonate polymer

Suppliers and Price of 1,3-dioxan-2-one

Supply Marketing:Edit

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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price

Total 63 raw suppliers

Chemical Property of 1,3-dioxan-2-one Edit

Chemical Property:

Melting Point:42.2 °C
Boiling Point:255.2°Cat760mmHg
Flash Point:148.6°C
PSA：35.53000
Density:1.2g/cm³
LogP:0.54330

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses 1,3-Dioxan-2-one homopolymer can be copolymerized with other lactone monomers to produce materials with tunable physical and chemical properties. After cross-linking a flexible and elastic (co-)polymer network is obtained, with properties similar to those of polydimethylsiloxane (PDMS) rubber.The materials can be used in biomedical applications. PTMC-based polymers degrade in vivo by an enzymatic surface erosion mechanism without releasing acidic degradation products, which makes these polymers well suited as matrices for the preparation of biodegradable composites for bone tissue engineering and drug delivery.

Technology Process of 1,3-dioxan-2-one

There total 33 articles about 1,3-dioxan-2-one which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 100.0%

: 503-30-0
trimethylene oxide

: 124-38-9,18923-20-1
carbon dioxide

: 2453-03-4,31852-84-3
trimethylene carbonate

Guidance literature:: With bis(acetylacetonate)oxovanadium; tetrabutylammomium bromide; In toluene; at 60 ℃; for 8h; under 26252.6 Torr; chemoselective reaction; Autoclave; Cooling with ice;
DOI:10.1039/c0gc00136h

Reference yield: 99.0%

: 332-25-2
4-(trifluoromethoxy)benzonitrile

: 504-63-2
trimethyleneglycol

: 2453-03-4,31852-84-3
trimethylene carbonate

Guidance literature:: With 3,7-di([1,1′-biphenyl]-4-yl)-10-(naphthalen-1-yl)-10H-phenoxazine; N-ethyl-N,N-diisopropylamine; In acetonitrile; at 20 ℃; for 24h; Reagent/catalyst; Inert atmosphere; Irradiation; Sealed tube;
DOI:10.1002/chem.201804603

Reference yield: 95.0%

: 124-38-9,18923-20-1
carbon dioxide

: 627-30-5
1-chloro-3-hydroxypropane

: 2453-03-4,31852-84-3
trimethylene carbonate

Guidance literature:: With caesium carbonate; In N,N-dimethyl-formamide; at 40 ℃; for 15h; under 760.051 Torr; Reagent/catalyst; Temperature; Inert atmosphere; Glovebox; Green chemistry;
DOI:10.1039/c3gc40790j