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Encyclopedia > Chloroprene
Chemical Structure of Chloroprene
Chemical Structure of Chloroprene

Chloroprene is the common name for the organic compound 2-chloro-1,3-butadiene, which has the chemical formula C4H5Cl. The chemical structure is shown at right. It is used as monomer for the production of the polymer polychloroprene, a type of synthetic rubber. Polychloroprene is better known to the public as Neoprene, the trade name DuPont gave it when the company first developed it and currently used by DuPont Dow. Image File history File links Chloroprene. ... An organic compound is any member of a large class of chemical compounds whose molecules contain carbon, with exception of carbides, carbonates and carbon oxides. ... A chemical formula (also called molecular formula) is a concise way of expressing information about the atoms that constitute a particular chemical compound. ... General Name, Symbol, Number carbon, C, 6 Chemical series nonmetals Group, Period, Block 14, 2, p Appearance black (graphite) colorless (diamond) Atomic mass 12. ... General Name, Symbol, Number hydrogen, H, 1 Chemical series nonmetals Group, Period, Block 1, 1, s Appearance colorless Atomic mass 1. ... General Name, Symbol, Number chlorine, Cl, 17 Chemical series halogens Group, Period, Block 17, 3, p Appearance yellowish green Atomic mass 35. ... Chemical structure is the arrangement of atoms within a molecule, usually linked by covalent bonds. ... In chemistry, a monomer (from Greek mono one and meros part) is a small molecule that may become chemically bonded to other monomers to form a polymer. ... A polymer is a generic term used to describe a substantially long molecule. ... Synthetic rubber is a type of artificially-made polymer material which acts as an elastomer. ... Neoprene is the trade name for a family of synthetic rubbers based on polychloroprene. ... This article is about the DuPont company. ...


Production of chloroprene

The acetylene process was used to produce chloroprene until the 1960s. In this process, acetylene and hydrogen chloride were used as shown here: The chemical compound acetylene, also called ethyne, was discovered in 1836 by Edmund Davy, in England; its chemical formula is C2H2 and its structure is: Acetylene is a colorless and extremely flammable gas at standard temperature and pressure, with a melting point of -80. ... Hydrogen chloride, also known under the name HCl, is a highly corrosive and toxic colorless gas that forms white fumes on contact with humidity. ...


Wikipedia does not have an article with this exact name. ...


This process had disadvantages in that it was very energy-intensive and had high investment costs.


The modern chloroprene process which is currently used by nearly all makers uses butadiene differently. 1,3-Butadiene undergoes addition of chlorine across one of its double bonds in its molecule to give 3,4-dichloro-1-butene. Then this compound undergoes an elimination of a hydrogen atom in the #3 position and the chlorine atom in the #4 position as HCl forming a double bond between the #3 and #4 carbon atoms in the molecule, yielding chloroprene. Butadiene can refer to either one of two hydrocarbon chemical compounds which are alkenes that are isomers of each other. ... General Name, Symbol, Number chlorine, Cl, 17 Chemical series halogens Group, Period, Block 17, 3, p Appearance yellowish green Atomic mass 35. ... Covalent bonding is a form of chemical bonding characterized by the sharing of one or more pairs of electrons between atoms, in order to produce a mutual attraction, which holds the resultant molecule together. ... A molecule is the smallest particle of a pure chemical substance that still retains its chemical composition and properties. ... Properties For alternative meanings see atom (disambiguation). ... Hydrogen chloride, also known under the name HCl, is a highly corrosive and toxic colorless gas that forms white fumes on contact with humidity. ...


References

Polychloroprene (CR), chloroprene rubber


  Results from FactBites:
 
Chloroprene (2-Chloro-1,3-Butadiene) | Technology Transfer Network Air Toxics Web site | US EPA (1497 words)
Chloroprene is polymerized to form polychloroprene (neoprene), a synthetic rubber used for wire and cable covers, gaskets, automotive parts, adhesives, caulks, flame-resistant cushioning and other applications requiring chemical, oil and weather resistance or high gum strength.
Acute oral exposure of rats caused inflammation of the mucous membranes; damage to the lungs, liver, spleen, and kidneys; and irritation of the gastrointestinal tract.
Chloroprene occurs as a colorless, mobile, flammable, and volatile liquid that is slightly soluble in water.
Chloroprene (IARC Summary & Evaluation, Volume 71, 1999) (359 words)
Chloroprene was tested for carcinogenicity in two studies in mice, in two studies in rats and in one study in hamsters, all by inhalation with samples of purity > 99%.
In one study in rats, chloroprene caused increased incidences of tumours of the oral cavity, thyroid gland, lung, mammary gland and kidney.
The observation of excretion of mercapturates of chloroprene indicates that glutathione conjugation occurs in rats.
  More results at FactBites »


 

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