| | 2-chloro-1,3-butadiene Basic information |
| Product Name: | 2-chloro-1,3-butadiene | | Synonyms: | 2-chloro-1,3-butadiene(chloroprene);2-chloro-1,3-butadiene(chloroprene)(50%inxylene);2-chloro-3-butadiene;2-chloro-buta-1,3-diene;2-Chlorobuta-1,3-diene;2-Chlorobutadiene;2-Chlorobutadiene 1,3;2-chlorobutadiene-1,3 | | CAS: | 126-99-8 | | MF: | C4H5Cl | | MW: | 88.54 | | EINECS: | 204-818-0 | | Product Categories: | monomer | | Mol File: | 126-99-8.mol |  |
| | 2-chloro-1,3-butadiene Chemical Properties |
| Melting point | -130°C | | Boiling point | 59.45°C | | density | 0,958 g/cm3 | | vapor pressure | 118 at 10 °C, 200 at 20 °C, 275 at 30 °C (quoted, Verschueren, 1983) | | refractive index | 1.4583 | | Fp | 11 °C | | storage temp. | 2-8°C | | solubility | Soluble in acetone, benzene, and ether (Weast, 1986) | | form | Colorless liquid | | Water Solubility | 256mg/L at 20℃ | | Henry's Law Constant | 3.20 x 10-2 atm?m3/mol using method of Hine and Mookerjee (1975) | | Exposure limits | Potential occupational carcinogen. NIOSH REL: 15-min ceiling 1 ppm (3.6
mg/m3), IDLH 300 ppm; OSHA PEL: TWA 25 ppm (90 mg/m3); ACGIH TLV: TWA 10 ppm
(adopted). | | LogP | 2.525 at 20℃ | | CAS DataBase Reference | 126-99-8(CAS DataBase Reference) | | IARC | 2B (Vol. Sup 7, 71) 1999 | | EPA Substance Registry System | Chloroprene (126-99-8) |
| | 2-chloro-1,3-butadiene Usage And Synthesis |
| Description | Chloroprene, 2-chloro-1,3-butadiene, is a colorless, volatile
synthetic liquid that has a pungent ether-like odor. Synthesis
of chloroprene was first reported by chemists of the E. I. du
Pont de Nemours Company in 1931 following studies of
acetylene polymerization with the objective of producing
synthetic rubber. The chloroprene monomer differs from
isoprene, the fundamental monomer of natural rubber, only
by substitution of chlorine for the methyl group of isoprene.
Chloroprene was observed to polymerize much more
quickly than did isoprene. In industrial processes prior to
1960, chloroprene was produced in relatively high yields by
reacting vinyl acetylene with hydrogen chloride. Today,
chloroprene is produced more efficiently by chlorination of
1,3-butadiene.
When compared with natural rubber the chloroprene
synthetic polymer, polychloroprene, was noted to be much
denser, more resistant to water and hydrocarbon solvents,
less permeable to many gases, and was more resistant
to degradation by oxygen, ozone, hydrogen chloride,
hydrogen fluoride, and other chemicals. Due to desirable
physical and chemical properties, polychloroprene and its
latex polymers are produced in quantities exceeding
200 000 metric tons at a limited number of facilities
around the world. Chloroprene production is closely tied to
demand for polychloroprene. | | Chemical Properties | Chloroprene (2-chloro-l,3-butadiene) was first synthesized by Carothers and
Collins (E.I. du Pont de Nemours and Co.) in 1930 during classical studies on
acetylene. The compound was found to undergo spontaneous polymerization
with the formation of a rubbery material. This product was shown to have
good resistance to oil, heat and weathering and commercial manufacture of
chloroprene rubber was started in 1932.
Chloroprene is a colourless liquid, b.p. 59℃. | | Chemical Properties | Chloroprene (2-chloro-1,3-butadiene) is a flammable, colorless liquid at room temperature with a characteristic ether-like odor. The Odor Threshold is 0.4 milligram per cubic meter. It is slightly soluble in water and more soluble in organic solvents. It has not been found to occur naturally. Chloroprene is very unstable and reacts in air with oxygen and other compounds to form epoxides, peroxides, and other hazardous compounds. | | Physical properties | Clear, colorless liquid with a pungent, ether-like odor. The odor threshold is 0.40 mg/m3 (CHRIS, 1984). | | Uses | Manufacture of neoprene. | | Uses | The only commercial use identified for chloroprene is as a monomer in the production of the elastomer polychloroprene (neoprene), a synthetic rubber used in the production of automotive and mechanical rubber goods, adhesives, caulks, flame-resistant cushioning,construction materials, fabric coatings, fiber binding, and footwear. Other uses of this polymer include applications requiring chemical, oil, or weather resistance or high gum strength. The U.S. Food and Drug Administration permits the use of chloroprene as a component of adhesives used in food packaging and also permits the use of polychloroprene in products intended for use with food (IARC 1979, 1999, NTP 1998). | | Uses | Almost all the chloroprene produced is used for the manufacture of these polychloroprene rubbers. Chloroprene is a volatile, toxic, flammable liquid and is especially susceptible to oxidation and polymerization. | | Preparation | Preparation of chloroprene from butadiene
In this method, the following route is used:
In the first step, butadiene is chlorinated in the vapour phase at 330-420??
and atmospheric pressure. The main products are 3,4-dichloro-l-butene and
1,4-dichloro-2-butene in approximately equal amounts. The latter material is
then isomerized to the former by heating with a copper catalyst such as
cuprous chloride. The 3,4-dichloro-l-butene is dehydrochlorinated by treatment with 10% aqueous sodium hydroxide at 85??. Chloroprene is isolated
by distillation under reduced pressure in the presence of polymerization
inhibitors. | | Production Methods | Chloroprene can be synthesized by addition of HCl to vinyl acetylene H2C=CH?C≡CH +HCl → H2C=CH?CCl=CH2, and by dehydrochlorination of dichlorobutenes or 2,2,3-trichlorobutane. | | Definition | A colorless liquid derivative of
butadiene used in the manufacture of neoprene
rubber. | | General Description | A clear colorless liquid. Flash point -4°F. May polymerize exothermically if heated or contaminated. If polymerization takes place inside a container, the container may rupture violently. Less dense than water. Vapors heavier than air. Used to make neoprene rubber. | | Air & Water Reactions | Highly flammable. Slightly soluble in water. | | Reactivity Profile | CHLOROPRENE emits highly toxic fumes of chlorine gas when heated to decomposition. Autooxidizes very rapidly with air and, even at 0°C, produces unstable peroxides that catalyze exothermic polymerization [Bretherick, 5th ed., 1995, p. 507]. This reactivity is greatly slowed by presence of an inhibitor. | | Hazard | Toxic by ingestion, inhalation, and skin
absorption. Flammable, dangerous fire risk, explosive limits in air 4.0–20%. Eye and upper respiratory
tract irritant. Possible carcinogen. | | Health Hazard | INHALATION: Fatigue, psychic changes, irritability, oppression in chest, occasionally substernal pain, tachycardia upon exertion. EYES: Can cause conjunctivitis, corneal necrosis and edema of eyelids. SKIN: May cause dermatitis and temporary loss of hair. Rapidly absorbed by skin. | | Safety Profile | Confirmed carcinogen. Poison by ingestion, intravenous, and subcutaneous routes. Moderately toxic by inhalation. An experimental teratogen. Experimental reproductive effects. Human mutation data reported. Human exposure has caused dermatitis, conjunctivitis, corneal necrosis, anemia, temporary loss of hair, nervousness, and irritabhty. Exposure to the vapor can cause respiratory tract irritation leading to asphyxia. Other effects are central nervous system depression, drop in blood pressure, severe degenerative changes in the liver, kidneys, lungs, and other vital organs. A very dangerous fire hazard when exposed to heat or flame. Explosive in the form of vapor when exposed to heat or flame. To fight fire, use alcohol foam. Auto-oxidlzes in air to form an unstable peroxide that catalyzes exothermic polymerization of the monomer. Incompatible with liquid or gaseous fluorine. When heated to decomposition it emits toxic fumes of Cl-. See also CHLORINATED HYDROCARBONS, ALIPHATIC . | | Potential Exposure | The major use of chloroprene is in the production of artificial rubber (Neoprene, duprene); polychloroprene elastomers. Chloroprene is extremely reactive, e.g., it can polymerize spontaneously at room temperatures; the process being catalyzed by light, peroxides, and other free radical initiators. It can also react with oxygen to form polymeric peroxides and because of its instability, flammability, and toxicity, chloroprene has no end-product uses as such. | | Carcinogenicity | Chloroprene is reasonably anticipated to be a human carcinogen based on evidence of carcinogenicity from studies in experimental
animals. | | Environmental Fate | Chemical/Physical. Anticipated products from the reaction of chloroprene with ozone or OH radicals in the atmosphere are formaldehyde, 2-chloroacrolein, OHCCHO, ClCOCHO, H2CCHCClO, chlorohydroxy acids, and aldehydes (Cupitt, 1980).
Chloroprene will polymerize at room temperature unless inhibited with antioxidants (NIOSH, 1997). Chloroprene is resistant to hydrolysis under neutral and alkaline conditions (Carothers et al., 1931).
Chloroprene is subject to hydrolysis forming 3-hydroxypropene and HCl. The reported hydrolysis half-life at 25 °C and pH 7 is 40 yr (Kollig, 1993). | | Shipping | UN1991 Chloroprene, stabilized, Hazard Class: 3; Labels: 3-Flammable liquid, 6.1-Poisonous material. | | Toxicity evaluation | Chloroprene is not generally available from chemical
supply firms. Concentrated chloroprene is extremely reactive
unless stored cold, under inert gas, and in presence of oxidation
inhibitors and free radical scavengers. With pure chloroprene
multiple undesirable reactions can occur, including spontaneous
dimerization, polymerization, oxidation, epoxide
formation, and nitration. Due to its reactivity, handling and
transportation of chloroprene are carefully regulated; shipment
of uninhibited chloroprene is forbidden by statute.
Chloroprene is not known to occur naturally. It is not widely
distributed in the environment due its reactivity and its use at
a limited number of facilitiesworldwide. Industrial productionof
chloroprene is accomplished in sealed reactor systems with very
limited fugitiveemissions.Polymerizationprocesses are designed
to be sealed, but must be opened to remove and manipulate
formed polymer. Such opening causes most environmental
release of chloroprene, the majority of which enters the atmosphere.
From National Library of Medicine Toxics Release
Inventory 2010 data, more than 270 000 pounds of chloroprene
was released into the environment. Of that amount more than
97% was released into air at one site in Louisiana, USA. | | Incompatibilities | Can form unstable peroxides; chloroprene may polymerize on standing with fire or explosion hazard. May form explosive mixture with air. Reacts with liquid or gaseous fluorine, alkali metals; metal powders, oxidizers, creating a fire or explosion hazard. Attacks some plastics, rubber, and coatings. May accumulate static electrical charges, and may cause ignition of its vapors. | | Waste Disposal | Incineration, preferably after mixing with another combustible fuel. Care must be exercised to assure complete combustion to prevent the formation of phosgene. An acid scrubber is necessary to remove the halo acids produced. |
| | 2-chloro-1,3-butadiene Preparation Products And Raw materials |
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