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Revision as of 12:09, 15 February 2012 editBeetstra (talk | contribs)Edit filter managers, Administrators172,031 edits Saving copy of the {{chembox}} taken from revid 476913276 of page Vinyl_chloride for the Chem/Drugbox validation project (updated: '').  Latest revision as of 01:57, 17 December 2024 edit Arthurfragoso (talk | contribs)Extended confirmed users1,841 edits Fixes image on dark mode 
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{{ambox | text = This page contains a copy of the infobox ({{tl|chembox}}) taken from revid of page ] with values updated to verified values.}}
{{chembox {{chembox
| Watchedfields = changed
| verifiedrevid = 447499154
| verifiedrevid = 476992265
| Name = Vinyl chloride
| ImageFileL1 = Vinyl-chloride-2D.png | Name = Vinyl chloride
| ImageFile = Vinyl-chloride-2D.png
| ImageSizeL1 = 100px
| ImageClass = skin-invert
| ImageNameL1 = Structural formula of vinyl chloride
| ImageFileR1 = Vinyl-chloride-3D-vdW.png | ImageFileL1 = Vinyl-chloride-3D-balls.png
| ImageNameL1 = Structural formula of vinyl chloride
| ImageSizeR1 = 120px
| ImageFileR1 = Vinyl-chloride-3D-vdW.png
| ImageNameR1 = Space-filling model
| ImageNameR1 = Space-filling model
| IUPACName = Chloroethene
| PIN = Chloroethene
| OtherNames = Vinyl chloride monomer<br />VCM<br />Chloroethylene
| OtherNames = Vinyl chloride monomer<br />VCM<br />Chloroethylene<br />Refrigerant-1140
| Section1 = {{Chembox Identifiers
| Section1 = {{Chembox Identifiers
| ChEBI_Ref = {{ebicite|correct|EBI}}
| CASNo = 75-01-4
| CASNo_Ref = {{cascite|correct|CAS}}
| Beilstein = 1731576
| ChEBI_Ref = {{ebicite|correct|EBI}}
| ChEBI = 28509 | ChEBI = 28509
| SMILES = ClC=C | ChEMBL = 2311071
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| PubChem = 6338
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 6098 | ChemSpiderID = 6098
| EC_number = 200-831-0
| Gmelin = 100541
| KEGG_Ref = {{keggcite|correct|kegg}} | KEGG_Ref = {{keggcite|correct|kegg}}
| KEGG = C06793 | KEGG = C06793
| PubChem = 6338
| RTECS = KU9625000
| UNNumber = 1086
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = WD06X94M2D
| SMILES = ClC=C
| InChI = 1/C2H3Cl/c1-2-3/h2H,1H2 | InChI = 1/C2H3Cl/c1-2-3/h2H,1H2
| InChIKey = BZHJMEDXRYGGRV-UHFFFAOYAW | InChIKey = BZHJMEDXRYGGRV-UHFFFAOYAW
Line 26: Line 36:
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = BZHJMEDXRYGGRV-UHFFFAOYSA-N | StdInChIKey = BZHJMEDXRYGGRV-UHFFFAOYSA-N
}}
| CASNo = 75-01-4
| Section2 = {{Chembox Properties
| CASNo_Ref = {{cascite|correct|CAS}}
|H=3|C=2|Cl=1
}}
| Appearance = Colorless gas
| Section2 = {{Chembox Properties
| Odor = pleasant<ref name=PGCH/>
| Formula = C<sub>2</sub>H<sub>3</sub>Cl
| MolarMass = 62.498 g/mol | Density = 0.911&nbsp;g/cc
| Solubility = 2.7&nbsp;g/L (0.0432 mol/L)
| Appearance = Colorless gas
| VaporPressure = 2580 mmHg at 20&nbsp;°C (68&nbsp;°F)
| Density = 0.911 g/ml
| MeltingPtC = −153.8
| Solubility = 2.7 g/L (0.0432 mol/L)
| BoilingPtC = −13.4
| MeltingPt = -153.8 °C (119.4 K)
| Viscosity =
| BoilingPt = -13.4 °C (259.8 K)
| MagSus = -35.9·10<sup>−6</sup> cm<sup>3</sup>/mol
| Viscosity =
}} }}
| Section3 = {{Chembox Structure | Section3 = {{Chembox Structure
| Dipole = | Dipole =
}} }}
| Section4 = {{Chembox Thermochemistry | Section4 = {{Chembox Thermochemistry
| DeltaHf = -94.12 kJ/mol (solid) | DeltaHf = −94.12&nbsp;kJ/mol (solid)
| HeatCapacity = 0.8592 J/K/g (gas)<br>0.9504 J/K/g (solid) | HeatCapacity = 0.8592&nbsp;J/K/g (gas)<br>0.9504&nbsp;J/K/g (solid)
}} }}
| Section7 = {{Chembox Hazards | Section7 = {{Chembox Hazards
| ExternalMSDS = | ExternalSDS = <!---->
| MainHazards = | MainHazards =
| FlashPt = -61.11°C | NFPA-H = 3
| NFPA-F = 4
}}
| NFPA-R = 2
| Section8 = {{Chembox Related
| Function = | NFPA-S =
| GHSPictograms = {{GHS02}}{{GHS08}}
| OtherFunctn =
| OtherCpds = | GHSSignalWord = Danger
| HPhrases = {{H-phrases|220|350}}
}}
| PPhrases = {{P-phrases|201|202|210|281|308+313|377|381|403|405|501}}
| FlashPtC = -61
| PEL = TWA 1 ppm C 5 ppm <ref name=PGCH>{{PGCH|0658}}</ref>
| ExploLimits = 3.6–33%<ref name=PGCH/>
| IDLH = Ca <ref name=PGCH/>
| REL = Ca<ref name=PGCH/>
}}
| Section8 = {{Chembox Related
| OtherFunction_label = chloroethenes
| OtherFunction = ]s, ], ], ]
| OtherCompounds =
}}
}} }}
'''Vinyl chloride''' is an ] with the ] H<sub>2</sub>C]CHCl. It is also called '''vinyl chloride monomer''' ('''VCM''') or '''chloroethene'''. It is an important industrial chemical chiefly used to produce the ] ] (PVC). Vinyl chloride is a colourless flammable gas that has a sweet odor and is ]ic. Vinyl chloride monomer is among the top twenty largest ]s (]-derived chemicals) in world production.<ref name=Ullmann/> The United States remains the largest vinyl chloride manufacturing region because of its low-production-cost position in chlorine and ethylene raw materials. China is also a large manufacturer and one of the largest consumers of vinyl chloride.<ref name="ihs.com">{{cite web|url=http://www.ihs.com/products/chemical/planning/ceh/vinyl-chloride-monomer.aspx|title=Vinyl Chloride Monomer (VCM) – Chemical Economics Handbook|publisher=]|access-date=5 April 2018|archive-date=18 August 2014|archive-url=https://web.archive.org/web/20140818011728/http://www.ihs.com/products/chemical/planning/ceh/vinyl-chloride-monomer.aspx|url-status=live}}</ref> It can be formed in the environment when ] organisms break down chlorinated solvents. Vinyl chloride that is released by industries or formed by the breakdown of other chlorinated chemicals can enter the air and drinking water supplies. Vinyl chloride is a common contaminant found near ]s.<ref>{{Cite web |date=2018-01-30 |title=Vinyl Chloride |url=https://dhs.wisconsin.gov/chemical/vc.htm |access-date=2023-02-07 |website=Wisconsin Department of Health Services |language=en |archive-date=2023-02-07 |archive-url=https://web.archive.org/web/20230207010917/https://dhs.wisconsin.gov/chemical/vc.htm |url-status=live }}</ref> Before the 1970s, vinyl chloride was used as an ] and ].<ref>{{cite web|url=https://pubmed.ncbi.nlm.nih.gov/31335054/|publisher=]|title=Vinyl Chloride Toxicity|author1=Fralish, Matthew S. |author2=Downs, John W.|language=en-US|url-status=live|date=June 21, 2022|pmid=31335054 |access-date=February 21, 2023|archive-date=February 21, 2023|archive-url=https://web.archive.org/web/20230221171747/https://pubmed.ncbi.nlm.nih.gov/31335054/}}</ref><ref name="npi.gov.au">{{Cite web |title=Vinyl Chloride Monomer (VCM)|url=https://www.dcceew.gov.au/environment/protection/npi/substances/fact-sheets/vinyl-chloride-monomer-vcm |url-status=live |archive-url=https://web.archive.org/web/20230206212928/https://www.dcceew.gov.au/environment/protection/npi/substances/fact-sheets/vinyl-chloride-monomer-vcm |archive-date=2023-02-06 |publisher=]}}</ref>

== Uses ==
] (PVC), the main end-product of vinyl chloride, is used extensively in sewage pipes due to its low cost, chemical resistance, and ease of jointing.|left]]
Vinyl chloride, also called vinyl chloride monomer (VCM), is exclusively used as a precursor to PVC. Due to its toxic nature, vinyl chloride is not found in other products. Poly(vinyl chloride) (PVC) is very stable, storable and not toxic.<ref name=Ullmann/>

Until 1974, vinyl chloride was used in ].<ref>{{Cite book |url=https://www.questia.com/read/124747742/deceit-and-denial-the-deadly-politics-of-industrial. |title=Deceit and Denial: The Deadly Politics of Industrial Pollution |last1=Markowitz |first1=Gerald |last2=Rosner |first2=David |publisher=University of California Press |year=2013 |location=Berkeley, California Press |pages=185 |url-access= |via=}}{{dead link|date=July 2021}}</ref> Vinyl chloride was briefly used as an ], in a similar vein to ], though its toxicity limited this use.<ref name="pmid572591">{{cite journal |vauthors=Tamburro CH |title=Health effects of vinyl chloride |journal=Texas Reports on Biology and Medicine |volume=37 |pages=126–44, 146–51 |date=1978 |pmid=572591}}</ref><ref name="pmid20255056">{{cite journal |vauthors=Oster RH, Carr CJ |title=Anesthesia; narcosis with vinyl chloride |journal=Anesthesiology |volume=8 |issue=4 |pages=359–61 |date=July 1947 |pmid=20255056 |doi=10.1097/00000542-194707000-00003 |s2cid=73229069 |url=https://pubs.asahq.org/anesthesiology/article/8/4/359/34257/ANESTHESIA-XXVII-NARCOSIS-WITH-VINYL-CHLORIDE |access-date=2023-02-15 |archive-date=2023-02-15 |archive-url=https://web.archive.org/web/20230215080851/https://pubs.asahq.org/anesthesiology/article/8/4/359/34257/ANESTHESIA-XXVII-NARCOSIS-WITH-VINYL-CHLORIDE |url-status=live |doi-access=free }}</ref>

==Production==
Globally, approximately 40 million tonnes of PVC resin are produced per year,<ref>{{cite web | title = PVC applications | publisher = The European Council of Vinyl Manufacturers | url = https://pvc.org/pvc-applications/ | accessdate = 2023-02-25}}</ref> requiring a corresponding amount of vinyl chloride monomer.<ref>{{cite web |title=Investigating the Safety of Vinyl Chloride in PVC Pipes for Drinking Water. Plumbing Navigator |url=https://plumbingnav.com/plumbing/safety-of-vinyl-chloride-in-pvc-pipes/ |website=Plumbingnav |publisher=Grabowski, B |access-date=April 12, 2023}}</ref>
===History===
Vinyl chloride was first synthesized in 1835 by ] and his student ]. They obtained it by treating ] with a solution of ] in ].<ref>{{cite journal |last1=Regnault |first1=H. V. |year=1835 |title=Sur la Composition de la Liqueur des Hollandais et sur une nouvelle Substance éthérée. |journal=Annales de Chimie et de Physique |publisher=Gay-Lussac & Arago |volume=5858 |pages=301–320 |url=https://gallica.bnf.fr/ark:/12148/bpt6k6569005x/f307.item.texteImage |access-date=2019-07-11 |archive-date=2019-07-11 |archive-url=https://web.archive.org/web/20190711155454/https://gallica.bnf.fr/ark:/12148/bpt6k6569005x/f307.item.texteImage |url-status=live }}</ref>
===Acetylene-based routes===
In 1912, Fritz Klatte, a German chemist working for Griesheim-Elektron, patented a means to produce vinyl chloride from ] and ] using ] as a ]. ] reacts with ] over a mercuric chloride catalyst to give vinyl chloride:
:C<sub>2</sub>H<sub>2</sub> + HCl → CH<sub>2</sub>=CHCl
The reaction is exothermic and highly selective. Product purity and yields are generally very high.<ref name=Ullmann/>

This route to vinyl chloride was common before ethylene became widely distributed. When vinyl chloride producers shifted to using the thermal cracking of EDC described below, some used byproduct HCl in conjunction with a colocated acetylene-based unit. The hazards of storing and shipping acetylene meant that the vinyl chloride facility needed to be located very close to the acetylene generating facility.<ref name="Ullmann" />

In view of mercury's toxicity, gold- and platinum-based catalysts have been proposed.<ref>{{cite journal | doi = 10.1126/science.aal3439| title = Identification of single-site gold catalysis in acetylene hydrochlorination| year = 2017| last1 = Malta| first1 = Grazia| last2 = Kondrat| first2 = Simon A.| last3 = Freakley| first3 = Simon J.| last4 = Davies| first4 = Catherine J.| last5 = Lu| first5 = Li| last6 = Dawson| first6 = Simon| last7 = Thetford| first7 = Adam| last8 = Gibson| first8 = Emma K.| last9 = Morgan| first9 = David J.| last10 = Jones| first10 = Wilm| last11 = Wells| first11 = Peter P.| last12 = Johnston| first12 = Peter| last13 = Catlow| first13 = C. Richard A.| last14 = Kiely| first14 = Christopher J.| last15 = Hutchings| first15 = Graham J.| journal = Science| volume = 355| issue = 6332| pages = 1399–1403| pmid = 28360324| bibcode = 2017Sci...355.1399M| s2cid = 206655247| url = https://figshare.com/articles/Identification_of_single-site_gold_catalysis_in_acetylene_hydrochlorination/9390182| doi-access = free}}</ref><ref>{{cite journal | doi = 10.1038/s41929-020-0431-3| title = Nanostructuring unlocks high performance of platinum single-atom catalysts for stable vinyl chloride production| year = 2020| last1 = Kaiser| first1 = Selina K.| last2 = Fako| first2 = Edvin| last3 = Manzocchi| first3 = Gabriele| last4 = Krumeich| first4 = Frank| last5 = Hauert| first5 = Roland| last6 = Clark| first6 = Adam H.| last7 = Safonova| first7 = Olga V.| last8 = López| first8 = Núria| last9 = Pérez-Ramírez| first9 = Javier| journal = Nature Catalysis| volume = 3| issue = 4| pages = 376–385| pmid = 32292878| pmc = 7156288}}</ref>

The mercury-based technology is the main production method in China due to low price on coal from which acetylene is produced,<ref name="ihs.com" /><ref name="Ullmann" /> with over 80% of national capacity as of 2018, even though the resulting PVC contains residues and is only suitable for low-end products like pipes.<ref>https://www.businesswire.com/news/home/20181102005262/en/China-Polyvinyl-Chloride-PVC-Industry-Report-2018-2022---ResearchAndMarkets.com</ref>

===Ethylene-based routes===
In the United States and Europe, mercury-catalyzed routes widely used in the 20th century have been superseded by more economical and ] processes based on ethylene. Ethylene is made by cracking ethane. Two steps are involved, chlorination and dehydrochlorination:
:{{chem2|H2C\dCH2 + Cl2 → H2ClC\sCH2Cl}}
:{{chem2|H2ClC\sCH2Cl → H2C\dCHCl + HCl}}

===Possible routes from ethane===
Numerous attempts have been made to convert ethane directly to vinyl chloride.<ref name=Ullmann>{{Ullmann |doi=10.1002/14356007.o06_o01 |title=Chlorethanes and Chloroethylenes |year=2011 |last1=Dreher |first1=Eberhard-Ludwig |last2=Torkelson |first2=Theodore R. |last3=Beutel |first3=Klaus K. |isbn=978-3527306732}}</ref> Ethane, which is even more readily available than ethylene, is a potential precursor to vinyl chloride. The conversion of ethane to vinyl chloride has been demonstrated by various routes:<ref name=Ullmann/>

High-temperature chlorination:
:{{chem2|H3C\sCH3 + 2 Cl2 → H2C\dCHCl + 3 HCl}}
High-temperature oxychlorination, which uses oxygen and hydrogen chloride in place of chlorine:
:{{chem2|H3C\sCH3 + O2 + HCl → H2C\dCHCl + 2 H2O}}

High-temperature oxidative chlorination:
{{chem2|4 H3C\sCH3 + 3 O2 + 2 Cl2 → 4 H2C\dCHCl + 6 H2O}}

====Thermal decomposition of dichloroethane====
], ClCH<sub>2</sub>CH<sub>2</sub>Cl (also known as ethylene dichloride, EDC), can be prepared by ] of ] or ], inexpensive starting materials. EDC thermally converts into vinyl chloride and anhydrous HCl. This production method has become the major route to vinyl chloride since the late 1950s.<ref name=Ullmann/>

:{{chem2|ClCH2\sCH2Cl → CH2\dCHCl + HCl}}

The thermal cracking reaction is highly endothermic, and is generally carried out in a fired heater. Even though residence time and temperature are carefully controlled, it produces significant quantities of chlorinated hydrocarbon side products. In practice, the yield for EDC conversion is relatively low (50 to 60 percent). The furnace effluent is immediately quenched with cold EDC to minimize undesirable side reactions. The resulting vapor-liquid mixture then goes to a purification system. Some processes use an absorber-stripper system to separate HCl from the chlorinated hydrocarbons, while other processes use a refrigerated ] system.<ref name=Ullmann/>

== Storage and transportation ==
Vinyl chloride is stored as a liquid. The accepted upper limit of safety as a health hazard is 500&nbsp;ppm. Often, the storage containers for the product vinyl chloride are high capacity spheres. The spheres have an inside sphere and an outside sphere. Several inches of space separate the inside sphere from the outside sphere. The interstitial space between the spheres is purged with an inert gas such as nitrogen. As the nitrogen purge gas exits the interstitial space it passes through an analyzer that detects whether any vinyl chloride is leaking from the internal sphere. If vinyl chloride starts to leak from the internal sphere or if a fire is detected on the outside of the sphere then the contents of the sphere are automatically dumped into an emergency underground storage container. Containers used for handling vinyl chloride at atmospheric temperature are always under pressure. Inhibited vinyl chloride may be stored at normal atmospheric conditions in suitable pressure vessels. Uninhibited vinyl chloride may be stored either under refrigeration or at normal atmospheric temperature in the absence of air or sunlight but only for a duration of a few days. If stored for longer periods, regular checks must be made to confirm no polymerization has taken place.<ref>{{Cite web |url=http://aseh.net/resources/restored/resources/teaching-units/teaching-unit-better-living-through-chemistry/historical-sources/lesson-1/MCA-Vinal%20Chloride%20Safety%20Sheet-1954.pdf |title=aseh.net |access-date=2013-10-06 |archive-date=2013-10-20 |archive-url=https://web.archive.org/web/20131020204308/http://aseh.net/resources/restored/resources/teaching-units/teaching-unit-better-living-through-chemistry/historical-sources/lesson-1/MCA-Vinal%20Chloride%20Safety%20Sheet-1954.pdf |url-status=dead }}</ref>{{better source needed|date=February 2023}}

In addition to its toxicity risk, transporting vinyl chloride also presents the same risks as transporting other flammable gases such as propane, butane, or natural gas.<ref>{{Cite web |title=Vinyl Chloride Monomer (VCM) Production |url=http://www.pvc.org/en/p/vinyl-chloride-monomer-vcm | publisher = The European Council of Vinyl Manufacturers | archive-url=https://web.archive.org/web/20190107005342/http://www.pvc.org:80/en/p/vinyl-chloride-monomer-vcm |archive-date=2019-01-07}}</ref> Examples of incidents in which this danger was observed include the ],<ref>{{Cite web |last1=Orsagos |first1=Patrick |last2=Seewer |first2=John |date=February 6, 2023 |title=Crews release toxic chemicals from derailed tankers in Ohio |url=https://apnews.com/article/ohio-train-derailment-updates-bf5a60de2243cd6f7f730096aa33294c |access-date=February 14, 2023|publisher=]|language=en-US|archive-date=February 7, 2023 |archive-url=https://web.archive.org/web/20230207084734/https://apnews.com/article/ohio-train-derailment-updates-bf5a60de2243cd6f7f730096aa33294c|url-status=live}}</ref><ref>{{Cite web |date=February 11, 2023 |title=Ohio catastrophe is 'wake-up call' to dangers of deadly train derailments|url=https://www.theguardian.com/us-news/2023/feb/11/ohio-train-derailment-wake-up-call|website=]|access-date=February 13, 2023|archive-date=February 13, 2023|archive-url=https://web.archive.org/web/20230213091852/https://www.theguardian.com/us-news/2023/feb/11/ohio-train-derailment-wake-up-call |url-status=live }}</ref> in which derailed tank cars dumped 100,000 gallons of hazardous materials, including vinyl chloride.<ref>{{Cite web |title=NTSB Issues Investigative Update on Ohio Train Derailment|publisher=] |url=https://www.ntsb.gov/news/press-releases/Pages/NR20230214.aspx|language=en-US|date=2023|access-date=April 19, 2023|archive-date=February 19, 2023|archive-url=https://web.archive.org/web/20230219060902/https://www.ntsb.gov/news/press-releases/Pages/NR20230214.aspx|url-status=live}}</ref><ref>{{cite web|title=TRAIN 32N - EAST PALESTINE.xlsx|publisher=]|url=https://www.epa.gov/system/files/documents/2023-02/TRAIN%2032N%20-%20EAST%20PALESTINE%20-%20derail%20list%20Norfolk%20Southern%20document.pdf|language=en-US|url-status=live|date=2023|access-date=April 19, 2023|archive-date=February 17, 2023|archive-url=https://web.archive.org/web/20230217230221/https://response.epa.gov/sites/15933/files/TRAIN%2032N%20-%20EAST%20PALESTINE%20-%20derail%20list%20Norfolk%20Southern%20document.pdf}}</ref>

==Fire and explosion hazard==
In the U.S., ] lists vinyl chloride as a Class IA Flammable Liquid, with a ] Flammability Rating of 4. Because of its low boiling point, liquid vinyl chloride will undergo ] (i.e., autorefrigerate) upon its release to atmospheric pressure. The portion vaporized will form a dense cloud (more than twice as heavy as the surrounding air). The risk of subsequent explosion or fire is significant. According to OSHA, the ] of vinyl chloride is −78&nbsp;°C (−108.4&nbsp;°F).<ref>{{Cite web |url=http://aseh.net/resources/restored/resources/teaching-units/teaching-unit-better-living-through-chemistry/historical-sources/lesson-1/MCA-Vinal%20Chloride%20Safety%20Sheet-1954.pdf |title=Aseh.net |access-date=2013-10-06 |archive-date=2013-10-20 |archive-url=https://web.archive.org/web/20131020204308/http://aseh.net/resources/restored/resources/teaching-units/teaching-unit-better-living-through-chemistry/historical-sources/lesson-1/MCA-Vinal%20Chloride%20Safety%20Sheet-1954.pdf |url-status=dead }}</ref> Its flammable limits in air are: lower 3.6 ] and upper 33.0 volume%. The ]s are: lower 4.0%, upper 22.05% by volume in air. Fire may release toxic ] (HCl) and ] (CO) and trace levels of ].<ref>"Occupational Safety and Health Guideline for Vinyl Chloride"1988."</ref><ref>{{cite journal |last1=O'Mara |first1=M. M. |last2=Grider |first2=L. B. |last3=Daniel |first3=R. L. |title=Combustion Products from Vinyl Chloride Monomer |journal=American Industrial Hygiene Association Journal |date=March 1971 |volume=32 |issue=3 |pages=153–156 |doi=10.1080/0002889718506429|pmid=5551110 }}</ref> Vinyl chloride can polymerise rapidly due to heating and under the influence of air, light and contact with a catalyst, strong oxidisers and metals such as copper and aluminium, with fire or explosion hazard. As a gas mixed with air, vinyl chloride is a fire and explosion hazard. On standing{{clarify|date=February 2023}}, vinyl chloride can form ], which may then explode. Vinyl chloride will react with iron and steel in the presence of moisture.<ref name="npi.gov.au"/><ref>{{cite web|url=https://www.gov.uk/government/publications/vinyl-chloride-properties-incident-management-and-toxicology|title=Vinyl chloride: health effects, incident management and toxicology|website=www.gov.uk|access-date=5 April 2018|archive-date=10 February 2018|archive-url=https://web.archive.org/web/20180210073756/https://www.gov.uk/government/publications/vinyl-chloride-properties-incident-management-and-toxicology|url-status=live}}</ref>

== Health effects ==
Since it is a gas under most ambient conditions, primary exposure is via inhalation, as opposed to the consumption of contaminated food or water, with occupational hazards being highest. Prior to 1974, workers were commonly exposed to 1,000&nbsp;ppm vinyl chloride, causing "vinyl chloride illness" such as ] and ]. The symptoms of vinyl chloride exposure are classified by ppm levels in ambient air with 4,000&nbsp;] having a threshold effect.<ref>Harrison, Henrietta (2008). , Health Protection Agency, UK</ref> The intensity of symptoms varies from acute (1,000–8,000 ppm), including dizziness, nausea, visual disturbances, headache, and ], to chronic (above 12,000&nbsp;ppm), including narcotic effect, ], and ].<ref name="IPCS19992">International Programme on Chemical Safety (IPCS) (1999). . Environmental Health Criteria 215. WHO. Geneva.</ref> ] (Reactive Airway Dysfunction Syndrome) may be caused by acute exposure to vinyl chloride.<ref>UK Department for Environment, Food, and Rural Affairs (DEFRA) and Environment Agency (EA) (2004). "Contaminants in soil: Collation of toxicological data and intake values for humans. Vinyl chloride."</ref>

Vinyl chloride is a mutagen having ]ic effects which affect lymphocyte chromosomal structure.<ref name="IPCS19992"/><ref name="ATSRD2">{{Cite report |url=https://stacks.cdc.gov/view/cdc/6948/cdc_6948_DS1.pdf |title=Toxicological profile for vinyl chloride |last=Agency for Toxic Substances and Disease Registry |date=July 2006 |publisher=] |location=Atlanta, US |access-date=2023-02-07 |archive-date=2023-02-15 |archive-url=https://web.archive.org/web/20230215200138/https://stacks.cdc.gov/view/cdc/6948/cdc_6948_DS1.pdf |url-status=live }}</ref> Vinyl chloride is a ] posing elevated risks of rare ], brain and lung tumors, and malignant ] lymphatic tumors.<ref>International Agency for Research on Cancer (IARC). "Vinyl chloride, polyvinyl chloride, and vinyl chloride-vinyl acetate copolymers." Vol 19, 1979. IARC. "Vinyl chloride." Supplement 7, 1987. Lyon.</ref> Chronic exposure leads to common forms of respiratory failure (], ]) and focused hepatotoxicity (], ]). Continuous exposure can cause CNS depression including euphoria and disorientation. Decreased male libido, miscarriage, and birth defects are known major reproductive defects associated with vinyl chloride.

Vinyl chloride can have acute dermal and ] effects. Dermal exposure effects are thickening of skin, edema, decreased elasticity, local frostbites, blistering, and irritation.<ref name="IPCS19992"/> The complete loss of skin elasticity expresses itself in Raynaud's Phenomenon.<ref name="ATSRD2" />

=== Liver toxicity ===
The ] of vinyl chloride has long been established since the 1930s when the PVC industry was just in its early stages. In the very first study about the dangers of vinyl chloride, published by Patty in 1930, it was disclosed that exposure of test animals to just a single short-term high dose of vinyl chloride caused liver damage.<ref>{{Cite journal |last1=Patty |first1=F. A. |last2=Yant |first2=W. P. |last3=Waite |first3=C. P. |date=1930 |title=Acute Response of Guinea Pigs to Vapors of Some New Commercial Organic Compounds: V. Vinyl Chloride |url=https://www.jstor.org/stable/4579760 |journal=Public Health Reports |language=en |volume=45 |issue=34 |pages=1963 |doi=10.2307/4579760 |jstor=4579760 |access-date=2023-02-08 |archive-date=2020-02-09 |archive-url=https://web.archive.org/web/20200209014604/https://www.jstor.org/stable/4579760 |url-status=live |url-access=subscription }}</ref> In 1949, a Russian publication discussed the finding that vinyl chloride caused liver injury among workers.<ref>Tribukh, S L et al. "Working Conditions and Measures for Their Improvement in Production and Use of Vinylchloride Plastics" (1949)</ref> In 1954, ] Chemical stated that vinyl chloride caused liver injury upon short-term exposures. Almost nothing was known about its long-term effects. They also recommended long-term animal toxicology studies. The study noted that if a chemical did justify the cost of testing, and its ill-effects on workers and the public were known, the chemical should not be made.<ref>Wilson, Rex H et al. "Toxicology of Plastics and Rubber – Plastomers and Monomers." Reprinted from Industrial Medicine and Surgery. 23:11, 479–786. November 1954.</ref> In 1963, research paid for in part by ] found liver damage in test animals from exposures below 500 parts per million (ppm).<ref>{{Cite journal |last1=Lester |first1=D. |last2=Greenberg |first2=L. A. |last3=Adams |first3=W. Robert |date=May 1963 |title=Effects of Single and Repeated Exposures of Humans and Rats to Vinyl Chloride |url=https://www.tandfonline.com/doi/full/10.1080/00028896309342963 |journal=American Industrial Hygiene Association Journal |language=en |volume=24 |issue=3 |pages=265–275 |doi=10.1080/00028896309342963 |pmid=13929916 |issn=0002-8894 |access-date=2023-02-07 |archive-date=2023-02-18 |archive-url=https://web.archive.org/web/20230218211332/https://www.tandfonline.com/doi/abs/10.1080/00028896309342963 |url-status=live }}</ref> Also in 1963, a Romanian researcher published findings of liver disease in vinyl chloride workers.<ref>{{Cite journal |last1=Suciu |first1=I. |last2=Prodan |first2=L. |last3=Ilea |first3=Elena |last4=Păduraru |first4=A. |last5=Pascu |first5=Livia |title=Clinical Manifestations in Vinyl Chloride Poisoning |date=January 1975 |url=https://onlinelibrary.wiley.com/doi/10.1111/j.1749-6632.1975.tb51080.x |journal=Annals of the New York Academy of Sciences |language=en |volume=246 |issue= 1|pages=53–69 |doi=10.1111/j.1749-6632.1975.tb51080.x |pmid=1054970 |bibcode=1975NYASA.246...53S |s2cid=30706677 |issn=0077-8923|url-access=subscription }}</ref> In 1968, Mutchler and Kramer, two ] researchers, reported their finding that exposures as low as 300&nbsp;ppm caused liver damage in vinyl chloride workers thus confirming earlier animal data in humans.<ref>Kramer, G.C., M.D. "The Correlation of Clinical and Environmental Measurements for Workers Exposed to Vinyl Chloride." The Dow Chemical Company. Midland Michigan.</ref> In a 1969 presentation given in Japan, P. L. Viola, a European researcher working for the European vinyl chloride industry, indicated, "every monomer used in V.C. manufacture is hazardous....various changes were found in bone and liver. Particularly, much more attention should be drawn to liver changes. The findings in rats at the concentration of 4 to 10&nbsp;ppm are shown in pictures." In light of the finding of liver damage in rats from just 4–10 ppm of vinyl chloride exposure, Viola added that he "should like some precautions to be taken in the manufacturing plants polymerizing vinyl chloride, such as a reduction of the threshold limit value of monomer."<ref>Viola, P.L. "Pathology of Vinyl Chloride" International Congress on Occupational Health. Japan. 1969.</ref>
Vinyl chloride was first reported to induce ] in 1974<ref>{{Cite journal |last=Wagoner |first=Joseph K. |date=1983 |title=Toxicity of Vinyl Chloride and Poly(Vinyl Chloride): A Critical Review |journal=Environmental Health Perspectives |volume=52 |pages=61–66 |doi=10.2307/3429651 |jstor=3429651 |pmid=6360677 |pmc=1569348 |issn=0091-6765}}</ref> and further research has demonstrated the carcinogenicity of VC to other organs and at lower concentrations,<ref>{{Cite book |url=https://catalogue.nla.gov.au/Record/4198902 |title=Origins of human cancer |publisher=Cold Spring Harbor Laboratory |year=1977 |isbn=978-0-87969-119-6 |editor-last=Winsten |editor-first=Jay A. |series=Cold Spring Harbor conferences on cell proliferation |volume=Book A. Incidence of cancer in humans. |location=Cold Spring Harbor, N.Y. |page=119 |editor-last2=Watson |editor-first2=James D. |editor-last3=Hiatt |editor-first3=Howard H. |editor-last4=Cold Spring Harbor Laboratory}}</ref><ref>{{Cite journal |last1=Maltoni |first1=C. |last2=Lefemine |first2=G. |last3=Ciliberti |first3=A. |last4=Cotti |first4=G. |last5=Carretti |first5=D. |date=1981-10-01 |title=Carcinogenicity bioassays of vinyl chloride monomer: a model of risk assessment on an experimental basis |journal=Environmental Health Perspectives |volume=41 |pages=3–29 |doi=10.1289/ehp.81413 |issn=0091-6765 |pmc=1568874 |pmid=6800782}}</ref> with evidence now extending to jobs associated with poly(vinyl chloride) exposure, indicating the need for prudent control of PVC dust in the industrial setting.<ref>{{Cite journal |last=Wagoner |first=J K |date=1983-10-01 |title=Toxicity of vinyl chloride and poly(vinyl chloride): a critical review. |journal=Environmental Health Perspectives |language=en |volume=52 |pages=61–66 |doi=10.1289/ehp.835261 |issn=0091-6765 |pmc=1569348 |pmid=6360677}}</ref>

Vinyl chloride is now an ] known to cause ] (HAS) in highly exposed industrial workers.<ref>{{Cite journal |last1=Sass |first1=Jennifer Beth |last2=Castleman |first2=Barry |last3=Wallinga |first3=David |date=2005-07-01 |title=Vinyl chloride: a case study of data suppression and misrepresentation |journal=Environmental Health Perspectives |volume=113 |issue=7 |pages=809–812 |doi=10.1289/ehp.7716 |issn=1552-9924 |pmc=1257639 |pmid=16002366}}</ref> Vinyl chloride monomer, a component in the production of poly(vinyl chloride) (PVC) resins, is a halogenated hydrocarbon with acute toxic effects, as well as chronic carcinogenic effects.<ref>{{Cite web |last=PMC |first=Europe |title=Europe PMC |url=https://europepmc.org/article/nbk/nbk544334 |access-date=2023-02-18 |website=europepmc.org |language=en}}</ref>

=== Cancerous tumors ===
Animals exposed to 30,000 ppm of vinyl chloride developed cancerous tumors. Studies on vinyl chloride workers were a "red flag" to B.F. Goodrich and the industry.<ref>Viola, P L. "Carcinogenic Effect of Vinyl Chloride" Presented at the Tenth International Cancer Congress. Houston, Texas. May 22–29, 1970.</ref> In 1972, Maltoni, another Italian researcher for the European vinyl chloride industry, found liver tumors (including angiosarcoma) from vinyl chloride exposures as low as 250&nbsp;ppm for four hours a day.<ref>Maltoni, C. "Cancer Detection and Prevention" (1972) Presented at the Second International Symposium on Cancer Detection and Prevention. Bologna, April 9–12, 1973.</ref>

In 1997 the U.S. ] (CDC) concluded that the development and acceptance by the PVC industry of a closed loop polymerization process in the late 1970s "almost completely eliminated worker exposures" and that "new cases of ] in vinyl chloride polymerization workers have been virtually eliminated."<ref> {{Webarchive|url=https://web.archive.org/web/20100916231603/http://www.cdc.gov/mmwr/preview/mmwrhtml/00046136.htm |date=2010-09-16 }}. Centers for Disease Control and Prevention. 1997.</ref>

The '']'' claimed in 1998 that the vinyl industry manipulated vinyl chloride studies to avoid liability for worker exposure and hid extensive and severe chemical spills in local communities.<ref>Jim Morris, "In Strictest Confidence. The chemical industry's secrets," ''Houston Chronicle''. Part One: "Toxic Secrecy," June 28, 1998, pp. 1A, 24A–27A; Part Two: "High-Level Crime," June 29, 1998, pp. 1A, 8A, 9A; and Part Three: "Bane on the Bayou," July 26, 1998, pgs. 1A, 16A.</ref>

=== Environment pollution ===
According to the ], "vinyl chloride emissions from poly(vinyl chloride) (PVC), ] (EDC), and vinyl chloride monomer (VCM) plants cause or contribute to air pollution that may reasonably be anticipated to result in an increase in mortality or an increase in serious irreversible, or incapacitating reversible illness. Vinyl chloride is a known human carcinogen that causes a rare cancer of the liver."<ref>National Emission Standards for Hazardous Air Pollutants (NESHAP) for Vinyl Chloride Subpart F, OMB Control Number 2060-0071, EPA ICR Number 0186.09 ( {{Webarchive|url=https://web.archive.org/web/20030322171842/http://www.epa.gov/fedrgstr/EPA-AIR/2001/September/Day-25/a23920.htm |date=March 22, 2003 }})</ref> EPA's 2001 updated Toxicological Profile and Summary Health Assessment for vinyl chloride in its ] (IRIS) database lowers EPA's previous risk factor estimate by a factor of 20 and concludes that "because of the consistent evidence for liver cancer in all the studies and the weaker association for other sites, it is concluded that the liver is the most sensitive site, and protection against liver cancer will protect against possible cancer induction in other tissues."<ref>EPA Toxicological Review of Vinyl Chloride in Support of Information on the IRIS. May 2000</ref>

===Mechanism===
The carcinogenicity of VC is attributed to the action of two metabolites, ] and ]. The former is produced by the action of cytochrome P-450 on VC. Both chloroethylene oxide and chloroacetaldehyde are ]s.

==Microbial remediation==
The bacteria species '']'' can degrade a variety of halogenated compounds including ], and vinyl chloride.<ref name="genome">{{cite web|url=http://genome.jgi-psf.org/finished_microbes/niteu/niteu.home.html|title=Home – Nitrosomonas europaea|website=genome.jgi-psf.org|access-date=5 April 2018|archive-url=https://web.archive.org/web/20090703071550/http://genome.jgi-psf.org/finished_microbes/niteu/niteu.home.html|archive-date=3 July 2009|url-status=dead}}</ref>

== See also ==
* ]
* ], for R-1140
* ], in which a large amount of vinyl chloride was spilled

== References ==
===Additional references for environmental pollution===
* ] (IPCS) (1999). ''. Environmental Health Criteria 215''. WHO, Geneva.
* ] (NPIS) (2004). "Vinyl chloride." TOXBASE®.
* World Health Organisation (WHO) (2000). "Air quality guidelines for Europe." WHO Regional Publications, European Series, No. 91. 2nd edition. WHO Regional Office for Europe. Copenhagen.
* Hathaway G.J. and Proctor N.H. (2004). ''Chemical Hazards of the Workplace''. 5th edition. John Wiley & Sons, New Jersey.
* Risk Assessment Information System (RAIS) (1993). "Toxicity summary for vinyl chloride. "Chemical Hazard Evaluation and Communication Group, Biomedical and Environmental Information Analysis Section, Health and Safety Research Division.

===Inline citations===
{{Reflist|2}}

==Further reading==
* {{cite news|url=http://www.time.com/time/magazine/article/0,9171,908587,00.html|archive-url=https://web.archive.org/web/20070612035903/http://www.time.com/time/magazine/article/0,9171,908587,00.html|url-status=dead|archive-date=June 12, 2007|title=Medicine: The Plastic Peril |date=May 13, 1974|magazine=]|access-date=2 July 2010}}

== External links ==
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{{HealthIssuesOfPlastics}}

{{Authority control}}

{{DEFAULTSORT:Vinyl Chloride}}
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