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创建页面，内容为“{{chembox | Watchedfields = changed | verifiedrevid = 406362547 | Name = 二氯苯基胂 | ImageFile = Phenyldichloroarsine.svg | ImageSize = 110px | ImageName = Sk...”
{{chembox
| Watchedfields = changed
| verifiedrevid = 406362547
| Name = 二氯苯基胂
| ImageFile = Phenyldichloroarsine.svg
| ImageSize = 110px
| ImageName = Skeletal formula
| ImageFile1 = Phenyldichloroarsine-3D-balls.png
| ImageSize1 = 190px
| ImageName1 = Ball-and-stick model
| IUPACName = 二氯苯基胂
| SystematicName =
| OtherNames = 苯二氯胂
| Section1 = {{Chembox Identifiers
| Abbreviations = PD (NATO)
| CASNo_Ref =
| CASNo = 696-28-6
| EINECS = 211-791-9
| EINECSCASNO =
| PubChem = 12762
| ChemSpiderID_Ref =
| ChemSpiderID = 12238
| SMILES = Cl[As](Cl)c1ccccc1
| StdInChI_Ref =
| StdInChI=1S/C6H5AsCl2/c8-7(9)6-4-2-1-3-5-6/h1-5H
| StdInChIKey_Ref =
| StdInChIKey = UDHDFEGCOJAVRE-UHFFFAOYSA-N
| RTECS = CH5425000
| MeSHName =
| ChEBI =
| KEGG_Ref =
| KEGG =
| ATCCode_prefix =
| ATCCode_suffix =
| ATC_Supplemental =}}
| Section2 = {{Chembox Properties
| Formula = C<sub>6</sub>H<sub>5</sub>AsCl<sub>2</sub>
| MolarMass = 222.9315 <nowiki>[g/mol]</nowiki>
| Appearance = 无色气体或液体
| Density = 1.65 g/cm<sup>3</sup> (at 20 °C)
| MeltingPt = -20 °C
| Melting_notes =
| BoilingPt = 252-255 °C
| Boiling_notes =
| Solubility = 与水反应| SolubleOther = 丙酮，乙醚，苯
| Solvent =
| LogP = 3.060
| VaporPressure = 0.033
| HenryConstant = 3.00E-05 atm·m<sup>3</sup>/mole
| AtmosphericOHRateConstant = 1.95E-12 cm<sup>3</sup>/molecule·s
| pKa =
| pKb = }}
| Section3 = {{Chembox Structure
| CrystalStruct =
| Coordination =
| MolShape = }}
| Section4 = {{Chembox Thermochemistry
| DeltaHf =
| DeltaHc =
| Entropy =
| HeatCapacity = }}
| Section5 = {{Chembox Pharmacology
| AdminRoutes =
| Bioavail =
| Metabolism =
| HalfLife =
| ProteinBound =
| Excretion =
| Legal_status =
| Legal_US =
| Legal_UK =
| Legal_AU =
| Legal_CA =
| PregCat =
| PregCat_AU =
| PregCat_US = }}
| Section6 = {{Chembox Explosive
| ShockSens =
| FrictionSens =
| ExplosiveV =
| REFactor = }}
| Section7 = {{Chembox Hazards
| ExternalMSDS = [http://nj.gov/health/eoh/rtkweb/documents/fs/1494.pdf New Jersey MSDS]
| EUClass =
| EUIndex =
| MainHazards = 易燃性，失能毒性，糜烂性
| NFPA-H = 4
| NFPA-F = 1
| NFPA-R = 0
| NFPA-O =
| RPhrases =
| SPhrases =
| RSPhrases =
| FlashPtC = 16
| AutoignitionC =
| ExploLimits =
| LD50 =2,500 mg·min/m<sup>3</sup>
| PEL = 0.5 mg/m<sup>2</sup>}}
| Section8 = {{Chembox Related
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'''二氯苯基胂'''，简称PD，是一种[[有机化学|有机]]、含砷的[[糜烂性毒剂|糜烂性]]和[[呕吐]]性毒剂，最初是由德国和法国在一战中发明的，在当时作为[[化学武器]]使用。
==历史==
1917至1918年间，德国和法国制备二氯苯基胂。二战期间，德国仍持续制备此种化学武器。
==化学性质==
===主要性质===
二氯苯基胂（PD）是一种无色无味的物质，与水接触可以生成[[盐酸]]<ref name=leikin/>。与水的这一反应很慢，二氯苯基胂会下沉至水底，反应没有危险<ref name=hazmat>Pohanish, Richard P. ''HazMat Data'', ([http://books.google.com/books?id=3Tbl2W8j-3oC&pg=PA895&dq=Phenyldichloroarsine&lr=&client=firefox-a#PPA895,M1 Google Books]), Wiley-IEEE, 2005, pp. 895-96, (ISBN 0471726109).</ref>。这一[[水解反应]]的另一产物是苯砷酸，会对[[粘膜]]和[[皮肤]]产生很强的刺激<ref name=leikin>Leikin, Jarrold B. and McFee, Robin B. ''Handbook of Nuclear, Biological, and Chemical Agent Exposures'',（《核、生物和化学武器暴露处理手册》） ([http://books.google.com/books?id=iB5pdQCKOZIC&pg=PA356&dq=Phenyldichloroarsine+chemical+weapon&client=firefox-a Google Books]), Informa Health Care, 2007, pp. 356-57, (ISBN 142004477X).</ref>。如果不纯净，二氯苯基胂可能带有一点棕色，当然在纯净的状态下，应为无色的并且有油状质地<ref name=ledgard/>。此外，不纯净的二氯苯基胂溶液还会散发[[辣根]]和类似[[大蒜]]的臭味，可检测浓度为 0.1 ppm。<ref name=ellison>Ellison, Hank D. ''Handbook of Chemical and Biological Warfare Agents'',（《化学和生物武器手册》） ([http://books.google.com/books?id=E58GAKMgcR4C&pg=PA156&dq=Phenyldichloroarsine&lr=&client=firefox-a#PPA156,M1 Google Books]), CRC Press, 2007, p. 156, (ISBN 0849314348).</ref>。
二氯苯基胂（PD）是[[糜烂性毒剂]]中四种含砷有机物中的一种，其他三种分别是[[二氯甲基胂]]、[[二氯乙基胂]]和[[路易氏剂]]<ref name=emed>Fitzgerald, Geoffrey M. and Vollmer, Timothy. "[http://emedicine.medscape.com/article/832158-overviewCBRNE - Vesicants, Organic Arsenicals: L, ED, MD, PD, HL]",''emedicine'' via ''WebMD'', June 19, 2006, accessed December 22, 2008.</ref>，二氯苯基胂即是路易氏剂的<ref name=armyrept/>。在凝固点-20 °C，二氯苯基胂转变为固体<ref name=hills>Hills, Terry.''The Illustrated Dictionary of Organic Chemistry'',（《插图本有机化学词典》） ([http://books.google.com/books?id=j4VHUen3bTYC&pg=PA149&dq=Phenyldichloroarsine&lr=&client=firefox-a Google Books]), Lotus Press, Tokyo: 2007, p. 149, (ISBN 8189093517).</ref>。
在[[分子]]结构上，苯环和砷[[原子]]由一个碳-类金属键连接，两个氯原子则由[[共价键]]与砷原子相连<ref name=manahan>Manahan, Stanley E.''Industrial Ecology: Environmental Chemistry and Hazardous Waste'',（《工业生态学：环境化学和有害废料》） ([http://books.google.com/books?id=_-GDMkpoA4YC&pg=PA189&dq=Phenyldichloroarsine&lr=&client=firefox-a Google Books]), CRC Press, 1999, p. 189, (ISBN 1566703816).</ref>。
===合成===
二氯苯基胂（PD）可由苯和三[[氯化]]砷经由[[无水氯化铝]][[催化]]反应制得<ref name=ledgard>Ledgard, Jared. ''A Laboratory History of Chemical Warfare Agents'',（《化学武器实验史》） ([http://books.google.com/books?id=atU4GuKE8x0C&pg=PA127&lpg=PA127&dq=Phenyldichloroarsine+chemical+weapon&source=web&ots=CA37Mk2pck&sig=9iUyjGqfuEUHDhuMHvkeKu8PhVU&hl=en&sa=X&oi=book_result&resnum=6&ct=result#PPA128,M1GoogleBooks]), Lulu.com, 2006, pp. 127-29, (ISBN 1411694325).</ref>。
==使用==
二氯苯基胂是一种现已过时的化学武器，在类别上，它属于糜烂性毒剂或呕吐性、[[失能性毒剂]]<ref name=cashman/>。在二张战场上，有军队使用二氯苯基胂，却发现它的效果不如其他呕吐性毒剂<ref name=cashman>Cashman, John R. ''Emergency Response Handbook for Chemical and Biological Agents and Weapons''（《生物和化学武器紧急应对手册》）, ([http://books.google.com/books?id=S4PW-5qHUU8C&pg=PA215&lpg=PA215&dq=Phenyldichloroarsine+chemical+weapon&source=bl&ots=yAI8IIobTk&sig=s-I7IDOWRw_oNT3dr9ly5aOUe4Y&hl=en&sa=X&oi=book_result&resnum=3&ct=result#PPA215,M1 Google Books]), CRC Press, 2008, pp. 215-19, (ISBN 1420052659).</ref>。此外，二氯苯基胂作为一种含砷的糜烂性毒剂，可以与[[芥子气]]混合，作为化学武器使用<ref name=emed2>Dire, Daniel J. "[http://emedicine.medscape.com/article/832060-overview CBRNE - Vesicants, Mustard: Hd, Hn1-3, H]", ''emedicine'' via ''WebMD'', December 21, 2007, accessed December 22, 2008.</ref>。
在一般环境条件下，二氯苯基胂可以存留2至7天<ref name=ledgard/>。在通风的条件下，它也可作为呕吐性毒剂产生一定效果。然而，由于二氯苯基胂可以在阴凉空气中持续生效，最初的发明者旨在将其用于潮湿环境中<ref name=byrnes/>。因此，在地下室、洞穴和壕沟，它就变得更加危险，因为这些地带往往极度潮湿<ref name=byrnes/>。此外，在诸如银行等安全要求极高的设施中，安保人员也用它作为对抗犯罪分子的武器<ref name=ledgard/>。
==生物效应==
二氯苯基胂（PD）损害眼睛、肺、[[喉咙]]和[[鼻粘膜]]<ref name=byrnes/>。它直接作用于[[眼部]]，并在大剂量的情况下导致[[失明]]<ref name=ledgard/>。它也导致[[恶心]]、呕吐，即使剂量在5-50毫克的吸入也会诱发剧烈呕吐<ref name=ledgard/>。由于体内钙被砷替换，长期暴露在二氯苯基胂下可以导致系统性损害，包括严重的[[骨髓]]损伤<ref name=byrnes/>。
然而总的来说，二氯苯基胂（PD）在野外很容易发现，且净化措施生效较快，它的效力不如其他糜烂性毒剂<ref name=ledgard/>。此外，它导致的[[糜烂]]效果并不立刻显现，少则延迟30分钟<ref name=armyrept>O'Connor,, Richard J., McGown, Evelyn L., Dill, Kilian. "[http://www.dtic.mil/cgi-bin/GetTRDoc?AD=ADA175296&Location=U2&doc=GetTRDoc.pdf Interaction of Phenyldicholoroarsine with Biological Molecules]", Department of Chemistry - Clemson University, Letterman Army Institute of Research, August 1986, accessed December 22, 2008.</ref>，多则32小时，这要取决于吸入的浓度<ref name=ledgard/>。
二氯苯基胂的毒理尚不完全清楚<ref name=armyrept/>，但1986年美国陆军资助的一项报告的确在这一领域有所进展。报告显示，二氯苯基胂可以穿透[[红细胞]]的[[细胞膜]]，与[[细胞]]内的某些物质反应。报告同时指出，[[血红蛋白]]不是把PD与红细胞结合在一起的物质，更有可能是[[谷胱甘肽]]<ref name=armyrept/><ref name=byrnes>Byrnes, Mark E. et al. ''Nuclear, Chemical, and Biological Terrorism: Emergency Response and Public Protection'',（《核、化学和生物恐怖主义：紧急应对和公众防护》） ([http://books.google.com/books?id=jOcXcdJuovgC&pg=PA57&dq=Phenyldichloroarsine+chemical+weapon&client=firefox-a#PPA57,M1Google Books]), CRC Press, 2003, p. 57, (ISBN 1566706513).</ref>。
==参见==
*[[二氯甲基胂]]
*[[二氯乙基胂]]
*[[路易氏剂]]
==参考来源==
[[Category:化学武器]] [[Category:有机砷化合物]] [[Category:糜烂性毒剂]]
==参考来源==
*[http://zh.wikipedia.org/wiki/%E4%BA%8C%E6%B0%AF%E8%8B%AF%E5%9F%BA%E8%83%82 维基百科-二氯苯基胂]
== 百科帮你涨知识 ==
[http://www.zk120.com/ji/ 查找更多中医古籍]
[http://www.zk120.com/an/ 查找更多名老中医的医案]
[http://www.zk120.com/fang/ 查找更多方剂]
| Watchedfields = changed
| verifiedrevid = 406362547
| Name = 二氯苯基胂
| ImageFile = Phenyldichloroarsine.svg
| ImageSize = 110px
| ImageName = Skeletal formula
| ImageFile1 = Phenyldichloroarsine-3D-balls.png
| ImageSize1 = 190px
| ImageName1 = Ball-and-stick model
| IUPACName = 二氯苯基胂
| SystematicName =
| OtherNames = 苯二氯胂
| Section1 = {{Chembox Identifiers
| Abbreviations = PD (NATO)
| CASNo_Ref =
| CASNo = 696-28-6
| EINECS = 211-791-9
| EINECSCASNO =
| PubChem = 12762
| ChemSpiderID_Ref =
| ChemSpiderID = 12238
| SMILES = Cl[As](Cl)c1ccccc1
| StdInChI_Ref =
| StdInChI=1S/C6H5AsCl2/c8-7(9)6-4-2-1-3-5-6/h1-5H
| StdInChIKey_Ref =
| StdInChIKey = UDHDFEGCOJAVRE-UHFFFAOYSA-N
| RTECS = CH5425000
| MeSHName =
| ChEBI =
| KEGG_Ref =
| KEGG =
| ATCCode_prefix =
| ATCCode_suffix =
| ATC_Supplemental =}}
| Section2 = {{Chembox Properties
| Formula = C<sub>6</sub>H<sub>5</sub>AsCl<sub>2</sub>
| MolarMass = 222.9315 <nowiki>[g/mol]</nowiki>
| Appearance = 无色气体或液体
| Density = 1.65 g/cm<sup>3</sup> (at 20 °C)
| MeltingPt = -20 °C
| Melting_notes =
| BoilingPt = 252-255 °C
| Boiling_notes =
| Solubility = 与水反应| SolubleOther = 丙酮，乙醚，苯
| Solvent =
| LogP = 3.060
| VaporPressure = 0.033
| HenryConstant = 3.00E-05 atm·m<sup>3</sup>/mole
| AtmosphericOHRateConstant = 1.95E-12 cm<sup>3</sup>/molecule·s
| pKa =
| pKb = }}
| Section3 = {{Chembox Structure
| CrystalStruct =
| Coordination =
| MolShape = }}
| Section4 = {{Chembox Thermochemistry
| DeltaHf =
| DeltaHc =
| Entropy =
| HeatCapacity = }}
| Section5 = {{Chembox Pharmacology
| AdminRoutes =
| Bioavail =
| Metabolism =
| HalfLife =
| ProteinBound =
| Excretion =
| Legal_status =
| Legal_US =
| Legal_UK =
| Legal_AU =
| Legal_CA =
| PregCat =
| PregCat_AU =
| PregCat_US = }}
| Section6 = {{Chembox Explosive
| ShockSens =
| FrictionSens =
| ExplosiveV =
| REFactor = }}
| Section7 = {{Chembox Hazards
| ExternalMSDS = [http://nj.gov/health/eoh/rtkweb/documents/fs/1494.pdf New Jersey MSDS]
| EUClass =
| EUIndex =
| MainHazards = 易燃性，失能毒性，糜烂性
| NFPA-H = 4
| NFPA-F = 1
| NFPA-R = 0
| NFPA-O =
| RPhrases =
| SPhrases =
| RSPhrases =
| FlashPtC = 16
| AutoignitionC =
| ExploLimits =
| LD50 =2,500 mg·min/m<sup>3</sup>
| PEL = 0.5 mg/m<sup>2</sup>}}
| Section8 = {{Chembox Related
| OtherAnions =
| OtherCations =
| OtherFunctn =
| Function =
| OtherCpds =
}}
}}
'''二氯苯基胂'''，简称PD，是一种[[有机化学|有机]]、含砷的[[糜烂性毒剂|糜烂性]]和[[呕吐]]性毒剂，最初是由德国和法国在一战中发明的，在当时作为[[化学武器]]使用。
==历史==
1917至1918年间，德国和法国制备二氯苯基胂。二战期间，德国仍持续制备此种化学武器。
==化学性质==
===主要性质===
二氯苯基胂（PD）是一种无色无味的物质，与水接触可以生成[[盐酸]]<ref name=leikin/>。与水的这一反应很慢，二氯苯基胂会下沉至水底，反应没有危险<ref name=hazmat>Pohanish, Richard P. ''HazMat Data'', ([http://books.google.com/books?id=3Tbl2W8j-3oC&pg=PA895&dq=Phenyldichloroarsine&lr=&client=firefox-a#PPA895,M1 Google Books]), Wiley-IEEE, 2005, pp. 895-96, (ISBN 0471726109).</ref>。这一[[水解反应]]的另一产物是苯砷酸，会对[[粘膜]]和[[皮肤]]产生很强的刺激<ref name=leikin>Leikin, Jarrold B. and McFee, Robin B. ''Handbook of Nuclear, Biological, and Chemical Agent Exposures'',（《核、生物和化学武器暴露处理手册》） ([http://books.google.com/books?id=iB5pdQCKOZIC&pg=PA356&dq=Phenyldichloroarsine+chemical+weapon&client=firefox-a Google Books]), Informa Health Care, 2007, pp. 356-57, (ISBN 142004477X).</ref>。如果不纯净，二氯苯基胂可能带有一点棕色，当然在纯净的状态下，应为无色的并且有油状质地<ref name=ledgard/>。此外，不纯净的二氯苯基胂溶液还会散发[[辣根]]和类似[[大蒜]]的臭味，可检测浓度为 0.1 ppm。<ref name=ellison>Ellison, Hank D. ''Handbook of Chemical and Biological Warfare Agents'',（《化学和生物武器手册》） ([http://books.google.com/books?id=E58GAKMgcR4C&pg=PA156&dq=Phenyldichloroarsine&lr=&client=firefox-a#PPA156,M1 Google Books]), CRC Press, 2007, p. 156, (ISBN 0849314348).</ref>。
二氯苯基胂（PD）是[[糜烂性毒剂]]中四种含砷有机物中的一种，其他三种分别是[[二氯甲基胂]]、[[二氯乙基胂]]和[[路易氏剂]]<ref name=emed>Fitzgerald, Geoffrey M. and Vollmer, Timothy. "[http://emedicine.medscape.com/article/832158-overviewCBRNE - Vesicants, Organic Arsenicals: L, ED, MD, PD, HL]",''emedicine'' via ''WebMD'', June 19, 2006, accessed December 22, 2008.</ref>，二氯苯基胂即是路易氏剂的<ref name=armyrept/>。在凝固点-20 °C，二氯苯基胂转变为固体<ref name=hills>Hills, Terry.''The Illustrated Dictionary of Organic Chemistry'',（《插图本有机化学词典》） ([http://books.google.com/books?id=j4VHUen3bTYC&pg=PA149&dq=Phenyldichloroarsine&lr=&client=firefox-a Google Books]), Lotus Press, Tokyo: 2007, p. 149, (ISBN 8189093517).</ref>。
在[[分子]]结构上，苯环和砷[[原子]]由一个碳-类金属键连接，两个氯原子则由[[共价键]]与砷原子相连<ref name=manahan>Manahan, Stanley E.''Industrial Ecology: Environmental Chemistry and Hazardous Waste'',（《工业生态学：环境化学和有害废料》） ([http://books.google.com/books?id=_-GDMkpoA4YC&pg=PA189&dq=Phenyldichloroarsine&lr=&client=firefox-a Google Books]), CRC Press, 1999, p. 189, (ISBN 1566703816).</ref>。
===合成===
二氯苯基胂（PD）可由苯和三[[氯化]]砷经由[[无水氯化铝]][[催化]]反应制得<ref name=ledgard>Ledgard, Jared. ''A Laboratory History of Chemical Warfare Agents'',（《化学武器实验史》） ([http://books.google.com/books?id=atU4GuKE8x0C&pg=PA127&lpg=PA127&dq=Phenyldichloroarsine+chemical+weapon&source=web&ots=CA37Mk2pck&sig=9iUyjGqfuEUHDhuMHvkeKu8PhVU&hl=en&sa=X&oi=book_result&resnum=6&ct=result#PPA128,M1GoogleBooks]), Lulu.com, 2006, pp. 127-29, (ISBN 1411694325).</ref>。
==使用==
二氯苯基胂是一种现已过时的化学武器，在类别上，它属于糜烂性毒剂或呕吐性、[[失能性毒剂]]<ref name=cashman/>。在二张战场上，有军队使用二氯苯基胂，却发现它的效果不如其他呕吐性毒剂<ref name=cashman>Cashman, John R. ''Emergency Response Handbook for Chemical and Biological Agents and Weapons''（《生物和化学武器紧急应对手册》）, ([http://books.google.com/books?id=S4PW-5qHUU8C&pg=PA215&lpg=PA215&dq=Phenyldichloroarsine+chemical+weapon&source=bl&ots=yAI8IIobTk&sig=s-I7IDOWRw_oNT3dr9ly5aOUe4Y&hl=en&sa=X&oi=book_result&resnum=3&ct=result#PPA215,M1 Google Books]), CRC Press, 2008, pp. 215-19, (ISBN 1420052659).</ref>。此外，二氯苯基胂作为一种含砷的糜烂性毒剂，可以与[[芥子气]]混合，作为化学武器使用<ref name=emed2>Dire, Daniel J. "[http://emedicine.medscape.com/article/832060-overview CBRNE - Vesicants, Mustard: Hd, Hn1-3, H]", ''emedicine'' via ''WebMD'', December 21, 2007, accessed December 22, 2008.</ref>。
在一般环境条件下，二氯苯基胂可以存留2至7天<ref name=ledgard/>。在通风的条件下，它也可作为呕吐性毒剂产生一定效果。然而，由于二氯苯基胂可以在阴凉空气中持续生效，最初的发明者旨在将其用于潮湿环境中<ref name=byrnes/>。因此，在地下室、洞穴和壕沟，它就变得更加危险，因为这些地带往往极度潮湿<ref name=byrnes/>。此外，在诸如银行等安全要求极高的设施中，安保人员也用它作为对抗犯罪分子的武器<ref name=ledgard/>。
==生物效应==
二氯苯基胂（PD）损害眼睛、肺、[[喉咙]]和[[鼻粘膜]]<ref name=byrnes/>。它直接作用于[[眼部]]，并在大剂量的情况下导致[[失明]]<ref name=ledgard/>。它也导致[[恶心]]、呕吐，即使剂量在5-50毫克的吸入也会诱发剧烈呕吐<ref name=ledgard/>。由于体内钙被砷替换，长期暴露在二氯苯基胂下可以导致系统性损害，包括严重的[[骨髓]]损伤<ref name=byrnes/>。
然而总的来说，二氯苯基胂（PD）在野外很容易发现，且净化措施生效较快，它的效力不如其他糜烂性毒剂<ref name=ledgard/>。此外，它导致的[[糜烂]]效果并不立刻显现，少则延迟30分钟<ref name=armyrept>O'Connor,, Richard J., McGown, Evelyn L., Dill, Kilian. "[http://www.dtic.mil/cgi-bin/GetTRDoc?AD=ADA175296&Location=U2&doc=GetTRDoc.pdf Interaction of Phenyldicholoroarsine with Biological Molecules]", Department of Chemistry - Clemson University, Letterman Army Institute of Research, August 1986, accessed December 22, 2008.</ref>，多则32小时，这要取决于吸入的浓度<ref name=ledgard/>。
二氯苯基胂的毒理尚不完全清楚<ref name=armyrept/>，但1986年美国陆军资助的一项报告的确在这一领域有所进展。报告显示，二氯苯基胂可以穿透[[红细胞]]的[[细胞膜]]，与[[细胞]]内的某些物质反应。报告同时指出，[[血红蛋白]]不是把PD与红细胞结合在一起的物质，更有可能是[[谷胱甘肽]]<ref name=armyrept/><ref name=byrnes>Byrnes, Mark E. et al. ''Nuclear, Chemical, and Biological Terrorism: Emergency Response and Public Protection'',（《核、化学和生物恐怖主义：紧急应对和公众防护》） ([http://books.google.com/books?id=jOcXcdJuovgC&pg=PA57&dq=Phenyldichloroarsine+chemical+weapon&client=firefox-a#PPA57,M1Google Books]), CRC Press, 2003, p. 57, (ISBN 1566706513).</ref>。
==参见==
*[[二氯甲基胂]]
*[[二氯乙基胂]]
*[[路易氏剂]]
==参考来源==
[[Category:化学武器]] [[Category:有机砷化合物]] [[Category:糜烂性毒剂]]
==参考来源==
*[http://zh.wikipedia.org/wiki/%E4%BA%8C%E6%B0%AF%E8%8B%AF%E5%9F%BA%E8%83%82 维基百科-二氯苯基胂]
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