Phosphorus trichloride


Phosphorus trichloride is a inorganic compound with the chemical formula PCl3. A colorless liquid when pure, it is an important industrial chemical, being used for the manufacture of phosphites and other organophosphorus compounds. It is toxic and reacts readily with water to release hydrogen chloride.

Phosphorus trichloride
Phosphorus trichloride
Phosphorus trichloride
Phosphorus trichloride 25ml.jpg
IUPAC name
Phosphorus trichloride
Systematic IUPAC name
Other names
Phosphorus(III) chloride
Phosphorous chloride
  • 7719-12-2 checkY
3D model (JSmol)
  • Interactive image
  • CHEBI:30334 checkY
  • 22798 checkY
ECHA InfoCard 100.028.864 Edit this at Wikidata
EC Number
  • 231-749-3
  • 24387
RTECS number
  • TH3675000
  • M97C0A6S8U ☒N
UN number 1809
  • DTXSID5029687 Edit this at Wikidata
  • InChI=1S/Cl3P/c1-4(2)3 checkY
  • ClP(Cl)Cl
Molar mass 137.33 g/mol
Appearance Colorless to yellow fuming liquid[1]
Odor unpleasant acrid, like hydrochloric acid[1]
Density 1.574 g/cm3
Melting point −93.6 °C (−136.5 °F; 179.6 K)
Boiling point 76.1 °C (169.0 °F; 349.2 K)
Solubility in other solvents soluble[vague] in benzene, CS2, ether, chloroform, CCl4, halogenated organic solvents
reacts with ethanol
Vapor pressure 13.3 kPa
−63.4·10−6 cm3/mol
1.5122 (21 °C)
Viscosity 0.65 cP (0 °C)
0.438 cP (50 °C)
0.97 D
−319.7 kJ/mol
GHS labelling:[3]
GHS06: Toxic GHS08: Health hazard GHS05: Corrosive
H300, H314, H330, H373
P260, P273, P284, P303+P361+P353, P304+P340+P310, P305+P351+P338
NFPA 704 (fire diamond)
Lethal dose or concentration (LD, LC):
18 mg/kg (rat, oral)[2]
104 ppm (rat, 4 hr)
50 ppm (guinea pig, 4 hr)[2]
NIOSH (US health exposure limits):
PEL (Permissible)
TWA 0.5 ppm (3 mg/m3)[1]
REL (Recommended)
TWA 0.2 ppm (1.5 mg/m3) ST 0.5 ppm (3 mg/m3)[1]
IDLH (Immediate danger)
25 ppm[1]
Safety data sheet (SDS) ICSC 0696
Related compounds
Related phosphorus chlorides
Phosphorus pentachloride
Phosphorus oxychloride
Diphosphorus tetrachloride
Related compounds
Phosphorus trifluoride
Phosphorus tribromide
Phosphorus triiodide
Supplementary data page
Phosphorus trichloride (data page)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references


Phosphorus trichloride was first prepared in 1808 by the French chemists Joseph Louis Gay-Lussac and Louis Jacques Thénard by heating calomel (Hg2Cl2) with phosphorus.[4] Later during the same year, the English chemist Humphry Davy produced phosphorus trichloride by burning phosphorus in chlorine gas.[5]


World production exceeds one-third of a million tonnes.[6] Phosphorus trichloride is prepared industrially by the reaction of chlorine with white phosphorus, using phosphorus trichloride as the solvent. In this continuous process PCl3 is removed as it is formed in order to avoid the formation of PCl5.

P4 + 6 Cl2 → 4 PCl3

Structure and spectroscopyEdit

It has a trigonal pyramidal shape. Its 31P NMR spectrum exhibits a singlet around +220 ppm with reference to a phosphoric acid standard.[citation needed]


The phosphorus in PCl3 is often considered to have the +3 oxidation state and the chlorine atoms are considered to be in the −1 oxidation state. Most of its reactivity is consistent with this description.[citation needed]


PCl3 is a precursor to other phosphorus compounds, undergoing oxidation to phosphorus pentachloride (PCl5), thiophosphoryl chloride (PSCl3), or phosphorus oxychloride (POCl3).

PCl3 as an electrophileEdit

Phosphorus trichloride is the precursor to organophosphorus compounds that contain one or more P(III) atoms, most notably phosphites and phosphonates. These compounds do not usually contain the chlorine atoms found in PCl3.

PCl3 reacts vigorously with water to form phosphorous acid (H3PO3) and hydrochloric acid:

PCl3 + 3 H2O → H3PO3 + 3 HCl

A large number of similar substitution reactions are known, the most important of which is the formation of phosphites by reaction with alcohols and phenols. For example, with phenol, triphenyl phosphite is formed:

3 PhOH + PCl3 → P(OPh)3 + 3 HCl

where "Ph" stands for the phenyl group, -C6H5. Alcohols such as ethanol react similarly in the presence of a base such as a tertiary amine:[7]

PCl3 + 3 EtOH + 3 R3N → P(OEt)3 + 3 R3NH+Cl

In the absence of base, however, the reaction proceeds with the following stoichiometry to give diethylphosphite:[8][9]

PCl3 + 3 EtOH → (EtO)2P(O)H + 2 HCl + EtCl

Secondary amines (R2NH) form aminophosphines. For example, bis(diethylamino)chlorophosphine, (Et2N)2PCl, is obtained from diethylamine and PCl3. Thiols (RSH) form P(SR)3. An industrially relevant reaction of PCl3 with amines is phosphonomethylation, which employs formaldehyde:

R2NH + PCl3 + CH2O → (HO)2P(O)CH2NR2 + 3 HCl

Aminophosphonates are widely used as sequestring and antiscale agents in water treatment. The large volume herbicide glyphosate is also produced this way. The reaction of PCl3 with Grignard reagents and organolithium reagents is a useful method for the preparation of organic phosphines with the formula R3P (sometimes called phosphanes) such as triphenylphosphine, Ph3P.

3 PhMgBr + PCl3 → Ph3P + 3 MgBrCl

Under controlled conditions or especially with bulky organic groups, similar reactions afford less substituted derivatives such as chlorodiisopropylphosphine.

PCl3 as a nucleophileEdit

Phosphorus trichloride has a lone pair, and therefore can act as a Lewis base,[10] e.g., forming a 1:1 adduct Br3B-PCl3. Metal complexes such as Ni(PCl3)4 are known, again demonstrating the ligand properties of PCl3.

This Lewis basicity is exploited in the Kinnear–Perren reaction to prepare alkylphosphonyl dichlorides (RP(O)Cl2) and alkylphosphonate esters (RP(O)(OR')2). Alkylation of phosphorus trichloride is effected in the presence of aluminium trichloride give the alkyltrichlorophosphonium salts, which are versatile intermediates:[11]

PCl3 + RCl + AlCl3 → RPCl+
+ AlCl

The RPCl+
product can then be decomposed with water to produce an alkylphosphonic dichloride RP(=O)Cl2.

PCl3 as a ligandEdit

PCl3, like the more popular phosphorus trifluoride, is a ligand in coordination chemistry. One example is Mo(CO)5PCl3.[12]


PCl3 is important indirectly as a precursor to PCl5, POCl3 and PSCl3, which are used in many applications, including herbicides, insecticides, plasticisers, oil additives, and flame retardants.

For example, oxidation of PCl3 gives POCl3, which is used for the manufacture of triphenyl phosphate and tricresyl phosphate, which find application as flame retardants and plasticisers for PVC. They are also used to make insecticides such as diazinon. Phosphonates include the herbicide glyphosate.

PCl3 is the precursor to triphenylphosphine for the Wittig reaction, and phosphite esters which may be used as industrial intermediates, or used in the Horner-Wadsworth-Emmons reaction, both important methods for making alkenes. It can be used to make trioctylphosphine oxide (TOPO), used as an extraction agent, although TOPO is usually made via the corresponding phosphine.

PCl3 is also used directly as a reagent in organic synthesis. It is used to convert primary and secondary alcohols into alkyl chlorides, or carboxylic acids into acyl chlorides, although thionyl chloride generally gives better yields than PCl3.[13]


Industrial production of phosphorus trichloride is controlled under the Chemical Weapons Convention, where it is listed in schedule 3, as it can be used to produce mustard agents.[18]

See alsoEdit


  1. ^ a b c d e NIOSH Pocket Guide to Chemical Hazards. "#0511". National Institute for Occupational Safety and Health (NIOSH).
  2. ^ a b "Phosphorus trichloride". Immediately Dangerous to Life or Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).
  3. ^ Sigma-Aldrich Co., Phosphorus trichloride.
  4. ^ Gay-Lussac; Thénard (27 May 1808). "Extrait de plusieurs notes sur les métaux de la potasse et de la soude, lues à l'Institut depuis le 12 janvier jusqu'au 16 mai" [Extracts from several notes on the metals potassium and sodium, read at the Institute from the 12th of January to the 16th of May]. Gazette Nationale, Ou le Moniteur Universel (in French). 40 (148): 581–582. From p. 582: "Seulement ils ont rapporté qu'en traitant le mercure doux par le phosphure, dans l'espérance d'avoir de l'acide muriatique bien sec, il ont trouvé une liqueur nouvelle très limpide, sans couleur, répandant de fortes vapeurs, s'enflammant spontanément lorsqu'on en imbibe le papier joseph; laquelle ne paraît être qu'une combinaison de phosphore, d'oxigène et d'acide muriatique, et par conséquent analogue à cette qu'on obtient en traitant le soufre par le gas acide muriatique oxigèné." (Only they reported that by treating calomel with phosphorus, in the hope of obtaining very dry hydrogen chloride, they found a new, very clear liquid, colorless, giving off strong vapors, spontaneously igniting when one soaks filter paper in it; which seems to be only a compound of phosphorus, oxygen, and hydrochloric acid, and thus analogous to what one obtains by treating sulfur with chlorine gas.)
  5. ^ Davy, Humphry (1809). "The Bakerian Lecture. An account of some new analytical researches on the nature of certain bodies, particularly the alkalies, phosphorus, sulphur, carbonaceous matter, and the acids hitherto undecomposed; with some general observations on chemical theory". Philosophical Transactions of the Royal Society of London. 99: 39–104. doi:10.1098/rstl.1809.0005. S2CID 98814859. On pp. 94–95, Davy mentioned that when he burned phosphorus in chlorine gas ("oxymuriatic acid gas"), he obtained a clear liquid (phosphorus trichloride) and a white solid (phosphorus pentachloride).
  6. ^ Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 978-0-08-037941-8.
  7. ^ A. H. Ford-Moore & B. J. Perry (1963). "Triethyl Phosphite". Organic Syntheses.; Collective Volume, vol. 4, p. 955
  8. ^ Malowan, John E. (1953). "Diethyl phosphite". Inorganic Syntheses. Inorganic Syntheses. Vol. 4. pp. 58–60. doi:10.1002/9780470132357.ch19. ISBN 9780470132357.
  9. ^ Pedrosa, Leandro (2011). "Esterification of Phosphorus Trichloride with Alcohols; Diisopropyl phosphonate". ChemSpider Synthetic Pages. Royal Society of Chemistry: 488. doi:10.1039/SP488.
  10. ^ R. R. Holmes (1960). "An examination of the basic nature of the trihalides of phosphorus, arsenic and antimony". Journal of Inorganic and Nuclear Chemistry. 12 (3–4): 266–275. doi:10.1016/0022-1902(60)80372-7.
  11. ^ Svara, J.; Weferling, N.; Hofmann, T. "Phosphorus Compounds, Organic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a19_545.pub2.
  12. ^ Frenking, Gernot; Wichmann, Karin; Fröhlich, Nikolaus; Grobe, Joseph; Golla, Winfried; Van, Duc Le; Krebs, Bernt; Läge, Mechtild (2002). "Nature of the Metal−Ligand Bond in M(CO)5PX3 Complexes (M = Cr, Mo, W; X = H, Me, F, Cl): Synthesis, Molecular Structure, and Quantum-Chemical Calculations". Organometallics. 21 (14): 2921–2930. doi:10.1021/om020311d.
  13. ^ L. G. Wade Jr. (2005). Organic Chemistry (6th ed.). Upper Saddle River, New Jersey, USA: Pearson/Prentice Hall. p. 477.
  14. ^ A. D. F. Toy (1973). The Chemistry of Phosphorus. Oxford, UK: Pergamon Press.
  15. ^ Documentation for Immediately Dangerous To Life or Health Concentrations (IDLHs)
  16. ^ OSHA: Phosphorus Trichloride
  17. ^ CDC - NIOSH Pocket Guide to Chemical Hazards
  18. ^ M. C. Forbes; C. A. Roswell; R. N. Maxson (1946). Phosphorus(III) Chloride. Inorg. Synth. Inorganic Syntheses. Vol. 2. pp. 145–7. doi:10.1002/9780470132333.ch42. ISBN 9780470132333.