Chemistry:Lead(II) acetate
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Acetate.jpg)
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| Names | |
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| IUPAC name
Lead(II) acetate
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| Systematic IUPAC name
Lead(II) ethanoate | |
| Other names
Plumbous acetate, Salt of Saturn, Sugar of Lead, Lead diacetate
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| Identifiers | |
3D model (JSmol)
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| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| EC Number |
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| MeSH | lead+acetate |
PubChem CID
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| RTECS number |
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| UNII |
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| Properties | |
| Pb(C2H3O2)2 | |
| Molar mass | 325.29 g/mol (anhydrous) 379.33g/mol (trihydrate) |
| Appearance | White powder or colourless, efflorescent crystals |
| Odor | Slightly acetic |
| Density | 3.25 g/cm3 (20 °C, anhydrous) 2.55 g/cm3 (trihydrate) 1.69 g/cm3 (decahydrate)[1] |
| Melting point | 280 °C (536 °F; 553 K) (anhydrous) 75 °C (167 °F; 348 K) (trihydrate) decomposes[4] at ≥ 200 °C 22 °C (72 °F; 295 K) (decahydrate)[1] |
| Boiling point | Decomposes |
| Anhydrous: 19.8 g/100 mL (0 °C) 44.31 g/100 mL (20 °C) 69.5 g/100 mL (30 °C)[2] 218.3 g/100 mL (50 °C)[1] | |
| Solubility | Anhydrous and trihydrate are soluble in alcohol, glycerol[2] |
| Solubility in methanol | Anhydrous:[2] 102.75 g/100 g (66.1 °C) Trihydrate:[3] 74.75 g/100 g (15 °C) 214.95 g/100 g (66.1 °C) |
| Solubility in glycerol | Anhydrous:[2] 20 g/100 g (15 °C) Trihydrate:[3] 143 g/100 g (20 °C) |
| −89.1·10−6 cm3/mol | |
Refractive index (nD)
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1.567 (trihydrate)[1] |
| Structure | |
| Monoclinic (anhydrous, trihydrate) Rhombic (decahydrate) | |
| Thermochemistry | |
Std enthalpy of
formation (ΔfH⦵298) |
−960.9 kJ/mol (anhydrous)[2] −1848.6 kJ/mol (trihydrate)[3] |
| Hazards | |
| Main hazards | Neurotoxic, probable human carcinogen |
| GHS pictograms |   [4]
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| GHS Signal word | Danger |
| H360, H373, H410[4] | |
| P201, P273, P308+313, P501[4] | |
| NFPA 704 (fire diamond) | |
| Flash point | Non-flammable |
| Lethal dose or concentration (LD, LC): | |
LD50 (median dose)
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400 mg/kg (mice, oral)[1] |
LCLo (lowest published)
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300 mg/kg (dog, oral)[5] |
| Related compounds | |
Other cations
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Lead(IV) acetate |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
 verify (what is   ?)
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| Infobox references | |
Lead(II) acetate, also known as lead acetate, lead diacetate, plumbous acetate, sugar of lead, lead sugar, salt of Saturn, or Goulard's powder, is a white crystalline chemical compound with a slightly sweet taste. Its chemical formula is usually expressed as Pb(CH
3COO)
2 or Pb(OAc)
2, where Ac represents the acetyl group. Like many other lead compounds, it causes lead poisoning. Lead acetate is soluble in water and glycerin. With water it forms the trihydrate, Pb(OAc)
2 · 3H2O, a colourless or white efflorescent monoclinic crystalline substance.
The substance is used as a reagent to make other lead compounds and as a fixative for some dyes. In low concentrations, it is the principal active ingredient in progressive types of hair colouring dyes.[6] Lead(II) acetate is also used as a mordant in textile printing and dyeing, and as a drier in paints and varnishes. It was historically used as a sweetener and preservative in wines and in other foods and for cosmetics.
Production
Lead(II) acetate can be made by boiling elemental lead in acetic acid and hydrogen peroxide. This method will also work with lead(II) carbonate or lead(II) oxide.
- Pb + H
2O
2 + 2 H+ → Pb2+ + 2 H
2O - Pb2+ + 2 AcO− → Pb(OAc)
2
Lead(II) acetate can also be made by dissolving lead(II) oxide in acetic acid:[7]
- PbO + 2 AcOH → Pb(OAc)
2 + H
2O
Lead(II) acetate can also be made via a single displacement reaction between copper acetate and lead metal:
- Cu(OAc)
2 + Pb → Cu + Pb(OAc)
2
Structure
The crystal structure of anhydrous lead(II) acetate has been described as a 2D coordination polymer. In comparison, lead(II) acetate trihydrate's structure is a 1D coordination polymer.[8] In the trihydrate, the Pb2+ ion's coordination sphere consists of nine oxygen atoms belonging to three water molecules, two bidentate acetate groups and two bridging acetate groups. The coordination geometry at Pb is a monocapped square antiprism.[9][10] The trihydrate thermally decomposes to a hemihydrate, Pb(OAc)2·1⁄2H2O, and to basic acetates such as Pb4O(OAc)6 and Pb2O(OAc)2.[8]
| Anhydrous[8] Pb(OAc)2 |
Trihydrate[9][10] Pb(OAc)2·3H2O | |
|---|---|---|
| Lead coordination sphere |
-acetate-xtal-Pb-coordination-3D-bs-17.png)
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-acetate-trihydrate-xtal-Pb-coordination-3D-noH-bs-17.png)
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| Strongly bonded aggregation |
-acetate-xtal-one-layer-3D-bs-17.png) 2D sheet |
-acetate-trihydrate-xtal-chain-3D-noH-bs-17.png) 1D chain |
| Weakly bonded aggregation |
-acetate-xtal-layers-3D-bs-17.png) sheets stacked with hydrophobic surfaces in contact |
-acetate-trihydrate-xtal-packing-HB-3D-noH-bs-17.png) chains linked by hydrogen bonds |
Uses
Sweetener
Like other lead(II) salts, lead(II) acetate has a sweet taste, which led to its historical use as a sugar substitute in both wines and foods.[11] The ancient Romans, who had few sweeteners besides honey, would boil must (unfiltered grape juice) in lead pots to produce a reduced sugar syrup called defrutum, concentrated again into sapa. This syrup was used to sweeten wine and to sweeten and preserve fruit. It is possible that lead(II) acetate or other lead compounds leaching into the syrup might have caused lead poisoning in those who consumed it.[12] Lead acetate is no longer used in the production of sweeteners because of its recognized toxicity. Legislation prohibiting its use as a wine sweetener was ineffective until, decades later, chemical methods of detecting its presence had been developed.[13]
Historical incidents
The earliest confirmed poisoning by lead acetate was that of Pope Clement II who died in October 1047. A toxicological examination of his remains conducted in the mid-20th century confirmed centuries-old rumors that he had been poisoned with lead sugar.[14] It is not clear whether he was assassinated.
In 1787 painter and biographer Albert Christoph Dies swallowed, by accident, approximately 3/4 oz (20 g) of lead acetate. His recovery from this poison was slow and incomplete. He lived with illnesses until his death in 1822.[15][16]
Although the use of lead(II) acetate as a sweetener was already illegal at that time, composer Ludwig van Beethoven may have died of lead poisoning caused by wines adulterated with lead acetate (see also Beethoven's liver).[17][18]
In the 1850s, Mary Seacole applied lead(II) acetate, among other remedies, against an epidemic of cholera in Panama.[19][20]
In 1887, 38 hunting horses belonging to Captain William Hollwey Steeds were poisoned in their stables at Clonsilla House, Dublin, Ireland. At least ten of the hunters died. Captain Steeds, an "extensive commission agent", had previously supplied the horses for the Bray and Greystones Coach. It transpired that they had been fed a bran mash that had been sweetened with a toxic lead acetate.[21]
Cosmetics
Lead(II) acetate, as well as white lead, has been used in cosmetics throughout history.[22]
Until recently,[when?] it was still used in the USA in men's hair colouring products[23] like Grecian Formula. It was not until 2018 that the manufacturer removed lead acetate from the hair coloring product. Lead acetate has been replaced by bismuth citrate as the progressive colorant. Its use in cosmetics has been banned in Canada by Health Canada since 2005 (effective at the end of 2006) based on tests showing possible carcinogenicity and reproductive toxicity,[24] and it is also banned in the European Union[24] and has been on the California Proposition 65 warning list as a carcinogen since 1988.[25]
Medical uses
Lead(II) acetate solution was a commonly used folk remedy for sore nipples.[26] In modern medicine, for a time, it was used as an astringent, in the form of Goulard's extract, and it has also been used to treat poison ivy.[27]
Industrial uses
Lead(II) acetate paper is used to detect the poisonous gas hydrogen sulfide. The gas reacts with lead(II) acetate on the moistened test paper to form a grey precipitate of lead(II) sulfide.
An aqueous solution of lead(II) acetate is the byproduct of a 1:1 ratio of hydrogen peroxide and white vinegar (acetic acid) used in the cleaning and maintenance of stainless steel firearm suppressors (silencers) and compensators. The solution is agitated by the bubbling action of the hydrogen peroxide, with the main reaction being the oxidation of lead by hydrogen peroxide and subsequent dissolution of lead oxide by the acetic acid, which forms lead acetate. Because of its high toxicity, this chemical solution must be appropriately disposed by a chemical processing facility or hazardous materials centre. Alternatively, the solution may be reacted with sulfuric acid to precipitate nearly insoluble lead(II) sulfate. The solid may then be removed by mechanical filtration and is safer to dispose of than aqueous lead acetate.
Other uses
It was also used in making of slow matches during the Middle Ages. It was made by mixing a natural form of lead(II) oxide called litharge and vinegar.
Sugar of lead was a recommended agent added to linseed oil during heating to produce "boiled" linseed oil, the lead and heat acting to cause the oil to cure faster than raw linseed oil.[28]
Lead(II) acetate ("salt of Saturn") was used to synthesise acetone which was then known as "spirit of Saturn" for being made with the salt of Saturn and thought to be a lead compound in the 17th century.[29]
See also
- Saturn's Tree
References
- ↑ 1.0 1.1 1.2 1.3 1.4 Pradyot, Patnaik (2003). Handbook of Inorganic Chemicals. The McGraw-Hill Companies, Inc.. ISBN 0-07-049439-8.
- ↑ 2.0 2.1 2.2 2.3 2.4 "Lead(II) acetate". http://chemister.ru/Database/properties-en.php?dbid=1&id=1990.
- ↑ 3.0 3.1 3.2 "Lead(II) acetate trihydrate". http://chemister.ru/Database/properties-en.php?dbid=1&id=1762.
- ↑ 4.0 4.1 4.2 4.3 Sigma-Aldrich Co., Lead(II) acetate trihydrate. Retrieved on 2014-06-08.
- ↑ "Lead compounds (as Pb)". Immediately Dangerous to Life and Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH). https://www.cdc.gov/niosh/idlh/7439921.html.
- ↑ "Lead Acetate in 'Progressive' Hair Dye Products". 7 October 2021. https://www.fda.gov/cosmetics/cosmetic-products/lead-acetate-progressive-hair-dye-products.
- ↑ Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. pp. 373, 388. ISBN 978-0-08-037941-8.
- ↑ 8.0 8.1 8.2 Martínez-Casado, Francisco J.; Ramos-Riesco, Miguel; Rodríguez-Cheda, José A.; Cucinotta, Fabio; Matesanz, Emilio; Miletto, Ivana; Gianotti, Enrica; Marchese, Leonardo et al. (2016). "Unraveling the Decomposition Process of Lead(II) Acetate: Anhydrous Polymorphs, Hydrates, and Byproducts and Room Temperature Phosphorescence". Inorg. Chem. 55 (17): 8576–8585. doi:10.1021/acs.inorgchem.6b01116. PMID 27548299.
- ↑ 9.0 9.1 Rajaram, R. K.; Mohana Rao, J. K. (1982). "Crystal structure of lead acetate trihydrate". Z. Kristallogr. 160 (1–4): 225–233. doi:10.1524/zkri.1982.160.14.225.
- ↑ 10.0 10.1 Bryant, Robert G.; Chacko, V. P.; Etter, Margaret C. (1984). "Carbon-13 CP/MAS NMR and crystallographic investigations of the structure and solid-state transformations of lead(II) acetate trihydrate". Inorg. Chem. 23 (22): 3580–3584. doi:10.1021/ic00190a029.
- ↑ "The Disturbingly Long History of Lead Toxicity in Winemaking." Anna Archibald, 30 July 2020. Retrieved: 22 December, 2020.
- ↑ Lead Poisoning and Rome
- ↑ Stoeppler, M. (1992), Hazardous Metals in the Environment, Techniques and Instrumentation in Analytical Chemistry, 12, Elsevier, p. 60, ISBN 9780080875606, https://books.google.com/books?id=x1zrlwqHlkoC&pg=PA60, "From the results achieved so far it is obvious that the purity law for lead in wines in the last two centuries was frequently ignored."
- ↑ Specht, W. and Fischer, K. (1959). "Vergiftungsnachweis an den Resten einer 900 Jahre alten Leiche" [Evidence of poisoning in the remains of a 900-year-old corpse] (in German). Archiv für Kriminologie 124: 61–84.
- ↑
One or more of the preceding sentences incorporates text from a publication now in the public domain: Chisholm, Hugh, ed (1911). "Dies, Christoph Albert". Encyclopædia Britannica. 8 (11th ed.). Cambridge University Press. p. 211.
- ↑ Dies, Albert Christoph (1810). Biographische Nachrichten von Joseph Haydn nach mündlichen Erzählungen desselben entworfen und herausgegeben. Vienna: Camesinaische Buchhandlung. English translation in: Dies, Albert Christoph (1963). "Biographical Accounts of Joseph Haydn". in Gotwals, Vernon. Haydn: Two Contemporary Portraits. Milwaukee: University of Wisconsin Press. ISBN 0-299-02791-0.
- ↑ "Beethoven und Blei: Tödliches Zusammenspiel". https://www.pharmazeutische-zeitung.de/index.php?id=magazin_30_2001.
- ↑ "Beethoven litt unter Bleivergiftung". http://www.3sat.de/3sat.php?http%3A%2F%2Fwww.3sat.de%2Fnano%2Fnews%2F11258%2Findex.html.
- ↑ Mary Seacole (1990), Wonderful Adventures of Mrs. Seacole in Many Lands, Chapter IV, Oxford University Press reprint, ISBN:0-19-506672-3; (2005 Penguin 20th Century Classics reprint, ed. Sarah Salih) ISBN:0-14-043902-1
- ↑ Jane Robinson (2004), Mary Seacole: The Charismatic Black Nurse who became a heroine of the Crimea, p.53. Constable ISBN:1-84119-677-0
- ↑ Weekly Irish Times, Saturday 15 October 1887; Enniskillen Chronicle and Erne Packet, 24 October 1887, p. 3
- ↑ Gunn, Fenja. (1973) The Artificial Face: A History of Cosmetics. — as cited in Leisure Activities of an 18th Century Lady
- ↑ Lead Based Hair Products: Too Hazardous for Household Use - Results, Howard W. Mielke, PhD, Myiesha D. Taylor, Chris R. Gonzales, M. Kelley Smith, Pamela V. Daniels, and Ayanna V.Buckner. Journal of American Pharmaceutical Association (NS37, Jan/Feb 1997:85-89).
- ↑ 24.0 24.1 "Can West News Service: Grecian Formula in a grey zone after ban". http://www.canada.com/montreal/montrealgazette/news/story.html?id=6caa01c2-3fb0-4431-a559-43aeece93860.
- ↑ "The Proposition 65 List". https://oehha.ca.gov/proposition-65/proposition-65-list.
- ↑ The American Frugal Housewife, by Lydia M. Child
- ↑ Laboratory manual in biology. Sharpe. 1911, American Book Company. p. 351
- ↑ Andés, Louis Edgar, and Arthur Morris. Oil colours and printers' inks a practical handbook treating of linseed oil, boiled oil, paints, artists' colours, lampblack and printers' inks, black and coloured. London: Scott, Greenwood. 1903. 41. Print.
- ↑ Mel Gorman, History of acetone (1600-1850), 1962
External links
- Case Studies in Environmental Medicine - Lead Toxicity
- Essay on "Lead Poisoning and Rome"
- HowStuffWorks "What Kind of Hair Color Do Men Use?" discussion of progressive dyes containing lead acetate
- National Pollutant Inventory - Lead and Lead Compounds Fact sheet (Does Not Bring Up Lead)
- ToxFAQs: Lead
- US Food and Drug Administration (FDA) fact sheet "Lead Acetate in Hair Dye Products"
- US Food and Drug Administration (FDA)21CFR73.2396 "PART 73 -- LISTING OF COLOR ADDITIVES EXEMPT FROM CERTIFICATION, Subpart C--Cosmetics, Sec. 73.2396 Lead acetate"
Acetyl halides and salts of the acetate ion
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|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| AcOH | He | ||||||||||||||||||
| LiOAc | Be(OAc)2 BeAcOH |
B(OAc)3 | AcOAc ROAc |
NH4OAc | AcOOH | FAc | Ne | ||||||||||||
| NaOAc | Mg(OAc)2 | Al(OAc)3 ALSOL Al(OAc)2OH Al2SO4(OAc)4 |
Si | P | S | ClAc | Ar | ||||||||||||
| KOAc | Ca(OAc)2 | Sc(OAc)3 | Ti(OAc)4 | VO(OAc)3 | Cr(OAc)2 Cr(OAc)3 |
Mn(OAc)2 Mn(OAc)3 |
Fe(OAc)2 Fe(OAc)3 |
Co(OAc)2, Co(OAc)3 |
Ni(OAc)2 | Cu(OAc)2 | Zn(OAc)2 | Ga(OAc)3 | Ge | As(OAc)3 | Se | BrAc | Kr | ||
| RbOAc | Sr(OAc)2 | Y(OAc)3 | Zr(OAc)4 | Nb | Mo(OAc)2 | Tc | Ru(OAc)2 Ru(OAc)3 Ru(OAc)4 |
Rh2(OAc)4 | Pd(OAc)2 | AgOAc | Cd(OAc)2 | In | Sn(OAc)2 Sn(OAc)4 |
Sb(OAc)3 | Te | IAc | Xe | ||
| CsOAc | Ba(OAc)2 | Hf | Ta | W | Re | Os | Ir | Pt(OAc)2 | Au | Hg2(OAc)2, Hg(OAc)2 |
TlOAc Tl(OAc)3 |
Pb(OAc)2 Pb(OAc)4 |
Bi(OAc)3 | Po | At | Rn | |||
| Fr | Ra | Rf | Db | Sg | Bh | Hs | Mt | Ds | Rg | Cn | Nh | Fl | Mc | Lv | Ts | Og | |||
| ↓ | |||||||||||||||||||
| La(OAc)3 | Ce(OAc)x | Pr | Nd | Pm | Sm(OAc)3 | Eu(OAc)3 | Gd(OAc)3 | Tb | Dy(OAc)3 | Ho(OAc)3 | Er | Tm | Yb(OAc)3 | Lu(OAc)3 | |||||
| Ac | Th | Pa | UO2(OAc)2 | Np | Pu | Am | Cm | Bk | Cf | Es | Fm | Md | No | Lr | |||||
 |  |
