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301-04-2
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???(??):
?????;????;???(?????);?????;???? ?;? ??(?????);?????? ?;????, ?(2+) ?;????, ?(2+) ? (2:1);????, ?(II);????, ?(II) ?;???? ? ?????;?(II)?????
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Lead acetate
???(??):
LEAD (II) ACETATE;PbAc2;unichempba;LEAD ACETATE 3H2O;ACETIC ACID LEAD SALT;Diacetic acid lead(II);LEAD ACETATE-3-HYDRATE;LEAD SUGAR;bleiacetat;Sugaroflead
CBNumber:
CB3750317
???:
C4H6O4Pb
??? ??:
325.29
MOL ??:
301-04-2.mol
MSDS ??:
SDS

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???
75 °C (dec.)(lit.)
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decomposes at >280℃ [KIR78]
??
3.3 g/cm3
???
15.7hPa at 25℃
?? ??
2-8°C
???
DMSO(?? ???), ???(?? ???)
??? ??
??
??
???
???
g/100g H2O: 19.7(0°C), 55.2(25°C); ?? ???, Pb(CH3COO)2·3H2O [KRU93]; g/100mL H2O: 44.3(20°C), 221(50°C) [KIR78]
?? ??(λmax)
260nm(H2O)(lit.)
Merck
14,5397
Solubility Product Constant (Ksp)
pKsp: 2.75
Dielectric constant
2.5(0.0℃)
??? ?? ??
?? ??
LogP
-0.17
CAS ??????
301-04-2(CAS DataBase Reference)
EPA
Lead(II) acetate (301-04-2)
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  • ?? ? ?? ??
  • ?? ? ???? ?? (GHS)
??? ?? T,N
?? ???? ?? 61-33-48/22-50/53-62
????? 53-45-60-61
????(UN No.) UN 1616
WGK ?? 2
RTECS ?? OF8050000
TSCA TSCA listed
HS ?? 2915.29.5000
?? ?? 6.1
???? III
?? ?? ??? 301-04-2(Hazardous Substances Data)
?? LD50 i.p. in rats: 15 mg Pb/100g (Bradley, Fredrick)
???? ?? KE-21888
?????? ??? 97-1-9
?????? ??? ??1-78
?, ??????? ??? 355
?? ? ???? ????: ????; ???(??)????: ????(lead tetraoxide), ???(lead sulfate), ??????(basic lead carbonate)? ??? ????(Lead compounds) ? ?? 25% ?? ??? ???. ??, ???(lead acetate), ????(lead alkyls), ?????(lead azide), ????(lead di(acetate)), ??????(lead(Ⅲ) methansulfonate), ???(lead phosphate(3:2)), ?????(lead styphate)? ??? ?? 0.5% ?? ??? ???
????(GHS): Corrosion (GHS05)Health Hazard (GHS08)Environment (GHS09)
?? ?: Danger
??·?? ??:
?? ??·?? ?? ?? ?? ?? ?? ? ?? ?? P- ??
H303 ??? ??? ? ?? ?? ?? ?? - ?? ?? 5 P312
H318 ?? ?? ??? ??? ?? ? ?? ?? ??? ?? ?? 1 ?? P280, P305+P351+P338, P310
H341 ???? ??? ??? ??? ??? (????? ???? ????? ???? ???? ???? ??? ?? ????? ??? ???? ??) ???? ???? ?? ?? 2 ?? P201,P202, P281, P308+P313, P405,P501
H351 ?? ??? ??? ??? (????? ?? ???? ???? ???? ??? ?? ????? ??? ???? ??) ??? ?? ?? 2 ?? P201, P202, P281, P308+P313, P405,P501
H360 ?? ?? ????? ??? ??? ? ?? ???? ?? ?? 1A, 1B ??
H370 ??(??, ??? ?? ??? ?? ??? ??)? ??? ???(????? ?? ???? ??? ???? ???? ???? ????? ??? ????? ??) ?? ???? ?? - 1? ?? ?? 1 ?? P260, P264, P270, P307+P311, P321,P405, P501
H372 ??? ?? ?? ???? ??(??, ??? ?? ??? ?? ??? ??)? ??? ??? ?? ???? ?? - ?? ?? ?? 1 ?? P260, P264, P270, P314, P501
H410 ??? ??? ?? ????? ?? ??? ?? ????? ?? - ?? ?? 1 ?? P273, P391, P501
??????:
P201 ?? ? ?? ???? ?????.
P202 ?? ?? ?? ??? ?? ???? ??? ???? ???.
P260 ??·?·??·???·??·...·????? ???? ???.
P264 ?? ??? ?? ??? ????.
P264 ?? ??? ?? ??? ????.
P270 ? ??? ??? ??? ???, ???? ???? ???.
P273 ???? ???? ???.
P280 ????/???/???/?????? ?????.
P391 ???? ????.
P405 ???? ?????.
P501 ...? ??? / ??? ?? ???.
NFPA 704
2
3 0

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Lead acetate is stable under ordinary conditions of use and storage. Lead acetate is incompatible with bromates, phenol, chloral hydrate, sulphides, hydrogen peroxide, resorcinol, salicylic acid, sulphites, vegetable infusions, alkalis, tannin, phosphates, citrates, chlorides, carbonates, tartrates, and acids. Lead (II) acetate, as well as white lead, has been used in cosmetics throughout history, though this practice has ceased in Western countries. It is still used in men’s hair colouring. Lead (II) acetate paper is used to detect the poisonous gas hydrogen sulphide. The gas reacts with lead (II) acetate on the moistened test paper to form a grey precipitate of lead (II) sulphide.

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Lead acetate is a white, flaky crystalline substance with a slight odor of acetic acid. Commercial grades may be powdered granules, or brown or gray lumps. Diacetate: Powder.

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2 – 1 - Sweetener
Like other lead (II) salts, lead (II) acetate has a sweet taste, which has led to its use as a sugar substitute throughout history. The ancient Romans, who had few sweeteners besides honey, would boil must (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 anyone consuming it . Lead acetate is no longer used in the production of sweeteners in most of the world because of its recognized toxicity. Modern chemistry can easily detect it, which has all but stopped the illegal use that continued decades after legal use as a sweetener was banned .
2 – 1 - Sweetener2 – 1 – 1 - Resultant deaths
Pope Clement II died in October 1047. A toxicologic examination of his remains conducted in the mid – 20 th century confirmed centuries-old rumors that he had been poisoned with lead sugar.It is not clear if he was assassinated.
In 1787 painter Albert Christoph Dies swallowed, by accident, approximately 21 g of lead acetate. His recovery from this poison was slow and incomplete. He lived with illnesses until his death in 1822 .
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.
Mary Seacole applied lead (II) acetate, among other remedies, against an epidemic of cholera in Panama.

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Lead acetate is made by dissolving lead monoxide (litharge) or lead carbonate in strong acetic acid. Several types of basic salts are formed when lead acetates are prepared from lead monoxide in dilute acetic acid or at high pH. The basic salts of lead acetate are white crystalline compounds, which are highly soluble in water and dissolve in ethyl alcohol.
Lead acetate can be made by boiling elemental lead in acetic acid and hydrogen peroxide.

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ChEBI: A lead coordination entity in which a central lead(2+) atom is coordinated to two acetate ions.

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Lead acetate is used as a color additive in hair dyes; as a mordant in cotton dyes, in the lead coating of metals; as a drier in paints; varnishes and pigment inks; and in medicinals, such as astringents. Incompatibilities: A strong reducing agent. Reacts violently with strong oxidizers, bromates, strong acids; chemically active metals; phosphates, carbonates, phenols. Contact with strong acids forms acetic acid. Incompatible with strong bases: ammonia, amines, cresols, isocyanates, alkylene oxides; epichlorohydrin, sulfites, resorcinol, salicylic acid, and chloral hydrat

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UN1616 Lead acetate, Hazard Class: 6.1; Labels: 6.1-Poisonous materials

Purification Methods

Crystallise it twice from anhydrous acetic acid and dry it under vacuum for 24hours at 100o. The solubility in H2O is 63% (at ~20o) and 200% (at boiling point). [Beilstein 2 IV 118.]

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A strong reducing agent. Reacts violently with strong oxidizers, bromates, strong acids; chemically active metals; phosphates, carbonates, phenols. Contact with strong acids forms acetic acid. Incompatible with strong bases: ammonia, amines, cresols, isocyanates, alkylene oxides; epichlorohydrin, sulfites, resorcinol, salicylic acid, and chloral hydrate

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Convert to nitrate using nitric acid; evaporate, then saturate with H2S; wash and dry the sulfide and ship to the supplier. Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (≥100 kg/mo) must conform with EPA regulations governing storage, transportation, treatment, and waste disposal

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Lead (II) acetate, as with any other lead salts, causes lead poisoning.

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