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Lead(II) acetate

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Lead(II) acetate
Systematic name Lead acetat trihydrate
Other names Lead (II) acetat trihydrate
Molecular formula Pb(C2H3O2)2·3H2O
Molar mass 379.34 g/mol
CAS number [6080-56-4]
Density 2.55 g/cm3
Solubility (water) 75 g/l
Melting point 75 °C
Boiling point decomp
Hazards
MSDS [External MSDS]
Main Hazards toxic
Flash point Non-flammable.
R/S statement R61, R33, E48/22, R50/R53, R62,
S53, S45, S60, S61
RTECS number
[Chemical infoboxDisclaimer and references]
Lead(II) acetate is a chemical compound, a white crystalline substance with a sweetish taste. It is made by treating litharge (lead monoxide, PbO) with acetic acid. Like other lead compounds, it is very toxic. Lead acetate is soluble in water and glycerin. With water it forms the trihydrate, Pb(CH3COO)2·3H2O, a colorless or white efflorescent monoclinic crystalline substance. Lead(II) acetate is also known as lead acetate, lead diacetate, plumbous acetate, sugar of lead, salt of Saturn, and Goulard's powder (after Thomas Goulard). 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 coloring dyes. Lead(II) acetate is also used as a mordant in textile printing and dyeing, as a drier in paints and varnishes, and in preparing other lead compounds.

Ancient use

The Romans, who had few sweeteners besides honey, would boil grape juice (must) in lead pots to produce a reduced sugar syrup called sapa. This syrup was used to sweeten wine, and to sweeten and preserve fruit. It is possible that its widespread consumption is responsible for the recorded insanity and death of several prominent figures in Ancient Rome.

In some countries, lead acetate is used deliberately to sweeten candy. This has resulted in criticism that children are being poisoned. [link]

Biological hazards

Lead(II) Acetate among other lead salts have been reported to cross the placenta and to the embryo leading to fetal mortality. Lead salts also have teratogenic effect in some animal species.

External links

 


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