Lead stearate
From Wikipedia the free encyclopedia
Names | |
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Other names Lead(2+) octadecanoate, lead(II) stearate, lead distearate | |
Identifiers | |
3D model (JSmol) | |
ChemSpider | |
ECHA InfoCard | 100.012.733 |
EC Number |
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PubChem CID | |
UNII | |
CompTox Dashboard (EPA) | |
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Properties | |
C 36H 70PbO 4 | |
Molar mass | 774.14 |
Appearance | White powder |
Density | 1.4 g/cm3 |
Melting point | 115.7 °C (240.3 °F; 388.8 K) |
Boiling point | 359.4 °C (678.9 °F; 632.5 K) |
Slightly soluble | |
Hazards | |
GHS labelling: | |
Danger | |
H302, H332, H360, H373 | |
P260, P261, P281, P304, P340, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). |
Lead stearate is a metal-organic compound, a salt of lead and stearic acid with the chemical formula C
36H
70PbO
4.[1] The compound is classified as a metallic soap, i.e. a metal derivative of a fatty acid.[2] The compound is toxic.
Synthesis
[edit]The compound can be prepared by reacting stearic acid, lead(II) oxide, and a catalyst acetic acid.[3]
Also, an exchange reaction between lead(II) acetate and sodium stearate:
Physical properties
[edit]White powder with a slight fatty odor. Sinks in water.[4] Hygroscopic in air.
Slightly soluble in water.[1] Soluble in hot ethanol.
Uses
[edit]The compound is used as a drier in oil paints and varnishes to speed the polymerization and oxidation processes. Also used as a lubricant and stabilizer in vinyl polymers and as a corrosion inhibitor in petroleum products.[5][6][7]
References
[edit]- ^ a b "Lead Stearate". American Elements. Retrieved 7 March 2023.
- ^ "T3DB: Lead stearate". t3db.ca. Retrieved 7 March 2023.
- ^ "Preparation process of lead stearate based on melting method". 18 December 2013. Retrieved 7 March 2023.
- ^ "LEAD STEARATE | CAMEO Chemicals | NOAA". cameochemicals.noaa.gov. Retrieved 7 March 2023.
- ^ "Lead Stearate » Waldies Co. Ltd". Waldies Co. Ltd. Retrieved 7 March 2023.
- ^ Encyclopedia of Chemical Technology: Fuel resources to heat stabilizers. Wiley. 1991. p. 1074. ISBN 978-0-471-52669-8. Retrieved 7 March 2023.
- ^ Titow, M. V. (6 December 2012). PVC Technology. Springer Science & Business Media. p. 269. ISBN 978-94-009-5614-8. Retrieved 7 March 2023.