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Lead palmitate is a chemical compound derived from lead and palmitic acid, characterized by its use as a heat stabilizer in various materials. It is known for its toxicity, which can lead to serious health risks, particularly affecting the nervous system and kidneys. Due to its potential harmful effects on human health and the environment, there has been a shift towards finding safer alternatives.

15773-56-5

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15773-56-5 Usage

Uses

Used in Plastics Industry:
Lead palmitate is used as a heat stabilizer for PVC plastics, providing thermal stability and preventing the degradation of the material at high temperatures.
Used in Paints and Coatings Industry:
In the paints and coatings industry, lead palmitate is used as a stabilizer in primers and paints to enhance their durability and performance.
However, due to the recognized toxicity of lead palmitate and the associated health and environmental concerns, there is a growing trend towards the development and adoption of safer alternatives in these applications.

Check Digit Verification of cas no

The CAS Registry Mumber 15773-56-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,7,7 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 15773-56:
(7*1)+(6*5)+(5*7)+(4*7)+(3*3)+(2*5)+(1*6)=125
125 % 10 = 5
So 15773-56-5 is a valid CAS Registry Number.
InChI:InChI=1/2C16H32O2.Pb/c2*1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16(17)18;/h2*2-15H2,1H3,(H,17,18);/q;;+2/p-2

15773-56-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name LEAD PALMITATE

1.2 Other means of identification

Product number -
Other names lead dipalmitate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:15773-56-5 SDS

15773-56-5Downstream Products

15773-56-5Related news

Molecular dynamics of palmitic acid and LEAD PALMITATE (cas 15773-56-5) in cross-linked linseed oil films: Implications from deuterium magnetic resonance for lead soap formation in traditional oil paintings☆09/05/2019

Many oil paintings, dating from the 15th century to the present, are affected by the formation of heavy-metal carboxylates (soaps) that alter the structural integrity and appearance of the works. Through transport phenomena not yet understood, free fatty acids formed from oils used as binders mi...detailed

15773-56-5Relevant academic research and scientific papers

Preparation of metal carboxylates and their stabilizing performance under intense high-pressure shear treatment

Akhmetkhanov,Kolesov,Kadyrov,Karmilov,Zaikov

, p. 842 - 845 (2004)

Solid-phase synthesis of certain metal carboxylates and their effect on stabilization of polyvinyl chloride under intense high-pressure shear treatment were studied.

The characterisation of lead fatty acid soaps in 'protrusions' in aged traditional oil paint

Plater, M. John,De Silva, Ben,Gelbrich, Thomas,Hursthouse, Michael B.,Higgitt, Catherine L.,Saunders, David R.

, p. 3171 - 3179 (2003)

Lead(II) carboxylate soaps of two fatty acids, palmitic (C 15H31COOH) and stearic acids (C17H 35COOH), and a dicarboxylic acid, azelaic acid (HOOCC 7H14COOH), have been synthesised and characterised by FTIR spectroscopy. These acids are all encountered in aged traditional oil paint, the azelaic acid resulting from the oxidative degradation of unsaturated fatty acids in the oil. Lead(II) azelate synthesised by hydrothermal methods was characterised by single crystal structure determination. This has a 3D polymeric structure with lead(II) ions linked by carboxylate bridges to form an infinite stack of (PbO4)n units. These layers are connected to adjacent layers by an infinite number of parallel C(CH 2)7C chains arranged perpendicularly to the stacks. The lead(II) ions display an unusual 7-fold coordination. The first direct evidence that the 'protrusions' encountered in aged traditional lead-containing oil paints contain lead soaps is reported. Their mechanism of formation is discussed.

Lead(ii) soaps: Crystal structures, polymorphism, and solid and liquid mesophases

Martínez-Casado,Ramos-Riesco,Rodríguez-Cheda,Redondo-Yélamos,Garrido,Fernández-Martínez,García-Barriocanal,Da Silva,Durán-Olivencia,Poulain

, p. 17009 - 17018 (2017/07/24)

The long-chain members of the lead(ii) alkanoate series or soaps, from octanoate to octadecanoate, have been thoroughly characterized by means of XRD, PDF analysis, DSC, FTIR, ssNMR and other techniques, in all their phases and mesophases. The crystal structures at room temperature of all of the members of the series are now solved, showing the existence of two polymorphic forms in the room temperature crystal phase, different to short and long-chain members. Only nonanoate and decanoate present both forms, and this polymorphism is proven to be monotropic. At higher temperature, these compounds present a solid mesophase, defined as rotator, a liquid crystal phase and a liquid phase, all of which have a similar local arrangement. Since some lead(ii) soaps appear as degradation compounds in oil paintings, the solved crystal structures of lead(ii) soaps can now be used as fingerprints for their detection using X-ray diffraction. Pair distribution function analysis on these compounds is very similar in the same phases and mesophases for the different members, showing the same short range order. This observation suggests that this technique could also be used in the detection of these compounds in disordered phases or in the initial stages of formation in paintings.

Coordination geometry of lead carboxylates - Spectroscopic and crystallographic evidence

Catalano, Jaclyn,Murphy, Anna,Yao, Yao,Yap, Glenn P. A.,Zumbulyadis, Nicholas,Centeno, Silvia A.,Dybowski, Cecil

, p. 2340 - 2347 (2015/01/30)

Despite their versatility, only a few single-crystal X-ray structures of lead carboxylates exist, due to difficulties with solubility. In particular, the structures of long-chain metal carboxylates have not been reported. The lone electron pair in Pb(ii) can be stereochemically active or inactive, leading to two types of coordination geometries commonly referred to as hemidirected and holodirected structures, respectively. We report 13C and 207Pb solid-state NMR and infrared spectra for a series of lead carboxylates, ranging from lead hexanoate (C6) to lead hexadecanoate (C18). The lead carboxylates based on consistent NMR parameters can be divided in two groups, shorter-chain (C6, C7, and C8) and longer-chain (C9, C10, C11, C12, C14, C16, and C18) carboxylates. This dichotomy suggests two modes of packing in these solids, one for the short-chain lead carboxylates and one for long-chain lead carboxylates. The consistency of the 13C and 207Pb NMR parameters, as well as the IR data, in each group suggests that each motif represents a structure characteristic of each subgroup. We also report the single-crystal X-ray diffraction structure of lead nonanoate (C9), the first single-crystal structure to have been reported for the longer-chain subgroup. Taken together the evidence suggests that the coordination geometry of C6-C8 lead carboxylates is hemidirected, and that of C9-C14, C16 and C18 lead carboxylates is holodirected.

Characterisation of metal carboxylates by Raman and infrared spectroscopy in works of art

Otero, Vanessa,Sanches, Diogo,Montagner, Cristina,Vilarigues, Mrcia,Carlyle, Leslie,Lopes, Joo A.,Melo, Maria J.

, p. 1197 - 1206 (2015/02/19)

This work introduces the complementary use of μ-Raman and μ-Fourier transform infrared (IR) spectroscopy for the detection of specific carbon chains and cations for the identification of metal carboxylates within oil paint microsamples. Metal carboxylates (metal soaps) form naturally when free fatty acids react with metal cations and may also be found as additives or degradation products. Twenty-two metal carboxylates were synthesised, and their spectra assembled in a reference database. Metal salts of cations commonly present in oil paintings were used, including lead, zinc, calcium, cadmium, copper and manganese. The fatty acids selected were the saturated acids palmitic (C1 6:0) and stearic (C18:0) and the polyunsaturated oleic acid (C1 8:1). Azelaic acid (C9 diacid), a product resulting from autoxidation of polyunsaturated acids, was also included. Metal carboxylates were characterised by Raman and IR spectroscopy, and their structures were confirmed by X-ray diffraction. Raman and IR spectroscopy proved to be complementary techniques for a full identification of the metal carboxylates in complex aged paint. Raman enables the differentiation of the carbon chain length in the C-C stretching region (1120-1040 cm-1), and IR distinguishes the metal cation in the COO- stretching absorption region (1650-1380cm-1). Principal component analysis was applied to the spectra in order to facilitate a fast and accurate method to discriminate between the different metal carboxylates and to aide in their identification. Finally, spectra from case studies were successfully projected in the principal component analysis models built, enabling a higher confidence level for the identification of copper palmitate and copper azelate in two 19th-century Portuguese oil paintings.

Phase diagrams of liquid-crystal binary systems of lanthanum(III) laurate with some divalent metal laurates

Bylina,Mirnaya,Volkov

, p. 639 - 641 (2008/10/09)

Phase equilibria in binary systems of lanthanum(III) laurate with laurates of divalent metals (lead, cadmium, zinc, and cobalt) are studied at temperatures from 0 to 350°C using differential thermal analysis (DTA) and polythermal polarized-light microscopy. Continuous or terminal smectic A liquid-crystal (LC) solutions are found to form in all systems. The temperature-concentration fields of formation of ionic LCs and glasses are determined. Pleiades Publishing, Inc., 2006.

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