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Palmitic Acid

Base Information
  • Chemical Name:Palmitic Acid
  • CAS No.:57-10-3
  • Deprecated CAS:116860-99-2,212625-86-0,60605-23-4,66321-94-6,212625-86-0,66321-94-6
  • Molecular Formula:C16H32O2
  • Molecular Weight:256.429
  • Hs Code.:29157015
  • European Community (EC) Number:200-312-9
  • ICSC Number:0530
  • NSC Number:5030
  • UNII:2V16EO95H1
  • DSSTox Substance ID:DTXSID2021602
  • Nikkaji Number:J1.378A
  • Wikipedia:Palmitic_acid
  • Wikidata:Q209727
  • NCI Thesaurus Code:C61873
  • RXCUI:1426390
  • Pharos Ligand ID:5QANM91XQ6LK
  • Metabolomics Workbench ID:23
  • ChEMBL ID:CHEMBL82293
  • Mol file:57-10-3.mol
Palmitic Acid

Synonyms:Acid, Hexadecanoic;Acid, Palmitic;Calcium Palmitate;Hexadecanoic Acid;Palmitate, Calcium;Palmitate, Sodium;Palmitic Acid;Sodium Palmitate

Suppliers and Price of Palmitic Acid
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Usbiological
  • Palmitic Acid
  • 250g
  • $ 368.00
  • TRC
  • Palmitic acid
  • 10g
  • $ 50.00
  • TCI Chemical
  • Palmitic Acid >97.0%(GC)(T)
  • 25g
  • $ 17.00
  • TCI Chemical
  • Palmitic Acid >97.0%(GC)(T)
  • 500g
  • $ 28.00
  • TCI Chemical
  • Palmitic Acid >99.5%(GC)
  • 5g
  • $ 89.00
  • Sigma-Aldrich
  • Palmitic acid ≥99%
  • 25g
  • $ 105.00
  • Sigma-Aldrich
  • Palmitic Acid
  • 25gm
  • $ 124.00
  • Sigma-Aldrich
  • Palmitic acid natural, 98%, FG
  • 1 kg
  • $ 113.00
  • Sigma-Aldrich
  • Palmitic acid ≥95%, FCC, FG
  • 10 kg
  • $ 148.00
  • Sigma-Aldrich
  • Palmitic acid European Pharmacopoeia (EP) Reference Standard
  • $ 190.00
Total 224 raw suppliers
Chemical Property of Palmitic Acid
Chemical Property:
  • Appearance/Colour:white chips, crystals or powder 
  • Vapor Pressure:10 mm Hg ( 210 °C) 
  • Melting Point:61-62.5 °C(lit.) 
  • Refractive Index:1.4273 
  • Boiling Point:340.616 °C at 760 mmHg 
  • PKA:4.78±0.10(Predicted) 
  • Flash Point:154.12 °C 
  • PSA:37.30000 
  • Density:0.893 g/cm3 
  • LogP:5.55230 
  • Storage Temp.:+15C to +30C 
  • Solubility.:chloroform: 0.5 M, clear, colorless 
  • Water Solubility.:insoluble 
  • XLogP3:6.4
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:14
  • Exact Mass:256.240230259
  • Heavy Atom Count:18
  • Complexity:178
Purity/Quality:

95%-98% *data from raw suppliers

Palmitic Acid *data from reagent suppliers

Safty Information:
  • Pictogram(s): IrritantXi 
  • Hazard Codes:Xi 
  • Statements: 36-36/38-36/37/38 
  • Safety Statements: 26-37/39-36 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Chemical Classes:Lipids -> Unambiguous Lipids,Other Classes -> Organic Acids
  • Canonical SMILES:CCCCCCCCCCCCCCCC(=O)O
  • Recent ClinicalTrials:Monitoring of Hepatic Fat Metabolism Using Magnetic Resonance Methods
  • Recent NIPH Clinical Trials:Intestinal absorption test using 13C-labeled compounds
  • Inhalation Risk:Evaporation at 20 °C is negligible; a nuisance-causing concentration of airborne particles can, however, be reached quickly when dispersed.
  • Description Palmitic acid is a kind of common saturated fatty acid of a 16-carbon backbone, which is contained in fats and waxes. It naturally exists in palm oil and palm kernel oil, and can also be found in butter, cheese, milk, meat, cocoa butter, soybean oil and sunflower oil. It can be produced by many kinds of plants and organisms. It can be used for the production of soap, cosmetics, and industrial mold release agents. It is also a food processing aid. It can also be used to produce cetyl alocohol which is useful in the production of detergents and cosmetics. Recently, it has been also used for the manufacture of a long-acting antipsychotic medication, paliperidone palmitate.
  • Uses Palmitic Acid is a common fatty acid found in plants and animals. The body converts excess carbohydrates into Palmitic Acid, thus Palmitic Acid is the first fatty acid produced during fatty acid synt hesis as well as a precursor for longer fatty acids. palmitic acid is one of the skin’s major fatty acids produced by the sebaceous glands. In cosmetic preparations, it is used as a formula texturizer. This acid is naturally occurring in allspice, anise, calamus oil, cascarilla bark, celery seed, coffee, tea, and many animal fats and plant oils. It is obtained from palm oil, Japan wax, or Chinese vegetable tallow. Palmitic Acid is a fatty acid which is a mixture of solid organic acids from fats consisting principally of palmitic acid with varying amounts of stearic acid. it functions as a lubricant, binder, and defoaming agent.
Technology Process of Palmitic Acid

There total 224 articles about Palmitic Acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With Iron(III) nitrate nonahydrate; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; potassium chloride; oxygen; In 1,2-dichloro-ethane; at 25 ℃; for 12h; Time; Concentration; Reagent/catalyst;
DOI:10.1021/jacs.6b03948
Guidance literature:
With oxalyl dichloride; In 1,2-dichloro-ethane; at 20 ℃; for 2.66667h;
DOI:10.1016/j.tetlet.2015.01.061
Guidance literature:
With iron(III) chloride; In dichloromethane; at 20 ℃; for 0.0833333h; Reagent/catalyst; Solvent; Catalytic behavior; Inert atmosphere; Green chemistry;
DOI:10.1248/cpb.c16-00161
Refernces

Synthesis of specific deuterated derivatives of the long chained stratum corneum lipids [EOS] and [EOP] and characterization using neutron scattering

10.1002/jlcr.3504

The study focuses on the synthesis and characterization of specific deuterated derivatives of long-chain ceramides [EOS] and [EOP] found in the stratum corneum lipids, which are essential components of the skin's barrier function. The researchers replaced linoleic acid with a palmitic acid branched with a methyl group and introduced deuteration in the branched and terminal methyl groups to create these derivatives. The synthesized ceramides were then prepared for neutron scattering investigations. The chemicals used in the study included various fatty acids, deuterated compounds, and ceramide precursors, such as 6-bromohexanoic acid ethyl ester, malonic acid ethyl ester, and lithium aluminum deuteride. These chemicals served the purpose of creating the branched and deuterated fatty acids, which were then used to synthesize the ceramides [EOS] and [EOP]. The synthesized deuterated ceramides are valuable tools for investigating the influence of these long-chain ceramide species on the nanostructure of stratum corneum lipid model membranes, as they can be detected in the lipid model membranes and help to understand their structural role in the skin's barrier.

Pd/Nb2O5/SiO2 catalyst for the direct hydrodeoxygenation of biomass-related compounds to liquid alkanes under mild conditions

10.1002/cssc.201500053

The research focuses on the development and evaluation of a Pd/Nb2O5/SiO2 catalyst for the direct hydrodeoxygenation (HDO) of biomass-derived compounds into liquid alkanes under mild conditions. The study involves the conversion of model compounds such as 4-(2-furyl)-3-buten-2-one (derived from furfural and acetone), palmitic acid, tristearin, and diphenyl ether, which represent microalgae oils, vegetable oils, and lignin, respectively. The experiments utilize a Pd-loaded Nb2O5/SiO2 catalyst prepared via a sol-gel method, aiming to achieve high yields of alkanes with minimal C-C bond cleavage. The catalyst's performance is assessed through batch reactions in a stainless-steel autoclave under controlled temperature (170°C) and pressure (2.5 MPa H2), with product analysis conducted using GC-MS to quantify the liquid products against an internal standard. The research also includes characterization of the catalyst using techniques like XRD, N2 adsorption-desorption isotherms, TEM, and EDAX atomic mapping to understand its structure and active sites. The study demonstrates that the Pd/10%Nb2O5/SiO2 catalyst is highly effective, achieving over 94% yield of alkanes under the specified mild conditions, and exhibits excellent stability and activity, making it a promising candidate for biomass conversion to liquid alkanes.

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