ChemicalBook >> CAS DataBase List >>Palmitic acid

Palmitic acid

CAS No.
57-10-3
Chemical Name:
Palmitic acid
Synonyms
N-HEXADECANOIC ACID;HEXADECANOIC ACID;C16;palmitic;Palmic acid;CETYLIC ACID;FEMA 2832;Hexadecylic acid;1-Pentadecanecarboxylic acid;Hydrofol
CBNumber:
CB9388222
Molecular Formula:
C16H32O2
Molecular Weight:
256.42
MDL Number:
MFCD00002747
MOL File:
57-10-3.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-08-25 20:17:46

Palmitic acid Properties

Melting point 61-62.5 °C(lit.)
Boiling point 351.5 °C
Density 0.852 g/mL at 25 °C(lit.)
bulk density 415kg/m3
vapor pressure 10 mm Hg ( 210 °C)
refractive index 1.4273
FEMA 2832 | PALMITIC ACID
FLAVIS Number 08.014 | Hexadecanoic acid
Flash point >230 °F
storage temp. room temp
solubility chloroform: 0.5 M, clear, colorless
form Flakes
pka 4.78±0.10(Predicted)
color White or almost white
Odor at 100.00 %. slightly waxy fatty
Odor Type waxy
biological source plant (vegetable)
Water Solubility insoluble
Specific Heat Capacity Cp(crystal): 1.8 J/(g·K), at 25℃
JECFA Number 115
Merck 14,6996
BRN 607489
Henry's Law Constant 4.9×10-1 mol/(m3Pa) at 25℃, Duchowicz et al. (2020)
Dielectric constant 2.3(71℃)
Stability Stable. Combustible. Incompatible with bases, oxidizing agents, reducing agents.
Cosmetics Ingredients Functions SURFACTANT - EMULSIFYING
SKIN CONDITIONING - EMOLLIENT
Cosmetic Ingredient Review (CIR) Palmitic acid (57-10-3)
InChI 1S/C16H32O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16(17)18/h2-15H2,1H3,(H,17,18)
InChIKey IPCSVZSSVZVIGE-UHFFFAOYSA-N
SMILES CCCCCCCCCCCCCCCC(O)=O
LogP 7.170
CAS DataBase Reference 57-10-3(CAS DataBase Reference)
Substances Added to Food (formerly EAFUS) PALMITIC ACID
FDA 21 CFR 357.210
EWG's Food Scores 1
FDA UNII 2V16EO95H1
NIST Chemistry Reference Hexadecanoic acid(57-10-3)
EPA Substance Registry System Palmitic acid (57-10-3)
UNSPSC Code 85151701
NACRES NA.77

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H319
Precautionary statements  P305+P351+P338
Hazard Codes  Xi
Risk Statements  36-36/38-36/37/38
Safety Statements  26-37/39-36
WGK Germany  -
RTECS  RT4550000
TSCA  TSCA listed
HS Code  29157015
Storage Class 13 - Non Combustible Solids
Hazardous Substances Data 57-10-3(Hazardous Substances Data)
Toxicity LD50 i.v. in mice: 57±3.4 mg/kg (Or, Wretlind)
REACH Registrations Active
NFPA 704
1
1 0

Palmitic acid price More Price(118)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich W283215 Palmitic acid natural, 98%, FG 57-10-3 1 each $62.3 2026-04-30 Buy
Sigma-Aldrich W283215 Palmitic acid natural, 98%, FG 57-10-3 1kg $108 2026-04-30 Buy
Sigma-Aldrich W283207 Palmitic acid ≥98%, FCC, FG 57-10-3 1 each $58 2026-04-30 Buy
Sigma-Aldrich W283215 Palmitic acid natural, 98%, FG 57-10-3 10Kg $494 2026-04-30 Buy
Sigma-Aldrich W283207 Palmitic acid ≥95%, FCC, FG 57-10-3 1kg $80.9 2026-04-30 Buy
Product number Packaging Price Buy
W283215 1 each $62.3 Buy
W283215 1kg $108 Buy
W283207 1 each $58 Buy
W283215 10Kg $494 Buy
W283207 1kg $80.9 Buy

Palmitic acid Chemical Properties, Uses, Production

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.

Chemical Properties

Palmitic acid occurs as white crystalline scales with a slight characteristic odor and taste. It is one of the most common saturated fatty acids found in animals and plants. It is a mixture of solid organic acids obtained from fats consisting chiefly of palmitic acid (C16H35O2) with varying amounts of stearic acid (C16H36O2). As its name tells us, it is found in palm oil but also in butter, cheese, milk and meat.

Occurrence

Reported found in apple, beef fat, preferments of bread, celery, cheddar cheese, blue cheese, roquefort cheese, other cheeses, roasted cocoa bean, cognac, country cured ham, essential oil of lemon, heated milk, essential oil of sweet orange, pork fat, potato, black tea, tomato, banana, grapefruit juice, cranberry, guava, grapes, melon, papaya, pear, raspberry, strawberry, cinnamon, ginger, saffron, milk powder, fatty fish, chicken, lamb, hop oil, beer, rum, whiskies, grape wines, peanut oil, popcorn, soybean, coconut meat, avocado, cloudberry, plums, beans, mushroom, starfruit, marjoram, fenugreek, mango, tamarind, fig, kelp, cardamom,rice, prickly pear, dill, licorice, sake, buckwheat, corn oil, malt, wort, roasted chicory root, lemon balm, shrimp, crab, clam, scallop, Chinese quince, pawpaw and sweet grass oil.

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.

Uses

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.

Uses

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.

Production Methods

Palmitic acid occurs naturally in all animal fats as the glyceride, palmitin, and in palm oil partly as the glyceride and partly uncombined. Palmitic acid is most conveniently obtained from olive oil after removal of oleic acid, or from Japanese beeswax. Synthetically, palmitic acid may be prepared by heating cetyl alcohol with soda lime to 270°C or by fusing oleic acid with potassium hydrate.

Definition

ChEBI: Palmitic acid is a saturated long-chain fatty acid with a 16-carbon backbone. It is a metabolite found in the aging mouse brain. It is found naturally in palm oil and palm kernel oil, as well as in butter, cheese, milk and meat.

Preparation

Palmitic acid is prepared from Palm kernel oil, Olive oil, Japan wax or Chinese vegetable tallow by saponification of the natural glycerylesters.

Application

Palmitic acid is mainly used to produce soaps, cosmetics, and release agents. These applications utilize sodium palmitate, which is commonly obtained by saponification of palm oil. To this end, palm oil, rendered from the coconut palm nut, is treated with sodium hydroxide (in the form of caustic soda or lye), which causes hydrolysis of the ester groups. This procedure affords glycerol and sodium palmitate.
Because it is inexpensive and adds texture to processed foods (convenience food), palmitic acid and its sodium salt find wide use including foodstuffs. Sodium palmitate is permitted as a natural additive in organic products.
Hydrogenation of palmitic acid yields cetyl alcohol, which is used to produce detergents and cosmetics.
Recently, a long-acting antipsychotic medication, paliperidone palmitate (marketed as INVEGA Sustenna), used in the treatment of schizophrenia, has been synthesized using the oily palmitate ester as a long-acting release carrier medium when injected intramuscularly. The underlying method of drug delivery is similar to that used with decanoic acid to deliver long-acting depot medication, in particular, neuroleptics such as haloperidol decanoate.

Synthesis Reference(s)

The Journal of Organic Chemistry, 27, p. 2950, 1962 DOI: 10.1021/jo01055a527
Tetrahedron Letters, 17, p. 4697, 1976 DOI: 10.1016/S0040-4039(00)92999-X

Pharmaceutical Applications

Palmitic acid is used in oral and topical pharmaceutical formulations. Palmitic acid has been used in implants for sustained release of insulin in rats.

Biochem/physiol Actions

Palmitic acid (PA) is a component of membrane phospholipids (PL) and adipose triacylglycerols (TAG). Elevated levels of palmitic acid contributes to the pathophysiology of atherosclerosis, type 2 diabetes mellitus, neurodegenerative diseases, obesity and cancer. PA promotes apoptosis in the endothelial cell by modulating the p38 mitogen-activated protein kinase (MAPK) pathway and favors expression of TNF-α and reactive oxygen species accumulation. PA promotes interleukin 8 (IL-8) synthesis in hepatocytes contributing to hepatic inflammation. PA by interacting with toll-like receptor 4 (TLR4) induces inflammatory injury in cardiomyoctes.

Biotechnological Applications

Excess carbohydrates in the body are converted to palmitic acid. Palmitic acid is the first fatty acid produced during fatty acid synthesis and the precursor to longer fatty acids. Palmitate negatively feeds back on acetyl-CoA carboxylase (ACC), which is responsible for converting acetyl-CoA to malonyl-CoA, which in turn is used to add to the growing acyl chain, thus preventing further palmitate generation. In biology, some proteins are modified by the addition of a palmitoyl group in a process known as palmitoylation. Palmitoylation is important for membrane localisation of many proteins.

Mechanism of action

Contact action

Safety Profile

A poison by intravenous route. A human skin irritant. Questionable carcinogen with experimental neoplastigenic data. When heated to decomposition it emits acrid smoke and irritating fumes

Safety

Palmitic acid is used in oral and topical pharmaceutical formulations and is generally regarded as nontoxic and nonirritant at the levels employed as an excipient. However, palmitic acid is reported to be an eye and skin irritant at high levels and is poisonous by intravenous administration.
LD50 (mouse, IV): 57 mg/kg

storage

The bulk material should be stored in a well-closed container in a cool, dry, place.

Purification Methods

Purify palmitic acid by slow (overnight) recrystallisation from hexane. Some samples are also crystallised from acetone, EtOH or EtOAc. The crystals are kept in air to lose solvent, or are pumped dry of solvent on a vacuum line. [Iwahashi et al. J Chem Soc, Faraday Trans 1 81 973 1985, pK: White J Am Chem Soc 72 1858 1950, Beilstein 2 IV 1157.]

Incompatibilities

Palmitic acid is incompatible with strong oxidizing agents and bases.

Toxics Screening Level

The initial threshold screening level (ITSL) for palmitic acid is 50 microgram per cubic meter (μg/m3) based on an annual averaging time.

Regulatory Status

GRAS listed. Included in the FDA Inactive Ingredients Database (oral tablets). Included in nonparenteral medicines licensed in the UK.

Pesticide Type

Insecticide

Global Suppliers ( 854)
Supplier Tel Email Country ProdList Advantage
Changzhou Xichenxi Biotechnology Co., Ltd 13900000000 497839497@qq.com China 961 58
Shanghai Aladdin Bio-Chem Technology Co.,LTD 400-6206333 13167063860 anhua.mao@aladdin-e.com China 29977 65
Nanjing F&S Pharmatech Co., Ltd. 025-86950358 13390612682 wangjinyu@fshpharm.com China 185 58
Shandong Juntai Pharmaceutical Co., LTD. 15006412179 sales@h2opharm.com China 208 55
Shanghai shengyue international trading co., ltd 021-66690837 13166269258 2570384992@qq.com China 53 58
JIANGSU BSECHEM CHEMICAL TECHNOLOGY Co., Ltd 87161895 15651337098 15651337098@163.com China 4932 58
Quzhou Rundong Chemical (Technology) Co. 0570-8789886 18892685668 info@rundongchemical.com China 4045 60
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
Meryer (Shanghai) Chemical Technology Co., Ltd. 4006356688 18621169109 market03@meryer.com China 40202 62
Alfa Aesar 400-6106006 saleschina@alfa-asia.com China 30103 84

Related articles

View Latest Price from Palmitic acid manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Palmitic acid pictures 2026-09-17 Palmitic acid
57-10-3
1kg 99% 100 T/Month Hebei Qujie Technology Co., Ltd.
Palmitic acid pictures 2026-09-17 Palmitic acid
57-10-3
0.99 RongNa Biotechnology Co.,Ltd
Palmitic acid Neo-Fat16 pictures 2026-09-17 Palmitic acid Neo-Fat16
57-10-3
$1.00 1g 99% 1000kg RongNa Biotechnology Co.,Ltd
industrene4516 Kortacid1698 LoxiolEP278 LunacP95 LunacP95KC NAA160 Neo-Fat16 pentadecanecarboxylicacid Prifac 2960 Prifrac 2960 Univol U332 PALMITIC ACID PALMITIC ACID N.F. GRADE (FINE POWDER) PALMITIC ACID N.F. GRADE (FLAKE) PALMITIC ACID, NATURAL PALMITIC ACID extrapure 99+% Lunac P-70 Palmitic acid,90% Palmitic acid,98% PALMITICACID(RG) Hexadecanoic acid (Palmitic) Palmitic acid,Hexadecanoic acid Palmitic acid, synthesis grade Palmitic Acid (500 mg) Palmitic acid ,97.5% A 1600 Edenor C 16-98-100 Edenor C16 FA 1695 KortAcid 1695 Lunac P 98 PalMitic acid, 98% 1KG acidehexadecylique acidepalmitique Emersol 140 Emersol 143 emersol140 emersol143 Glycon P-45 Hexadecansαure Hydrofol 1-Pentadecanecarboxylic acid 1-pentadecanecarboxylicacid HydrofolAcid1690 Hystrene 8016 Hystrene 9016 hystrene8016 hystrene9016 Industrene 4516 Hexadecoic acid mitic Acid Palmitic acid (16:0), ultrapure Palmitic Acid - CAS 57-10-3 - Calbiochem PALMITIC ACID, 95%PALMITIC ACID, 95%PALMITIC ACID, 95%PALMITIC ACID, 95% n-hexadecoicacid n-hexadecyclicacid n-hexadecylicacid PA900