Stearic acid

Stearic acid (/ˈstɪərɪk/ STEER-ik, /stiˈærɪk/ stee-ARR-ik) is a saturated fatty acid with an 18-carbon chain. The IUPAC name is octadecanoic acid. It is a waxy solid and its chemical formula is C17H35CO2H. Its name comes from the Greek word στέαρ "stéar", which means tallow. The salts and esters of stearic acid are called stearates. As its ester, stearic acid is one of the most common saturated fatty acids found in nature following palmitic acid.[11] The triglyceride derived from three molecules of stearic acid is called stearin.

[1]
Skeletal formula of stearic acid
Ball-and-stick model of stearic acid
Stearic acid
Names
Preferred IUPAC name
Octadecanoic acid
Other names
Stearic acid
C18:0 (Lipid numbers)
Identifiers
CAS Number
  • 57-11-4 check
3D model (JSmol)
  • Interactive image
ChEMBL
  • ChEMBL46403 check
ChemSpider
  • 5091 check
DrugBank
  • DB03193 check
ECHA InfoCard100.000.285 Edit this at Wikidata
EC Number
  • 200-313-4
IUPHAR/BPS
  • 3377
PubChem CID
  • 5281
RTECS number
  • WI2800000
UNII
  • 4ELV7Z65AP check
CompTox Dashboard (EPA)
  • DTXSID8021642 Edit this at Wikidata
SMILES
  • CCCCCCCCCCCCCCCCCC(=O)O
Properties
Chemical formula
C18H36O2
Molar mass284.484 g·mol−1
AppearanceWhite solid
OdorPungent, oily
Density0.9408 g/cm3 (20 °C)[2]
0.847 g/cm3 (70 °C)
Melting point69.3 °C (156.7 °F; 342.4 K) [2]
Boiling point361 °C (682 °F; 634 K)
decomposes
232 °C (450 °F; 505 K)
at 15 mmHg[2]
Solubility in water
0.00018 g/100 g (0 °C)
0.00029 g/100 g (20 °C)
0.00034 g/100 g (30 °C)
0.00042 g/100 g (45 °C)
0.00050 g/100 g (60 °C)[3]
SolubilitySoluble in alkyl acetatesalcoholsHCOOCH3phenylsCS2CCl4[4]
Solubility in dichloromethane3.58 g/100 g (25 °C)
8.85 g/100 g (30 °C)
18.3 g/100 g (35 °C)[4]
Solubility in hexane0.5 g/100 g (20 °C)
4.3 g/100 g (30 °C)
19 g/100 g (40 °C)
79.2 g/100 g (50 °C)
303 g/100 g (60 °C)[4]
Solubility in ethanol1.09 g/100 mL (10 °C)
2.25 g/100 g (20 °C)
5.42 g/100 g (30 °C)
22.7 g/100 g (40 °C)
105 g/100 g (50 °C)
400 g/100 g (60 °C)[3]
Solubility in acetone4.73 g/100 g[5]
Solubility in chloroform15.54 g/100 g[5]
Solubility in toluene13.61 g/100 g[5]
Vapor pressure0.01 kPa (158 °C)[2]
0.46 kPa (200 °C)
16.9 kPa (300 °C)[6]
Magnetic susceptibility (χ)
−220.8·10−6 cm3/mol
Thermal conductivity0.173 W/m·K (70 °C)
0.166 W/m·K (100 °C)[7]
Refractive index (nD)
1.4299 (80 °C)[2]
Structure
Crystal structure
B-form = Monoclinic[8]
Space group
B-form = P21/a[8]
Point group
B-form = Cs
2h
[8]
Lattice constant
a = 5.591 Å, b = 7.404 Å, c = 49.38 Å (B-form)[8]
α = 90°, β = 117.37°, γ = 90°
Thermochemistry
Heat capacity (C)
501.5 J/mol·K[2][6]
Std molar
entropy (So298)
435.6 J/mol·K[2]
Std enthalpy of
formation fH298)
−947.7 kJ/mol[2]
Std enthalpy of
combustion cH298)
−11342.4 kJ/mol[9]
Hazards
NFPA 704 (fire diamond)
1
1
0
Flash point113 °C (235 °F; 386 K)
Lethal dose or concentration (LD, LC):
LD50 (median dose)
4640 mg/kg (rats, oral)[10]
21.5 mg/kg (rats, intravenous)[4]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Occurrence and productionEdit

Stearic acid is more abundant in animal fat (up to 30%) than in vegetable fat (typically <5%). The important exceptions are the foods cocoa butter (34%)[12] and shea butter, where the stearic acid content (as a triglyceride) is 28–45%.[13]

In terms of its biosynthesis, stearic acid is produced from carbohydrates via the fatty acid synthesis machinery wherein acetyl-CoA contributes two-carbon building blocks.[citation needed]

Stearic acid is obtained from fats and oils by the saponification of the triglycerides using hot water (about 100 °C). The resulting mixture is then distilled.[14] Commercial stearic acid is often a mixture of stearic and palmitic acids, although purified stearic acid is available.[citation needed] Commercially, fats high in oleic acid such as palm and soy may be hydrogenated to convert oleic into stearic acid.[15][16]

UsesEdit

In general, the applications of stearic acid exploit its bifunctional character, with a polar head group that can be attached to metal cations and a nonpolar chain that confers solubility in organic solvents. The combination leads to uses as a surfactant and softening agent. Stearic acid undergoes the typical reactions of saturated carboxylic acids, a notable one being reduction to stearyl alcohol, and esterification with a range of alcohols. This is used in a large range of manufactures, from simple to complex electronic devices.[citation needed]

As food additiveEdit

Stearic acid (E number E570) is found in some foods.[17]

Soaps, cosmetics, detergentsEdit

Stearic acid is mainly used in the production of detergents, soaps, and cosmetics such as shampoos and shaving cream products. Soaps are not made directly from stearic acid, but indirectly by saponification of triglycerides consisting of stearic acid esters. Esters of stearic acid with ethylene glycol (glycol stearate and glycol distearate) are used to produce a pearly effect in shampoos, soaps, and other cosmetic products. They are added to the product in molten form and allowed to crystallize under controlled conditions. Detergents are obtained from amides and quaternary alkylammonium derivatives of stearic acid.[citation needed]

Lubricants, softening and release agentsEdit

In view of the soft texture of the sodium salt, which is the main component of soap, other salts are also useful for their lubricating properties. Lithium stearate is an important component of grease. The stearate salts of zinc, calcium, cadmium, and lead are used to soften PVC. Stearic acid is used along with castor oil for preparing softeners in textile sizing. They are heated and mixed with caustic potash or caustic soda. Related salts are also commonly used as release agents, e.g. in the production of automobile tires. As an example, it can be used to make castings from a plaster piece mold or waste mold, and to make a mold from a shellacked clay original. In this use, powdered stearic acid is mixed in water and the suspension is brushed onto the surface to be parted after casting. This reacts with the calcium in the plaster to form a thin layer of calcium stearate, which functions as a release agent.[18]

When reacted with zinc it forms zinc stearate, which is used as a lubricant for playing cards (fanning powder) to ensure a smooth motion when fanning. Stearic acid is a common lubricant during injection molding and pressing of ceramic powders.[19] It is also used as a mold release for foam latex that is baked in stone molds.[citation needed]

Niche usesEdit

Being inexpensive, nontoxic, and fairly inert, stearic acid finds many niche applications.[14] Stearic acid is used as a negative plate additive in the manufacture of lead-acid batteries. It is added at the rate of 0.6 g per kg of the oxide while preparing the paste. It is believed to enhance the hydrophobicity of the negative plate, particularly during dry-charging process. It also reduces the extension of oxidation of the freshly formed lead (negative active material) when the plates are kept for drying in the open atmosphere after the process of tank formation. As a consequence, the charging time of a dry uncharged battery during initial filling and charging (IFC) is comparatively lower, as compared to a battery assembled with plates which do not contain stearic acid additive. Fatty acids are classic components of candle-making. Stearic acid is used along with simple sugar or corn syrup as a hardener in candies. In fireworks, stearic acid is often used to coat metal powders such as aluminium and iron. This prevents oxidation, allowing compositions to be stored for a longer period of time.[citation needed]

MetabolismEdit

An isotope labeling study in humans[20] concluded that the fraction of dietary stearic acid that oxidatively desaturates to oleic acid is 2.4 times higher than the fraction of palmitic acid analogously converted to palmitoleic acid. Also, stearic acid is less likely to be incorporated into cholesterol esters. In epidemiologic and clinical studies, stearic acid was found to be associated with lowered LDL cholesterol in comparison with other saturated fatty acids.[21]

Salts and estersEdit

Stearates are the salts or esters of stearic acid. The conjugate base of stearic acid, C17H35COO, is also known as the stearate anion.

ExamplesEdit

Salts
  • Calcium stearate
  • Lithium stearate
  • Magnesium stearate
  • Sodium stearate
  • Zinc stearate
Esters
  • Estradiol stearate
  • Glycol stearate
  • Stearin
  • Testosterone stearate


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