Hydrogenated Palm Oil
If you find any inaccurate information, please let us know by providing your feedback here

This article is compiled based on the United States Pharmacopeia (USP) – 2025 Edition
Issued and maintained by the United States Pharmacopeial Convention (USP)
DOWNLOAD PDF HERE
R1COOCH –CH(OOCR2)–CH2OOCR3, where R1, R2, and R3 are mainly C15 and C17;
Hydrogenated palm oil
CAS RN: 68514-74-9.
1 DEFINITION
Hydrogenated Palm Oil is the product obtained by refining and hydrogenating the oil obtained from the pulp of the fruit of the oil palm Elaeis guineensis Jacq. (Fam. Aracaceae). The product consists mainly of triglycerides of palmitic and stearic acids.
2 IDENTIFICATION
A. It meets the requirements of the test for Fats and Fixed Oils, Fatty Acid Composition 〈401〉.
B. It meets the requirements of the test for Melting Range or Temperature 〈741〉.
3 IMPURITIES
Residue on Ignition 〈281〉
Sample: 5 g
Acceptance criteria: NMT 0.1%
Limit of Nickel
Sample solution: Weigh 5.0 g of Hydrogenated Palm Oil into a previously tared platinum or silica crucible. Cautiously heat the substance, and introduce into it a wick formed from twisted, ashless filter paper. Ignite the wick. When the substance ignites, stop heating. After combustion, ignite in a muffle furnace at about 600°. Continue the incineration until a white ash is obtained. After cooling, with the aid of two 2-mL portions of diluted hydrochloric acid, transfer the residue to a 25-mL volumetric flask, add 0.3 mL of nitric acid, and dilute with water to volume.
Nickel standard solution: Immediately before use, dilute 10 mL of nickel standard solution TS with water to 500 mL. This solution contains the equivalent of 0.2 μg/mL of nickel.
Standard solutions: Into four separate identical 10-mL volumetric flasks introduce respectively 0, 1.0, 2.0, and 4.0 mL of Nickel standard solution. To each flask add a 2.0-mL portion of the Sample solution, and dilute with water to volume to obtain four Standard solutions containing added quantities of 0, 0.2, 0.4, and 0.8 μg of nickel, respectively.
Instrumental conditions
(See Atomic Absorption Spectroscopy 〈852〉.)
Mode: Atomic absorption spectrophotometer equipped with a graphite furnace
Analytical wavelength: 232.0 nm
Lamp: Nickel hollow-cathode
Analysis
Samples: Standard solutions
Concomitantly determine the absorbances of the Standard solutions at least three times each. Record the average of the steady readings for each of the Standard solutions. Plot the absorbances of the Standard solutions versus the added quantity, in μg, of nickel.
Extrapolate the line joining the points on the graph until it meets the quantity axis. The distance between this point and the intersection of the axes represents the quantity of nickel in the 2-mL portion of the Sample solution added to the Standard solutions.
Calculate the content of nickel in the portion of Hydrogenated Palm Oil taken:
Result = [V × (A/VA)]/W
V = volume of the Sample solution, 25 mL
A = quantity of nickel (μg)
VA = volume of the Sample solution added to the Standard solutions, 2 mL
W = weight of Hydrogenated Palm Oil taken to prepare the Sample solution (g)
Acceptance criteria: NMT 1 μg/g
Alkaline Impurities
Sample: A mixture of 2.0 g of Hydrogenated Palm Oil, 1.5 mL of alcohol, and 3.0 mL of toluene
Analysis: Dissolve the Sample by gentle heating. Add 0.05 mL of bromophenol blue TS, and titrate with 0.01 N hydrochloric acid VS until the
mixture turns yellow.
Acceptance criteria: NMT 0.4 mL of 0.01 N hydrochloric acid is required.
4 SPECIFIC TESTS
Melting Range or Temperature 〈741〉: 58°–62°
Fats and Fixed Oils, Acid Value, Method II 〈401〉: NMT 2.0
Fats and Fixed Oils, Fatty Acid Composition 〈401〉: Hydrogenated Palm Oil exhibits the composition profile of fatty acids as shown in Table 1.
Table 1
| Carbon-Chain Length | Number of Double Bonds | Percentage |
| ≤12 | 0 | ≤2.5 |
| 14 | 0 | 0.5-5.9 |
| 16 | 0 | 32.0-47.0 |
| 18 | 0 | 49.0-57.0 |
| 20 | 0 | ≤1.0 |
| 22 | 0 | ≤1.0 |
| 16 | 1 | ≤2.5 |
| 18 | 1 | ≤2.5 |
| 18 | 2 | ≤0.5 |
| 18 | 3 | ≤0.5 |
Fats and Fixed Oils, Peroxide Value 〈401〉: NMT 5.0
Fats and Fixed Oils, Unsaponifiable Matter 〈401〉: NMT 0.8%
Loss on Drying 〈731〉
Analysis: Dry a sample at 105° for 4 h.
Acceptance criteria: NMT 0.1%
5 ADDITIONAL REQUIREMENTS
Packaging and Storage: Preserve in tight, light-resistant containers. No storage requirement specified.

