Literature DB >> 31372470

Complete fatty acid analysis data of flaxseed oil using GC-FID method.

Mohammed Danish1, Maniruddin Nizami2.   

Abstract

The data presented in this article were generated through the gas chromatography (GC) with a flame ionization detector (FID). The flaxseed oil was converted into fatty acid methyl ester (FAME) then used in the GC with FID and observe the retention time of different fatty acid present in the flaxseed oil. The observed retention time was compared with the standard fatty acid to confirm the specific fatty acid presence in the flaxseed oil. The part of the data is used in the article "Optimization of the process variable for biodiesel production by transesterification of flaxseed oil and produced biodiesel characterizations" Renewable Energy journal (Ahmad et al., 2019).

Entities:  

Keywords:  Fatty acid methyl ester (FAME); Fatty acids; Flaxseed oil; Gas chromatography; Trans-fats

Year:  2019        PMID: 31372470      PMCID: PMC6661239          DOI: 10.1016/j.dib.2019.103845

Source DB:  PubMed          Journal:  Data Brief        ISSN: 2352-3409


Specifications table The data give complete information about the fatty acids present in the flaxseed oil. Standard of each fatty acid data can be used for the reference for the other oil analysis. The percentage information of the saturated fats (SAFA), Trans-fats (TFA), Monounsaturated fats (MUFA), polyunsaturated fats (PUFA), and total unsaturated fats (TUFA) in flaxseed oil will help researchers in food and nutrition. Fatty acid profiling of the oil will help in converting flaxseed oil into biodiesel.

Data

The data collected for fatty acid are given in the below tables. Table 1 represents the standard Supelco 37 FAME data for comparison purpose. Table 2 shows the GC-FID data for flaxseed oil converted FAME. The chromatogram of standard Supelco 37 is shown Fig. 1 and flaxseed oil converted FAME chromatogram is shown in Fig. 2.
Table 1

Supelco 37 component FAME Mix FAME analysis data used for calibration for quantitation & identification of the unknown peaks in the oil samples.

SNFatty acids in CRMFatty acid groupsRTShort name% Area
1C4:0–Butyric acidSAFA6.519C4:01.69614
2C6:0–Caproic acidSAFA6.913C6:03.13618
3C8:0–Caprylic acidSAFA7.606C8:03.22269
4C10:0–Capric acidSAFA8.706C10:03.3805
5C11:0–Undecanoic acidSAFA9.424C11:01.84709
6C12:0–Lauric acidSAFA10.264C12:03.94123
7C13:0–Triundecanoic acidSAFA11.242C13:02.06048
8C14:0–Myristic acidSAFA12.394C14:04.32965
9C14:1–Myristoleic acidMUFA13.479C14:12.13117
10C15:0–Pentadecanoic acidSAFA13.771C15:02.23474
11C15:1–cis-10-Pentadecenoic acidMUFA15.103C15:12.15963
12C16:0–Palmitic acidSAFA15.456C16:06.3978
13C16:1–Palmitoleic acidMUFA16.810C16:12.24513
14C17:0–Heptadecanoic acidSAFA17.488C17:01.56535
15C17:1–cis-Heptadecenoic acidMUFA18.882C17:12.21837
16C18:0–Stearic acidSAFA19.553C18:04.69103
17C18:1–trans-9-Elaidic acidTFA20.348C18:1n9t2.28174
18C18:1 (n-9)–Oleic acidMUFA/ω9FA20.723C18:1n9c4.5848
19C18:2–trans-Linolelaidic acidTFA21.617C18:2n6t2.10519
20C18:2 (n-6)–Linoleic acidPUFA22.423C18:2n6c2.09427
21C20:0–Arachidic acidSAFA23.401C20:04.68651
22C18:3 (n-6)–g-Linolenic acidPUFA/ω6FA23.601C18:3n61.91131
23C18:3 (n-3)–a-Linolenic acid (ALA)PUFA/ω3FA24.314C18:3n31.84683
24C20:1 (n-9)–cis-11-Eicosenic acidMUFA24.458C20:12.3618
25C21:0–Heneicosanoic acidSAFA25.262C21:02.36044
26C20:2–cis-11,14-Eicosadienoic acidPUFA26.203C20:22.07894
27C22:0–Behenic acidSAFA27.281C22:04.67455
28C22:3n6–cis-8,11,14-Eicostrienoic acidPUFA/ω6FA27.548C20:3n61.69522
29C20:3n3–cis-11,14,17-Eicosatrienoic acidPUFA/ω3FA28.407C20:3n31.38465
30C22:1 (n-9)–Erucic acidMUFA/ω9FA28.553C22:1n92.32792
31C20:4 (n-6)–Arachidonic acidPUFA/ω6FA28.591C20:4n61.74384
32C23:0–Tricosanoic acidSAFA29.504C23:02.46567
33C22:2–cis-13,16-Docasadienoic acidPUFA30.705C22:22.114
34C20:5 (n-3)–cis-5,8,11,14,17-Eicosapentaenoic acid (EPA)PUFA/ω3FA31.251C20:5n31.53761
35C24:0–Lignoceric acidSAFA32.030C24:04.75565
36C24:1–Nervonic acidMUFA33.684C24:12.14213
37C22:6 (n-3)–cis-4,7,10,13,16,19-Docosahexaenoic acid (DHA)PUFA37.833C22:6n31.58971
Table 2

Fatty acids with their relative percentage in the total fat of the flaxseed oil.

SNFatty acids in flaxseed oilFatty acid groupsRTPeak area (FAME)% Fat (of total fat)
1C14:0–Myristic acidSAFA12.3880.5699510.046
2C16:0–Palmitic acidSAFA15.45770.399295.687
3C16:1–Palmitoleic acidMUFA16.8061.193020.096
4C18:0–Stearic acidSAFA19.57168.690445.578
5C18:1–trans-9-Elaidic acidTFA20.4411.064640.086
6C18:1 (n-9)–Oleic acidMUFA/ω9FA20.757253.643120.591
7C18:2–trans-Linolelaidic acidTFA21.6491.108710.09
8C18:2 (n-6)–Linoleic acidPUFA/ω6FA22.445194.6987915.801
9C20:0–Arachidic acidSAFA23.4122.505810.204
10C18:3 (n-6)–g-Linolenic acidPUFA23.7052.879350.234
11C18:3 (n-3)–a-Linolenic acid (ALA)PUFA/ω3FA24.37633.3297151.376
12C22:0–Behenic acidSAFA27.2752.174240.178
13C24:0–Lignoceric acidSAFA32.0140.3948520.034
14Sum of Omega-3 (n-3)ω3FA51.376
15Sum of Omega-6 (n-6)ω6FA15.801
16Sum of Omega-9 (n-9)ω9FA20.591
17Saturated fats (SAFA)SAFA11.727
18Trans-fats (TFA)TFA0.176
19Monounsaturated fats (MUFA)MUFA20.687
20Polyunsaturated fats (PUFA)PUFA67.41
21Total Unsaturated fats (TUFA)TUFA88.097

ω3FA = Omega-3 Fatty Acids, ω6FA = Omega-6 Fatty Acids, ω9FA = Omega-9 Fatty Acids, SAFA = Saturated Fatty Acids, TFA = Trans Fatty Acids, MUFA = Monounsaturated Fatty Acids, PUFA = Polyunsaturated Fatty Acids, TUFA = Total Unsaturated Fatty Acids.

Fig. 1

GC-FID chromatogram of supelco 37 component FAME mix, Cat: CRM47885, Lot: XA19807V.

Fig. 2

GC-FID Chromatogram of flaxseed oil with peak label (Retention Time & Name of Fatty Acid).

Supelco 37 component FAME Mix FAME analysis data used for calibration for quantitation & identification of the unknown peaks in the oil samples. Fatty acids with their relative percentage in the total fat of the flaxseed oil. ω3FA = Omega-3 Fatty Acids, ω6FA = Omega-6 Fatty Acids, ω9FA = Omega-9 Fatty Acids, SAFA = Saturated Fatty Acids, TFA = Trans Fatty Acids, MUFA = Monounsaturated Fatty Acids, PUFA = Polyunsaturated Fatty Acids, TUFA = Total Unsaturated Fatty Acids. GC-FID chromatogram of supelco 37 component FAME mix, Cat: CRM47885, Lot: XA19807V. GC-FID Chromatogram of flaxseed oil with peak label (Retention Time & Name of Fatty Acid).

Experimental design, materials, and methods

FAME preparation from flaxseed oil

For conversion of flaxseed oil into FAME the following methods was adopted: around 0.1 g flaxseed oil was taken into 40 mL glass vial then mix with 5 mL of 0.50 N methanolic NaOH (Methanol: VWR Chemicals, 20864.320, Batch 14C030509. NaOH: PanReac, 141687.1211, Lot # 0001070723), the mixture was heated for 3 mins at 60 °C. The mixture was allowed to cool at room temperature, then 6 mL of 14% BF3 solution (Aldrich, B1250-500mL, Lot # BCBW8950) was added [2] to the mixture and again heated for 3 mins at 60 °C. The mixture was again cool at room temperature then added 10 mL isooctane (Carlo Erba, 412460 2.5 L) and shake it well, then keep it to settling down. After settling the mixture, the upper layer of the mixture was transferred to the tube containing sodium sulfate (Ajax Finechem, 503-500G, B/No. 1608224929) to remove the moisture. The extract was analyzed with GC-FID (Agilent 7890B), the flow chart of the flaxseed oil analysis method condition shown in Scheme 1 The quantity and identification of fatty acid in the flaxseed oil was done through the comparison of standard supelco 37 FAME component [3].
Scheme 1

Flow chart of the flaxseed oil fatty acid analysis.

Flow chart of the flaxseed oil fatty acid analysis.

GC acquisition method

Following are the detail of the gas chromatography instrumentation and methods [4]. GC oven program: Initial Temperature: 120 °C, Hold Time: 1 min. Rate 1: 10 °C/min to 175 °C, Hold Time: 10 min. Rate 2: 5 °C/min to 210 °C, Hold Time: 10 min. Rate 3: 5 °C/min to 230 °C, Hold Time: 9.5 min. Equilibration Time: 0.5 min. Max Temperature: 260 °C. Automatic Liquid Sampler Injector: Syringe Size: 10 μL, Injection Volume: 1 μL, Injection Dispense Speed: 6000 μL/min, Viscosity Delay: 0 sec. Sample inlet parameters: Split/Splitless Inlet. Mode: Split, Heater: 250 °C, Pressure: 20.863 psi, Total Flow: 54 mL/min, Septum Purge Flow: 3 mL/min, Split Ratio: 50:1, Split Flow: 50 mL/min. Column Parameters: Initial Flow: 1 mL/min, Post Run: 1.4 mL/min. Column Specifications: Agilent 112-88A7, HP-88, 0 °C - 250 °C (260 °C): 100 m × 250 μm x 0.2 μm. Detector Parameters: Flame Ionization Detector (FID), Heater: 260 °C, H2 Flow: 40 mL/min, Air Flow: 450 mL/min, Makeup Flow: Off.

Specifications table

Subject areaAnalytical chemistry
More specific subject areaFood analysis
Type of dataTable, image, text file, graph, figure
How data was acquiredGas chromatography with a flame ionization detector, model of the instrument: Agilent GC 7890B with Flame Ionization Detector.
Data formatRaw, filtered, analyzed.
Experimental factorsFlaxseed oil pretreated with methanolic NaOH, BF3, and filter through sodium sulfate.
Experimental featuresConversion of fatty acids into Fatty acid methyl ester (FAME) was an essential feature of the GC-FID analysis.
Data source locationDammam, Saudi Arabia.
Data accessibilityAll data related to the fatty acid analysis of flaxseed oil is included in this article.
Related research article“Optimization of process variable for biodiesel production by transesterification of flaxseed oil and produced biodiesel characterizations” Renewable Energy Journal [1].
Value of the data

The data give complete information about the fatty acids present in the flaxseed oil.

Standard of each fatty acid data can be used for the reference for the other oil analysis.

The percentage information of the saturated fats (SAFA), Trans-fats (TFA), Monounsaturated fats (MUFA), polyunsaturated fats (PUFA), and total unsaturated fats (TUFA) in flaxseed oil will help researchers in food and nutrition.

Fatty acid profiling of the oil will help in converting flaxseed oil into biodiesel.

  1 in total

1.  Concentration-Emission Matrix (CEM) Spectroscopy Combined with GA-SVM: An Analytical Method to Recognize Oil Species in Marine.

Authors:  Yunan Chen; Ruifang Yang; Nanjing Zhao; Wei Zhu; Xiaowei Chen; Ruiqi Zhang; Jianguo Liu; Wenqing Liu
Journal:  Molecules       Date:  2020-11-04       Impact factor: 4.411

  1 in total

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