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The sunflower (Helianthus annus L.) native to the Americas, arrived in Europe in the 16th century. It is an annual plant that reaches full maturity after about 4 months from sowing. There are two varieties: one with a high content of linoleic acid, the other of oleic acid. The main producing countries are Ukraine, Russia and Argentina. Sunflower oil is extracted by means of solvents. Upon pressing, the seed provides an oil yield of 40-45%. The crude oil extracted is yellow in color. It has a high content of phosphatides and waxes. After the refining and “winterization” process, the oil is bright yellow. It is used as table oil, for frying and for the manufacture of margarines. According to the regulations in force, the oil must meet the requirements indicated in the following technical data sheet:

CARATTERISTICAREQUISITIMETODO DI ANALISI 
Relative density at a 20/20°Cfrom 0,918 to 0,923See A.1.1
Refractive index nD at 40°Cfrom 1,461 to 1,468See A.1.2
Number of iodinefrom 118 to 141See A.1.3
Content in sterols mg / kgfrom 1700 to 5000See A.1.5
Acidity, expressed as oleic acid,%max 0,5See A.1.6
Number of peroxides, meq oxygen / kgmax 7,0See A.1.7
Impurities (petroleum ether)%max 0,05UNI EN ISO 663
Soaps, expressed as sodium oleate, mg / kgmax 10See A.1.8
Metals, mg / kg (**)
ironmax 1,5UNI EN ISO 8294
coppermax 0,1UNI EN ISO 8294
lead (1) max 0,1UNI EN ISO 12193
arsenicmax 0,1See A.2.1
Solvents, mg / kg (***)
hexanemax 1
CARATTERI ORGANOLETTICI
smell and tasteDelicate flavor characteristic of the oil, free from anomalous or unpleasant odors or tastes
appearanceclear 20°C
colorthe spectrophotometric absorptions, measured on diluted oil with the same volume of hexane, in a 1 cm tray, with reference to normal hexane, must not exceed the values ​​of 0.20 and 0.10 respectively at 420 and 453 nm
Permitted additives and relative limitsAccording to current legislation (2)
Aromatic polycyclic hydrocardidesAccording to CE 333/07 and subsequent amendments
Composition of fatty acids, GLC (capillary),% ISO 5508Composition of sterols, GLC (capillary),% See A.1.4
CHARACTERISTICREQUIREMENTSCHARACTERISTICREQUIREMENTS
C12:0 - Lauric AcidND - 0,1CholesterolND - 0,5
C14:0 - Myristic acidND - 0,2BrassicasteroloND - 0,2
C16:0 - Palmitic acidfrom 5 to 7,624-Methylene cholesterol§
C16:1 - Palmitoleic acid *ND - 0,3Campesterolfrom 6,5 to13,0
C17:0 - Heptadecenoic acidND - 0,2Campestanol§
C17:1 - Heptadecenoic acidND - 0,1Stigmasterolo6,0 to13,0
C18:0 - Stearic acidfrom 2,7 to 6,5Delta 7 - Campesterol§
C18:1 - Oleic acid *from 14,0 to 39,4Delta 5.23 - Stigmastadienol §
C18:2 - Linoleic acidfrom 48,3 to 74,0Clerosterol§
C18:3 - Linoleic acidND - 0,3Beta - sitosterolfrom 50,0 to 70,0
C20:0 - Arachic acidfrom 0,1 to 0,5Sitostanol§
C20:1 - Eicosenoic acidND 0,3Delta5 - AvenasteroloND - 6,9
C20:2 - Eicosadienoic acidNDDelta 7.9 (0.11) - Stigmastadienol§
C22:0 - Behenic acidfrom 0,3 to 1,5Delta 5.24 - Stigmastadienol§
C22:1 - Erucic acidND - 0,1Delta 7 - Stigmastenolfrom 6,5 to 24,0
C22:2 - Docosadienoic acidND - 0,3Delta7 - Avenasterolfrom 3,0 to 7,5
C24:0 - Lignoceric acidND - 0,5
C24 :1 - Tetracosenoic acidND

* Sum of positional isomers which may or may not be separated under the test conditions
** Codex Alimentarius
*** Law Decree n. 64/1993
(1) EC Regulation 466 of 08/03/2001
(2) At the date of publication of this standard, the D.M. n. 209 – 27.2.1996, (Official Gazette no. 96 – 24.4.1996)
§ The components indicated with § and for which no limit value has been set must not be taken into consideration for the purity assessment.
NORMATIVE REQUIREMENTS
ISO 5508 – Animal and Vegetable fats and oils – Analysis by gaschromatografy of methilesthers of fatty acids
ISO 5509 – Animal and Vegetable fats and oils – Preparation of methyl esters of fatty acids
UNI EN ISO 663 – Vegetable and animal oils and fats – Determination of the content of insoluble impurities
UNI EN ISO 8294 – vegetable and animal oils and fats – Determination of the content of copper, iron and nickel. Method for atomic absorption spectrometry with a graphite furnace.
UNI EN ISO 12193 – Vegetable and animal oils and fats – Determination of lead content. Method for atomic absorption spectrometry with a graphite furnace.

APPENDIX (information)
A BIBLIOGRAPHY
A.1 NGD REFERENCE METHODS (GRASS STANDARDS AND DERIVATIVES)
A.1.1 NGD C18- Determination of the relative density
A.1.2 NGD C31 – Determination of the refractive index
A.1.3 NGD C32- Determination of the iodine number according to Wijs
A.1.4 NGD C71 – Determination of sterol composition by capillary column gas chromatography
A.1.5 NGD C72 – Determination of sterol content by capillary column gas chromatography
A.1.6 NGD C10 – Determination of acidity
A.1.7 NGD C35 – Determination of the number of peroxides
A.1.8 NGD C8 – Determination of soaps
A.2 OTHER REFERENCE METHODS
A.2.1 AOAC 963.21 – 1990 Arsenic in food. Kjeldahl Flask Digestion. Final action.
AOAC 952.13- 1990 Arsenic in food. Silver Diethyldithiocarbamate method. Final action.