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Commission Directive 2011/3/EU (repealed)Show full title

Commission Directive 2011/3/EU of 17 January 2011 amending Directive 2008/128/EC laying down specific purity criteria on colours for use in foodstuffs (Text with EEA relevance) (repealed)

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ANNEXU.K.

In Annex I to Directive 2008/128/EC the entry on E 160 d is replaced by the following:

E 160 D LYCOPENE

(i) synthetic lycopene
SynonymsLycopene from chemical synthesis
DefinitionSynthetic lycopene is a mixture of geometric isomeres of lycopenes and is produced by the Wittig condensation of synthetic intermediates commonly used in the production of other carotenoids used in food. Synthetic lycopene consists predominantly of all-trans-lycopene together with 5-cis-lycopene and minor quantities of other isomers. Commercial lycopene preparations intended for use in food are formulated as suspensions in edible oils or water-dispersible or water- soluble powder.
Colour Index No75125
EINECS207-949-1
Chemical nameΨ,Ψ-carotene, all-trans-lycopene, (all-E)-lycopene, (all-E)-2,6,10,14,19,23,27,31-octamethyl-2,6,8,10,12,14,16,18,20,22,24,26,30-dotriacontatridecaene
Chemical formulaC40H56
Molecular weight536,85
Assay

Not less than 96 % total lycopenes (not less than 70 % all-translycopene)

E1 cm 1 % at 465 - 475 nm in hexane (for 100 % pure all-translycopene) is 3 450

DescriptionRed crystalline powder
Identification
SpectrophotometryA solution in hexane shows an absorption maximum at approximately 470 nm
Test for carotenoidsThe colour of the solution of the sample in acetone disappears after successive additions of a 5 % solution of sodium nitrite and 1N sulphuric acid
SolubilityInsoluble in water, freely soluble in chloroform
Properties of 1 % solution in chloroformIs clear and has intensive red-orange colour
Purity
Loss on dryingNot more than 0,5 % (40 °C, 4 h at 20 mm Hg)
Apo-12’-lycopenalNot more than 0,15 %
Triphenyl phosphine oxideNot more than 0,01 %
Solvent residues

Methanol not more than 200 mg/kg,

Hexane, Propan-2-ol: Not more than 10 mg/kg each.

Dichloromethane: Not more than 10 mg/kg (in commercial preparations only)

LeadNot more than 1 mg/kg
(ii) from red tomatoes
SynonymsNatural Yellow 27
Definition

Lycopene is obtained by solvent extraction of red tomatoes (Lycopersicon esculentum L.) with subsequent removal of the solvent. Only the following solvent may be used:

carbon dioxide, ethyl acetate, acetone, propan-2-ol, methanol, ethanol, hexane. The major colouring principle of tomatoes is lycopene, minor amounts of other carotenoid pigments may be present. Besides the colour pigments the product may contain oil, fats, waxes and flavour components naturally occurring in tomatoes.

Colour Index No75125
EINECS207-949-1
Chemical nameΨ,Ψ-carotene, all-trans-lycopene, (all-E)-lycopene, (all-E)-2,6,10,14,19,23,27,31-octamethyl-2,6,8,10,12,14,16,18,20,22,24,26,30-dotriacontatridecaene
Chemical formulaC40H56
Molecular weight536,85
Assay

E1 cm 1 % at 465 - 475 nm in hexane (for 100 % pure all-translycopene) is 3 450.

Content not less than 5 % total colouring matters

DescriptionDark red viscous liquid
Identification
SpectrophotometryMaximum in hexane at ca 472 nm
Purity
Solvent residues

Propane-2-ol

Hexane

Acetone

Ethanol

Methanol

Ethylacetate

Not more than 50 mg/kg, singly or in combination

Sulphated ashNot more than 1 %
MercuryNot more than 1 mg/kg
CadmiumNot more than 1 mg/kg
ArsenicNot more than 3 mg/kg
LeadNot more than 2 mg/kg
(iii) from Blakeslea trispora
SynonymsNatural Yellow 27
DefinitionLycopene from Blakeslea trispora is extracted from the fungal biomass and purified by crystallisation and filtration. It consists predominantly of all-trans-lycopene. It also contains minor quantities of other carotenoids. Isopropanol and isobutyl acetate are the only solvents used in the manufacture. Commercial lycopene preparations intended for use in food are formulated as suspensions in edible oils or water-dispersible or water-soluble powder.
Colour Index No75125
EINECS207-949-1
Chemical nameΨ,Ψ-carotene, all-trans-lycopene, (all-E)-lycopene, (all-E)-2,6,10,14,19,23,27,31-octamethyl-2,6,8,10,12,14,16,18,20,22,24,26,30-dotriacontatridecaene
Chemical formulaC40H56
Molecular weight536,85
Assay

Not less than 95 % total lycopenes and not less than 90 % all-translycopene of all colouring matters

E1 cm 1 % at 465 - 475 nm in hexane (for 100 % pure all-translycopene) is 3 450

DescriptionRed crystalline powder
Identification
SpectrophotometryA solution in hexane shows an absorption maximum at approximately 470 nm
Test of carotenoidsThe colour of the solution of the sample in acetone disappears after successive additions of a 5 % solution of sodium nitrite and 1N sulphuric acid
SolubilityInsoluble in water, freely soluble in chloroform
Properties of 1 % solution in chloroformIs clear and has intensive red-orange colour
Purity
Loss on dryingNot more than 0,5 % (40 °C, 4 h at 20 mm Hg)
Other carotenoidsNot more than 5 %
Solvent residues

Propan-2-ol: Not more than 0,1 %

Isobutyl acetate: Not more than 1,0 %

Dichloromethane: Not more than 10 mg/kg (in commercial preparations only)

Sulphated ashNot more than 0,3 %
LeadNot more than 1 mg/kg

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