Residue Monograph prepared by the meeting of the Joint FAO/WHO Expert Committee on Food Additives (JECFA), 82 nd meeting 2016.

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Residue Monograph prepared by the meeting of the Joint FAO/WHO Expert Committee on Food Additives (JECFA), 82 nd meeting 2016 Allura Red AC This monograph was also published in: Compendium of Food Additive Specifications. Joint FAO/WHO Expert Committee on Food Additives (JECFA), 82 nd meeting 2016. FAO JECFA Monographs 19

1 of 4 ALLURA RED AC Prepared at the 82 nd JECFA and published in JECFA Monograph 19 (2016) superseding specifications prepared at the 28th JECFA (1984) and published in FNP 31/1 (1984) and FNP 52 (1992). Metals and arsenic specifications revised at the 59th JECFA (2002). An ADI of 0-7 mg/kg bw was established at the 25th JECFA (1981). SYNONYMS INS No. 129, CI Food Red 17, CI (1975) No.16035, FD&C Red No. 40 DEFINITION Consists of disodium 6-hydroxy-5-(2-methoxy-5-methyl-4- sulfonatophenylazo)-2-naphthalenesulfonate and subsidiary colouring matters together with sodium chloride and/or sodium sulfate as the principal uncoloured components. It is manufactured by coupling diazotized 4- amino-5-methoxy-2-methylbenzenesulfonic acid with 6-hydroxy-2- naphthalene sulphonic acid. The resulting dye is purified and isolated as the sodium salt. May be converted to the corresponding aluminium lake in which case only the General Specifications for Aluminium Lakes of Colouring Matters applies. Chemical names Disodium 6-hydroxy-5-(2-methoxy-5-methyl-4-sulfonatophenylazo)-2- naphthalenesulfonate C.A.S. number 25956-17-6 Chemical formula C 18 H 14 N 2 Na 2 O 8 S 2 Structural formula Formula weight 496.43 Assay DESCRIPTION FUNCTIONAL USES CHARACTERISTICS Not less than 85% total colouring matters Dark red powder or granules Colour

2 of 4 IDENTIFICATION Solubility Spectrophotometry PURITY Loss on drying, chloride and sulfate as sodium salts Water insoluble matter Subsidiary colouring matters Organic compounds other than colouring matters Freely soluble in water, insoluble in ethanol Maximum wavelength approximately 501 nm. Determine the UV-visible absorption spectrum of the sample solution dissolved in water. Not more than 15% as total amount Determine according to chloride as sodium chloride, sulfate as sodium sulfate, and water content (loss on drying at 135 C) in Volume 4 (under Specific Methods, Food Colours ). Not more than 0.2% Not more than 3% See description under TESTS Not more than 0.3% of sodium 6-hydroxy-2-naphthalenesulfonate Not more than 0.2% of 4-amino-5-methoxy-2-methylbenzenesulfonic acid Not more than 1.0% of disodium 6,6'-oxybis(2-naphthalenesulfonate) See description under TESTS Unsulfonated primary aromatic amines Ether extractable matter Lead TESTS PURITY TESTS Subsidiary colouring matters Not more than 0.01% calculated as aniline Not more than 0.2% Not more than 2 mg/kg Determine using a method appropriate to the specified level. The selection of sample size and method of sample preparation may be based on the principles of the method described in Volume 4 (under General Methods, Metallic Impurities ). Determine subsidiary colouring matters by reversed-phase HPLC using the following conditions: Column: C18 (250 mm x 4.6 mm i.d., 5 µm particle size) Eluent A: 0.05 M ammonium acetate Eluent B: methanol Injection volume: 20 μl Detector: UV-visible/PDA at 500 nm Flow rate: 1 ml/min

3 of 4 Gradient: Min %A %B 0 95 5 3 95 5 19 25 75 20 0 100 25 0 100 Standards: Higher sulfonated subsidiary colors: 3-Hydroxy-4-[(2-methoxy-5-methyl-4-sulfophenyl)azo]-2,7- naphthalenedisulfonic acid, trisodium salt Wako, Cat. No. 037-23311 or equivalent 7-Hydroxy-8-[(2-methoxy-5-methyl-4-sulfophenyl)azo]-1,3- naphthalenedisulfonic acid, trisodium salt Wako, Cat. No. 034-23321 or equivalent Lower sulfonated subsidiary color: 4-[(2-Hydroxy-1-naphthalenyl)azo]-5-methoxy-2-methylbenzenesulfonic acid, sodium salt Wako, Cat. No. 030-23301 or equivalent Organic compounds other than colouring matters Sample preparation: Dissolve 150 mg of sample in 100 ml of 0.05 M ammonium acetate. Determine sodium 6-hydroxy-2-naphthalenesulfonate, 4-amino-5- methoxy-2-methylbenzenesulfonic acid, and disodium 6,6'-oxybis(2- naphthalenesulfonate) by reversed-phase HPLC (under Specific Methods, Food Colours ) using the following conditions: Column: C18 (250 mm x 4.6 mm i.d., 5 µm particle size) Eluent A: 0.05 M ammonium acetate Eluent B: methanol Injection volume: 20 μl Detector: UV-visible/PDA at 235 and 254 nm Flow rate: 1 ml/min Gradient: Min %A %B 0 95 5 3 95 5 19 25 75 20 0 100 25 0 100 Note: A general gradient for the separation of organic compounds other than colouring matters in food colours is given in Vol. 4. Analyst may use above gradient for the analytes in Allura Red AC. Standards: Sodium 6-hydroxy-2-naphthalenesulfonate Wako, Cat. No. 010-25141 or equivalent 4-Amino-5-methoxy-2-methylbenzenesulfonic acid Wako, Cat. No. 196-17301 or equivalent Disodium 6,6'-oxybis(2-naphthalenesulfonate) Santa Cruz

4 of 4 Biotechnology, Cat. No. 210553 or equivalent METHOD OF ASSAY Sample preparation: Dissolve 150 mg of sample in 100 ml of 0.05 M ammonium acetate. Determine total colouring matters content by spectrophotometry using Procedure 1 in Volume 4 (under Specific Methods, Food Colours ) and an appropriate solvent. Using water as the solvent: absorptivity (a) = 54.0 l/(g cm) and wavelength of maximum absorbance = 501 nm.