Registration Dossier
Registration Dossier
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EC number: 222-093-9 | CAS number: 3344-18-1
Endpoint summary
Administrative data
Description of key information
Read across from a fairly limited reliable report of a non-standard oral feeding study using citric acid in the rat, conducted without GLP compliance, identified 5-day NOAEL values in the rat of 4000 mg/kg bw/day (which corresponds to 4680 mg tri magnesium dicitrate /kg (bw)/d*). (Hoffman, 1976; rel 2) In addition read across from a fairly limited reliable report of a non-standard 10 day feeding study using citric acid conducted without GLP compliance in mice and rats, identified 10-day NOAEL values in the mouse of 1000 and 4000 g/kg bw/day, (which corresponds to 1170 and 4680 mg tri magnesium dicitrate /kg (bw)/d*)respectively.
* based on a conversion factor of 1.17 derived by: (Mass of one mole of salt)/(mass of citric acid produced when trimagnesium dicitrate dissociates) = 451.1 / (2 * 192.9) = 1.29.
Key value for chemical safety assessment
Additional information
In accordance with Annex 11, Section 1 of REACH, the repeated dose toxicity endpoint has been waived has been waived based on the following information:
(1) The available read across repeat dose toxicity studies with citric acidin their diet reported no treatment related abnormalities.
(2) The low acute toxicity of citric acid LD50 = 5.4g/kg
(3) A long history of human exposure to citric acid and its derived salts.
In conclusion, the available read across data from citric acid, is sufficient to fulfil the information requirements for this endpoint. Information available in the public domain on tests carried out on other salts of this metal indicates that the magnesium ions are not expected to contribute to the toxicity of the substance. Additionally, the substance will dissociate when in solution, so test organisms exposure will be to the citrate and the metal ions separately.
Therefore, the hazard assessment fortri magnesium dicitrate canbe based on the properties of citric acid. All of which are sufficient to fulfil the requirements for long term repeat dose toxicity.
Justification for classification or non-classification
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