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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Administrative data

Description of key information

Acute oral toxicity with Dresinate 835 A (Reaction mass of Resin acids and Rosin acids, hydrogenated, sodium salts and sodium [1R-(1a,4aß,10aa)]-1,2,3,4,4a,9,10,10a-octahydro-7-isopropyl-1,4a-dimethylphenanthren-1-carboxylate) (OECD 401, EU Method B.1): LD50 >2000 mg/kg bw.
Acute dermal toxicity with Resin 835 A (Reaction mass of Rosin, hydrogenated and [1R-(1a,4aß,10aa)]-1,2,3,4,4a,9,10,10a-octahydro-7-isopropyl-1,4a-dimethylphenanthren-1-carboxylic acid)(OECD 402, EU Method B.3): >2000 mg/kg bw

Key value for chemical safety assessment

Acute toxicity: via oral route

Endpoint conclusion
Dose descriptor:
LD50
Value:
2 000 mg/kg bw

Acute toxicity: via dermal route

Endpoint conclusion
Dose descriptor:
LD50
Value:
2 000 mg/kg bw

Additional information

Acute oral toxicity with the related substance Dresinate 835 A ( Reaction mass of Resin acids and Rosin acids, hydrogenated, sodium salts and sodium [1R-(1a,4aß,10aa)]-1,2,3,4,4a,9,10,10a-octahydro-7-isopropyl-1,4a-dimethylphenanthren-1-carboxylate): The LD50 was 2130 mg/kg bw for males and >2000 mg/kg bw for females

Mortality occurred at 2000 mg/kg bw (2/5 males, 1/5 females) and at 2240 mg/kg bw (3/5 males). No mortality occurred at 1600 mg/kg bw.

Acute dermal toxicity with the related substance Resin 835 A ( Reaction mass of Rosin, hydrogenated and [1R-(1a,4aß,10aa)]-1,2,3,4,4a,9,10,10a-octahydro-7-isopropyl-1,4a-dimethylphenanthren-1-carboxylic acid): The LD50 was >2000 mg/kg bw and no adverse effects were noted in the animals. A justification for read-across is given in section 13, Assessment reports.

Justification for classification or non-classification

According to Commission Directive 2001/59/EC and to EU-GHS the test item does not require classification for acute oral toxicity.