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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Link to relevant study record(s)

Description of key information

Due to the high water solubility and the low logP value, dermal uptake will be very unlikely and a ratio of 0.1 for oral to dermal absorption is therefore used for DNEL derivation. For the oral and inhalatory route, the default absorption values from the REACH guidance (Chapter 8, R.8.4.2) are used for DNEL derivation, namely: 100% for inhalation, and 50% for oral absorption.

Key value for chemical safety assessment

Bioaccumulation potential:
low bioaccumulation potential
Absorption rate - oral (%):
Absorption rate - dermal (%):
Absorption rate - inhalation (%):

Additional information

Since no toxicokinetic studies are available for the test substance the following assessment is based on the available physicochemical properties and results from other toxicological studies.

The test substance is a dark red powder with a molecular weight of 1030.98 g/mol. The calculated log Pow value is -6.1 and the solubility in water is 86.3 g/L.

Gastrointestinal absorption: Water-soluble substances may readily dissolve into the gastrointestinal fluids. However, absorption of very hydrophilic substances by passive diffusion may be limited by the rate at which the substance partitions out of the gastrointestinal fluid. The high molecular weight of the test substance does also not favor absorption. However, the 28-days repeated dose study shows toxic effects in the kidneys of rats receiving 1000 mg/kg/day (increased kidney weight, cytoplasmic vacuolization of cortical collecting tubules, and reddish discolored urine).

Dermal absorption: The high water solubility (>10000 mg/L) and the log Pow lower than -1 suggests that the substance may be too hydrophilic to cross the lipid rich environment of the stratum corneum. Furthermore, in the available acute dermal study, no effects were observed. Therefore, dermal uptake will be very unlikely and a ratio of 0.1 for oral to dermal absorption is therefore used for DNEL derivation.

Respiratory absorption: No experimental data is available concerning the respiratory hazard of the test substance. Water soluble dust would readily diffuse/dissolve into the mucus lining of the respiratory tract. However, very hydrophilic substances can be transported out of the respiratory tract, when molecular weights are larger than 200. Furthermore, the low log Pow does not favor absorption. However, signs of toxic effects in the kidney present in the oral toxicity study indicates the potential for absorption following ingestion and it is therefore possible that the substance will also be absorbed if it is inhaled.