Registration Dossier

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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

- An up to date acute oral toxicity study is available that reports no toxicity at the maximum dose of 2000 mg/kg bw.
- No studies on dermal toxicity are available.
- A set of non-standard studies with single inhalation exposure are available, but not suitable for setting a LC50.
- Only airborne exposures to soluble beryllium compounds are associated with acute beryllium disease. Exposure to beryllium metal has not been found to be associated with acute or short-term respiratory reactions.
Eisenbud M. The Standard for Control of Chronic Beryllium Disease. Appl Occup Environ Hyg 13(1): 25–31 (1998).

Key value for chemical safety assessment

Acute toxicity: via oral route

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

Additional information

Justification for classification or non-classification

- oral toxicity: Be metal is non-toxic via the oral route and does not need to be classified for acute oral toxicity according to CLP

(REGULATION (EC) No 1272/2008 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL) as implementation

of UN-GHS in the EU.

- dermal toxicity: The dermal toxicity Be metal cannot be assessed as no reliable study is available. Given the absence of oral toxicity a classification for acute dermal toxicity is deemed unjustified according to CLP (REGULATION (EC) No 1272/2008 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL) as implementation of UN-GHS in the EU.

- inhalation toxicity: Beryllium metal is non-toxic via the inhalation route and does not need to be classified for acute oral toxicity according to CLP (REGULATION (EC) No 1272/2008 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL)