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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Endpoint:
repeated dose toxicity: inhalation
Remarks:
other: Assessment
Type of information:
other: Expert Assessment
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Expert Assessment as opposed to experimental result

Data source

Reference
Reference Type:
other: Expert Assessment
Title:
Unnamed
Year:
2015
Report date:
2015

Materials and methods

Principles of method if other than guideline:
Assessment
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Reaction mass of disodium metasilicate and sodium hydroxide
EC Number:
910-245-3
Molecular formula:
NaOH Na2SiO3
IUPAC Name:
Reaction mass of disodium metasilicate and sodium hydroxide

Results and discussion

Effect levels

Remarks on result:
not measured/tested
Remarks:
It has an aqueous pH of >13; the high pH makes testing by the inhalation route inappropriate for animal welfare reasons

Target system / organ toxicity

Critical effects observed:
not specified

Any other information on results incl. tables

Assessment

Applicant's summary and conclusion

Executive summary:

This substance is a multi-constituent substance consisting of sodium hydroxide (215-185-5, 1310-73-2) and disodium metasilicate (229-912-9, 6834-92-0). It is the by-product of a reaction between zircon (EC no 239-019-6) and sodium hydroxide; after hydrolysis, this substance is the water-soluble fraction. It has an aqueous pH of >13; the high pH makes testing by the inhalation route inappropriate for animal welfare reasons. In addition, REACH Annex VIII requires testing by “the most appropriate route of exposure” where acute testing additional to the oral route is appropriate. As well as animal welfare considerations, testing by the inhalation route would be inappropriate as the severe irritancy affect would mask any systemic toxicity effects. An inhalation toxicity study has been conducted for silicic acid, potassium salt (215-199-1), which showed an LC50 of >2.06 mg/L air. Thus, running an acute inhalation study would add nothing to the hazard assessment for this substance, and risk management measures are driven primarily by its corrosive nature due to the high pH. Determination of acute toxicity by the inhalation route is therefore considered inappropriate and unnecessary.

The above should be considered as an expert statement to waive the requirement for testing for acute toxicity by the inhalation route REACH Annex VIII for endpoint 8.6.1.