Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
acute toxicity: other routes
Type of information:
experimental study
Adequacy of study:
disregarded due to major methodological deficiencies
Reliability:
3 (not reliable)
Rationale for reliability incl. deficiencies:
other: Documentation insufficient for assessment

Data source

Reference
Reference Type:
secondary source
Title:
The influence of chain length on the metabolic fate of condensed phosphates
Author:
Gosselin RE, Megirian R
Year:
1955
Bibliographic source:
J Pharmacol Exp Ther. 115(4):402-7; PMID: 13272192

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
The respective LD50 values are cited from another publication, namely: Gosselin RE, Tidball CS, Megirian R, Maynard EA, Downs WL, Hodge HC, Metabolic acidosis and hypocalcemia as toxic manifestations of polymeric phosphates, J Pharmacol Exp Ther. 1953 ;108(1):117-27.
GLP compliance:
no
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Sodium metaphosphate
EC Number:
233-343-1
EC Name:
Sodium metaphosphate
Cas Number:
10124-56-8
Molecular formula:
H6O18P6.6Na
IUPAC Name:
Sodium metaphosphate
Details on test material:
- Name of test material (as cited in study report): hexametaphosphate; NaMP-6

Test animals

Species:
rat
Strain:
not specified
Sex:
female
Details on test animals or test system and environmental conditions:
no data

Administration / exposure

Route of administration:
intraperitoneal
Vehicle:
not specified
Details on exposure:
single i.p. injections in rats weighing 200 to 300 grams.
Doses:
no data
No. of animals per sex per dose:
no data
Control animals:
not specified
Statistics:
All concentrations given were converted from grams phosphorus (as they were expressed in the article) to grams of the respective test compound.

Results and discussion

Effect levels
Sex:
female
Dose descriptor:
LD50
Effect level:
632.11 mg/kg bw
Remarks on result:
other: Calculated from the given value (59 mg P/kg bw) using the molecular masses of phosphorus (90.97 g/mol) and sodium hexametaphosphate (611.77 g/mol).
Other findings:
The main cause for the observed mortalities seems to be severe metabolic acidosis due to hydrolytic release of phosphate / phosphoric acid.

Applicant's summary and conclusion

Conclusions:
This article cites a LD50 (i.p. rat) for sodium hexametaphosphate of 632.11 mg/kg bw, as calculated from the given value (192 mg/kg bw) which is expressed as amount of phosphorus. The main cause for the observed mortalities seems to be severe metabolic acidosis due to hydrolytic release of phosphate / phosphoric acid.
Executive summary:

This article gives information on the acute toxicity of sodium hexametaphosphate after single i.p. injection. The given value is based on an earlier publication of the same author (Gosselin RE, Tidball CS, Megirian R, Maynard EA, Downs WL, Hodge HC, Metabolic acidosis and hypocalcemia as toxic manifestations of polymeric phosphates, J Pharmacol Exp Ther. 1953 ;108(1):117-27) which can be assumed to give further details on the experimental procedure.

The cited value for the LD50 (i.p., rat) is 192 mg phosphorus per kg body weight which can be converted into 632.11 mg/kg bw sodium hexametaphosphate using their molecular masses of 30.97 and 611.77 mg/kg bw, respectively. The main cause for the observed mortalities seems to be severe metabolic acidosis due to hydrolytic release of phosphate / phosphoric acid.