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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
acute toxicity: other routes
Type of information:
experimental study
Adequacy of study:
weight of evidence
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
abstract

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1976
Report date:
1976

Materials and methods

Principles of method if other than guideline:
No information available.
GLP compliance:
no
Remarks:
pre-GLP

Test material

Constituent 1
Chemical structure
Reference substance name:
Reaction products of 6-hydroxy-5-nitrosonaphthalene-2-sulfonic acid, chelated with iron (3+), sodium salts.
EC Number:
943-973-5
Molecular formula:
not available being an UVCB substance
IUPAC Name:
Reaction products of 6-hydroxy-5-nitrosonaphthalene-2-sulfonic acid, chelated with iron (3+), sodium salts.

Test animals

Species:
mouse
Strain:
not specified
Sex:
not specified

Administration / exposure

Route of administration:
intraperitoneal
Vehicle:
water
Doses:
10-50 % acqueous suspensions.
Control animals:
not specified
Details on study design:
- Duration of observation period following administration: 14 days

Results and discussion

Effect levels
Sex:
not specified
Dose descriptor:
LD50
Effect level:
> 1 500 - < 2 100 mg/kg bw
Based on:
test mat.
Other findings:
dyspnea, apathy, agitation, tumbling, cramps, partially belly-side position, tonic spasms, skin stained systemically green, urine stained green, intrabdominal colouration, general condition was bad.

Applicant's summary and conclusion

Conclusions:
1500 mg/kg b.w.< LD50 ( mouse, i.p.) < 2100 mg/kg b.w.
Executive summary:

Method

The acute toxicity, after intraperitoneal injection of the substance to mice, was evaluated. The animals were observed for 14 days.

Observations

The following signs were observed: dyspnea, apathy, agitation, tumbling, cramps, partially belly-side position, tonic spasms, skin stained systemically green, urine stained green, intrabdominal colouration, general condition was bad.

Results

The LD50 of the substance for the mouse over the period of 14 days is 1500 - 2100 mg/kg b.w.