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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
basic toxicokinetics
Type of information:
calculation (if not (Q)SAR)
Remarks:
Migrated phrase: estimated by calculation
Adequacy of study:
key study
Study period:
2001
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: The toxicokinetic assessment was derived from available physiochemical and toxicity data, not based on actual experimental examinations..

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2001
Report date:
2001

Materials and methods

Objective of study:
toxicokinetics
Test guideline
Qualifier:
no guideline followed
Deviations:
not applicable
Principles of method if other than guideline:
Toxicokinetic assessment was performed based on physicochemical properties and available toxicity data
GLP compliance:
not specified

Test material

Constituent 1
Details on test material:
- Physical state: blue powder
Radiolabelling:
no

Test animals

Species:
other: Prediction toxicokinetic behavior based on physicochemical properties and available toxicity data.
Strain:
other: Prediction toxicokinetic behavior based on physicochemical properties and available toxicity data.
Sex:
not specified

Administration / exposure

Route of administration:
other: Prediction toxicokinetic behavior based on physicochemical properties and available toxicity data.
Vehicle:
unchanged (no vehicle)
Duration and frequency of treatment / exposure:
Not Applicable
Doses / concentrations
Remarks:
Doses / Concentrations:
Not Applicable
No. of animals per sex per dose / concentration:
Not Applicable
Control animals:
other: Prediction toxicokinetic behavior based on physicochemical properties and available toxicity data.
Positive control reference chemical:
Not applicable
Details on study design:
Not applicable
Details on dosing and sampling:
Not applicable
Statistics:
Prediction toxicokinetic behavior based on physicochemical properties and available toxicity data.

Results and discussion

Preliminary studies:
Not Applicable

Toxicokinetic / pharmacokinetic studies

Details on absorption:
Not Applicable
Details on distribution in tissues:
Not Applicable
Transfer into organs
Transfer type:
other: Prediction toxicokinetic behavior based on physicochemical properties and available toxicity data.
Observation:
not determined
Details on excretion:
Not Applicable
Toxicokinetic parameters
Toxicokinetic parameters:
other: Prediction toxicokinetic behavior based on physicochemical properties and available toxicity data.

Metabolite characterisation studies

Metabolites identified:
not measured
Details on metabolites:
Not Applicable

Any other information on results incl. tables

The information used for toxicokinetic assessment was listed below:

Physicochemical Property And Toxicity Test Data Of 1779u

Property

Value

Molecular Formula

(C32H15CuN8).(O3S)x(C38H80N)x, x= 1.2~1.4

Physical

Blue powder

Particle Size

46.6% passed through a 38mm sieve

Melting Point

> 250oC

Specific Gravity

1.26 g/cm3

Water Solubility

< 0.24 mg/L

Acute Oral Toxicity, Rat

> 5000 mg/kg

Acute Dermal Toxicity, Rat

> 2000 mg/kg

Skin Irritation, Rabbit

Not classified

Eye Irritation, Rabbit

Not classified

Skin Sensitization, Guinea-pig

Not classified

Sub-acute Toxicity, Rat

NOEL 1000 mg/kg/day

Inhibition of Activated Sludge Respiration

LC50 > 1000 mg/L

Algal Toxicity

NOEC > 0.24 mg/L

 

There was evidence of systemic toxicity in the repeat dose toxicity study at 1000 mg/kg/day, with effects seen in the spleen, stomach and liver indicating that absorption, possible metabolism and excretion process were involved. 

Applicant's summary and conclusion

Conclusions:
Interpretation of results (migrated information): other: predicted no bioaccumulation.
Based on the representative chemical structure and available physicochemical property and toxicity data, a prediction of toxicokinetic behavior was created, and absorption, distribution to distance organs, possible metabolism and excretion process were involved.
Executive summary:

The test material has a molecular weight range from 1332.4 (x=1.2) to 1458.6 (x=1.4). It is poorly water soluble (< 0.24 mg/L). Based on the representative chemical structure and available physicochemical property and toxicity data, a prediction of toxicokinetic behavior was created