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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Ecotoxicological information

Toxicity to microorganisms

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Administrative data

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Endpoint:
activated sludge respiration inhibition testing
Type of information:
experimental study
Adequacy of study:
weight of evidence
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
guideline study with acceptable restrictions
Remarks:
The study was well documented and meets generally accepted scientific principles, but was not conducted in compliance with GLP.
Qualifier:
no guideline followed
Principles of method if other than guideline:
Non-quantitative study of effect of increasing concentration of test substance on the sewage treatment process
GLP compliance:
not specified
Analytical monitoring:
not specified
Vehicle:
no
Test organisms (species):
activated sludge
Test type:
not specified
Water media type:
not specified
Limit test:
no
Total exposure duration:
30 d
Duration:
30 d
Dose descriptor:
NOEC
Effect conc.:
200 mg/L
Nominal / measured:
nominal
Conc. based on:
not specified
Basis for effect:
other: sewage gas production volume
Duration:
30 d
Dose descriptor:
LOEC
Effect conc.:
500 mg/L
Nominal / measured:
nominal
Conc. based on:
not specified
Basis for effect:
other: sewage gas volume reduced and fermentation delayed
Details on results:
At 50 mg/L the test material showed no effects.
At 100 and 200 mg/L the start of fermentation was delayed, but constant gas volume was achieved in the same period as in the control.
At 500 mg/L the test material , the system was strongly disturbed, as indicated by a late beginning of fermentation, and greatly reduced sewage gas production volume.
Conclusions:
A non-standard study of effects on sewage treatment plant micro-organisms was conducted according to generally accepted scientific principles but lacks detail in the study report. The result of a lack of effects on respiration up to 200 mg/L provides reliable evidence.
Endpoint:
activated sludge respiration inhibition testing
Type of information:
experimental study
Adequacy of study:
weight of evidence
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
guideline study with acceptable restrictions
Remarks:
The study was well documented and meets generally accepted scientific principles, but was not conducted in compliance with GLP.
Qualifier:
no guideline followed
Principles of method if other than guideline:
Results determined in Sapromat test, derived from comparison of biochemical oxygen demand
GLP compliance:
not specified
Analytical monitoring:
not specified
Vehicle:
no
Test organisms (species):
activated sludge
Details on inoculum:
Klaeranlage-Muenchen-Grosslappen
Test type:
static
Water media type:
freshwater
Limit test:
no
Total exposure duration:
5 d
Remarks on exposure duration:
Whilst the exposure duration is not explicitly stated, BOD5 values are quoted and so it is deduced that the exposure period is at least 5 days duration.
Post exposure observation period:
Not reported
Hardness:
Not reported
Test temperature:
Not reported
pH:
Not reported
Dissolved oxygen:
Not reported
Salinity:
Not reported
Nominal and measured concentrations:
Not reported
Details on test conditions:
Test concentration series: 1, 5, 10, 50 and 100 mg/L
Reference substance (positive control):
no
Duration:
5 d
Dose descriptor:
EC0
Effect conc.:
>= 100 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
inhibition of total respiration
Remarks:
respiration rate
Validity criteria fulfilled:
not applicable
Conclusions:
A non-standard study of activated sludge respiration inhibition determined that the top concentration of 100 mg/L did not cause inhibition. The result is considered reliable.
Endpoint:
activated sludge respiration inhibition testing
Type of information:
read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
weight of evidence
Justification for type of information:
Please refer to Annex 3 of the CSR and IUCLID Section 13 for justification of read-across within the ATMP category.
Reason / purpose for cross-reference:
read-across source
Reason / purpose for cross-reference:
read-across source
Duration:
30 d
Dose descriptor:
NOEC
Effect conc.:
200 mg/L
Nominal / measured:
nominal
Conc. based on:
not specified
Basis for effect:
other: sewage gas production volume
Duration:
5 d
Dose descriptor:
EC0
Effect conc.:
>= 100 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
inhibition of total respiration
Remarks:
respiration rate

Description of key information

NOEC 200 mg/l activated sludge respiration inhibition (non-standard test, rel. 2) Henkel 1972. The data are read across from the parent acid ATMP-H.

Key value for chemical safety assessment

EC10 or NOEC for microorganisms:
200 mg/L

Additional information

A number of non-standard studies are available giving evidence that ATMP has no inhibitory effect on micro-organisms at concentrations up to ca. 200 mg/L (Henkel, 1972; Huber, 1975; Schoberl and Huber, 1988).

A study of seven Swiss WWTPs in 1996 shows a maximum concentration of ATMP in WWTP untreated influent of ca. 0.8 µmol/L, equivalent to ca. 0.26 mg/L (Nowack, 1998, see IUCLID Section 5.5.1).

The data set is further supported by the findings of an activated sludge respiration inhibition test conducted with an ammonium salt of ATMP (Worth and Mead, 1995). In this reliable study conducted in accordance with OECD Test Guideline 209, an EC50 >1000 mg/l was determined based on a 3-hour exposure period.

The acid, sodium, potassium and ammonium salts in the ATMP category are freely soluble in water. The ATMP anion can be considered fully dissociated from its sodium, potassium or ammonium cations when in dilute solution. Under any given conditions, the degree of ionisation of the ATMP species is determined by the pH of the solution. At a specific pH, the degree of ionisation is the same regardless of whether the starting material was ATMP-H, ATMP.4Na, ATMP.7K or another salt of ATMP.

 

Therefore, when a salt of ATMP is introduced into test media or the environment, the following is present (separately):

  1. ATMP is present as ATMP-H or one of its ionised forms. The degree of ionisation depends upon the pH of the media and not whether ATMP (3-5K) salt, ATMP (3-5Na) salt, ATMP-H (acid form), or another salt was used for dosing.
  2. Disassociated potassium, sodium or ammonium cations. The amount of potassium or sodium present depends on which salt was dosed.
  3. It should also be noted that divalent and trivalent cations would preferentially replace the sodium or potassium ions. These would include calcium (Ca2+), magnesium (Mg2+) and iron (Fe3+). These cations are more strongly bound by ATMP than potassium, sodium and ammonium. This could result in ATMP-dication (e.g. ATMP-Ca, ATMP-Mg) and ATMP-trication (e.g. ATMP-Fe) complexes being present in solution.