Registration Dossier
Registration Dossier
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 944-552-9 | CAS number: -
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data

Biodegradation in water: screening tests
Administrative data
Link to relevant study record(s)
- Endpoint:
- biodegradation in water: ready biodegradability
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2000.07.28 to 2000.08.25
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 301 F (Ready Biodegradability: Manometric Respirometry Test)
- Version / remarks:
- Adopted July 1992
- Deviations:
- no
- GLP compliance:
- not specified
- Specific details on test material used for the study:
- Batch no.: QX14202042-ISO
Purity: X14DesB30 contained a colloidal mixture of active ingredient, ethanol and water. According to information from sponsor, the purity of the active ingredient X14DesB30 was >89%
Expiry date 2000.31.12 - Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge, non-adapted
- Details on inoculum:
- Activated sludge collected from Usserød sewage treatment plant, Usserød, Denmark
- Duration of test (contact time):
- ca. 28 d
- Initial conc.:
- 20 mg/L
- Based on:
- test mat.
- Parameter followed for biodegradation estimation:
- O2 consumption
- Remarks:
- ThOD
- Details on study design:
- pH: 7.6
T: 22°C+/-1°C - Reference substance:
- other: sodium benzoate
- Key result
- Parameter:
- % degradation (O2 consumption)
- Remarks:
- ThOD
- Value:
- ca. 83
- Sampling time:
- 28 d
- Details on results:
- At the end of the 10 day window covering day 1-11, the BOD was 75+/-8% of the ThOD for complete oxidation of the test product. After 28 days, the BOD corresponded to 83+/-3% of the ThOD.
- Results with reference substance:
- Sodium benzoate was applied as a reference substance: After 14 days, a biodegradation of 93+/-6 % had been reached and after 28 days, a biodegradation of 99+/-9% was reached. Oxygen consumption of activity controls therefore showed that the activity of the inoculum was satisfactory
- Validity criteria fulfilled:
- yes
- Interpretation of results:
- readily biodegradable
- Conclusions:
- The biodegradation of X14DesB30 was studied according to the OECD Guideline No. 301F (Ready Biodegradability: Manometric Respirometry Test).
At the end of the 10 day window covering day 1-11, the BOD was 75+/-8% of the ThOD for complete oxidation of the test product.
After 28 days, 83+/-3% biodegradation was achieved. This is above 60% and therefore the test product is composed, or mainly composed, of readily biodegradable substances. - Executive summary:
The biodegradation of X14DesB30 was studied according to the OECD Guideline No. 301F (Ready Biodegradability: Manometric Respirometry Test).
At the end of the 10 day window covering day 1-11, the BOD was 75+/-8% of the ThOD for complete oxidation of the test product.
After 28 days, 83+/-3% biodegradation was achieved. This is above 60% and therefore the test product is composed, or mainly composed of readily biodegradable substances.
Sodium benzoate was applied as a reference substance: After 14 days a biodegradation of 93+/-6 % had been reached and after 28 days a biodegradation of 99+/-9% was reached. Oxygen consumption of activity controls therefore showed that the activity of the inoculum was satisfactory.
- Endpoint:
- biodegradation in water: ready biodegradability
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2003.01.16 to 2003.02.13
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 301 F (Ready Biodegradability: Manometric Respirometry Test)
- Version / remarks:
- Adopted July, 1992
- GLP compliance:
- yes
- Specific details on test material used for the study:
- UM 306-4990
Batch no. MMO404501
Production date 2002.12.19
Purity: > 98%
Dry matter content 94.9%
The test substance is Human Insulin. The test substance name used in the test report is Insulin. - Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge, non-adapted
- Details on inoculum:
- Activated sludge collected from Usserød sewage treatment plant, Usserød, Denmark
- Duration of test (contact time):
- 28 d
- Initial conc.:
- 20 mg/L
- Based on:
- ThOD
- Remarks:
- ThOD-NO3: 42 mg O2/L
- Details on study design:
- T: 22°C+/-1°C
- Reference substance:
- other: sodium benzoate
- Key result
- Parameter:
- % degradation (O2 consumption)
- Remarks:
- ThOD-NO3
- Value:
- 98
- Sampling time:
- 28 d
- Details on results:
- At the end of the 10 day window covering day 1-11 the BOD was 92+/-1% of the ThOD-NO3 for complete oxydation of the test product. After 28 days the BOD corresponded to 98+/-1% of the ThOD-NO3.
- Results with reference substance:
- The biodegradation of sodium benzoate was 94.4% and 97.5% after 14 and 28 days, respectively. (BOD of % of ThOD)
- Validity criteria fulfilled:
- yes
- Interpretation of results:
- readily biodegradable
- Conclusions:
- The biodegradation of Insulin was studied according to the OECD Guideline No. 301F (Ready Biodegradability: Manometric Respirometry Test).
At the end of the 10 day window covering day 1-11 the BOD was 92+/-1% of the ThOD-NO3 for complete oxydation of the test product.
After 28 days 98+/-1% biodegradation was achieved. This is above 60% and therefore Insulin is considered as readily biodegradable. - Executive summary:
The biodegradation of Insulin was studied according to the OECD Guideline No. 301F (Ready Biodegradability: Manometric Respirometry Test).
At the end of the 10 day window covering day 1-11, the BOD was 92+/-1% of the ThOD-NO3 for complete oxidation of the test product. After 28 days 98+/-1% biodegradation was achieved. This is above 60% and therefore Insulin is considered as readily biodegradable.
Sodium benzoate was applied as a reference substance: After 14 days a biodegradation of 94+/-4 % had been reached and after 28 days a biodegradation of 97+/-5% was reached. Oxygen consumption of activity controls therefore showed that the activity of the inoculum was satisfactory.
- Endpoint:
- biodegradation in water: ready biodegradability
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Read across: Please refer to setion "Justification for type of information"
- Reason / purpose for cross-reference:
- read-across source
- Reason / purpose for cross-reference:
- read-across source
- Reason / purpose for cross-reference:
- read-across source
- Key result
- Parameter:
- % degradation (O2 consumption)
- Value:
- > 60
- Sampling time:
- 28 d
- Remarks on result:
- other:
- Remarks:
- study result
- Validity criteria fulfilled:
- not applicable
- Interpretation of results:
- readily biodegradable
- Conclusions:
- Liraglutide precursor is predicted to be readily biodegradable based on the results in the ready biodegradability studies of the source substances (S1, S2, S3).
The biodegradation of Liraglutide precursor is assumed to follow the same pattern as that of the source substances because of the high degree of structural similarity.
The results from the ready biodegradability studies with the source substances revealed a biodegradability of 98% (S1), 103% (S2) and 83% (S3). - Executive summary:
The biodegradation of Liraglutide precursor is assumed to follow the same pattern as that of the source substances because of the high degree of structural similarity:
• Liraglutide precursor and the source substances belong to the same chemical categories: human insulins, polypeptides and proteins
• Liraglutide precursor and the source substances are composed of polypeptide containing amino acids
• The ready biodegradability prediction is supported by the fact that the amino acids in Liraglutide precursor and the source substances are readily biodegradable.
Liraglutide precursor is predicted to be readily biodegradable based on the results in the ready biodegradability studies of the source substances (S1, S2, S3).
The results from the ready biodegradability studies with the source substances revealed a biodegradability of 98% (S1), 103% (S2) and 83% (S3).
- Endpoint:
- biodegradation in water: ready biodegradability
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2000.07.28 to 2000.08.25
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 301 F (Ready Biodegradability: Manometric Respirometry Test)
- Version / remarks:
- Adopted July 1992
- Deviations:
- no
- GLP compliance:
- yes
- Specific details on test material used for the study:
- Batch no.: QA204979
Expiry date 2000.12.31
MI3 contained 297 mg active ingredient per g of a purity of 98.62% - Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge, non-adapted
- Details on inoculum:
- Activated sludge, municipal waste water treatment plant, Usserød, Denmark
- Duration of test (contact time):
- ca. 28 d
- Initial conc.:
- 20 mg/L
- Based on:
- test mat.
- Parameter followed for biodegradation estimation:
- O2 consumption
- Remarks:
- ThOD
- Details on study design:
- pH: 7.6
T: 22°C+/-1°C - Reference substance:
- other: sodium benzoate
- Key result
- Parameter:
- % degradation (O2 consumption)
- Remarks:
- ThOD
- Value:
- 103
- Sampling time:
- 28 d
- Remarks on result:
- other: 103+/-16%
- Details on results:
- At the end of the 10 day window covering day 1-11, the BOD was 90+/-7% of the ThOD for complete oxidation of the test product. After 28 days, the BOD corresponded to 103+/-16% of the ThOD. From day 23 to 25 the temperature dropped to 20°C. However, the degradation had already reached the pass level at this time, and therefore it did not influence the result.
- Results with reference substance:
- Sodium benzoate was applied as a reference substance: After 14 days, a biodegradation of 93+/-6 % had been reached and after 28 days, a biodegradation of 99+/-9% was reached. The oxygen consumption in activity controls showed that the activity of the inoculum was satisfactory.
- Validity criteria fulfilled:
- yes
- Interpretation of results:
- readily biodegradable
- Conclusions:
- The biodegradation of MI3 was studied according to the OECD Guideline No. 301F.
After 28 days, 103+/-16% biodegradation was achieved. This is above 60% and therefore MI3 is considered as readily biodegradable. - Executive summary:
The biodegradation of MI3 was studied according to the OECD Guideline No. 301F (Ready Biodegradability: Manometric Respirometry Test).
At the end of the 10 day window covering day 1-11, the BOD was 90+/-7% of the ThOD for complete oxidation of the test product.
After 28 days, 103+/-16% biodegradation was achieved. This is above 60% and therefore MI3 is considered as readily biodegradable.
Sodium benzoate was applied as a reference substance: After 14 days, a biodegradation of 93+/-6 % had been reached and after 28 days, a biodegradation of 99+/-9% was reached. Oxygen consumption of activity controls therefore showed that the activity of the inoculum was satisfactory.
Referenceopen allclose all
Description of key information
The biodegradation of Liraglutide precursor is assumed to follow the same pattern as that of the source substances because of the high degree of structural similarity:
• Liraglutide precursor and the source substances belong to the same chemical categories: human insulins, polypeptides and proteins
• Liraglutide precursor and the source substances are composed of polypeptide containing amino acids
• The ready biodegradability prediction is supported by the fact that the amino acids in Liraglutide precursor and the source substances are readily biodegradable.
Liraglutide precursor is predicted to be readily biodegradable based on the results in the ready biodegradability studies of the source substances (S1, S2, S3).
The results from the ready biodegradability studies with the source substances revealed a biodegradability of 98% (S1), 103% (S2) and 83% (S3).
Key value for chemical safety assessment
- Biodegradation in water:
- readily biodegradable
Additional information
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.
