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Diss Factsheets
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EC number: 215-199-1 | CAS number: 1312-76-1
- 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
Toxicity to microorganisms
Administrative data
Link to relevant study record(s)
- Endpoint:
- toxicity to microorganisms
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Principles of method if other than guideline:
- Method: other: growth inhibition test; Umweltbundesamt, Berlin: Bewertung wassergefaehrdender Stoffe. Erarbeitet von der ad-hoc-Arbeitsgruppe 1 "Bewertung wassergefaehrdender Stoffe"
- GLP compliance:
- yes
- Remarks:
- TNO Division of Technology for Society, Delft, The Netherlands
- Analytical monitoring:
- no
- Test organisms (species):
- Pseudomonas putida
- Details on test conditions:
- Type: aquatic
- Duration:
- 18 h
- Dose descriptor:
- EC0
- Effect conc.:
- > 3 480 mg/L
- Basis for effect:
- growth inhibition
- Remarks on result:
- other: for neutralised concentrations (pH 7.6-7.8)
- Duration:
- 18 h
- Dose descriptor:
- EC0
- Effect conc.:
- > 348 mg/L
- Basis for effect:
- growth inhibition
- Remarks on result:
- other: for unneutralised concentrations (pH>9)
- Endpoint:
- toxicity to microorganisms
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Guideline study, but no information on purity of test substance.
- Principles of method if other than guideline:
- Method: other: DIN 38412, Teil 27 (Bacterial oxygen consumption test)
- GLP compliance:
- yes
- Remarks:
- Henkel KGaA, Forschung Biologie Ökologie.
- Test organisms (species):
- Pseudomonas putida
- Duration:
- 30 min
- Dose descriptor:
- EC0
- Effect conc.:
- 3 454 mg/L
- Endpoint:
- toxicity to microorganisms
- Type of information:
- read-across based on grouping of substances (category approach)
- Adequacy of study:
- key study
- Justification for type of information:
- Refer to category justification provided in IUCLID section 13.
- Reason / purpose for cross-reference:
- read-across source
- Reason / purpose for cross-reference:
- read-across source
- Duration:
- 18 h
- Dose descriptor:
- EC0
- Effect conc.:
- > 3 480 mg/L
- Basis for effect:
- growth inhibition
- Remarks on result:
- other: for neutralised concentrations (pH 7.6-7.8)
- Remarks:
- Source, key, 1344-09-8, Hanstveit 1989
- Duration:
- 18 h
- Dose descriptor:
- EC0
- Effect conc.:
- > 348 mg/L
- Basis for effect:
- growth inhibition
- Remarks on result:
- other: for unneutralised concentrations (pH>9)
- Remarks:
- Source, key, 1344-09-8, Hanstveit 1989
- Duration:
- 30 min
- Dose descriptor:
- EC0
- Effect conc.:
- 3 454 mg/L
- Remarks on result:
- other:
- Remarks:
- Source, key, 1344-09-8, Kirch 1993
Referenceopen allclose all
RESULTS EXPOSED:
- Nominal/measured concentrations: Not reported
- EC0 (toxicity threshold): > 10000 mg/l for neutralised
concentrations (pH 7.6-7.8). Equivalent to >3480 mg active
matter/l.
- EC0 (toxicity threshold): > 1000 mg/l for unneutralised
concentrations (pH > 9). Equivalent to > 348 mg active
matter/l.
RESULTS CONTROL: No effects
RESULTS TEST WITH REFERENCE SUBSTANCE: No reference
substance was tested
RESULTS: EXPOSED
- Nominal concentrations: 10000 mg product/l
- Effect data (Immobilisation): EC0 10000 mg product/l (3454
mg active matter/l) (pH 11.1, at start 8.0), oxygen
consumption was reduced by 8.13% i.e. 10%
- Concentration / response curve: not reported
- Cumulative immobilisation: not reported
- Effect concentration vs. test substance solubility: not
reported
- Other effects: not reported
RESULTS CONTROL: not reported
RESULTS: TEST WITH REFERENCE SUBSTANCE
- Concentrations: not reported
- Results: not reported
Description of key information
EC0 (18h, growth inhibition) > 10000 mg/L for neutralized concentrations (pH 7.6-7.8). Equivalent to > 3480 mg active matter/L (Pseudomonas putida)
EC0 (18h, growth inhibition) > 1000 mg/L for unneutralised concentrations (pH > 9). Equivalent to > 348 mg active matter/L (Pseudomonas putida)
EC0 (30min, oxygen consumption inhibition) 3454 mg/L
Key value for chemical safety assessment
Additional information
No study available on potassium silicate. Data are read-across to sodium silicate. The toxicity of a sodium silicate solution (MR 3.46, 34.8 wt%) has been determined with a growth inhibition test in compliance with German standards and GLP using the bacterium Pseudomonas putida (Hanstveit 1989). The 18 h toxicity threshold (EC10, 10 % inhibition) of a neutralised silicate solution of pH 7.6 - 7.8 was > 3480 mg active matter/L, the highest concentration tested, while for the unneutralised solution (pH 7.9 - 10.4) effects were found at concentrations above 348 mg active matter/L. In a further GLP guideline study complying with German standards corresponding to OECD 209, the toxicity to Pseudomonas putida was tested in an oxygen consumption inhibition test. Concentrations of a sodium silicate solution (MR 3.0, 34.54 wt%) of up to 3454 mg active matter/L at pH 8.0 - 11.1 did not cause toxic effects (Kirch 1993).
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