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Diss Factsheets
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EC number: 208-863-7 | CAS number: 544-17-2
- 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
Acute Toxicity: oral
Administrative data
- Endpoint:
- acute toxicity: oral
- Type of information:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- weight of evidence
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- other: see 'Remark'
- Remarks:
- Summary with tables and figures of a pre-guideline study. Meets generally accepted scientific standards, well documented and acceptable for assessment. This report was submitted to the MAK commission of the Deutsche Forschungsgemeinschaft (DFG) assessing hazardous materials.
Data source
Reference
- Reference Type:
- publication
- Title:
- Die akute und chronische Toxizität der Ameisensäure und ihrer Formiate.
- Author:
- Malorny G
- Year:
- 1 969
- Bibliographic source:
- Zeitschrift Ernährungswissenschaft 9, 332-339.
Materials and methods
- Principles of method if other than guideline:
- Pre-guideline study. LD50 determination was presumably conducted similar to the method used in OECD guideline 401.
- GLP compliance:
- no
- Test type:
- standard acute method
- Limit test:
- no
Test material
- Reference substance name:
- Sodium formate
- EC Number:
- 205-488-0
- EC Name:
- Sodium formate
- Cas Number:
- 141-53-7
- Molecular formula:
- CHO2Na
- IUPAC Name:
- sodium formate
- Details on test material:
- - Name of test material (as cited in study report): Na-Formiat
Constituent 1
Test animals
- Species:
- mouse
- Strain:
- not specified
- Sex:
- not specified
- Details on test animals or test system and environmental conditions:
- no data
Administration / exposure
- Route of administration:
- oral: gavage
- Vehicle:
- water
- Details on oral exposure:
- no data
- Doses:
- Applied doses not specified
- No. of animals per sex per dose:
- Total number of animals: 45
- Control animals:
- not specified
Results and discussion
Effect levels
- Sex:
- not specified
- Dose descriptor:
- LD50
- Effect level:
- 9 600 - 12 800 mg/kg bw
Any other information on results incl. tables
Table: oral LD50 of formic acid and its salts in the mouse:
Substance |
LD50 (mg/kg bw) |
LD50range (mg/kg bw) |
LD50,formate (mg/kg bw)# |
No of animals |
Formic acid |
1100 |
1000-1200 |
1076 |
55 |
Na-formate |
11200 |
9600-12800 |
7410 |
45 |
K-formate |
5500 |
5000-6000 |
2950 |
50 |
NH4-formate |
2250 |
2050-2460 |
1610 |
50 |
Ca-formate |
1920 |
1280-1330 |
1330 |
45 |
# =
calculated proportion of formate anion of the LD50dose.
Thus, the order of oral toxicity in mice was formic acid > Ca, NH4, K
salts > sodium formate.
Applicant's summary and conclusion
- Conclusions:
- The oral LD50 of sodium formate was approx. 11200
mg/kg bw in mice.
The oral toxicity formic acid and its salts depended largely
on the presence of H-ions, not on the presence of formate.
Therefore formic acid was more toxic than the salts.
- Executive summary:
The acute oral toxicity of formic acid and several of its salts was examined in male and female mice in a pre-guideline study. The aim was to establish LD50 values and elucidate the mode of action. Sodium formate was tested in a total of 45 mice. The oral LD50was 11200 mg/kg bw (range: 9600-12800) in mice. The acute oral toxicity was therefore low (Malorny, 1969).
This pre-guideline publication reviews the results of a variety of studies including metabolism and excretion, acute and repeated toxicity, and toxicity to reproduction. These results were used in the course of an early MAK-assessment. Though formal requirements for modern studies are not met, the published results are valuable for the assessment of formic acid and its salts. The study is considered to be valid (low reliability of 4 is assigned for formal reasons) and is used in a Weight of Evidence approach.
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.
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