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EC number: 203-481-7 | CAS number: 107-31-3
- 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
Toxicological Summary
- Administrative data
- Workers - Hazard via inhalation route
- Workers - Hazard via dermal route
- Workers - Hazard for the eyes
- Additional information - workers
- General Population - Hazard via inhalation route
- General Population - Hazard via dermal route
- General Population - Hazard via oral route
- General Population - Hazard for the eyes
- Additional information - General Population
Administrative data
Workers - Hazard via inhalation route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 120 mg/m³
- Most sensitive endpoint:
- repeated dose toxicity
- Route of original study:
- By inhalation
DNEL related information
- DNEL derivation method:
- other: OEL and MAK value
Acute/short term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 240 mg/m³
- Most sensitive endpoint:
- repeated dose toxicity
- Route of original study:
- By inhalation
DNEL related information
- DNEL derivation method:
- other: OEL and MAK value
- DNEL extrapolated from long term DNEL
Local effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 120 mg/m³
- Most sensitive endpoint:
- repeated dose toxicity
DNEL related information
- DNEL derivation method:
- other: OEL and MAK value
Acute/short term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 240 mg/m³
- Most sensitive endpoint:
- repeated dose toxicity
DNEL related information
- DNEL derivation method:
- other: OEL and MAK value
- DNEL extrapolated from long term DNEL
Workers - Hazard via dermal route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 17.1 mg/kg bw/day
- Most sensitive endpoint:
- repeated dose toxicity
- Route of original study:
- By inhalation
DNEL related information
- DNEL derivation method:
- other: OEL for inhalation (MAK)
Acute/short term exposure
- Hazard assessment conclusion:
- medium hazard (no threshold derived)
- Most sensitive endpoint:
- repeated dose toxicity
- Route of original study:
- By inhalation
DNEL related information
Local effects
Long term exposure
- Hazard assessment conclusion:
- medium hazard (no threshold derived)
- Most sensitive endpoint:
- repeated dose toxicity
Acute/short term exposure
- Hazard assessment conclusion:
- medium hazard (no threshold derived)
- Most sensitive endpoint:
- repeated dose toxicity
Workers - Hazard for the eyes
Local effects
- Hazard assessment conclusion:
- medium hazard (no threshold derived)
Additional information - workers
Following absorption, methyl formate is quickly cleaved by non-enzymatic reactions and esterases to form methanol and formic acid. Methanol is in a second step further metabolized to formaldehyde and formic acid. There is a clear species-specific difference in toxicokinetic. While formic acid is primarily oxidized to CO2 and finally exhaled in rodents, primates are less efficient in the formation of CO2. This difference is due to the hepatic levels of tetrahydrofolate and of 10-formyltetrahydrofolate dehydrogenase activity, the enzyme catalyzing the final step of formate oxidation to carbon dioxide. Thus, formic acid accumulates in humans in blood and other tissues (including CNS and the retina), thereby leading to metabolic acidosis and blindness. In contrast, such effects are not observed in rodents due to their higher formate detoxification capacity. Based on this species difference and the higher susceptibility of humans as compared to experimental animals, methanol has been classified as toxic by all three routes of exposure (H301, H311, H331). Considering that methyl formate quickly forms methanol following up-take, it is reasonable to use this classification for methyl formate as well. Accordingly, methanol was shown to be an ocular toxicant due to the formation of formic acid in Mueller cells of the retina. Thus, classification of methyl formate as STOT SE category 1 is warranted.
Based on the available data, it is not possible to derive an acute systemic/local inhalation and dermal DNEL based on missing dose response curves. However, since methyl formate is irritating to eyes (H319) and the respiratory system (H335) and acute toxic for all three routes of exposure (H301/311/331), a qualitative assessment according to ECHA guidance document 15 has been performed.
Inhalation:
The German MAK commission and SCOEL derived an occupational exposure level for methyl formate of 50 ppm (120 mg/m3). A study with human volunteers exposed to 100 ppm methyl formate for 8 hours indicated a possible effect of methyl formate exposure on the subjective feeling of fatigue without measurable impairment of neurobehavioral performance (Sethre et al., 1998 and 2000). Due to only minimal subjective effects in volunteers exposed to 100 ppm methyl formate for 8 hours and no effects in workers exposed to 36 ppm methyl formate and 44 ppm isopropanol (Sethre et al. 2000), the recommended 8-hour TWA is 50 ppm (120 mg/m3). SCOEL further states that multifocal degeneration of the olfactory epithelium of the nasal cavity occurred in rats exposed to 500 and 1500 ppm methyl formate for 14 days, whereas no effects were observed at 100 ppm; systemic effects as indicated by changes in body and organ weights were only observed at 1500 ppm. Based on this study, the NOAEC for local effects was 100 ppm and for systemic effects 500 ppm.
In a limited 90-days inhalation rat study (results have been derived from abstract, graphics and tables) atrophy of respiratory epithelium was observed after exposure to 1600 ppm (3.92 mg/l). After exposure to 400 ppm (0.98 mg/l) systemic effects were indicated by body and organ weight changes.
Based on this study, the NOAEC for local effects was 400 ppm and for systemic effects 100 ppm (0.25 mg/l).
In accordance with the derived OEL of 50 ppm from the human volunteer study, the same OEL is derived in consideration of interspecies differences and increased effects after chronical exposure from the NOAEC for local and systemic effects of the 90-days rat study.
Considering that the derived OEL is based on human data (related to neurobehavioral effects) and animal data (related to local olfactory effects and systemic effects indicated by body and organ weight changes), this OEL can be used as long-term systemic as well as long-term local DNEL.
Dermal:
Available dermal data for DNEL derivation is poor and insufficient for DNEL derivation. Skin contact should be avoided due to dermal absorption properties of methyl formate. Nevertheless a systemic dermal DNEL may be calculated on the basis of the accepted internal systemic dose based on the inhalative DNEL.
Assuming a breathing volume of 10 m3 for workers at light activity for 8-hours, exposure to 120 mg/m3 during a working shift is roughly equivalent to a dose of 1.2 g/person/day. Taking the average body weight of 70 kg into consideration, this yields a systemic dermal DNEL of 17 mg/kg bw/day. This calculation depicts a worst case scenario assuming that the dermal uptake is the same as from inhalation and neglecting the high volatility of the material.
General Population - Hazard via inhalation route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 14.29 mg/m³
- Most sensitive endpoint:
- repeated dose toxicity
- Route of original study:
- By inhalation
Acute/short term exposure
- Hazard assessment conclusion:
- medium hazard (no threshold derived)
- Most sensitive endpoint:
- repeated dose toxicity
- Route of original study:
- By inhalation
DNEL related information
Local effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 14.29 mg/m³
- Most sensitive endpoint:
- repeated dose toxicity
Acute/short term exposure
- Hazard assessment conclusion:
- medium hazard (no threshold derived)
- Most sensitive endpoint:
- repeated dose toxicity
DNEL related information
General Population - Hazard via dermal route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 2.02 mg/kg bw/day
- Most sensitive endpoint:
- repeated dose toxicity
- Route of original study:
- By inhalation
DNEL related information
- DNEL derivation method:
- other: DNEL is calculated based on the occupational exposure limit for workers, which has been derived by the German MAK commission and by the Scientific Committee of Exposure Limits (EU).
Acute/short term exposure
- Hazard assessment conclusion:
- medium hazard (no threshold derived)
- Most sensitive endpoint:
- repeated dose toxicity
- Route of original study:
- By inhalation
DNEL related information
Local effects
Long term exposure
- Hazard assessment conclusion:
- medium hazard (no threshold derived)
- Most sensitive endpoint:
- repeated dose toxicity
Acute/short term exposure
- Hazard assessment conclusion:
- medium hazard (no threshold derived)
- Most sensitive endpoint:
- repeated dose toxicity
General Population - Hazard via oral route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 2.02 mg/kg bw/day
- Most sensitive endpoint:
- repeated dose toxicity
- Route of original study:
- By inhalation
DNEL related information
- DNEL derivation method:
- other: DNEL is calculated based on the occupational exposure limit for workers, which has been derived by the German MAK commission and by the Scientific Committee of Exposure Limits (EU).
Acute/short term exposure
- Hazard assessment conclusion:
- medium hazard (no threshold derived)
- Most sensitive endpoint:
- repeated dose toxicity
- Route of original study:
- By inhalation
DNEL related information
General Population - Hazard for the eyes
Local effects
- Hazard assessment conclusion:
- medium hazard (no threshold derived)
Additional information - General Population
DNEL (consumer)
There is no intended consumer use for methyl formate. However, a DNEL is calculated based on the occupational exposure limit for workers, which has been derived by the German MAK commission and by the Scientific Committee of Exposure Limits (EU). This value protects against local as well as systemic effects and needs to be corrected considering the following alterations:
- Increased intraspecies variability (5 for workers vs. 10 for consumers)→factor 2
- Increased exposure time (8 h for 5 days per week for workers vs. 24 h for 7 days a week for consumers)→factor 4.2
- Total factor: 2 x 4.2 = 8.4
DNEL inhalation long-term systemic and local = 120 mg/m3 / 8.4 = 14.29 mg/m3
DNEL dermal and oral long-term systemic = 17 mg/kg/d / 8.4 = 2.02 mg/kg/d
Due to missing dose-response relationship, acute DNELs (inhalation or dermal or oral) are not calculated and such effects thought to be covered by the systemic DNELs. Since methyl formate is not classified with respect to skin irritation and dose-response information is missing, no dermal local DNEL has been calculated.
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