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EC number: 200-289-5 | CAS number: 56-81-5
- 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
Endpoint summary
Administrative data
Key value for chemical safety assessment
Effects on fertility
Description of key information
Glycerin was administered by oral gavage to groups of male and female rats through two generations.
There was no effect noted on growth, fertility and reproductive performance through two generations at 2000 mg/kg/day.
Effect on fertility: via oral route
- Endpoint conclusion:
- no adverse effect observed
- Dose descriptor:
- NOAEL
- 2 000 mg/kg bw/day
- Study duration:
- chronic
- Species:
- rat
- Quality of whole database:
- The study has limitations but there was no evidence of any adverse effects on reproductive parameters.
Additional information
Two additional studies were evaluated and summarised by EFSA 2017 (Johnson et al 1933, Guerrant et al. 1947), however these studies were very old and had significant limitations.
No additional relevant studies were summarised by any of the other official bodies (MAK 2007 and 2016, OECD 2002).
The overall conclusion was that the reports of the two- and multigeneration reproductive toxicity studies have limitations but there was no evidence of any adverse effects on reproductive parameters.
There was no new relevant information identified up to and including 2021 (most recent literature research).
Re-evaluation of glycerol (E 422) as a food additive, EFSA Journal 2017;15(3):4720
Glycerol, CAS Number 56-81-5, OECD SIDS Initial Assessment Report For SIAM 14 Paris, France, 26-28 March 2002
Glycerin [MAK Value Documentation in German language, 2007]
The MAK Collection for Occupational Health and Safety 2017, Vol 2, No 2
Effects on developmental toxicity
Description of key information
A developmental toxicity study was conducted in rats, mice and rabbits. There was no effect on developmental toxicity of offspring of female rats dosed with glycerin at doses as high as 1310 mg/kg/day. There was no effect on developmental toxicity of offspring of female mice dosed with glycerin at doses as high as 1280 mg/kg/day. There was no effect on developmental toxicity of offspring of female rabbits dosed with glycerin at doses as high as 1180 mg/kg/day.
Effect on developmental toxicity: via oral route
- Endpoint conclusion:
- no adverse effect observed
- Dose descriptor:
- NOAEL
- 1 180 mg/kg bw/day
- Species:
- other: rat, mouse and rabbit
Additional information
There is no evidence of a developmental toxicity effect in rats, mice and rabbits. The highest dose levels ranged from 1180 mg/kg/day in rabbits to 1310 mg/kg/day in rats.
No additional relevant studies were summarised by any of the official bodies (MAK 2007 and 2016, OECD 2002, EFSA 2017).
The overall conclusion was that there was no evidence of teratogenicity for glycerol. All NOAEL values for several species are above the limit dose given in the OECD Test Guideline.
There was no new relevant information identified up to and including 2021 (most recent literature research).
Re-evaluation of glycerol (E 422) as a food additive, EFSA Journal 2017;15(3):4720
Glycerol, CAS Number 56-81-5, OECD SIDS Initial Assessment Report For SIAM 14 Paris, France, 26-28 March 2002
Glycerin [MAK Value Documentation in German language, 2007]
The MAK Collection for Occupational Health and Safety 2017, Vol 2, No 2
Toxicity to reproduction: other studies
Additional information
No additional information available.
Justification for classification or non-classification
There is no justification for classification based on data from available studies.
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.
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