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EC number: 275-164-1 | CAS number: 71076-48-7
- 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
Exposure related observations in humans: other data
Administrative data
- Endpoint:
- exposure-related observations in humans: other data
- Type of information:
- migrated information: read-across based on grouping of substances (category approach)
- Adequacy of study:
- other information
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Basic data given
Data source
Reference
- Reference Type:
- publication
- Title:
- Percutanous absorption of azelaic acid in humans
- Author:
- Taeuber U., Weiss C. and Matthes H.
- Year:
- 1 992
- Bibliographic source:
- Exp Dermatol. 1992 Nov;1(4):176-9
Materials and methods
- Type of study / information:
- Six healthy male volunteers received a single topical treatment with 5 g of an anti-acne cream containing 20% azelaic acid (AzA) onto the face, the chest and the upper back. One week later 1 g of AzA was given orally to the same subjects as aqueous microcrystalline suspension. Following the two treatments the renal excretion of the unchanged compound was measured
- Endpoint addressed:
- basic toxicokinetics
- Principles of method if other than guideline:
- Excretion of azelaic acid was analyzed in urine after dermal application of six healthy male volunteers with a singlel treatment with 5 g of an anti-acne cream containing 20% azelaic acid and after oral application.
- GLP compliance:
- no
Test material
- Reference substance name:
- Azelaic acid
- EC Number:
- 204-669-1
- EC Name:
- Azelaic acid
- Cas Number:
- 123-99-9
- Molecular formula:
- C9H16O4
- IUPAC Name:
- azelaic acid
Constituent 1
Method
- Ethical approval:
- confirmed and informed consent free of coercion received
- Details on study design:
- Six healthy male volunteers received a single topical treatment with 5 g of an anti-acne cream containing 20% azelaic acid (AzA) onto the face, the chest and the upper back. One week later 1 g of AzA was given orally to the same subjects as aqueous microcrystalline suspension. Following the two treatments the renal excretion of the unchanged compound was measured
- Exposure assessment:
- measured
- Details on exposure:
- TYPE OF EXPOSURE:
- Dermal: 1 g azelaic acid in 5 g cream (Skinoren, Schering AG) was applied to ca. 5 cm2 skin. 2 g to chest, 2 g onto the back and 1 g to the face.
One hour after application, the skin areas treated on the back and chest were covered with cotton tissue fixed with adhesive tape. After 24 h of exposure, the covering material was removed and the treated areas were washed with 25 ml of ethanol 70% (v /v)
- Oral: 1 week after dermal application subjects received 100 ml of an aqueous micro-crystalline suspension containing 1 g azelaic acid in the morning before the breakfast was served
TYPE OF EXPOSURE MEASUREMENT: Biomonitoring (urine) by HPLC
EXPOSURE PERIOD:
- Dermal: 24 hours
- Oral: single application
POSTEXPOSURE PERIOD:
- Dermal: up to 3 days
- Oral: up to 4 days
Results and discussion
- Results:
- After dermal application of 5 g of cream containing 20% of Azelaic acid at a skin area dose of 5 mg /cm2 maximum concentrations 7.8 ± 3.2 µg/ ml (11.29 ± 0.5% of the dose applied) have been measured in the urine within the first 24 h. During the 2nd and 3rd d 0.76 +0.49% and 0.12 + 0.15% of the dose, respectively, was excreted unchanged with the urine. The total amount of Azelaic acid excreted unchanged with the urine within 3 d was determined to 2.2 ± 0.7% of the dose.
After oral administration a mean concentration of Azelaic acid of 424 + 104 µg/ml was found in the 0-24 h urine samples, corresponding to 61.2+ 8.8% of the dose administered. Excretion was complete within 24 h.
Any other information on results incl. tables
Urinary excretion of unchanged azelaic acid alter oral and dermal administration of 1 g azelaic acid to 6 male volunteers. Percentage of dose per fraction:
Time post aplication | Subjects | |||||||
1 | 2 | 3 | 4 | 5 | 6 | mean ± SD | ||
Oral | 0 - 24 h | 49.4 | 59.5 | 72.5 | 65.7 | 53.4 | 66.9 | 61.2 ± 0.88 |
24 -48 h | 0 | 0 | 0 | 0 | 0 | 0 | 0.0 ± 0.0 | |
Dermal | 0 - 24 h | 0.68 | 1.52 | 1.01 | 1.73 | 2.06 | 0.75 | 1.29 ± 0.56 |
24 -48 h | 0.48 | 1.01 | 1.46 | 0 | 0.75 | 0.83 | 0.76 ± 0.49 | |
48 - 72 h | 0.17 | 0.37 | 0.19 | 0 | 0 | 0 | 0.12 ± 0.15 | |
72 - 96 h | 0 | 0 | 0.49 | 0 | 1.01 | 0 | 0.25 ± 0.42 |
Applicant's summary and conclusion
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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