Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 268-219-6 | CAS number: 68037-95-6 This substance is identified by SDA Substance Name: C16-C18 and C18 unsaturated alkyl amine and SDA Reporting Number: 11-029-00.
- 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
Skin irritation / corrosion
Administrative data
- Endpoint:
- skin irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1988
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Guideline study according to GLP
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 988
- Report date:
- 1988
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Deviations:
- no
- GLP compliance:
- yes
Test material
- Reference substance name:
- Amines, tallow alkyl
- EC Number:
- 263-125-1
- EC Name:
- Amines, tallow alkyl
- Cas Number:
- 61790-33-8
- IUPAC Name:
- 61790-33-8
- Reference substance name:
- Tallow Alkylamines
- IUPAC Name:
- Tallow Alkylamines
- Details on test material:
- - Name of test material (as cited in study report): Genamin TA 100 D
Constituent 1
Constituent 2
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Hoechst AG, Germany
- Age at study initiation: ca. 3 - 5 month
- Weight at study initiation: 2.2 - 3.0 kg
- Housing: individually, stainless steel cages
- Diet (e.g. ad libitum): ad libitum
- Water (e.g. ad libitum): ad libitum
- Acclimation period: 5 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20 +/- 3 °C
- Humidity (%): 50 +/- 20
- Photoperiod (hrs dark / hrs light): 12 hour interval
Test system
- Type of coverage:
- semiocclusive
- Preparation of test site:
- shaved
- Vehicle:
- unchanged (no vehicle)
- Controls:
- no
- Amount / concentration applied:
- 500mg/patch
- Duration of treatment / exposure:
- 3 min (3 animals)
4 h (1 animal) - Observation period:
- 0.5 - 1, 24, 48, and 72 h
7, 14, and 21 days - Number of animals:
- 4 (3 for 3 min exposure, 1 for 4 h exposure)
- Details on study design:
- TEST SITE
- Area of exposure: dorsal area of the trunk
- % coverage: approx. 6.25 cm²
REMOVAL OF TEST SUBSTANCE
- Washing: water
TEST SITE
- Area of exposure: 2.5 x 2.5 cm
- % coverage: 100
- Type of wrap if used: semi-occlusive bandage
REMOVAL OF TEST SUBSTANCE
- Washing (if done): yes
- Time after start of exposure: after exposure period of 4 hours or 3 minutes
SCORING SYSTEM: Draize
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- mean
- Remarks:
- 3 min exposure
- Time point:
- other: 0.5 - 1 h
- Score:
- 1.67
- Max. score:
- 2
- Irritation parameter:
- edema score
- Basis:
- mean
- Remarks:
- 3 min exposure
- Time point:
- other: 0.5 - 1 h
- Score:
- 2
- Max. score:
- 2
- Irritation parameter:
- erythema score
- Basis:
- animal #1
- Remarks:
- 3 min exposure
- Time point:
- other: mean 24, 48, 72 h
- Score:
- 2
- Max. score:
- 2
- Remarks on result:
- other: redness around sclerosis
- Irritation parameter:
- edema score
- Basis:
- animal #1
- Remarks:
- 3 min exposure
- Time point:
- other: mean 24, 48, 72 h
- Score:
- 2.33
- Max. score:
- 3
- Remarks on result:
- other: swelling around sclerosis at 72 h observation
- Irritation parameter:
- erythema score
- Basis:
- animal #2
- Remarks:
- 3 min exposure
- Time point:
- other: mean 24, 48, 72 h
- Score:
- 2.67
- Max. score:
- 3
- Remarks on result:
- other: redness around sclerosis
- Irritation parameter:
- edema score
- Basis:
- animal #2
- Score:
- 3.33
- Max. score:
- 4
- Remarks on result:
- other: swelling around sclerosis at 72 h observation
- Irritation parameter:
- erythema score
- Basis:
- animal #3
- Remarks:
- 3 min exposure
- Time point:
- other: mean 24, 48, 72 h
- Score:
- 2
- Max. score:
- 2
- Remarks on result:
- other: redness around sclerosis
- Irritation parameter:
- edema score
- Basis:
- animal #3
- Remarks:
- 3 min exposure
- Time point:
- other: mean 24, 48 h
- Score:
- 3
- Max. score:
- 3
- Remarks on result:
- other: edema not evaluable after 72 h due to sclerosis
- Irritation parameter:
- other: overall erythema score
- Basis:
- mean
- Time point:
- other: mean 24, 48, 72 h
- Score:
- 2.22
- Max. score:
- 3
- Remarks on result:
- other: redness around sclerosis
- Irritation parameter:
- other: overall edema score
- Basis:
- mean
- Time point:
- other: mean 24, 48, 72 h
- Score:
- 2.88
- Max. score:
- 4
- Remarks on result:
- other: swelling around sclerosis at 72 h observation; in one animal, edema not evaluable after 72 h due to sclerosis
- Irritation parameter:
- erythema score
- Basis:
- animal #1
- Remarks:
- 4 h exposure
- Time point:
- other: 0.5 - 1 h
- Score:
- 3
- Irritation parameter:
- edema score
- Basis:
- animal #1
- Remarks:
- 4 h exposure
- Time point:
- other: 0.5 - 1 h
- Score:
- 3
- Irritation parameter:
- erythema score
- Basis:
- animal #1
- Time point:
- other: mean 24, 48, 72 h
- Score:
- 3
- Max. score:
- 3
- Remarks on result:
- other: around sclerosis
- Irritation parameter:
- edema score
- Basis:
- animal #1
- Remarks:
- 4 h exposure
- Time point:
- other: mean 24, 48, 72 h
- Score:
- 3
- Max. score:
- 3
- Irritant / corrosive response data:
- 3 min exposure: The test item caused very slight to moderate erythema and slight to moderate oedema. Both, erythema and oedema was partly evaluable only around sclerosis or not evaluable due to sclerosis. 24 h until 14 days after patch removal, the skin was sclerotic, arched upward, discoloured (brown), fissured, scabbed, incrusted, dry, scaled, parchmenty, and pink. Additionally, ablation of the skin was observed. After 14 days, all animals showed scars.
4 h exposure: From 0.5 - 72 h after patch removal, moderate erythema and oedema were observed. Up to day 7, the skin was sclerotic, arched upward, incrusted, scabbed, discoloured (white or brown-white, respectively) and showed exudation. On day 7, a very slight erythema around the sclerosis was observed. Oedma was not evaluable due to sclerosis. The skin was destructed in full thickness. The animal was humanely killed.
Applicant's summary and conclusion
- Interpretation of results:
- corrosive
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- Based on the study results, Genamin TA 100 D was corrosive to skin.
- Executive summary:
- In a GLP conform study, Genamin TA 100 D was tested for skin irritation / corrosion according to OECD test guideline 404. for this 0.5 g of undiluted Genamin TA 100 D was applied semi-occlusively for 3 minutes or 4 hours to the shaved skin of three or one New Zealand White rabbits, respectively. The skin then was examined 30 minutes, 1 hour, 24, 48 and 72 hours after removal of the dressing. Since effects were still present after 72 hours, additional readings were performed after 7 and 14 days. Results for the 3 minute exposure period (3 animals): From 30 minutes to 14 days after patch removal, the treated skin sites showed mild to moderate erythema and mild to strong oedema. Between 24 hours and 14 days, the treated skin areas were sclerotic, vaulted, brownish discoloured, cracked, dry-brittle, scaly, translucent and pink-coloured. Additionally scaling was observed. After 14 days, all animals showed scars. Due to the severity of effects, scoring of erythema and oedema was restricted. Results for the 4 hour exposure period (1 animal): From 30 minutes to 7 days after application, the skin was temporarily sclerotic, vaulted, encrusted, scabby, white and brown-white discoloured. Additionally, exudations were observed. Full thickness destruction of the epidermis had occurred after 7 days and the animal was killed for human reasons on day 7. Due to the severity of effects, scoring of erythema and oedema was restricted. Based on the results of this study, Genamin TA 100 D was corrosive to skin.
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.