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EC number: 204-679-6 | CAS number: 124-09-4
- 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
Description of key information
- Skin irritation: Corrosive (OECD 435, Kr: 1)
- Eye irritation: highly irritating, induced irreversible effects ( 92/69/EEC, B.5, Kr: 2)
- Respiratory irritation: Irritating (See results of sub-chronic studies by inhalation in rat and mice)
Key value for chemical safety assessment
Skin irritation / corrosion
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (corrosive)
Eye irritation
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (irritating)
Respiratory irritation
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (irritating)
Additional information
1- Skin irritation:
There are several skin irritation studies, all showing evidence of HMD corrosivity.The study identified as the key study (Ladies, 1998), 35%, 70% and 85% of HMD aqueous solutions were corrosive and were assigned to Packing Group II (OECD 435, in vitro test, Kr: 1). The results were confirmed in vivo by a test conducted according to the Directive 92/69/EEC, B.4 (Marzin, 1978, Kr: 2), the mean scores were 4 for both erythema and oedema and all these effects were not reversible at 72 hours after application..
2- Eye irritation:
Eye irritation is severe following HMD contact. In an eye irritation/corrosion study (Marzin, 1978, Key study, Kr: 2), four rabbits were treated with 0.1 g of HMD. The method followed is similar to 92/69/EEC, B.5. The mean irritation scores for all animals within 24, 48 and 72 hours was 4 for corneal opacity and 2 for iris without reversibility after 72-hour observation period. Due to the corrosivity of the HMD, the study was finished after 3 days of exposure. Based on this study, HMD is highly irritating to eyes and induced irriversible effects (the worst case).
3- Respiratory irritation: HMD is classified with STOT SE3 in the
CLP (1272/2008). In sub-chronic studies conducted in rats and mice
exposed by inhalation (NTP, 1993 and Ben-Dyke, 1981), clinical signs
were primarily related to upper respiratory tract irritation and
included dyspnea and nasal discharge both in rats and mice. Moreover,
clinical signs were accompanied by histopathological examinations
showing irritation in the nasal cavity and larynx in both species from
31 mg HMD/m3 (see "7.5.3 Repeated dose toxicity: inhalation").
Effects on skin irritation/corrosion: corrosive
Effects on eye irritation: highly irritating
Effects on respiratory irritation: irritating
Justification for classification or non-classification
Hexamethylenediamine (Cas: 124 -09 -4) is classified in the Annex VI (Table 3.1 and 3.2) of CLP regulation (1272/2008) as:
- Skin Corr. 1B (H314)
- and STOT SE 3 (H335)
According to the results of key studies, no self classification is proposed.
Remark/eye irritation:
Based on the key study (cited above), HMD is considered in Category 1 (irreversible effects on the eye) according to the CLP Regulation (Regulation (EC) No 1272/2008). Since HMD is classified as Skin Corr. 1B (H314: Causes severe skin burns and eye damage) the corresponding hazard statement for serious eye damage (H318) does not need to be used for labelling to avoid redundancy.
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