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EC number: 931-312-3 | CAS number: 53880-05-0
- 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
Toxicity to reproduction
Administrative data
- Endpoint:
- screening for reproductive / developmental toxicity
- Type of information:
- other: Grouping and read-across according to Reg (EC) No 1907/2006, Annex XI, 1.5 and for weight of evidence according to Reg (EC) No 1907/2006, Annex XI, 1.2 with respect to reproductive toxicity for aliphatic diisocyanate monomers and their polyisocyanates
- Remarks:
- see also "Justification for type of information"
- Adequacy of study:
- weight of evidence
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: According to ECHA Practical Guide 6 the maximum score for read across is rel. 2
- Justification for type of information:
- Remark regarding read across approach IPDI oligomers, isocyanurate type:
3-Isocyanatomethyl-3,5,5-trimethylcyclohexyl isocyanate oligomers, isocyanurate type, CAS 53880-05-0, is a prepolymerised aliphatic polyisocyanate compound, used in manufacture of polyurethanes. The idealised structure is built of 3 units of 3-isocyanatomethyl-3,5,5-trimethylcyclohexyl isocyanate (= Isophorondiisocyanat, IPDI), but actually the product contains a range of oligomeric structures with also 5, 7, 9, and > 11 IPDI units and an average molecular weight of MW = 930 g/mol (Mn 790).
The only reactive functional group in the molecule, the isocyanate group (NCO-group; N=C=O; common functional group), is responsible for the toxicological mode of action (MoA) of the substances.No toxic effect is anticipated from the aliphatic backbone of the molecules or the species that is yield from the NCO-conversion. The MoA is characterised by the local irritant effect at the first site of contact/port-of-entry (e.g. respiratory tract, skin, eyes) and is, moreover, the common MoA for other aliphatic monomeric and homopolymeric isocyanates. This defines the applicability domain of substances that should belong to the group: aliphatic monomeric and homopolymeric isocyanates without any other functional groups. Examples are hexamethylene 1,6-diisocyanate (HDI)-based or 4,4'-methylenedicyclohexyl diisocyanate (H12MDI)-based polyisocyanates. A comprehensive database is available for some of these substances pointing to that common primary toxicological profile, dominated by the irritation potential at the first site of contact/port-of-entry.
A full and detailed text "Justification for grouping and read-across according to Regulation (EC) No 1907/2006, Annex XI, 1.5 and for weight of evidence according to Regulation (EC) No 1907/2006, Annex XI, 1.2 with respect to reproductive toxicity for aliphatic diisocyanate monomers and their polyisocyanates" is attached to chapter 13 of IUCLID. Based on this comparative evaluation the conclusion is drawn that in this case grouping and read-across of toxicological data according to Regulation (EC) No. 1907/2006 (REACH), Annex XI, 1.5 is justified.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 004
- Report date:
- 2004
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 421 (Reproduction / Developmental Toxicity Screening Test)
- Version / remarks:
- (1995)
- GLP compliance:
- yes (incl. QA statement)
- Limit test:
- no
Test material
- Reference substance name:
- 4,4'-methylenedicyclohexyl diisocyanate
- EC Number:
- 225-863-2
- EC Name:
- 4,4'-methylenedicyclohexyl diisocyanate
- Cas Number:
- 5124-30-1
- Molecular formula:
- C15H22N2O2
- IUPAC Name:
- 1-isocyanato-4-[(4-isocyanatocyclohexyl)methyl]cyclohexane
- Details on test material:
- - Purity: 99.5%
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Wistar
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Strain: Wistar Hsd Cpb:WU (SPF)
- Source: Harlan-Winkelmann GmbH, Borchen, Germany
- Age at study initiation: 13 weeks
- Weight at study initiation: males 365 (344-388) g, females 218 (198-233) g
- Housing: singly in Makrolon Type IIIh cages except during their overnight co-housing during the matings
- Diet and Water: ad libitum
- Acclimation period: at least 7 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 22 +/- 2
- Humidity (%): approx. 50
- Air changes (per hr): approx. 10
- Photoperiod (hrs dark / hrs light): 12/12
Administration / exposure
- Route of administration:
- inhalation: aerosol
- Type of inhalation exposure (if applicable):
- nose only
- Vehicle:
- unchanged (no vehicle)
- Details on exposure:
- GENERATION OF TEST ATMOSPHERE / CHAMBER DESCRIPTION
- Mode of exposure: Animals were nose-only exposed to the aerosolized test article in restrainers made of Plexiglas. The type of exposure is comparable with a directed-flow exposure design (Moss and Asgharian, Respiratory Drug Delivery IV, 1994, 197-201).
- Exposure apparatus: Chambers used are commercially available (TSE, Bad Homburg, Germany) and the performance as well as their validation has been published (e.g. Pauluhn, Journal of Applied Toxicology, 14, 55-62, 1994). Each segment of the aluminum inhalation chamber has the following dimensions: inner diameter = 14 cm, outer diameter = 35 cm (two-chamber system), height = 25 cm (internal volume = about 3.8 I).
- Generation of aerosol: In order to increase the efficiency of the generation of respirable particles and to prevent larger particles from entering the chamber a preseparator/baffle system was used. Under dynamic conditions the various concentrations of the test substance were nebulized into the baffle (pre-separator) which entrained the substance into the intake of the cylindrical inhalation chamber. For nebulization a binary nozzle (maintained at a temperature of 30°C) and conditioned compressed air (15 L/min and 10 µL/min test substance; dispersion pressure approximately 600 kPa). The test substance was fed into the nozzle by a digital pump (Hamilton Microlab M). This atmosphere was diluted further with 45 L/min prior to entering the inhalation chamber. The targeted concentrations were achieved by using air extraction/substitution dilution cascades.
- Inhalation chamber equilibrium concentration: The test atmosphere generation conditions provide an adequate number of air exchanges per hour (> 200 x, continuos generation of test atmosphere). Under such test conditions used chamber equilibrium is attained in less than one minute of exposure (t99% = 4.6 x chamber volume/chamber airflow). The ratio between the air supplied and exhausted was chosen so that approximately 90% of the supplied air is removed via the exhaust system.
- Conditioning the compressed air: Compressed air was supplied by Boge compressors and was conditioned (i.e. freed from water, dust, and oil) automatically by a VIA compressed air dryer. Adequate control devices were employed to control supply pressure.
- Exhaust air treatment: The exhaust air was purified via cotton woll and HEPA filters.
- Temperature and humidity measurements were performed by the computerized Data Acquisition and Control System using FTF11-Sensoren (Fa. Elka Electronic, Lüdenscheid, Germany).
TEST ATMOSPHERE
- The integrity end stability of the aerosol generation and exposure system was monitored using a RAM-1 (MIE, Bedford, MA, USA) and FhG (Fraunhofer Institute, Hannover, Germany) real-time aerosol photometer.
- Samples taken from breathing zone: yes
- Brief description of analytical method used: gravimetric analysis of filter samples (filter: Glass-Fibre-Filter, Sartorius, Göttingen, Germany; digital balance).
- Particle size distribution: The particle-size distribution was analyzed using a BERNER-Type Aeras low-pressure critical orifice cascade impactor. > 92 % of the particle mass had an aerodynamic diameter = 3 µm.
- MMAD (Mass median aerodynamic diameter): The respirability of the aerosol was adequate, i.e. the mass median aerodynamic diameter (MMAD) was 1.1 µm at 1 mg/m³, 1.1 µm at 6 mg/m³ and 1.0 µm at 36 mg/m³ (geometric standard deviation (GSD) approx. 2). - Details on mating procedure:
- MATING PROCEDURES: During the following mating period the first F0 male was cohoused with the first female F0 animal within the group and so on over night at a maximum of 12 times during the two-week mating period. As a rule inseminated females were not further co-housed. Insemination was established by investigating vaginal smears prepared in the morning.
- Analytical verification of doses or concentrations:
- yes
- Details on analytical verification of doses or concentrations:
- Actual target concentrations were measured in each chamber up to 3 times per day per gravimetric analysis. Chamber samples were taken in the viscinity of the breathing zone.
- Duration of treatment / exposure:
- The test substance was administered to parental (F0) animals two weeks prior to and during their mating, during the resultant pregnancy up day
19 p.c. Males were dosed 28 days at a minimum. For technical reasons (to avoid withdrawal from their pups) females were not treated during lactation. - Frequency of treatment:
- 6 hours/day, 7 days/week, for 2 weeks
- Details on study schedule:
- After a gestation period of about 22 days litters were born and the dams were allowed to rear them up to day 4-6 p.p. Then dams and their pups were killed.
Doses / concentrationsopen allclose all
- Remarks:
- Doses / Concentrations:
1, 6, 36 mg/m³
Basis:
other: target concentration
- Remarks:
- Doses / Concentrations:
1.06, 5.95, 34.04 mg/m³
Basis:
analytical conc.
- Remarks:
- Doses / Concentrations:
5, 20, 119 mg/m³
Basis:
nominal conc.
- No. of animals per sex per dose:
- 12 test animals / 12 controls
- Control animals:
- other: conditioned air
- Details on study design:
- - Dose selection rationale: An orientating aerosol inhalation pilot study with 5 male and 5 female rats exposed nose-only for 1 week to target concentrations of 1, 6 and 36 mg/m³ establishes a NOAEL of 6 mg/m³ and serves for dose selection rationale
Examinations
- Parental animals: Observations and examinations:
- CAGE SIDE OBSERVATIONS: Yes, all F0 parental animals
- Time schedule: Twice daily (once daily on weekends and public holidays); Any findings such as course of birth e.g. prolonged parturition, morbidity and mortality as well as lactation behavior noticed during this cage side observation were recorded. Furthermore, all rats were clinically observed before and after inhalation exposure especially for symptoms concerning nose and breathing.
DETAILED CLINICAL OBSERVATIONS: Yes, all F0 parental animals
- Time schedule: Prior to the study and at least once weekly as routine at their cage change. This investigation includes the evaluation of the general state of health, behavior, condition of the fur, and the orifices as well as excretory products. During gestation periods females were clinically examined on day 0, 7, 14,20, and during lactation on day 0 and 4 in the same way.
BODY WEIGHT: Yes, all F0 parental animals
- Time schedule for examinations: at study-start (first day of dosing), then weekly for male animals up to necropsy and for female animals up to established insemination. After that female animals were weighed on postcoital days 0, 7, 14 and 20; and on days 0 and 4 after birth of their pups. F0 animals were weighed at the day of necropsy to permit calculations of the relative organ weights.
FOOD CONSUMPTION: Yes, all F0 parental animals
- Food consumption for each animal determined and mean daily diet consumption calculated as g food/kg body weight/day: Yes
WATER CONSUMPTION AND COMPOUND INTAKE (if drinking water study): No data - Oestrous cyclicity (parental animals):
- At necropsy also the number of corpora lutea in the right and left ovary was determined.
- Sperm parameters (parental animals):
- Parameters examined in male parental generation:
- Organ weight of left epididymis and testes were done during the scheduled necropsy
- Examination on Sperms and Spermatids: Determination of spermatozoa motility and viability, determination of spermatozoa morphology, determination of spermatozoa in epididymis (spermatozoa density per mg epididymis), determination of homogenization resistant spermatid heads in the testis (number of spermatid heads per mg testis) - Litter observations:
- PARAMETERS EXAMINED
The following parameters were examined in F1 offspring shortly after birth and on day 4 p.p.:
- number of live and dead pups
- sex of the pups
- body weights
- clinical signs
- apparent malformations were determined - Postmortem examinations (parental animals):
- SACRIFICE
- Unscheduled Necropsies: Parental animals that died or were killed in moribund condition (under diethyl ether narcosis) during the study were necropsied and macroscopically examined.
- Scheduled Necropsies: When pups were 4 to 6 days old dams were anesthetized with carbon dioxide and killed by exsanguination (at carotid artery) and examined for gross pathology. F0 males were killed as scheduled under carbon dioxide narcosis when they were administered 28 days to a minimum.
GROSS NECROPSY
In F0 females implantation sites were counted and documented. Implantation sites were stained with 10% ammoniumsulfide. At necropsy also the number of corpora lutea in the right and left ovary was determined.
HISTOPATHOLOGY / ORGAN WEIGHTS
- Organ weight determinations of the lungs (with trachea), left epididymis and testes were done during the scheduled necropsy.
- Fixed organs/organ specimen of the F0 parental animals(in 10 % neutral buffered formalin solution): lungs (instilled) with trachea, head, one testis, ovaries with oviducts, one epididymis, seminal vesicles, coagulation glands, prostate, tattooed ears and all organs/organ specimen exhibiting macroscopic changes.
- Histopathological evaluation of testes, epididymides and ovaries of control and high dose rats. - Postmortem examinations (offspring):
- GROSS NECROPSY
- Unscheduled Necropsies: Pups that were found dead at birth, that died during lactation as well as those killed (with carbon dioxide) in moribund condition were macroscopically inspected after opening the body cavities, with particular attention on the organs of reproduction except for cases of autolysis or cannibalism. This includes also visible skeletal abnormalities as far as possible. A lung flotation in water was performed during the necropsy of pups found dead on the day of the first litter inspection to determine whether pups had breathed at birth or not. Macroscopically changed organs were fixed in 10% formalin.
- Scheduled Necropsies
When they were 4 to 6 days old pups were killed under carbon dioxide anesthesia and were examined for macroscopical alterations as described above. - Statistics:
- Dunnett-Test with a variance analysis; Fisher’s exact CHI-SQUARE (positive ANOVA probability test with a significance levels of alpha = 5%).
- Reproductive indices:
- - Indices: insemination, fertility, gestation
- Offspring viability indices:
- - Indices: live birth, viability
Results and discussion
Results: P0 (first parental generation)
Details on results (P0)
CLINICAL SIGNS AND MORTALITY (PARENTAL ANIMALS)
At 36 mg/m³ changes in breathing behavior and/or serous nasal discharge (nostrils with red encrustation) were noted in the majority of F0 rats. At 36 mg/m³ in single animals also signs of poor general conditions occurred and slightly increased (2 of 24 rats) mortality was observed. One male of the high dose group was found dead during the premating period and one female of the high dose group has to be killed in moribund condition. At 6 mg/m³ only serous nasal discharge and red encrusted nostrils were noted in F0 rats.
BODY WEIGHT AND FOOD CONSUMPTION (PARENTAL ANIMALS)
No toxic effect was seen on body weights of F0 rats up to 6 mg/m³. At 36 mg/m³ reduced body weight gain was noted at some time points in both sexes (males: week 5-6: 2.8g vs. 9.8g in controls, week 4-5: 10.2g vs. -1.2g in controls; females: week 1-2: -11.2g vs -4.7g in controls). The food intake of 36 mg/m³ F0 males was transiently reduced. The absolute (14%) and relative (18%) weights of the lungs were increased in 36 mg/m3 F0 male rats.
REPRODUCTIVE FUNCTION: SPERM MEASURES (PARENTAL ANIMALS)
Results of sperm analysis were excluded from the study evaluation, because mechanical stress on the epididymides and testes caused by the narrowness of exposure restrainers had induced untypical and test-compound independent low sperm motility (below 30%) and increase in sperm abnormalities (higher than 50%) in all groups which corroborate with testicular and epididymal changes seen histologically.
Dose mg/m³: 0 / 1 / 6 / 36
Sperm motility, (first min) %: 21 / 7 / 26 / 16
Sperm motility (fifth min) %: 18 / 6 / 25 / 15
Abnormal sperms %: 59.4 / 87.4 / 60.9 / 66.4
Mean number of spermatids per mg testis: 52773 / 41767 / 41989 / 49707
Mean number of sperms per mg epididymis: 490037 / 138194 / 347913 / 323042
REPRODUCTIVE PERFORMANCE (PARENTAL ANIMALS)
At 36 mg/m³ a slightly reduced fertility index was noted. No other reproduction parameter was affected.
Dose mg/m³: 0/ 1/ 6/ 36
Insemination index %: 100.0/ 91.7/ 100.0/ 100.0
Fertility index %: 91.7/ 81.8/ 83.8/ 66.7 (p > 0.05)
Gestation index %: 90.9/ 100.0/ 100.0/ 100.0
Gestation length Days: 22.11/ 22.25/ 22.22/ 22.00
Co-housed females n: 12/ 12/ 12/ 12
Number of implantation sites (per litter): 10.8 / 10.56 / 11.50 / 9.88
Litters alive n: 10/ 9/ 10/ 8
Live birth index %: 98.57 / 99.07 / 97.22 / 96.36
Viability index %: 99.00 / 100.0 / 92.17 / 98.96
HISTOPATHOLOGY (PARENTAL ANIMALS)
No test compound-related effects were seen in the testes and epididymides of F0 rats. In the testes of both groups evaluated (control and high dose) tubular degeneration (mainly multi/focal) was seen in the majority of animals:
dose mg/m³: 0 ; 36
Focal tubular degeneration: 5/12 ; 8/12
Dif. tubular degeneration: 2/12 ; 0/12
In the epididymides, spermatic debris and oligospermia occurred in almost all rats.
dose mg/m³: 0 ; 36
Spermatic debris: 12/12 ; 11/12
Oligospermia: 11/12 ; 10/12
The morphology of the ovaries of F0 females was not affected.
Effect levels (P0)
open allclose all
- Dose descriptor:
- NOAEL
- Effect level:
- 1 mg/m³ air
- Sex:
- male/female
- Basis for effect level:
- other: General toxicity: signs of respiratory irritation (breathing behaviour, nose discharge) at higher dose group (6 and 36 mg/m3)
- Dose descriptor:
- NOAEL
- Effect level:
- 6 mg/m³ air
- Sex:
- male/female
- Basis for effect level:
- other: Reproduction Toxicity: slightly reduced fertility index at next higher dose group (36 mg/m3)
Results: F1 generation
Details on results (F1)
dose mg/m³: 0 / 1 / 6 / 36
- Live birth index %: 98.57 / 99.07 / 97.22 / 96.36
- Viability index %: 99.00 / 100.0 / 92.17 / 98.96
- Males %: 54.31 / 50.56 / 49.23 /53.90
CLINICAL SIGNS (OFFSPRING)
No remarkable clinical signs were observed during the four day lactation period up to 36 mg/m³.
GROSS PATHOLOGY (OFFSPRING)
No effect on body weights and no macroscopical alterations were noted at pup necropsies up to 36 mg/m³.
Effect levels (F1)
- Key result
- Dose descriptor:
- NOAEL
- Generation:
- F1
- Effect level:
- >= 36 mg/m³ air (nominal)
- Sex:
- male/female
- Basis for effect level:
- other: no adverse effects were observed up to 36 mg/m3
Overall reproductive toxicity
- Reproductive effects observed:
- not specified
Any other information on results incl. tables
Remark regarding read across approach IPDI oligomers, isocyanurate type:
3-Isocyanatomethyl-3,5,5-trimethylcyclohexyl isocyanate oligomers, isocyanurate type, CAS 53880-05-0, is a prepolymerised aliphatic polyisocyanate compound, used in manufacture of polyurethanes. The idealised structure is built of 3 units of 3-isocyanatomethyl-3,5,5-trimethylcyclohexyl isocyanate (= Isophorondiisocyanat, IPDI), but actually the product contains a range of oligomeric structures with also 5, 7, 9, and > 11 IPDI units and an average molecular weight of MW = 930 g/mol (Mn 790).
The only reactive functional group in the molecule, the isocyanate group (NCO-group; N=C=O; common functional group), is responsible for the toxicological mode of action (MoA) of the substances.No toxic effect is anticipated from the aliphatic backbone of the molecules or the species that is yield from the NCO-conversion. The MoA is characterised by the local irritant effect at the first site of contact/port-of-entry (e.g. respiratory tract, skin, eyes) and is, moreover, the common MoA for other aliphatic monomeric and homopolymeric isocyanates. This defines the applicability domain of substances that should belong to the group: aliphatic monomeric and homopolymeric isocyanates without any other functional groups. Examples are hexamethylene 1,6-diisocyanate (HDI)-based or 4,4'-methylenedicyclohexyl diisocyanate (H12MDI)-based polyisocyanates. A comprehensive database is available for some of these substances (see list below) pointing to that common primary toxicological profile, dominated by the irritation potential at the first site of contact/port-of-entry.
A full and detailed text "Justification for grouping and read-acrossaccording to Regulation (EC) No 1907/2006, Annex XI, 1.5 and for weight of evidence according to Regulation (EC) No 1907/2006, Annex XI, 1.2 with respect to reproductive toxicity for aliphatic diisocyanate monomers and their polyisocyanates" is attached to chapter 13 of IUCLID. Based on this comparative evaluation the conclusion is drawn that in this case grouping and read-across of toxicological data according to Regulation (EC) No. 1907/2006 (REACH), Annex XI, 1.5 is justified.
Short name |
Name used for registration |
CAS no |
EC /ECHA list no |
IPDI |
3-Isocyanatomethyl-3,5,5-trimethylcyclohexyl isocyanate |
4098-71-9 |
223-861-6 |
IPDI oligomers, isocyanurate type |
3-Isocyanatomethyl-3,5,5-trimethylcyclohexyl isocyanate homopolymer, isocyanurate type |
53880-05-0 |
931-312-3 |
HDI |
Hexamethylene diisocyanate |
822-06-0 |
212-485-8 |
HDI oligomers, isocyanurate type |
HDI oligomers, isocyanurate |
28182-81-0 |
931-274-8 |
HDI oligomers, iminooxadiazindione type |
HDI oligomers, iminooxadiazindione |
28182-81-0 |
931-297-3 |
HDI oligomers, biuret type |
HDI oligomers, biuret |
28182-81-0 |
939-340-8 |
HDI oligomers, uretdione type |
HDI oligomers, uretdione |
28182-81-0 |
931-288-4 |
H12MDI |
4,4'-Methylenedicyclohexyl diisocyanate |
5124-30-1 |
225-863-2 |
Applicant's summary and conclusion
- Executive summary:
4,4´-Methylenedicyclohexyl diisocyanate has already been assessed in the OECD HPV programme.
Cited from SIAR for SIAM20 (Paris, April 19 -22, 2005): "In a reproduction/developmental toxicity screening test according to OECD TG 421 (...) Wistar rats (12 animals/sex/dose) were exposed to 4,4´-methylenedicyclohexyl diisocyanate aerosol. The rats were exposed nose-only daily for 6 hours/day to concentrations of 0, 1, 6 and 36 mg/m³ (= target concentrations). F0male and female rats were exposed for 2 weeks (premating exposure period), which was continued during the approximately 2 week mating period. Males were exposed for at least 28 days (prior to necropsy) whereas the exposure of the F0females continued during the pregnancy up to day 19 post coitum (p.c.). Exposure of the F0females was suspended up to the day of necropsy on day 4 - 6 p.p. (post partum), i.e., the time points at which F1pups were sacrificed. In all exposure groups, the aerosol was highly respirable to rats, i.e., the average mass median aerodynamic diameter (MMAD) was ≈ 1 μm, the geometric standard deviation (GSD) was ≈ 2. Clinical signs as changes in breathing behavior and/or serous nasal discharge were documented for F0animals of the 6 and 36 mg/m³ groups. One male of the high dose group was found dead during the premating period and one female of the high dose group had to be killed in moribund condition. No effect on body weights gain, food consumption and necropsy findings, were observed at ≤ 6 mg/m3. Significant increases of absolute and relative weights of the lungs were detected at 36 mg/m³ in male rats. No effects of 4,4´-methylenedicyclohexyl diisocyanate on reproductive parameters such as insemination index, gestation index and length and the number of implantation sites were described. At 36 mg/m³ a slightly reduced fertility index was noted (0, 1, 6, 36 mg/m³: fertility index: 91.7, 81.8, 83.8, 66.7* % (*= p > 0.05)). No remarkable clinical signs were seen in any F1pubs during the 4 day lactation period and body weight gain was comparable to the control animals. In the testes of both groups evaluated (control and high concentration F0animals) tubular degeneration (mainly multi/focal) was seen in the majority of animals. In the epididymides, spermatic debris and oligospermia occurred in almost all rats. These histopathological findings are concordant with the results of the spermatological evaluation of all animals (no or very low sperm motility and high percentage of abnormal sperms in control rats and in all concentration groups). Nevertheless the findings seen in the testes are not substance-related because they were found also in the control animals and they are dose independent. Mechanical stress on the epididymides and testes caused by the narrowness of exposure restrainers seems to be responsible for the effects seen in all 4,4´-methylenedicyclohexyl diisocyanate and air exposed animals.
Based on these findings, the NOAELs were considered to be 1 mg/m³ in males and females for general toxicity. Due to a slightly reduced fertility index at 36 mg/m³, 6 mg/m³ is the NOAEL for reproductive toxicity in rats."
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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