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EC number: 200-838-9 | CAS number: 75-09-2
- 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:
- two-generation reproductive toxicity
- Remarks:
- based on test type (migrated information)
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Klimisch code: 1. Reliable without restrictions. “Key study” Well-defined, GLP compliant study
Data source
Reference
- Reference Type:
- publication
- Title:
- Methylene Chloride: Two-Generation Inhalation Reproductive Study in Rats.
- Author:
- Nitschke et al
- Year:
- 1 988
- Bibliographic source:
- Fundamental and Applied Toxicology, Vol. 11: 60-67.
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 416 (Two-Generation Reproduction Toxicity Study)
- Principles of method if other than guideline:
- test method EU B.35
- GLP compliance:
- not specified
Test material
- Reference substance name:
- Methylene chloride
- IUPAC Name:
- Methylene chloride
- Test material form:
- other: vapour
- Details on test material:
- Methylene chloride (99.86% pure)
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Fischer 344
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source:Charles River Breeding Laboratory, Kingston, NY
- Age at study initiation: 7 weeks
- Weight at study initiation: (P) Males: x-x g; Females: x-x g; (F1) Males: x-x g; Females: x-x g
- Fasting period before study:
- Housing: singly in wire-mesh stainless steel cages
- Use of restrainers for preventing ingestion (if dermal): yes/no
- Diet (e.g. ad libitum):ad libitum, except for during exposure
- Water (e.g. ad libitum):ad libitum
- Acclimation period: 1 week
ENVIRONMENTAL CONDITIONS
- Temperature (°F):72
- Humidity (%): 40 -60
- Air changes (per hr):
- Photoperiod (hrs dark / hrs light):12 hour
Administration / exposure
- Route of administration:
- inhalation: vapour
- Type of inhalation exposure (if applicable):
- whole body
- Details on exposure:
- Whole body inhalation chamber exposure to test substance vapour.
Exposure chambers: 14.5 m3 chambers with stainless steel pyramidal-shaped ceilings with resin-coated floors and walls. - Details on mating procedure:
- F0: after 14-week exposure; F1: after 17-week exposure
Breeding programme: two 5-day cohabitation periods
M/F ratios per cage: 1M/1F;
F1: avoided breeding of females and males from the same litter. - Duration of treatment / exposure:
- For 14 weeks (F0 rats); for 17 weeks (F1 rats).
Dams were not exposed from gestation Day 21 until postpartum Day 4. - Frequency of treatment:
- 6 h/day, 5 days/week –premating period
6 h/day, 7 days/week –mating, gestation and lactation.
Doses / concentrations
- Remarks:
- Doses / Concentrations:
0, 100, 500, or 1500 ppm
Basis:
- No. of animals per sex per dose:
- F0 and F1: 30 male and 30 female rats per group/per dose.
- Control animals:
- yes
Examinations
- Parental animals: Observations and examinations:
- CAGE SIDE OBSERVATIONS: Yes / Daily observation for signs of toxicity and changes in demeanour.
- Time schedule:
- Cage side observations checked in table [No.?] were included.
body weights measured prior to exposure start and weekly thereafter prior to mating; then after mating females – bodyweights measured on gestation Days 0, 7, 14 & 21; males - bodyweights measured weekly. - Litter observations:
- Offspring: sex, body weights, number of live pups (on Days 1, 4, 7, 14, 21, & 28 after delivery.
F1 (10/sex/dose group) and F2 (30/sex/dose group): complete necropsy examination. Complete histopathology performed on F1 and F2 of control and high dose group. - Postmortem examinations (parental animals):
- F0 and F1: gross necropsy of organs and tissues, histopathology was not performed.
- Statistics:
- Bartlett’s test, ANOVA, Dunnett’s test, Wilcoxon’s rank sum test with Bonferroni’s correction (for body weights), Fisher exact probability test (for fertility indices), binominal distribution test (for neonatal sex ratio).
Results and discussion
Overall reproductive toxicity
- Reproductive effects observed:
- not specified
Any other information on results incl. tables
NOAEC parental toxicity:
1500 ppm
NOAEC developmental & reproduction toxicity:
1500 ppm
F0 Generation:
Mortality:
No treatment-related mortality or signs of toxicity were observed.
Body weight:
No treatment-related significant reductions in body weights were observed.
Fertility and gestation:
No treatment related changes in survival, letter size and pup weights were observed.
Necropsy & Gross examination:
No treatment-related lesions were observed.
F1 Generation:
Mortality:
No treatment-related mortality or signs of toxicity were observed.
Body weight:
No treatment-related significant reductions in body weights were observed.
Fertility and gestation:
No treatment related changes in survival, letter size and pup weights were observed.
Necropsy & Gross examination:
No treatment-related lesions were observed.
Histopathologic examination:
No treatment-related histopathologic changes were observed.
Applicant's summary and conclusion
- Conclusions:
- Under the study conditions, a level of 1500 ppm methylene chloride vapour is considered as a no observed adverse effect concentration (NOAEC) for both parental and developmental/ reproductive toxicity in Fischer 344 rats.
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