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EC number: 200-880-8 | CAS number: 75-57-0
- 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:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study without detailed documentation
- Remarks:
- Study conducted following OECD guideline 421 and GLP principles. However, only limited data were available for review (data from SIDS Initial Assessment Report).
- Justification for type of information:
- The rationale to read across the data is attached in section 14.
Cross-reference
- Reason / purpose for cross-reference:
- reference to same study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 005
- Report date:
- 2005
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 421 (Reproduction / Developmental Toxicity Screening Test)
- GLP compliance:
- yes
- Limit test:
- no
Test material
- Reference substance name:
- TMAH
- IUPAC Name:
- TMAH
- Details on test material:
- - Name of test material (as cited in study report): TMAH
- Analytical purity: >99.9%
- Lot No.: 40914
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Sprague-Dawley
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: not reported
- Age at study initiation: (P) 9 wks; (F1) 4 days
No further details provided.
Administration / exposure
- Route of administration:
- oral: gavage
- Vehicle:
- water
- Details on exposure:
- No details reported.
- Details on mating procedure:
- No details reported.
- Analytical verification of doses or concentrations:
- not specified
- Duration of treatment / exposure:
- Male: 14 days before mating to the day before scheduled death through mating (total 32 days).
Female: 14 days before mating to 3 days after delivery through mating and gestation periods. - Frequency of treatment:
- daily
- Details on study schedule:
- No details reported
Doses / concentrationsopen allclose all
- Dose / conc.:
- 1 mg/kg bw/day
- Dose / conc.:
- 5 mg/kg bw/day
- Dose / conc.:
- 20 mg/kg bw/day
- No. of animals per sex per dose:
- 10
- Control animals:
- yes, concurrent vehicle
- Details on study design:
- For mating, one male to one female mating was used. A female rat was placed together with a male rat until copulation occurred. When no copulation was observed, the female animal was mated with another male animal of the same dose group for additional 14 days. Day 0 of gestation (GD 0) was defined as the day a vaginal plug or sperm was found.
- Positive control:
- No
Examinations
- Parental animals: Observations and examinations:
- CAGE SIDE OBSERVATIONS: Yes
DETAILED CLINICAL OBSERVATIONS: Yes, twice daily
BODY WEIGHT: Yes, males were weighed on Day 1 and 3 of dosing, and weekly thereafter. Females were weighed on Day 1, 3 and 7 of dosing, weekly thereafter until delivery, and PND 0 and 4. - Litter observations:
- Clinical signs and body weights of the live pups were recorded.
- Postmortem examinations (parental animals):
- Autopsy at end of experiment.
- Postmortem examinations (offspring):
- Autopsy at end of experiment.
- Statistics:
- Statistical analysis : Bartlett's test, one-way analysis of variance, Dunnett's test, Kruskal-wallis test, chi-square test
Results and discussion
Results: P0 (first parental generation)
General toxicity (P0)
- Clinical signs:
- effects observed, treatment-related
- Description (incidence and severity):
- Salivation was observed on the 4th day of administration and later in male and female rats at 5 mg/kg bw/day and higher. Salivation was considered to be due to strong alkaline property of TMAH, but not due to toxic effects of TMAH. In the female animals at 20 mg/kg bw/day, a decrease in locomotor activity, incomplete eyelid opening or eyelid closure, and loss of hair were observed on GD 21 and thereafter.
- Mortality:
- mortality observed, treatment-related
- Description (incidence):
- One female rat at 20 mg/kg bw/day died on GD 22 and another one on GD 23 during parturition. Although the two deaths occurred at highest dose level, no further details are included on cause of death. therefore it is unclear if mortality was substance-related or incidental.
- Body weight and weight changes:
- effects observed, treatment-related
- Description (incidence and severity):
- Significant decrease in body weight females after parturition.
- Organ weight findings including organ / body weight ratios:
- not specified
- Histopathological findings: non-neoplastic:
- not specified
Reproductive function / performance (P0)
- Reproductive function: oestrous cycle:
- not examined
- Reproductive function: sperm measures:
- not specified
- Reproductive performance:
- no effects observed
- Description (incidence and severity):
- Tetramethylammonium hydroxide showed no effect on number of days required for successful copulation, copulation index, fertility indices of males and females, implantation index, gestation length and delivery index.
Effect levels (P0)
open allclose all
- Key result
- Dose descriptor:
- NOAEL
- Effect level:
- 5 mg/kg bw/day (actual dose received)
- Based on:
- test mat.
- Sex:
- female
- Basis for effect level:
- mortality
- body weight and weight gain
- Key result
- Dose descriptor:
- NOAEL
- Effect level:
- >= 20 mg/kg bw/day
- Based on:
- test mat.
- Sex:
- male/female
- Basis for effect level:
- reproductive performance
Results: F1 generation
General toxicity (F1)
- Clinical signs:
- no effects observed
- Mortality / viability:
- mortality observed, treatment-related
- Description (incidence and severity):
- At 20 mg/kg, one stillborn was observed (male). The number of total newborns per dam that delivered newborns was 13.2, 14.0, 13.5 and 12.3 at respectively 0, 1, 5 and 20 mg/kg bw/day.
- Body weight and weight changes:
- not examined
- Sexual maturation:
- not examined
- Organ weight findings including organ / body weight ratios:
- not specified
- Gross pathological findings:
- not specified
- Histopathological findings:
- not examined
Developmental neurotoxicity (F1)
- Behaviour (functional findings):
- not examined
Developmental immunotoxicity (F1)
- Developmental immunotoxicity:
- not examined
Details on results (F1)
The percentage of live newborns at day 4 after birth was 97.7%, 98.4%, 100% and 85.4% for 0, 1, 5 and 20 mg/kg bw respectively.
Effect levels (F1)
- Key result
- Dose descriptor:
- NOAEL
- Generation:
- F1
- Effect level:
- >= 20 mg/kg bw/day (actual dose received)
- Based on:
- test mat.
- Sex:
- male/female
- Basis for effect level:
- other: No effects seen at highest test concentration.
- Remarks on result:
- other: Mortality of pups during day 1-4 after birth was seen at 20 mg/kg bw/day, but in absence of more detailed information this effect is considered to be related to maternal toxicity and not a direct effect of TMAH.
Overall reproductive toxicity
- Key result
- Reproductive effects observed:
- no
Any other information on results incl. tables
Table
1. Mating and fertility findings in the reproductive/developmental
toxicity screening test of tetramethylammonium hydroxide.
============================================================
Parameter Dose
(mg/kg bw/day)
--------------------------------
0 1 5 20
-----------------------------------------------------------
[Male]
No. of animals mated 10 10 10 11
No. of animals that copulated
10 10 10 10
No. of animals that produced pregnant female
10 10 10 10
-----------------------------------------------------------
[Female]
No. of animals mated 10 10 10 10
No. of animals that copulated
10 10 10 10
No. of pregnant animals 10 10 10 10
-----------------------------------------------------------
Duration of mating(days required for successful copulation)
Mean 3.0 2.7 3.2 4.7
S.D. 1.49 1.42 1.03 5.44
============================================================
Table
2. Postnatal outcomes in the reproductive/developmental toxicity
screening test of tetramethylammonium hydroxide.
============================================================
Parameter Dose
(mg/kg bw/day)
----------------------------------
0 1 5 20
-----------------------------------------------------------
[Dam]
No. of dams 10 10 10 9
No. of
dams delivered live newborns
10 9 10 8
Duration of pregnancy(day)
Mean 22.0 22.0 21.8 22.3
S.D. 0.00 0.50 0.42 0.46
No. of implantation sites 1)
141(14.1) 147(14.7) 148(14.8) 123(13.7)
-----------------------------------------------------------
[Newborns]
No. of newborns
Total
2) 132(13.2) 126(14.0) 135(13.5) 98(12.3)
Male 61 65 71 45
Female 71 61 64 52
No. of stillborns 0 0 0 1(Male)
Sex ratio of live newborns at birth (male/female)
61/71 65/61 71/64 44/52
No. of deads 3 2 0 14
No. of live newborns on PND 4
Total
3) 129(97.7) 124(98.4) 135(100) 82(85.4)
Male
3) 58(95.1) 64(98.5) 71(100) 37(84.1)
Female
3) 71(100) 60(98.4) 64(100) 45(86.5)
============================================================
1)
The value in parentheses is the number of implantation sites per dam.
2) The value in parentheses is the number of total newborns per dam
delivered live newborns.
3) The value in parentheses is percentage of live newborns at birth.
Table
3. External findings on newborns in the reproductive/developmental
toxicity screening test of tetramethylammonium hydroxide.
============================================================
Parameter Dose(mg/kg
bw/day)
------------------------------------
0 1 5 20
-----------------------------------------------------------
No. of dams 10 9 10 8
-----------------------------------------------------------
[PND 0]
No. of newborns examined 132 126 135 82
No. of newborns with abnormalities
0 0 0 0
-----------------------------------------------------------
[PND 4]
No. of newborns examined 129 124 135 82
No. of newborns with abnormalities
0 0 0 0
============================================================
Applicant's summary and conclusion
- Conclusions:
- In a reproductive/developmental toxicity screening test in rats according to OECD guideline 421 and GLP principles, the NOAEL for parental toxicity was found to be 5 mg/kg bw/d. Since no effects were seen on fertility and development, the NOAELs for these endpoint were found to be >=20 mg/kg bw/d.
- Executive summary:
A reproductive/developmental toxicity screening test was performed with rats according to OECD guideline 421 and GLP principles. TMAH was dosed by oral gavage at 0, 1, 5 and 20 mg/kg bw/d. A significant decrease in food consumption was observed at 20 mg/kg bw/day on Day 3 in male animals and on gestation day (GD) 20 in female animals. In the female animals at 20 mg/kg bw/day, a decrease in locomotor activity, incomplete eyelid opening or eyelid closure, and loss of hair were observed on GD 21 and thereafter, and a significant decrease in body weight on days 0 and 4 after parturition (PND 0 and 4). One female rat at 20 mg/kg bw/day died on GD 22 and another one on GD 23 during parturition. Tetramethylammonium hydroxide showed no effect on any of the following parental reproductive parameters; days required for successful copulation, copulation index, fertility indices of males and females, implantation index, gestation length and delivery index. There was no effect of tetramethylammonium hydroxide on either the numbers of total newborns, sex ratio. No compound-related abnormality was observed either in external features.
Based on these observations, the NOAEL for parental toxicity was found to be 5 mg/kg bw/day and for reproduction/developmental toxicity >=20 mg/kg bw/day in rats.
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