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EC number: 233-140-8 | CAS number: 10043-52-4
- 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
Developmental toxicity / teratogenicity
Administrative data
- Endpoint:
- developmental toxicity
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Comparable to OECD guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 974
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 414 (Prenatal Developmental Toxicity Study)
- GLP compliance:
- not specified
- Limit test:
- no
Test material
- Reference substance name:
- Calcium chloride
- EC Number:
- 233-140-8
- EC Name:
- Calcium chloride
- Cas Number:
- 10043-52-4
- Molecular formula:
- CaCl2
- IUPAC Name:
- calcium dichloride
- Details on test material:
- Test substance: Tine white granular material marked with FDA 71-87.
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- Dutch
Administration / exposure
- Route of administration:
- oral: gavage
- Duration of treatment / exposure:
- 6th to 18th day of pregnancy
- Frequency of treatment:
- daily
Doses / concentrations
- Remarks:
- Doses / Concentrations:
1.69, 7.85, 35.6, 169 mg/kg/day
Basis:
- Control animals:
- other: sham-treated
- Details on study design:
- Sex: female
Duration of test: up to the last day of pregnancy
Results and discussion
Results: maternal animals
Effect levels (maternal animals)
- Dose descriptor:
- NOAEL
- Effect level:
- > 169 mg/kg bw/day
- Basis for effect level:
- other: maternal toxicity
Results (fetuses)
Effect levels (fetuses)
- Dose descriptor:
- NOAEL
- Effect level:
- > 169 mg/kg bw/day
- Basis for effect level:
- other: teratogenicity
Fetal abnormalities
- Abnormalities:
- not specified
Overall developmental toxicity
- Developmental effects observed:
- not specified
Any other information on results incl. tables
Table 1: Fate Summary
-------------------------------------------------------
Group Material Dose*** Total Surviving at Term
---------------- ---------------
mg/kg Mated Pregnant Total Pregnant*
-------------------------------------------------------
341 Sham 0.0 18 13 18 13
342 6-AN** 2.5 20 10 19 10
347 CaCl2 1.69 22 13 18 12
348 CaCl2 7.85 22 14 16 11
349 CaCl2 35.6 17 14 14 12
350 CaCl2 169.0 16 16 14 14
--------------------------------------------------------
* Includes all dams examined at term
** Positive Control: 2.5 mg/kg of 6-aminonicotinamide
dosed on Day 9
*** Administered as a water solution
- Table 2: Reproduction Data
--------------------------------------------------------
Group 341 342 347 348 349 350
Dose (mg/kg) Sham 6-AN* 1.69 7.85 35.6 169.0
--------------------------------------------------------
-----Pregnancies-----
Total No. 13 10 13 14 14 16
Died or Aborted (before Day 29)
0 1 1 3 2 2
To term (on Day 29)13 10 12 11 12 14
-----Corpora Lutea-----
Total No. 174 122 148 129 138 146
Average/dam mated 9.67 6.42 7.40 7.17 8.63 10.4
-----Live Litters-----
Total No.** 12 10 12 9 11 12
-----Implant Sites-----
Total No. 69 56 86 63 69 72
Average/dam** 5.31 5.60 7.17 7.73 5.75 5.14
-----Resorptions-----
Total No.** 4 2 12 8 8 4
Dams with 1 or more sites resorbed
3 1 4 4 6 3
Dams with all sites resorbed
1 - - 2 1 -
Per cent partial resorptions
23.1 10.0 33.3 36.4 50.0 21.4
Per cent complete resorptions
7.69 - - 18.2 8.33 -
-----Live Fetuses-----
Total No. 65 54 74 55 61 58
Average/dam** 5.00 5.40 6.17 5.00 5.55 4.83
Sex ratio (M/F) 0.86 0.74 1.47 1.04 1.16 1.24
-----Dead Fetuses-----
Total** - - - - - 10
Dams with 1 or more dead
- - - - - 2
Dams with all dead
- - - - - 1
Per cent partial dead
- - - - - 14.3
Per cent all dead - - - - - 7.14
-----Average Fetus Weight (g)-----
38.2 33.8 37.3 38.0 36.8 39.2
---------------------------------------------------------
* Positive Control: 2.5 mg/kg of 6-aminonicotinamide dosed
on Day 9
** Includes only those dams examined at term.
- Table 3: Summary of Skeletal Findings***
---------------------------------------------------------
Group No. 341 342 347 348 349 350
Dose (mg/kg) Sham 6-AN** 1.69 7.85 35.6 169.0
---------------------------------------------------------
Live Fetuses Examined
(at term) 65/12 53/10* 74/12 54/9* 61/11 58/12
-----Sternebrae-----
Incomplete oss. - - 2/1 - 1/1 -
Scrambled
Bipartite - - 1/1 - - -
Fused - 1/1 - - - -
Extra
Missing
Other
-----Rids-----
Incomplete oss.
Fused/split - 2/1 - - - -
Wavy
Less than 12
More than 13
Other
-----Vertebrae-----
Incomplete oss.
Scrambled - 5/1 - - - -
Fused
Extra ctrs. oss.
Scoliosis - 1/1 - - - -
Tail defects - 10/3 - - - -
Other; spina bifida
-----Skull-----
Incomplete closure
1/1 - - - - -
Missing
Craniostosis - - 2/1 - - -
Other
-----Extremities-----
Incomplete oss.
Missing
Extra
-----Miscellaneous-----
---------------------------------------------------------
* One pup lost in processing
** Positive Control: 2.5 mg/kg of 6-aminonicotinamide
dosed on Day 9
*** Numerator = Number of fetuses affected
- Table 4: Summary of Soft Tissue Abnormalities
---------------------------------------------------------
Group Material Dose Level Dam Number Description
(mg/kg) of Pups
---------------------------------------------------------
342 6-AN* 2.5 Z7640 2 Medial rotation
of hind limbs
----------------------------------------------------------
* Positive Control: 2.5 mg/kg of 6-aminonicotinamide dosed
on Day 9
- Table 5: Average body Weights*** (g)
---------------------------------------------------------
Group Material Dose Day0 Day6 Day12 Day18 Day29**
Level
(mg/kg)
---------------------------------------------------------
341 Sham 0.0 2.23 2.32 2.40 2.48 2.59
(13)
342 6-AN* 2.5 1.86 1.94 2.03 2.08 2.18
(10)
347 CaCl2 1.69 2.20 2.31 2.43 2.51 2.64
(12)
348 CaCl2 7.85 2.12 2.16 2.16 2.25 2.33
(11)
349 CaCl2 35.6 2.22 2.31 2.34 2.40 2.50
(12)
350 CaCl2 169.0 2.27 2.39 2.41 2.46 2.50
(14)
---------------------------------------------------------
* Positive Control: 2.5 mg/kg of 6-aninonicotinamide dosed
on Day 9
** Number of surviving dams in parentheses (c.f. Table 1)
*** Of pregnant dams
Applicant's summary and conclusion
- Conclusions:
- The administration of up to 169 mg/kg (body weight) of the
test material to pregnant rats for 13 consecutive days had
no clearly discernible effect on nidation or on maternal or
fetal survival. The number of abnormalities seen in either
soft or skeletal tissues of the test groups did not differ
from the number occurring spontaneously in the sham-treated
controls.
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