Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 231-887-4 | CAS number: 7775-09-9
- 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: other studies
Administrative data
- Endpoint:
- toxicity to reproduction: other studies
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- study well documented, meets generally accepted scientific principles, acceptable for assessment
- Remarks:
- The study provides scientific evidence that heparin binding autocrine factors modulate testosterone production by the adult rat Leydig cell.
Data source
Reference
- Reference Type:
- publication
- Title:
- Evidence that heparin binding autocrine factors modulate testosterone production by the adult rat Leydig cell
- Author:
- McFarlane JR, Laslett A, de Kretser DM and Risbridger GP
- Year:
- 1 996
- Bibliographic source:
- Molecular and Cellular Endocrinology 118: 57-63
Materials and methods
- Principles of method if other than guideline:
- Leydig cells obtained from testes of adult rats aged between 90-120 days, and purified (purity of the resulting Leydig cell preparations was 96 ± 3%). These cells were incubated in the absence or presence of a maximally stimulating dose of LH, together with the test substances (sodium chlorate, protamine sulphate, and sodium chlorate/heparin). Controls of nonspecific binding were included in the test.
- GLP compliance:
- not specified
- Type of method:
- in vitro
Test material
- Reference substance name:
- Sodium chlorate
- EC Number:
- 231-887-4
- EC Name:
- Sodium chlorate
- Cas Number:
- 7775-09-9
- Molecular formula:
- ClHO3.Na
- IUPAC Name:
- sodium chlorate
- Details on test material:
- - Name of test material (as cited in study report): Sodium Chlorate
Constituent 1
Results and discussion
Effect levels
- Remarks on result:
- not measured/tested
Observed effects
Testosterone production by dibutryl-cAMP stimulated Leydig cells was also inhibited by sodium chlorate.
Any other information on results incl. tables
The sodium chlorate (25 mM) inhibited testosterone production by LH stimulated cells by over 50%, but had no effect on unstimulated cells. Testosterone production by dibutryl-cAMP stimulated Leydig cells was also inhibited by sodium chlorate.
The LH responsiveness and testosterone production returned to normal after the sodium chlorate was removed from the culture media
Applicant's summary and conclusion
- Conclusions:
- The sodium chlorate (25 mM) was able to significantly suppress testosterone production by adult rats LH stimulated cells (over 50%) and also the testosterone production by dibutryl-cAMP stimulated Leydig cells.
- Executive summary:
The aim of this study was to determine the role of cell surface heparan sulfate proteoglycans in the regulation of testosterone secretion by adult rat Leydig cells. In some experiments the effect of sodium chlorate was evaluated. The sodium chlorate (25 mM) inhibited testosterone production by LH stimulated cells by over 50%, but had no effect on unstimulated cells. Testosterone production by dibutryl-cAMP stimulated Leydig cells was also inhibited by sodium chlorate. The LH responsiveness and testosterone production returned to normal after the sodium chlorate was removed from the culture media.
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.