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EC number: 276-763-0 | CAS number: 72676-55-2
- 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
Endpoint summary
Administrative data
Description of key information
Additional information
Appearance
5,5'-Dithiodi-1,3,4-thiadiazole-2(3H)-thione is a yellow powder.
Melting Point
Key Study:
In an EU Method A.1 study, not conducted according to GLP, the melting temperature of 5,5'-Dithiodi-1,3,4-thiadiazole-2(3H)-thione is 164.5°C (Intertek Pharmaceutical Services Manchester, 2014).
Boiling Point
Key Study:
In an EU Method A.2 study, not conducted according to GLP, the boiling temperature of 5,5'-Dithiodi-1,3,4-thiadiazole-2(3H)-thione could not be measured due to possible thermal decomposition (Intertek Pharmaceutical Services Manchester, 2014).
Density
Key Study:
In an EU Method A.3 study, not conducted according to GLP, the relative density of 5,5'-Dithiodi-1,3,4-thiadiazole-2(3H)-thione is 2.01 +/- 0.01 at 20°C +/- 0.5°C (Intertek Pharmaceutical Services Manchester, 2014).
Particle Size
Key Study:
In an OECD 110 study, not conducted according to GLP, the median particle size of 5,5'-Dithiodi-1,3,4-thiadiazole-2(3H)-thione is 6.456 µm, with a mass median aerodynamic diameter of 4.554 µm. The particle size distribution is 10% of the substance <2.719 µm, 50% of the substance <6.456 µm and 90% of the substance <11.816 µm (Intertek Pharmaceutical Services Manchester, 2014).
Vapour Pressure
Key Study:
In an EU Method A.4 study, using the Grain-Watson Correction for Solids and accounting for the enthalpy of melting and a theoretical boiling point, the vapour pressure of 5,5'-Dithiodi-1,3,4-thiadiazole-2(3H)-thione is estimated to be 0.000041 Pa at 25°C (Intertek Pharmaceutical Services Manchester, 2014).
Partition Coefficient
Key Study:
In a study conducted according to GLP, the partition coefficient (log Pow) of 5,5'-Dithiodi-1,3,4-thiadiazole-2(3H)-thione estimated based on the ratio of n-octanol solubility and water solubility is 1.46 at 25 ± 1°C (Intertek Pharmaceutical Services Manchester, 2016).
Water Solubility
Key Study:
In an EU Method A.6 (shake flask) study, conducted according to GLP, the water solubility of 5,5'-Dithiodi-1,3,4-thiadiazole-2(3H)-thione is 167 mg/L at 25°C ± 1°C (Intertek Pharmaceutical Services Manchester, 2016).
Surface Tension
Key Study:
In an EU Method A.5 (plate method), not conducted according to GLP, the mean surface tension of 5,5'-Dithiodi-1,3,4-thiadiazole-2(3H)-thione is 65 mN/m at 25 ± 0.5°C over a measured concentration range of 322 to 434 mg/L (Intertek Pharmaceutical Services Manchester, 2014).
Flash Point
A flash point study is applicable for liquid substances, while a flammability study is applicable for solids. 5,5'-Dithiodi-1,3,4-thiadiazole-2(3H)-thione is a solid, therefore the flammability study is more applicable for testing and the flash point study is waived.
Auto Flammability
Key Study:
In an EU Method A.16 study, not conducted according to GLP, 5,5'-Dithiodi-1,3,4-thiadiazole-2(3H)-thione did not auto ignite (Intertek Pharmaceutical Services Manchester, 2014).
Flammability
Key Study:
In an EU Method A.10 study, not conducted according to GLP, 5,5'-Dithiodi-1,3,4-thiadiazole-2(3H)-thione is not flammable (Intertek Pharmaceutical Services Manchester, 2014).
Explosivity
Key Study:
Based on a comprehensive examination of the structural formula, according to guidance in the UN Transport of Dangerous Goods, Manual of Tests and Criteria, 5,5'-Dithiodi-1,3,4-thiadiazole-2(3H)-thione does not exhibit explosive properties and is not considered capable of rapid gas or heat release (Intertek Pharmaceutical Services Manchester, 2014). Conduct of an explosivity study according to EU Method A.14 therefore is waived.
Oxidising Properties
Key Study:
In an EU Method A.17 study, not conducted according to GLP, 5,5'-Dithiodi-1,3,4-thiadiazole-2(3H)-thione is not oxidising (Intertek Pharmaceutical Services Manchester, 2014).
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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