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EC number: 206-462-1 | CAS number: 345-78-8
- 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
Key value for chemical safety assessment
Additional information
An Ames Test (OECD TG 471, GLP) is available where the tester strains Salmonella typhimurium TA 1535, TA 1537, TA 98 and TA 100 were used to examine the mutagenic potential of the test substance up to concentrations of 5000 µg/plate in a standard plate test a preincubation test with and without metabolic activation (BASF 1991). Neither cytotoxic nor genotoxic effects have been observed, thus the test substance possessed no mutagenic potential in the bacterial system used.
In addition, two bacterial reverse mutation studies performed with two different structural analogues of pseudoephedrine hydrochloride are available. The mutagenicity of (-)-Norephedrin S krist has been tested with 4 Salmonella typhimurium strains (TA 1535, TA 1537, TA 98, and TA 100) and one E. Coli strain (WP2 uvrA) in a standard plate test and a preincubation test (BASF 2000). The mutagenicity of ephedrine sulfate has been tested with four strains of Salmonella typhimurium (TA 1535, TA 100, TA98, TA 97) in a preincubation test (NTP 1986). In none of these studies an increase in the number of revertants was observed either without S9 mix or after the addition of a metabolizing system.
In the study performed with pseudoephedrine hydrochloride, Salmonella typhimurium strains TA 1535, TA 1537, TA 98 and TA 100 were used. In accordance with OECD Guideline 471, mutagenicity in bacteria should also be tested in Salmonella typhimurium strain TA102 or E.coli WP2. In the studies performed with the two analogues of pseudoephedrine hydrochloride no mutagencity was observed in these Salmonella and E.coli strains. It was therefore concluded that these test substances are not mutagenic in bacteria and as a result pseudoephedrine hydrochloride is considered to be not mutagenic to bacteria.
Justification for selection of genetic toxicity endpoint
One Genetic toxixity study is available. This study is adequate for covering this endpoint.
Short description of key information:
It is concluded that there is no evidence of induction of gene mutations by the test substance and its metabolites in the four S. typhimurium strains used in an OECD 471 guideline study. In addition two bacterial reverse mutation studies are available, performed with two different structural analogous of pseudoephedrine hydrochloride. These two structural analogues: (-)-Norephedrin S krist, and ephedrine sulphate do not induce the number of revertants either without S9 mix or after the addition of a metabolizing system. It was therefore concluded that pseudoephedrine hydrochloride is not mutagenic.
Endpoint Conclusion: No adverse effect observed (negative)
Justification for classification or non-classification
Pseudoephedrine hydrochloride and the structural analogues of pseudoephedrine hydrochloride: (-)-Norephedrin S krist, and ephedrine sulfate are all non-mutagenic in the different Ames tests performed. Based on this, classification for genetic toxicity is not warranted in accordance with EU Directive 67/548 (DSD) and EU Classification, Labeling and Packaging of Substances and Mixtures (CLP) Regulation No. 1272/2008.
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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