The ratings reflect potential health hazards but do not account for the level of exposure or individual susceptibility, factors which determine actual health risks, if any. Registrant can provide information on eye exposure as mentioned above for ‘Data for workers – eye exposure.’. Log Pow provides substance information on the partition coefficient type Pow at a temperature measured in °C and acidity in pH. ECHA’s Guidance Chapter R.12: Use Descriptor system of ECHA’s Guidance on information requirements and chemical safety assessment, ECHA guidance chapter R.12: Use Descriptor system of ECHA Guidance on information requirements and chemical safety assessment, Guidance on the safe use of the substance, Endocrine disrupter testing in aquatic vertebrates – in vivo. If so, the data provided is not processed for the Brief Profile. Displayed are the RANGES of min – max of the PRIORITISED value(s) within the five highest priority groupings of provided data. Degradation rate constant with OH radicals provides substance information on the substance’s degradation rate constant with OH Radicals as a reaction type in cm3molecule-1s-1, cm3molecule-1d-1, m3molecule-1s-1 or m3molecule-1d-1. Therefore this does not constitute official and legally binding information. This section summarises the boiling point values from all registered dossiers for the substance. Long-term EC10 or LC10 or NOEC for soil microorganisms provides substance information on the substance’s effect concentration or lethal concentration (long term) for 10% of the soil microorganisms in the test, or the no observed effect concentration for soil microorganisms. European Commission. While the Agency tries to aggregate the information on chemicals in the best possible way, ECHA cannot check whether all the information provided by industry is free of errors. 1 000 g will be displayed as 1 kg. Guidance on the safe use of the substance provided by manufacturers and importers of this substance. Note: Registrants can also select ‘other’ as the test species, dose descriptor type and/or the unit of measure. Applicant’s summary and conclusion – Interpretation of results (inhalation). No or insufficient data available at present, Hazard related to composition of atmosphere identified, No potential to cause toxic effects if accumulated (in higher organisms) via the food chain, bw/day (mg/kg bw/day; mg/kg bw/day; mg/kg bw/day), DMEL (Derived Minimum Effect Level) - not included for short–term effects, Insufficient data available (further information necessary), Hazard unknown (no further information necessary), Hazard unknown but no further hazard information necessary as no exposure expected, ‘No DNEL required: short term exposure controlled by conditions for long-term’ is added, Hamster (combine hamster, Armenian; hamster, Chinese and hamster, Syrian), No adverse effect observed (not irritating), Adverse effect observed (irreversible damage), mg/kg bw/day (nominal/actual dose received), See ‘Study results oral: Prioritization by test species’, mg/L air (combining mg/L air, mg/L air (nominal), mg/L air (analytical), mg/m³ air, mg/m³ air (nominal), mg/m³ air (analytical)), ppm (combine ppm, ppm (nominal), ppm (analytical), mg/kg bw/day (actual dose received), mg/kg bw/day (combining mg/kg bw/day (nominal), mg/kg bw/day (actual dose received) and mg/kg bw/day), mg/cm² per day (combining mg/cm² per day, mg/cm² per day (nominal), mg/cm² per day (analytical)), No study available / no study available (further information necessary). More information on processable studies and data-waiving is available in the section help of the ‘Scientific properties’. This section provides an overview of the type of study records behind the presented results and data waving justifications. Note: Registrants can also select ‘BMD’, ‘BMC’, ‘dose level’ and ‘conc. 90028-68-5 Access full datasheet Displayed is the most conservative of the prioritised value(s). Water solubility provides substance information on the substance’s solubility in water in grams per litre at a temperature measured in °C. Processable data is prioritised by the toxicity descriptor type (see list below) and subsequently further prioritised by duration (longer prioritised over shorter). This substance is used by consumers, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing. For substance’s physical state at 20°C and 1 013 hPa, registrants can classify their substance as: For substance’s form, registrants can classify their substance as: For substance’s odour, registrants can classify their substance as: For substance’s type, registrants can classify their substance as: Summary data is collected from the endpoint summary(ies) provided by registrants of REACH dossiers. Appears as: listid: IFRA-458; Chemical_Name: Oakmoss Extracts; Synonyms: Oakmoss absoluteEvernia absoluteEvernia prunastri, ext. This section summarises the values related to adsorption/desorption from all registered dossiers for the substance. level’ as the dose descriptor. This section provides an overview of the type of study records behind the presented results and – if applicable - data-waving justifications. Please see Registrants/Suppliers details. Sed elementum odio augue, eget iaculis lorem faucibus vel. ECHA maintains the C&L Inventory, but does not review or verify the accuracy of the information. The quality and correctness of the information remains the responsibility of the data submitter. The Restriction list describes the conditions for the manufacture, placing on the market or use of certain substances, either on their own or in mixtures or articles. The availability of additional data beyond the five results displayed is indicated by (…).Processable data is prioritised by the toxicity descriptor type (see list below) and subsequently further prioritised by duration (longer prioritised over shorter). Applicant’s summary and conclusion – Interpretation of results. This substance has not been registered under the REACH Regulation, therefore as yet ECHA has not received any data about this substance from registration dossiers. If only waived data is available for the substance, following justifications for data-waiving can be displayed in the Brief Profile: Some endpoints are not included in the Brief Profile due to the use of free text and/or complex field(s) in the reporting of information, which cannot be easily summarised by an automatic algorithm. This section displays the values related to repeated dose toxicity from all registered dossiers for the substance. The PIC regulatory processes identified for the Brief Profile are: The ’About this substance’ section provides an overview of the volume in which this substance is manufactured or imported to the European Economic Area (EU28 + Iceland, Liechtenstein and Norway).
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