On these pages, ECHA publishes the following non-confidential data in IUCLID 6 format.
Reference substances: A Reference substance is a software entity in IUCLID that is used to define the identity of a Substance, or a component within it, in such a way that the definition may be re-used in more than one location. This provides consistency and avoids duplication of work. A Reference substance contains chemical identifiers and structural information. Reference substances can be created in IUCLID but you may find it more efficient to take a ready-made one from this collection and import it in to IUCLID. There are thousands available, but it is possible to search for and download only what you need.
IUCLID inventories: Chemical inventories are a type of data in IUCLID that is used as a source of chemical identifiers that have been defined outside IUCLID. A link can be created from a Reference substance to an inventory entry. This provides the Reference substance with information on chemical identity in a re-usable way, and in a standard format. For example, the EC Inventory contains chemical identifiers such as EC numbers, CAS numbers and molecular formulae. It is delivered with IUCLID 6 Desktop, but not with IUCLID 6 Server. The EC Inventory is available for download here.
REACH Study Results: REACH Study Results is a collection of non-confidential substance data that was submitted to ECHA under the REACH regulation. It contains results from studies that relate to physical-chemical properties, environmental fate and pathways, and ecotoxicology and toxicological information.
Industry data contribution: Previously unpublished data on chemicals tested to develop medicines is now publicly available. The information can contribute, among other purposes, to the development of predictive computational testing models.
US FDA toxicity data: These data, provided by the United States Food and Drug Administration, contain pre-clinical animal, and clinical human data. The animal data are based on test results extracted from pharmacological reviews, including studies of types: repeat-dose, carcinogenicity, developmental and reproductive toxicity. The human data are derived from structured product labels.
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