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Related Concept Videos

Halogens03:01

Halogens

Group 17 elements, known as halogens, are nonmetals. At room temperature, fluorine and chlorine are gases, bromine is a liquid, and iodine a solid. Astatine is a highly unstable radioactive element, so currently, most of its properties are unknown due to its short half-life. Tennessine is a synthetic element also predicted to be in this group.
Supercritical Fluid Chromatography01:18

Supercritical Fluid Chromatography

Supercritical fluid chromatography (SFC) provides a beneficial substitute for gas chromatography (GC) and liquid chromatography (LC) for certain samples because it merges the top attributes of both techniques. SFC allows the separation and analysis of compounds that GC or LC does not easily manage. These compounds are traditionally nonvolatile or thermally unstable, making GC unsuitable and lacking functional groups required for HPLC analysis.
SFC utilizes a supercritical fluid mobile phase,...
Molecular Shape and Polarity03:37

Molecular Shape and Polarity

Dipole Moment of a Molecule
Gas Chromatography: Types of Detectors-II01:19

Gas Chromatography: Types of Detectors-II

In gas chromatography, different detectors are employed to meet specific analytical needs. These detectors are often categorized based on their detection mechanisms and the types of compounds they are best suited to analyze. Thermal Conductivity Detectors (TCD), Flame Ionization Detectors (FID), and Electron Capture Detectors (ECD) represent common categories, each with unique operating principles and applications. However, beyond these, several other detectors are designed for more specialized...
Alkyl Halides02:45

Alkyl Halides

Structural Properties
Alkyl halides are halogen-substituted alkanes wherein one or more hydrogen atoms of an alkane is replaced by a halogen atom such as fluorine, chlorine, bromine, or iodine. The carbon atom in an alkyl halide is bonded to the halogen atom, which is sp3-hybridized and exhibits a tetrahedral shape.
Unlike alkyl halides, compounds in which a halogen atom is bonded to an sp2 -hybridized carbon atom of a carbon-carbon double bond (C=C) are called vinyl halides. Whereas aryl...
Electrophilic Aromatic Substitution: Fluorination and Iodination of Benzene01:13

Electrophilic Aromatic Substitution: Fluorination and Iodination of Benzene

Bromination and chlorination of aromatic rings by electrophilic aromatic substitution reactions are easily achieved, but fluorination and iodination are difficult to achieve. Fluorine is so reactive that its reaction with benzene is difficult to control, resulting in poor yields of monofluoroaromatic products. To address this, Selectfluor reagent is used as a fluorine source in which a fluorine atom is bonded to a positively charged nitrogen.

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Related Experiment Video

Updated: May 19, 2026

Identifying Per- and Polyfluorinated Chemical Species with a Combined Targeted and Non-Targeted-Screening High-Resolution Mass Spectrometry Workflow
09:04

Identifying Per- and Polyfluorinated Chemical Species with a Combined Targeted and Non-Targeted-Screening High-Resolution Mass Spectrometry Workflow

Published on: April 18, 2019

Perfluorinated compounds.

Christopher Lau1

  • 1Toxicity Assessment Division, National Health and Environment Effects Research Laboratory, Office of Research and Development, U.S. Environmental Protection Agency, Research Triangle Park, NC, 27711, USA, lau.christopher@epa.gov.

Experientia Supplementum (2012)
|September 5, 2012
PubMed
Summary
This summary is machine-generated.

Per- and polyfluoroalkyl substances (PFAS) are widespread synthetic chemicals. Recent research reveals their environmental persistence, bioaccumulation, and potential adverse health effects, prompting global concern.

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Area of Science:

  • Environmental Science and Toxicology
  • Public Health
  • Chemical Risk Assessment

Background:

  • Per- and polyfluoroalkyl substances (PFAS) are synthetic chemicals with widespread industrial and consumer applications since the 1950s.
  • Historically considered biologically inactive, recent findings highlight their global distribution, environmental persistence, and presence in humans and wildlife.
  • Growing evidence links PFAS to adverse health effects observed in laboratory animals, increasing scientific, regulatory, and public scrutiny.

Purpose of the Study:

  • To provide an overview of recent advancements in understanding PFAS.
  • To summarize current knowledge on environmental and human exposure pathways.
  • To review toxicological data, modes of action in animal models, and epidemiological findings.

Main Methods:

  • Literature review of recent scientific publications on PFAS.
  • Synthesis of data on environmental monitoring and human biomonitoring studies.
  • Analysis of toxicological studies in animal models and epidemiological research.

Main Results:

  • PFAS are globally distributed and environmentally persistent.
  • Evidence indicates bioaccumulation in humans and wildlife.
  • Toxicological studies in animals suggest potential adverse health outcomes.
  • Epidemiological studies are emerging to assess human health impacts.

Conclusions:

  • Significant scientific, regulatory, and public interest surrounds PFAS due to their persistence and potential health risks.
  • Further research is needed to fully elucidate the long-term health effects of PFAS exposure in humans.
  • Understanding exposure, toxicology, and epidemiology is crucial for risk assessment and management of PFAS.