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  2. Benzylamine - Wikipedia

    en.wikipedia.org/wiki/Benzylamine

    Benzylamine, also known as phenylmethylamine, is an organic chemical compound with the condensed structural formula C 6 H 5 CH 2 NH 2 (sometimes abbreviated as PhCH 2 NH 2 or BnNH 2).It consists of a benzyl group, C 6 H 5 CH 2, attached to an amine functional group, NH 2.

  3. Benzyl group - Wikipedia

    en.wikipedia.org/wiki/Benzyl_group

    Benzyl is most commonly abbreviated Bn. For example, benzyl alcohol can be represented as BnOH. Less common abbreviations are Bzl and Bz, the latter of which is ambiguous as it is also the standard abbreviation for the benzoyl group C 6 H 5 C(O)−.

  4. Occupational toxicology - Wikipedia

    en.wikipedia.org/wiki/Occupational_toxicology

    Additionally, these sectors involve directly handling various substances that can possibly contain harmful chemical compounds. Toxicological studies are experimental laboratory studies on the response of organisms and biological pathways to a substance, and can generate data that are used for other occupational safety and health activities. [4]

  5. Xylamine - Wikipedia

    en.wikipedia.org/wiki/Xylamine

    Xylamine is a monoaminergic neurotoxin and benzylamine derivative that is closely related to DSP-4. [1] [2] It is a relatively selective noradrenergic neurotoxin, which is attributed to its high affinity for the norepinephrine transporter (NET). [1]

  6. Chemical hazard - Wikipedia

    en.wikipedia.org/wiki/Chemical_hazard

    Chemical exposure to the skin is a common workplace injury and may also occur in domestic situations with chemicals such as bleach or drain-cleaners. The exposure of chemicals to the skin most often results in local irritation to the exposed area. [9] In some exposures, the chemical will be absorbed through the skin and will result in poisoning ...

  7. Histone deacetylase inhibitor - Wikipedia

    en.wikipedia.org/wiki/Histone_deacetylase_inhibitor

    To carry out gene expression, a cell must control the coiling and uncoiling of DNA around histones.This is accomplished with the assistance of histone acetyl transferases (HAT), which acetylate the lysine residues in core histones leading to a less compact and more transcriptionally active euchromatin, and, on the converse, the actions of histone deacetylases (HDAC), which remove the acetyl ...

  8. Isopropylbenzylamine - Wikipedia

    en.wikipedia.org/wiki/Isopropylbenzylamine

    N-isopropylbenzylamine is a compound that has appeared in chemical literature often playing an intermediary role in applications of experimental synthesis and novel organic transformations.

  9. Globally Harmonized System of Classification and Labelling of ...

    en.wikipedia.org/wiki/Globally_Harmonized_System...

    The pictogram for harmful substances of the Globally Harmonized System of Classification and Labelling of Chemicals.. The Globally Harmonized System of Classification and Labelling of Chemicals (GHS) is an internationally agreed-upon standard managed by the United Nations that was set up to replace the assortment of hazardous material classification and labelling schemes previously used around ...