WebOct 13, 2024 · Phenylalanine is a type of amino acid. Amino acids are molecules that combine to form proteins. Phenylalanine is an essential amino acid in humans, meaning that the body cannot synthesize its own... WebAug 21, 2014 · Phenylketonuria (PKU) is an inherited disorder of metabolism that causes an increase in the blood of a chemical known as phenylalanine. Phenylalanine comes from a person's diet and is used by the body to make proteins. Phenylalanine is found in all food proteins and in some artificial sweeteners. Without dietary treatment, phenylalanine can ...
Phenylalanine in diet soda: Is it harmful? - Mayo Clinic
WebApr 1, 2024 · aniline (countable and uncountable, plural anilines) (organic chemistry) The simplest aromatic amine, C 6 H 5 NH 2, synthesized by the reduction of nitrobenzene; it is a colourless oily basic poisonous liquid used in the manufacture of dyes and pharmaceuticals. Synonyms . aminobenzene; phenylamine; Derived terms . WebDec 23, 2024 · Phenylalanine can cause intellectual disabilities, brain damage, seizures and other problems in people with PKU. Phenylalanine occurs naturally in many protein-rich … how to wire a downlight
Phenylamine - definition of phenylamine by The Free Dictionary
WebDec 23, 2024 · Phenylalanine can cause intellectual disabilities, brain damage, seizures and other problems in people with PKU. Phenylalanine occurs naturally in many protein-rich foods, such as milk, eggs and meat. Phenylalanine is also sold as a dietary supplement. The artificial sweetener aspartame (Equal, NutraSweet), which is added to many medications ... WebAniline, phenylamine or aminobenzene is a toxic organic compound with the formula C6H5NH2. Consisting of a phenyl group attached to an amino group, aniline is the prototypical aromatic amine. Its main use is in the manufacture of precursors to polyurethane and other industrial chemicals. WebAniline is an organic molecule with the chemical formula C 6 H 5 NH 2 that consists of a phenyl group connected to an amino group. Aniline has an excess of negative charge or electron in the ortho and para positions of a benzene ring than in the meta position; thus, the o and p locations are directed towards the electrophilic substitution ... origin of madeleine