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  2. Glycine - Wikipedia

    en.wikipedia.org/wiki/Glycine

    Glycine is not widely used in foods for its nutritional value, except in infusions. Instead, glycine's role in food chemistry is as a flavorant. It is mildly sweet, and it counters the aftertaste of saccharine. It also has preservative properties, perhaps owing to its complexation to metal ions.

  3. Glycine (data page) - Wikipedia

    en.wikipedia.org/wiki/Glycine_(data_page)

    Chemical formula: C 2 H 5 N O 2 Molar mass: 75.067 g·mol −1 Systematic name: 2-aminoacetic acid Abbreviations: G, Gly Synonyms: Aciport Aminoacetic acid Aminoethanoic acid Amitone Corilin Glicoamin Glycocoll Glycolixir Glycosthene Glykokoll Glyzin Gyn-hydralin Hampshire glycine Hgly Padil Sucre de gelatine

  4. Glycine N-carboxyanhydride - Wikipedia

    en.wikipedia.org/wiki/Glycine_N-carboxyanhydride

    Glycine N-carboxyanhydride is an organic compound with the formula HNCH(CO) 2 O. A colorless solid, it is the product of phosgenation (reaction with phosgene) of glycine. [4] [5] Glycine N-carboxyanhydride is the simplest member of the amino acid N-carboxyanhydrides. It is also the parent of the 2,5-oxazolidinedione family of heterocycles.

  5. Glycylglycine - Wikipedia

    en.wikipedia.org/wiki/Glycylglycine

    Glycylglycine is the dipeptide of glycine, making it the simplest peptide. [1] The compound was first synthesized by Emil Fischer and Ernest Fourneau in 1901 by boiling 2,5-diketopiperazine (glycine anhydride) with hydrochloric acid. [2] Shaking with alkali [1] and other synthesis methods have been reported. [3]

  6. Dimethylglycine - Wikipedia

    en.wikipedia.org/wiki/Dimethylglycine

    Dimethylglycine (DMG) is a derivative of the amino acid glycine with the structural formula (CH 3) 2 NCH 2 COOH. It can be found in beans and liver, and has a sweet taste. It can be formed from trimethylglycine upon the loss of one of its methyl groups. It is also a byproduct of the metabolism of choline.

  7. Glycocyamine - Wikipedia

    en.wikipedia.org/wiki/Glycocyamine

    Glycocyamine (or guanidinoacetate) is a metabolite of glycine in which the amino group has been converted into a guanidine by guanylation (transfer of a guanidine group from arginine). In vertebrate organism it is then transformed into creatine by methylation. Glycocyamine is used as a supplement and as a feed additive in poultry farming.

  8. Triglycine sulfate - Wikipedia

    en.wikipedia.org/wiki/Triglycine_sulfate

    Triglycine sulfate (TGS) is a chemical compound with a formula (NH 2 CH 2 COOH) 3 ·H 2 SO 4. The empirical formula of TGS does not represent the molecular structure, which contains protonated glycine moieties and sulfate ions. TGS with protons replaced by deuterium is called deuterated TGS or DTGS; alternatively, DTGS may refer to doped TGS.

  9. Glycin - Wikipedia

    en.wikipedia.org/wiki/Glycin

    Glycin, or N-(4-hydroxyphenyl)glycine, is N-substituted p-aminophenol. It is a photographic developing agent used in classic black-and-white developer solutions. [2] It is not identical to, but derived from glycine, the proteinogenic amino acid. It is typically characterized as thin plates of white or silvery powder, although aged samples ...