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  2. Guanidine - Wikipedia

    en.wikipedia.org/wiki/Guanidine

    It is a highly stable +1 cation in aqueous solution due to the efficient resonance stabilization of the charge and efficient solvation by water molecules. As a result, its pK aH is 13.6 [2] (pK b of 0.4) meaning that guanidine is a very strong base in water; in neutral water, it exists almost exclusively as guanidinium. Due to this, most ...

  3. Guanidinium chloride - Wikipedia

    en.wikipedia.org/wiki/Guanidinium_chloride

    The equilibrium is not complete because the acidity difference between guanidinium and water is not large. The approximate pK a values: 13.6 vs 15.7. Complete deprotonation should be done with extremely strong bases, such as lithium diisopropylamide. C(NH 2) + 3 Cl − + Li + N(C 3 H 7) − 2 → HNC(NH 2) 2 + HN(C 3 H 7) 2 + LiCl

  4. Guanine - Wikipedia

    en.wikipedia.org/wiki/Guanine

    6, and 50 mL of water, followed by a subsequent acid hydrolysis. However, it is unknown whether the presence of guanine was not simply a resultant contaminant of the reaction. [5] 10NH 3 + 2CH 4 + 4C 2 H 6 + 2H 2 O → 2C 5 H 8 N 5 O (guanine) + 25H 2. A Fischer–Tropsch synthesis can also be used to form guanine, along with adenine, uracil ...

  5. Guanidinium thiocyanate - Wikipedia

    en.wikipedia.org/wiki/Guanidinium_thiocyanate

    Guanidinium thiocyanate can be used to deactivate a virus, such as the influenza virus that caused the 1918 "Spanish flu", so that it can be studied safely.. Guanidinium thiocyanate is also used to lyse cells and virus particles in RNA and DNA extractions, where its function, in addition to its lysing action, is to prevent activity of RNase enzymes and DNase enzymes by denaturing them.

  6. Guanidine nitrate - Wikipedia

    en.wikipedia.org/wiki/Guanidine_nitrate

    Guanidine nitrate is the chemical compound with the formula [C(NH 2) 3]NO 3. It is a colorless, water-soluble salt. It is produced on a large scale and finds use as precursor for nitroguanidine, [1] fuel in pyrotechnics and gas generators. Its correct name is guanidinium nitrate, but the colloquial term guanidine nitrate is widely used.

  7. Guanosine - Wikipedia

    en.wikipedia.org/wiki/Guanosine

    Guanosine (symbol G or Guo) is a purine nucleoside comprising guanine attached to a ribose (ribofuranose) ring via a β-N 9-glycosidic bond.Guanosine can be phosphorylated to become guanosine monophosphate (GMP), cyclic guanosine monophosphate (cGMP), guanosine diphosphate (GDP), and guanosine triphosphate (GTP).

  8. Nitroguanidine - Wikipedia

    en.wikipedia.org/wiki/Nitroguanidine

    Nitroguanidine is an extremely insensitive but powerful high explosive. Wetting it with > 20 wt.-% water effects desensitization from HD 1.1 down to HD 4.1 (flammable solid). [2] Nitroguanidine is used as an energetic material, i.e., propellant or high explosive, precursor for insecticides, and for other purposes.

  9. Purine metabolism - Wikipedia

    en.wikipedia.org/wiki/Purine_metabolism

    Purines are biologically synthesized as nucleotides and in particular as ribotides, i.e. bases attached to ribose 5-phosphate.Both adenine and guanine are derived from the nucleotide inosine monophosphate (IMP), which is the first compound in the pathway to have a completely formed purine ring system.

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