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2,5-Hexanedione reacts with lysine residues in axonal proteins by Schiff base formation followed by cyclization to give pyrroles. Oxidation of the pyrrole residues then causes cross-linking and denaturation of proteins, which perturbs axonal transport and function and causes damage to nerve cells.
It dissolves cellulose nitrate, vinyl polymers and copolymers, and natural and synthetic resins. It is recommended as a solvent because it is photochemically inactive; [5] however it has a very low safe threshold limit value. 2-Hexanone is absorbed through the lungs, orally and dermally and its metabolite, 2,5-hexanedione, is neurotoxic. [6]
NO 2: nitrogen dioxide: 10102–44–0 N 2: nitrogen: 7727-37-9 [1] N 2 F 2: dinitrogen difluoride: 13812–43–6 N 2 F 4: dinitrogen tetrafluoride: 10036–47–2 N 2 O: dinitrogen monoxide: 10024–97–2 N 2 O 3: dinitrogen trioxide: 10544–73–7 N 2 O 4: dinitrogen tetroxide: 10544–72–6 N 2 O 5: dinitrogen pentoxide: 10102–03–1 ...
2,5-Hexanediol is an organic compound with the formula CH 3 CH(OH)CH 2 CH 2 CH(OH)CH 3. It is both a glycol and a secondary alcohol. [1] It is a colorless water-soluble viscous liquid. [2] [3] [4] The chemical properties are well understood and have been extensively reported and studied. [5]
The following is a list of chemicals published as a requirement of Safe Drinking Water and Toxic Enforcement Act of 1986, commonly known as California Proposition 65, that are "known to the state to cause cancer or reproductive toxicity" as of January 3, 2020. [1]
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Add 1 to 2 tablespoons lemon juice and more salt and pepper to taste. Add 1 to 2 tablespoons of the reserved pasta water at a time, if desired, to loosen the sauce. The pasta will absorb the sauce ...
I 2 + 2 NaCH(C(O)CH 3) 2 → [CH(C(O)CH 3) 2] 2 + 2 NaI. Reminiscent of the case of acetylacetone, tetraacetylethane exists as the enol, as established by X-ray crystallography. The two C 3 O 2 H rings are twisted with a dihedral angle near 90°. [2] Many metal complexes have been prepared from the conjugate base of this ligand.