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δ-Aminolevulinic acid (also dALA, δ-ALA, 5ALA or 5-aminolevulinic acid), an endogenous non-proteinogenic amino acid, is the first compound in the porphyrin synthesis pathway, the pathway that leads to heme [3] in mammals, as well as chlorophyll [4] in plants. 5ALA is used in photodynamic detection and surgery of cancer. [5] [6] [7] [8]
Lipoic acid (LA), also known as α-lipoic acid, alpha-lipoic acid (ALA) and thioctic acid, is an organosulfur compound derived from caprylic acid (octanoic acid). [3] ALA, which is made in animals normally, is essential for aerobic metabolism. It is also available as a dietary supplement or pharmaceutical drug in some countries.
The traditional ‘Made in France’ label is an incontestable draw for customers – the Pro France Ifop survey [3] (September 2018) reported that two thirds of French people ‘often’ or ‘systematically’ take the product’s origin into account when they buy a product or service, and that three quarters of French people would be ...
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The crust formed on the lid was ground to powder and boiled with water to remove the calomel. Calx – calcium oxide; was also used to refer to other metal oxides. Chalcanthum – the residue produced by strongly roasting blue vitriol (copper sulfate); it is composed mostly of cupric oxide. Chalk – a rock composed of porous biogenic calcium ...
Sodium bis(2-methoxyethoxy)aluminium hydride (SMEAH; [1] trade names Red-Al, Synhydrid, Vitride) is a hydride reductant with the formula NaAlH 2 (OCH 2 CH 2 OCH 3) 2. The trade name Red-Al refers to its being a reducing aluminium compound. It is used predominantly as a reducing agent in organic synthesis.
BASF SE is the most important manufacturer of α-ADA under the brand name Trilon M, has large-scale plants in Ludwigshafen and Lima, Ohio, and is currently expanding its existing capacities with another large-scale plant at Evonik's site in Theodore, Alabama.
Alanine (symbol Ala or A), [4] or α-alanine, is an α-amino acid that is used in the biosynthesis of proteins. It contains an amine group and a carboxylic acid group, both attached to the central carbon atom which also carries a methyl group side chain. Consequently it is classified as a nonpolar, aliphatic α-amino acid.