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Summary Of: Ascorbic acid

of ascorbic acid is commonly known as... Ascorbic acid synthesis in non... Another way to look at ascorbic acid is to consider it as an... Ascorbic acid also interconverts into two unstable... The concentration of a solution of ascorbic acid can be determined in many ways... ascorbic acid can be reacted with iodine in excess... generate the iodine in the presence of the ascorbic acid by the reaction of... Ascorbic acid is easily oxidized and so is used as a reductant in photographic developer solutions... of ascorbic acid is also known as... Ascorbic acid and its sodium... s supply of ascorbic acid is produced in China... ascorbic acid can be used to assemble molecular chains more quickly and with less waste than traditional... Ascorbic acid synthesis in non... Ascorbic acid synthesis in non... Ascorbic acid is found in plants... Reptiles and older orders of birds make ascorbic acid in their kidneys... Recent orders of birds and most mammals make ascorbic acid in their livers where the enzyme... genetic defect and are therefore unable to make ascorbic acid in their livers... a tropical environment where plenty of foodstuffs containing ascorbic acid were available throughout the year... Although ascorbic acid is a vital food nutrient for humans and is therefore termed a vitamin... a discussion of the medical properties of ascorbic acid as well as its historic and social role... The Natural History of Ascorbic Acid in the Evolution of Mammals and Primates... The Effect of Ascorbic Acid on Bleaching Coral... The Effect of Ascorbic Acid on Fragmented Coral...

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Vitamin C | | | IUPAC name | CAS number | PubChem | EINECS number | InChI | ChemSpider | Molecular formula | Molar mass | Density | Melting point | Solubility | water | Solubility | ethanol | Solubility | glycerol | Solubility | propylene glycol | Solubility | Acidity | MSDS | LD50 | standard state
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| Infobox references | sugar acid | antioxidant | enantiomer | vitamin C | alpha privative | scurvy | Nobel Prize | Walter Haworth | Paul Karrer | vitamins | Albert Szent-Györgyi | vinylogous | carboxylic acid | resonance structures | enol | enolate | | | | Nucleophilic attack | diketone | tautomers | proton | enol | titration | oxidizing agent | DCPIP | solution | iodine | starch | indicator | iodate | acid | N-bromosuccinimide | potassium iodide | | | reduced form | Vitamin C | dehydroascorbic acid | oxidized form | Vitamin C | preservative | L-enantiomer | vitamin C | scurvy | Primates | guinea pig | salts | antioxidant | food additives | fats | soluble | esters | fatty acids | E numbers | sodium ascorbate | calcium ascorbate | potassium ascorbate | ascorbyl palmitate | ascorbyl stearate | water | tooth decay | citation needed | reactive oxygen species | hydrogen peroxide | nucleic acid | scurvy | L-gulonolactone oxidase | Vitamin C | Dehydroascorbic acid | Erythorbic acid | diastereomer | Mineral ascorbates | Acids in wine | ISBN 0-19-850346-6 | University of York | ISBN 0-85186-333-7 | ISBN 0-85404-513-9 | Oxford University | 2005 | 10-09 | April 25 | 1932 | National Library of Medicine | May 20 | 2007 | University of Oxford | v | d | Vitamins | A11 | Fat soluble | A | Retinol | Beta-carotene | Tretinoin | Alpha-carotene | D | Ergosterol | Ergocalciferol (D2) | 7-Dehydrocholesterol | Previtamin D3 | Cholecalciferol (D3) | 25-hydroxycholecalciferol | Calcitriol | 1,25-dihydroxycholecalciferol, active form | Calcitroic acid | Dihydroergocalciferol | Vitamin D5 | Dihydrotachysterol | Calcipotriol | Tacalcitol | Paricalcitol | E | Tocopherol | Alpha | Beta | Tocotrienol | K | Naphthoquinone | Phylloquinone/K1 | Menatetrenone/K2 | Water soluble | B vitamins | Thiamine | Riboflavin | Niacin | Nicotinamide | Pantothenic acid | Dexpanthenol | Pantethine | B6 | Pyridoxine | Pyridoxal phosphate | Pyridoxamine | Biotin | Folic acid | Folinic acid | B12 | Cyanocobalamin | Hydroxocobalamin | Methylcobalamin | Cobamamide | C | Choline | enzyme cofactors | enzymes | v | d | Enzyme | cofactors | Coenzymes | vitamins | NAD+ | NADP+ | Coenzyme A | THF / H4F | DHF | MTHF | Menaquinone | Coenzyme F420 | ATP | CTP | SAM | PAPS | GSH | Coenzyme B | Coenzyme M | Coenzyme Q | Methanofuran | BH4 | H4MPT | prosthetic groups | TPP / ThDP | FMN | FAD | PLP / P5P | Biotin | Methylcobalamin | Cobamamide | Haem / Heme | Lipoic acid | Molybdopterin | PQQ | Ca2+ | Cu2+ | Fe2+, Fe3+ | Mg2+ | Mn2+ | Mo | Ni2+ | Se | Zn2+ | biochemicals | Saccharides | Carbohydrates | Glycosides | Amino acids | Peptides | Proteins | Glycoproteins | Lipids | Terpenes | Steroids | Carotenoids | Alkaloids | Nucleobases | Nucleic acids | Enzyme cofactors | Flavonoids | Polyketides | Tetrapyrroles | Categories | Organic acids | Antioxidants | Dietary antioxidants | Coenzymes | Corrosion inhibitors | All articles with unsourced statements | Articles with unsourced statements since July 2008 |
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Ascorbic acid".