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Chemical Structure| 56-82-6 Chemical Structure| 56-82-6
Chemical Structure| 56-82-6

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DL-Glyceraldehyde is an important intermediate metabolite involved in glycolysis and gluconeogenesis. In metabolic studies, DL-Glyceraldehyde is used to study enzyme activity and its role in energy metabolism.

4.5 *For Research Use Only !

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Product Details of DL-Glyceraldehyde

CAS No. :56-82-6
Formula : C3H6O3
M.W : 90.08
SMILES Code : OCC(O)C=O
MDL No. :MFCD00064379

Safety of DL-Glyceraldehyde

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H312-H332
Precautionary Statements:P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P330-P362-P403+P233-P501

Application In Synthesis of DL-Glyceraldehyde

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 56-82-6 ]

[ 56-82-6 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 56-82-6 ]
  • bacterium coli [ No CAS ]
  • yeast water [ No CAS ]
  • calcium dicarbonate [ No CAS ]
  • [ 453-17-8 ]
  • [ 497-09-6 ]
  • 2
  • [ 56-82-6 ]
  • bacterium lactis aerogenes [ No CAS ]
  • yeast water [ No CAS ]
  • calcium dicarbonate [ No CAS ]
  • [ 453-17-8 ]
  • [ 497-09-6 ]
  • 3
  • [ 67-56-1 ]
  • sucrose [ No CAS ]
  • [ 530-26-7 ]
  • [ 27871-49-4 ]
  • [ 1663-35-0 ]
  • [ 5837-73-0 ]
  • [ 1186-47-6 ]
  • [ 56-82-6 ]
  • [ 621-63-6 ]
YieldReaction ConditionsOperation in experiment
72% With potassium carbonate; at 160℃; for 16h;Flow reactor; The stainless steel pressure vessel (40 cc, Swagelok) is filled in with the methanol (15.0 g: Sigma-Aldrich, 003e99.8percent) solution of the metal salt (metal ion supply source), and sucroses (0.450 g: Fluka, 003e99.0percent) and catalyst (0.150 g). The reactor is closed and it heats up under the mixing (700 rpm) with 160. In 160 reaction, it makes maintained for 16 hours and the container reaction rapidly is cooled in the cold water after this period as the dipping. Sample from the reaction container was filtered and it analyzed with the HPLC (the Agilent 1200, the Biorad Aminex HPX-87H column, 65, 0.05 M H2SO4, 0.6 ml min-1) and it was the art exhibition ring hexose and dihydroxy acetone (DHA), the methyllactate (ML) using the fixed quantity: and GC (the Agilent 7890 in which the Phenomenex Solgelwax column is comprehended) the glyceraldehyde (GLA), and methyl vinyl glycol rate (MVG, and the methyl 2- hydroxy -3- butenoate) and glycol aldehyde dimethylacetal (GADMA) the fixed quantity.
  • 4
  • [ 56-82-6 ]
  • [ 497-09-6 ]
  • (R)-glyceraldehyde 3-phosphate [ No CAS ]
 

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Technical Information

• Appel Reaction • Barbier Coupling Reaction • Baylis-Hillman Reaction • Bucherer-Bergs Reaction • Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions • Chugaev Reaction • Clemmensen Reduction • Complex Metal Hydride Reductions • Corey-Chaykovsky Reaction • Corey-Fuchs Reaction • Corey-Kim Oxidation • Dess-Martin Oxidation • Fischer Indole Synthesis • Grignard Reaction • Hantzsch Dihydropyridine Synthesis • Heat of Combustion • Henry Nitroaldol Reaction • Horner-Wadsworth-Emmons Reaction • Hydride Reductions • Jones Oxidation • Julia-Kocienski Olefination • Knoevenagel Condensation • Leuckart-Wallach Reaction • Martin's Sulfurane Dehydrating Reagent • McMurry Coupling • Meerwein-Ponndorf-Verley Reduction • Mitsunobu Reaction • Moffatt Oxidation • Mukaiyama Aldol Reaction • Nozaki-Hiyama-Kishi Reaction • Oxidation of Alcohols by DMSO • Passerini Reaction • Paternò-Büchi Reaction • Petasis Reaction • Pictet-Spengler Tetrahydroisoquinoline Synthesis • Preparation of Alcohols • Preparation of Aldehydes and Ketones • Preparation of Amines • Prins Reaction • Reactions of Alcohols • Reactions of Aldehydes and Ketones • Reactions of Amines • Reactions with Organometallic Reagents • Reformatsky Reaction • Ritter Reaction • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Sharpless Olefin Synthesis • Stetter Reaction • Stobbe Condensation • Swern Oxidation • Tebbe Olefination • Ugi Reaction • Wittig Reaction • Wolff-Kishner Reduction

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