Home Cart Sign in  
Chemical Structure| 59-23-4 Chemical Structure| 59-23-4
Chemical Structure| 59-23-4

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

D-Galactose is a naturally occurring monosaccharide that plays a crucial role in various metabolic pathways. D-Galactose is mainly used in cell culture, metabolic research, and biochemical analysis.

Synonyms: D-Galactopyranose; D-(+)-Galactose

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of D-Galactose

CAS No. :59-23-4
Formula : C6H12O6
M.W : 180.16
SMILES Code : O=C[C@@H]([C@H]([C@H]([C@@H](CO)O)O)O)O
Synonyms :
D-Galactopyranose; D-(+)-Galactose
MDL No. :MFCD00151230

Safety of D-Galactose

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312+P330-P302+P352-P304+P340+P312-P305+P351+P338-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of D-Galactose

* 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 [ 59-23-4 ]

[ 59-23-4 ] Synthesis Path-Downstream   1~7

  • 2
  • [ 7493-95-0 ]
  • [ 59-23-4 ]
  • 3
  • [ 59-23-4 ]
  • [ 7493-95-0 ]
  • [ 902-54-5 ]
  • 4
  • [ 57-50-1 ]
  • [ 7493-95-0 ]
  • [ 59-23-4 ]
  • [ 470-55-3 ]
  • 5
  • [ 7493-95-0 ]
  • [ 59-23-4 ]
  • [ 499-39-8 ]
YieldReaction ConditionsOperation in experiment
With recombinant alpha-galactosidase AgaAHJG4 from Streptomyces; In aq. phosphate buffer; at 37.0℃; for 24.0h;Catalytic behavior; General procedure: Transglycosylation reactions were carried out using pNPG as the donor at 40mM with various acceptors at 400mM including Xyl, Glc, Gal, Sor, Fru, Man, Lac, Suc, Raf, Sta, Mant, Sort, methanol (MeOH), ethanol (EtOH), ethylene glycol (EgOH), 2-propanol (PrOH), n-butanol (BuOH), 3-methyl-1-butanol (mBuOH), and glycerol (GlOH). Donor and acceptors were preincubated for 10min at 37C. The mixtures were incubated at 37C for 24h after the addition of 0.2UmL-1 rAgaAJB07 or rAgaAHJG4. Reactions were stopped by rapid freezing. Transglycosylation products were analyzed by thin layer chromatography (TLC) using the method of Shivam and Mishra (2010) with some modifications as follows:
With recombinant alpha-galactosidase AgaAJB07 from Mesorhizobium; In aq. phosphate buffer; at 37.0℃; for 24.0h;Catalytic behavior; General procedure: Self-condensation reactions were carried out using 40mM pNPG or 400mM Mel, Raf, or Sta as the substrates. Transglycosylation reactions were carried out using pNPG as the donor at 40mM with various acceptors at 400mM including Xyl, Glc, Gal, Sor, Fru, Man, Lac, Suc, Raf, Sta, Mant, Sort, methanol (MeOH), ethanol (EtOH), ethylene glycol (EgOH), 2-propanol (PrOH), n-butanol (BuOH), 3-methyl-1-butanol (mBuOH), and glycerol (GlOH). Donor and acceptors were preincubated for 10min at 37C. The mixtures were incubated at 37C for 24h after the addition of 0.2UmL-1 rAgaAJB07 or rAgaAHJG4. Reactions were stopped by rapid freezing. Transglycosylation products were analyzed by thin layer chromatography (TLC) using the method of Shivam and Mishra (2010) with some modifications as follows:
  • 7
  • [ 59-23-4 ]
  • [ 30065-27-1 ]
  • C15H20N4O6S [ No CAS ]
YieldReaction ConditionsOperation in experiment
90% With acetic acid; In ethanol; for 10.0h;Reflux; General procedure: To solution of 4 (10 mmol) in absolute ethanol, different sugars (10 mmol) were added and then glacial acetic acid (1 ml) was added to the reaction mixture which was refluxed for 10h (TLC).The solvent was evaporated or concentrated under reduced pressure and the product was filtered off to afford 5(a-d) (83 - 88%) yields.
 

Historical Records

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

Categories