L-Galactose

Base Information

• Chemical Name: L-Galactose
• CAS No.: 93780-23-5
• Molecular Formula: C6H12 O6
• Molecular Weight: 180.158
• European Community (EC) Number: 227-780-7,219-994-4,239-630-8,217-870-4,224-118-9,822-986-9
• NSC Number: 406891,224293,83659,26247,2573
• DSSTox Substance ID: DTXSID70860057
• Nikkaji Number: J2.733.971I
• Wikidata: Q105024342
• NCI Thesaurus Code: C61716,C83903
• RXCUI: 349730
• ChEMBL ID: CHEMBL1206211
• Mol file: 93780-23-5.mol

Synonyms:Anhydrous Dextrose;D Glucose;D-Glucose;Dextrose;Dextrose, Anhydrous;Glucose;Glucose Monohydrate;Glucose, (alpha-D)-Isomer;Glucose, (beta-D)-Isomer;Glucose, (DL)-Isomer;Glucose, (L)-Isomer;L Glucose;L-Glucose;Monohydrate, Glucose;Hexose;Hexoses

Chemical Property of L-Galactose

Chemical Property:

• PSA: 118.22000
• LogP: -3.37880
• XLogP3: -2.9
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 5
• Exact Mass: 180.06338810
• Heavy Atom Count: 12
• Complexity: 138

Purity/Quality:

Hexose ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C(C(C(C(C(C=O)O)O)O)O)O
• Recent ClinicalTrials: Effects of HMOs on the Faecal Microbiota and on Host Metabolism in Obese Children
• Uses: Hexose is a tissue glycoproteins that increase in diabetic rats from the effects of oral administration of Helicteres isora plants. It is also an important components of biological relevant compounds as well as precursors for certain pharmaceutical drugs.

Technology Process of L-Galactose

There total 110 articles about L-Galactose which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

β-glucan FoHA2 from fruit bodies Fomitopsis officinalis → D-xylose (58-86-6) + D-Mannose (3458-28-4) + D-Fucose (3615-37-0,478518-52-4) + D-glucose (50-99-7) + galactose (93780-23-5)

Guidance literature:

With trifluoroacetic acid; In water; at 100 ℃; for 5h;

DOI:10.1016/j.phytochem.2020.112313

Reference yield:

β-glucan FoHA4 from fruit bodies Fomitopsis officinalis → D-xylose (58-86-6) + D-Mannose (3458-28-4) + D-Fucose (3615-37-0,478518-52-4) + D-glucose (50-99-7) + galactose (93780-23-5)

Guidance literature:

With trifluoroacetic acid; In water; at 100 ℃; for 5h;

DOI:10.1016/j.phytochem.2020.112313

Reference yield:

β-glucan FoCA from fruit bodies Fomitopsis officinalis → D-xylose (58-86-6) + D-Mannose (3458-28-4) + D-Fucose (3615-37-0,478518-52-4) + D-glucose (50-99-7) + galactose (93780-23-5)

Guidance literature:

With trifluoroacetic acid; In water; at 100 ℃; for 5h;

DOI:10.1016/j.phytochem.2020.112313

upstream raw materials:

mannitol

para-xylene

water

D-sorbitol

Downstream raw materials:

p-benzosemiquinone radical anion

succinic acid

L-Lactic acid

LACTIC ACID

Refernces

• 1、 Cai, Charles M.,Zhang, Taiying,Kumar, Rajeev,Wyman, Charles E.. "THF co-solvent enhances hydrocarbon fuel precursor yields from lignocellulosic biomass". . p. 3140 - 3145. Retrieved 2013.
• 2、 Jain, Namrata,Tamura, Kazune,Déjean, Guillaume,Van Petegem, Filip,Brumer, Harry. "Orthogonal Active-Site Labels for Mixed-Linkage endo-β-Glucanases". . p. 1968 - 1984. Retrieved 2021/05/26.
• 3、 Golovchenko, Victoria V.,Naranmandakh, Shinen,Ganbaatar, Jamsranjav,Prilepskii, Artur Yu.,Burygin, Gennady L.,Chizhov, Alexander O.,Shashkov, Alexander S.. "Structural investigation and comparative cytotoxic activity of water-soluble polysaccharides from fruit bodies of the medicinal fungus quinine conk". . . Retrieved 2020/04/28.