Glyceraldehyde

Base Information

• Chemical Name: Glyceraldehyde
• CAS No.: 367-47-5
• Deprecated CAS: 367-47-5
• Molecular Formula: C3H6O3
• European Community (EC) Number: 200-290-0,206-695-9
• NSC Number: 67934
• UNII: DI19XSG16H
• DSSTox Substance ID: DTXSID90861586
• Nikkaji Number: J5.790H
• Wikipedia: Glyceraldehyde
• Wikidata: Q423211
• Pharos Ligand ID: LPXRBM1A5KKY
• Metabolomics Workbench ID: 124294
• ChEMBL ID: CHEMBL173813
• Mol file: 367-47-5.mol

Synonyms:Glyceraldehyde

Chemical Property of Glyceraldehyde

Chemical Property:

• Vapor Pressure: 0.0146mmHg at 25°C
• XLogP3: -1.6
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 90.031694049
• Heavy Atom Count: 6
• Complexity: 43.3

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Biological Agents -> Monosaccharides and Derivatives
• Canonical SMILES: C(C(C=O)O)O

Technology Process of Glyceraldehyde

There total 205 articles about Glyceraldehyde 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: 85.0%

D-glyceraldehyde 3-phosphate (20283-52-7) → (S)-glyceraldehyde (497-09-6,367-47-5,26793-98-6)

Guidance literature:

With Potato acid phosphatase (Pase); In water; for 4h; pH 3-4 (adjusted with 2 N NaOH);

DOI:10.1021/jo00167a012

Reference yield:

ethylene glycol (107-21-1) → methanol (67-56-1) + formaldehyd (50-00-0,30525-89-4,61233-19-0) + formic acid (64-18-6) + methane (34557-54-5,27936-85-2) + carbon dioxide (124-38-9,18923-20-1) + carbon monoxide (201230-82-2) + hydrogen (1333-74-0) + acetaldehyde (75-07-0,9002-91-9) + acetic acid (64-19-7,77671-22-8) + Glyceraldehyde (56-82-6,367-47-5,26793-98-6)

Guidance literature:

With 1 wt.percent mixtures of Rh and RhOx/TiO₂; In water; at 14.84 ℃; for 12h; under 750.075 Torr; Wavelength; Reagent/catalyst; UV-irradiation; Inert atmosphere;

DOI:10.1016/j.jcat.2016.02.021

Reference yield:

glycerol (56-81-5,25618-55-7,64333-26-2,8013-25-0) → dihydroxyacetone (96-26-4,26776-70-5) + 3-hydroxy-2-oxo-propionaldehyde (997-10-4) + Glyceraldehyde (56-82-6,367-47-5,26793-98-6)

Guidance literature:

With oxygen; In water; at 20 ℃; for 3h; Irradiation;

DOI:10.1039/d1cy00360g

upstream raw materials:

D-Fructose

L-sorbose

2-Phenyl-4H-[1,3]dioxin

3,3-diethoxypropane-1,2-diol

Downstream raw materials:

LACTIC ACID

ethanol

acetaldehyde

acetic acid

Refernces

• 1、 Arnold,Evans. "-". . p. 1950. Retrieved 1936.
• 2、 Waldmann,Prey. "". . p. 543,550. Retrieved 1953.
• 3、 Duo, Jia,Jin, Binbin,Jin, Fangming,Shi, Xiaoyu,Wang, Tianfu,Ye, Xin,Zhong, Heng. "Photothermal strategy for the highly efficient conversion of glucose into lactic acid at low temperatures over a hybrid multifunctional multi-walled carbon nanotube/layered double hydroxide catalyst". . p. 813 - 822. Retrieved 2022/02/09.
• 4、 Fryszkowska, Anna,Klapars, Artis,Marshall, Nicholas,Ruccolo, Serge,Strotman, Neil A.,Zhang, Shaoguang. "Electrochemical Activation of Galactose Oxidase: Mechanistic Studies and Synthetic Applications". . p. 7270 - 7280. Retrieved 2021/06/30.