RIBONIC ACID

Base Information

• Chemical Name: RIBONIC ACID
• CAS No.: 642-98-8
• Molecular Formula: C5H10O6
• Molecular Weight: 166.131
• Hs Code.: 2918199090
• DSSTox Substance ID: DTXSID801021863
• Nikkaji Number: J921.158F
• Wikidata: Q27109369
• Metabolomics Workbench ID: 37474
• Mol file: 642-98-8.mol

Synonyms:RIBONIC ACID;D-()-Ribonic acid

Chemical Property of RIBONIC ACID

Chemical Property:

• PSA: 118.22000
• LogP: -2.85400
• Storage Temp.: 2-8°C
• XLogP3: -2.7
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 4
• Exact Mass: 166.04773803
• Heavy Atom Count: 11
• Complexity: 135

Purity/Quality:

99%, ^*data from raw suppliers

D-Ribonic acid lithium salt ≥95.0%(TLC) ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C(C(C(C(C(=O)O)O)O)O)O
• Isomeric SMILES: C([C@H]([C@H]([C@H](C(=O)O)O)O)O)O

Technology Process of RIBONIC ACID

There total 65 articles about RIBONIC ACID 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: 98.0%

D-xylose (58-86-6) → D-xylonic acid (488-30-2,526-91-0,526-92-1,608-53-7,642-98-8,4172-43-4,4172-44-5,13171-74-9,13752-83-5,17812-24-7,17828-56-7,20663-19-8,28223-40-7)

Guidance literature:

With sodium carbonate; In water; at 30 ℃; for 40h; Wavelength; Irradiation;

DOI:10.1039/c6gc03022j

Reference yield: 35.0%

D-glucose (50-99-7) + chloroamine-T (127-65-1) → D-glyceric acid (473-81-4,600-19-1,6000-40-4,28305-26-2,118916-26-0) + D-threonic acid (20246-26-8) + D-erythronic acid (488-16-4) + arabinoic acid (488-30-2) + D-ribonic acid (642-98-8) + gluconic acid (526-95-4)

Guidance literature:

In water; at 35 ℃; Kinetics; Thermodynamic data; Mechanism; E_a; ΔH excit.; ΔG excit.; ΔS excit; add. of NaOH, var. solv. D2O;

DOI:10.1016/S0008-6215(97)00243-7

Reference yield: 3.0%

D-xylose (58-86-6) → D-lyxonic acid (526-92-1) + D-xylonic acid (488-30-2,526-91-0,526-92-1,608-53-7,642-98-8,4172-43-4,4172-44-5,13171-74-9,13752-83-5,17812-24-7,17828-56-7,20663-19-8,28223-40-7)

Guidance literature:

With sodium anthraquinone-2-sulfonate; calcium chloride; In sodium hydroxide; at 50 ℃;

DOI:10.1016/0008-6215(84)85210-6

upstream raw materials:

pyridine

arabinoic acid

D-ribose

D-ribonic acid 5-phosphate

Downstream raw materials:

D-ribose

(E)-but-2-enoic acid

5-methyl-dihydro-furan-2-one

2-furanoic acid

Refernces

• 1、 Nishida. "". . . Retrieved 1951.
• 2、 Zdarta, Jakub,Pinelo, Manuel,Jesionowski, Teofil,Meyer, Anne S.. "Upgrading of Biomass Monosaccharides by Immobilized Glucose Dehydrogenase and Xylose Dehydrogenase". . p. 5164 - 5173. Retrieved 2018/10/25.
• 3、 Zhou, Baowen,Song, Jinliang,Zhang, Zhanrong,Jiang, Zhiwei,Zhang, Pei,Han, Buxing. "Highly selective photocatalytic oxidation of biomass-derived chemicals to carboxyl compounds over Au/TiO2". . p. 1075 - 1081. Retrieved 2017/03/17.