meso-erythritol

Base Information

• Chemical Name: meso-erythritol
• CAS No.: 909878-64-4
• Molecular Formula: C₄H₁₀O₄
• Molecular Weight: 122.121
• Mol file: 909878-64-4.mol

Synonyms:meso-erythritol

Chemical Property of meso-erythritol

Chemical Property:

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of meso-erythritol

There total 125 articles about meso-erythritol 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:

α-cellulose → β-D-glucose (492-61-5) + meso-erythritol (909878-64-4,10030-58-7,188346-77-2,149-32-6) + sorbitol (50-70-4,69-65-8,87-78-5,133-43-7,488-44-8,488-45-9,608-66-2,643-01-6,643-03-8,5552-13-6,6706-59-8,24557-79-7,25878-23-3,26566-34-7,45007-61-2,60660-56-2,60660-57-3,60660-58-4,132747-27-4)

Guidance literature:

With 5% active carbon-supported ruthenium; water; hydrogen; toluene-4-sulfonic acid; at 159.84 ℃; for 7h; under 37503.8 Torr; Autoclave;

DOI:10.1039/c0cc02263b

Reference yield:

alginic acid (9005-32-7) → meso-erythritol (909878-64-4,10030-58-7,188346-77-2,149-32-6) + rac-threitol (6968-16-7,10030-58-7,188346-77-2,149-32-6) + 1,2,3,4,5-pentapentanol (6018-27-5) + XYLITOL (87-99-0) + Adonitol (488-81-3) + mannitol (69-65-8) + D-sorbitol (50-70-4) + D-galactitol (608-66-2)

Guidance literature:

With hydrogen; In water; at 180 ℃; under 37503.8 Torr; Temperature; Reagent/catalyst; Autoclave;

DOI:10.1016/j.apcata.2019.04.003

Reference yield:

cellulose (9004-34-6) → D-threitol (2418-52-2,10030-58-7,188346-77-2,149-32-6) + meso-erythritol (909878-64-4,10030-58-7,188346-77-2,149-32-6) + D-Arabitol (488-82-4) + XYLITOL (87-99-0) + hydroxy-2-propanone (116-09-6)

Guidance literature:

With water; hydrogen; at 210 ℃; for 0.5h; under 45004.5 Torr; Autoclave;

DOI:10.1016/j.molcata.2013.11.016

upstream raw materials:

formaldehyd

3,4-butenediol

1,4-butenediol

erythronic acid butyl ester

Downstream raw materials:

(+/-)-phosphoric acid mono-(erythro-2,3,4-trihydroxy-butyl ester)

2,5-dihydrofuran

thiophene

propylene glycol

Refernces

• 1、 Gao, Lou,Hou, Wenrong,Hui, Yingshuang,Tang, Yi,Zhan, Yulu,Zhang, Yahong. "Product Control and Insight into Conversion of C6 Aldose Toward C2, C4 and C6 Alditols in One-Pot Retro-Aldol Condensation and Hydrogenation Processes". . p. 560 - 566. Retrieved 2021/06/25.
• 2、 Tindall, Daniel J.,Mader, Steffen,Kindler, Alois,Rominger, Frank,Hashmi, A. Stephen K.,Schaub, Thomas. "Selective and Scalable Synthesis of Sugar Alcohols by Homogeneous Asymmetric Hydrogenation of Unprotected Ketoses". supporting information. p. 721 - 725. Retrieved 2020/10/19.