2,3,4-Trihydroxybutanoicacid

Base Information

• Chemical Name: 2,3,4-Trihydroxybutanoicacid
• CAS No.: 10191-35-2
• Molecular Formula: C4H8O5
• Molecular Weight: 136.105
• Hs Code.: 2918199090
• Mol file: 10191-35-2.mol

Synonyms:trihydroxybutiric acid;2,3,4-trihydroxy-benzoic acid hydrazide;2,3,4-trihydroxybutyric acid;L-glycero-tetronic acid;2,3,4-trihydroxybutanedioic acid;2,3,4-Trihydroxy-benzoesaeure-hydrazid;Butanoic acid,2,3,4-trihydroxy;Benzoic acid,2,3,4-trihydroxy-,hydrazide;trihydroxybutyric acid;

Chemical Property of 2,3,4-Trihydroxybutanoicacid

Chemical Property:

• Melting Point: 97-99 °C
• Boiling Point: 518.9±50.0 °C(Predicted)
• PKA: 3.47±0.17(Predicted)
• PSA: 97.99000
• Density: 1.650±0.06 g/cm3(Predicted)
• LogP: -2.21490
• Storage Temp.: 2-8°C

Purity/Quality:

98%,99%, ^*data from raw suppliers

2,3,4-Trihydroxybutanoicacid 98% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 2,3,4-Trihydroxybutanoicacid

There total 33 articles about 2,3,4-Trihydroxybutanoicacid 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: 12.0%

D-lyxose (87-72-9,608-45-7,608-46-8,608-47-9,2460-44-8,6748-95-4,6763-34-4,7261-26-9,7283-06-9,7283-07-0,7296-55-1,7296-56-2,7296-58-4,7296-59-5,7296-60-8,7296-61-9,7296-62-0,7322-30-7,10257-31-5,10257-32-6,10257-33-7,10257-34-8,10257-35-9,19982-83-3,20242-88-0,28697-53-2,36562-42-2,41546-41-2,89299-64-9,107655-34-5,115794-06-4,115794-07-5,130550-15-1,130606-21-2) → formic acid (64-18-6) + glycolic Acid (79-14-1) + glyceric acid (473-81-4,118916-26-0) + carbon dioxide (124-38-9,18923-20-1) + 2,3,4-Trihydroxybutanoic acid (10191-35-2)

Guidance literature:

With copper(II) sulfate; at 100 ℃; Product distribution; Rate constant; Thermodynamic data; study of the oxidation reaction of D-lyxose by cupric ion, kinetic mesurements, ΔS(excit.),;

Reference yield:

D-Glucose (2280-44-6) → glycolic Acid (79-14-1) + LACTIC ACID (849585-22-4,106989-11-1,26811-96-1,31587-11-8,26100-51-6) + erythrosone (496-56-0) + 3-deoxyglucosone (82399-12-0) + glyceric acid (473-81-4,118916-26-0) + 2,4-dihydroxybutanoic acid (1518-62-3) + 2,4,5-trihydroxypentanoic acid (50480-12-1,29625-78-3) + xylo-3-deoxy-hexonic acid (87420-95-9) + Glyoxal (131543-46-9,107-22-2) + 3-hydroxy-2-oxo-propionaldehyde (997-10-4) + 4-hydroxy-2-oxobutanal (28119-61-1) + 2,3,4-Trihydroxybutanoic acid (10191-35-2) + 3-deoxypentos-2-ulose + 2-oxopropanal (78-98-8)

Guidance literature:

With water; oxygen; calcium chloride; magnesium chloride; L-histidine; at 121 ℃; for 1h; Product distribution / selectivity;

Reference yield:

alpha-D-mannopyranoside (7296-15-3) + sodium hydrogensulfite → formic acid (64-18-6) + 2,3,4-Trihydroxybutanoic acid (10191-35-2)

Guidance literature:

In not given;

upstream raw materials:

D-Fructose

D-Mannose

silver(I) acetate

L-arabinose

Downstream raw materials:

DL-tartaric acid

oxalic acid

formic acid

LACTIC ACID

Refernces

• 1、 -. "TREATMENT OF SUGAR SOLUTIONS". Page/Page column 12; 13; Sheets 5-8. . Retrieved 2008/06/13.
• 2、 Krupenskii, V. I.. "OXIDATION OF D-LYXOSE BY CUPRIC, SILVER, AND MERCURY IONS IN ACID MEDIA". . p. 1479 - 1481. Retrieved 2007/10/02.