XYLITOL

Base Information

• Chemical Name: XYLITOL
• CAS No.: 16277-71-7
• Molecular Formula: C₅H₁₂O₅
• Molecular Weight: 152.147
• Hs Code.: 2905491000
• Mol file: 16277-71-7.mol

Synonyms:Xylenolorange;Xylolorange;o-Cresolphthalexon S;xylitol CM 50;BIX1004;cresol phthalexon s;UNII-S2VDY878QD;m-Cresolphthalexon S;

Chemical Property of XYLITOL

Chemical Property:

• Melting Point: 94-97oC(lit.)
• PSA: 101.15000
• LogP: -2.94630
• Storage Temp.: 2-8°C
• Solubility.: H2O: 0.1 g/mL, clear, colorless
• Water Solubility.: SOLUBLE

Purity/Quality:

99% ^*data from raw suppliers

Xylitol,98.5-101.0%(AnhydrousBasis),meetsNF/FCCspecifications 98.5-101.0%(AnhydrousBasis) ^*data from reagent suppliers

Safty Information:

• Safety Statements: S24/25:

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of XYLITOL

There total 11 articles about XYLITOL 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: 96.0%

D-Xylose (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) → D-xylitol (87-99-0,488-81-3,488-82-4,2152-56-9,6018-27-5,6917-36-8,7643-75-6,16277-71-7,84709-28-4,84709-42-2)

Guidance literature:

With hydrogen; In 2-methyltetrahydrofuran; water; at 150 ℃; for 4h; under 3 Torr;

Reference yield:

XYLITOL (87-99-0) → formic acid (64-18-6) + LACTIC ACID (849585-22-4,106989-11-1,26811-96-1,31587-11-8,26100-51-6) + propylene glycol (57-55-6,63625-56-9) + ethylene glycol (107-21-1) + arabitol (87-99-0,488-81-3,488-82-4,2152-56-9,6018-27-5,6917-36-8,7643-75-6,16277-71-7,84709-28-4,84709-42-2) + glycerol (56-81-5,25618-55-7,64333-26-2,8013-25-0)

Guidance literature:

With platinum on activated charcoal; water; hydrogen; calcium hydroxide; at 199.84 ℃; under 30003 Torr; Autoclave;

DOI:10.1039/c0gc00571a

Reference yield:

D-glucose (50-99-7) → formic acid (64-18-6) + D-xylose (58-86-6) + gluconic acid (526-95-4) + D-xylitol (87-99-0,488-81-3,488-82-4,2152-56-9,6018-27-5,6917-36-8,7643-75-6,16277-71-7,84709-28-4,84709-42-2)

Guidance literature:

With cetyltrimethylammonim bromide; titanium(IV) oxide; for 2h; Reagent/catalyst; Concentration;

DOI:10.1016/j.materresbull.2017.08.016

upstream raw materials:

D-glucose

D-Xylose

D-ribulose

xylulose

Downstream raw materials:

furan

furfural

carbon dioxide

carbon monoxide

Refernces

• 1、 -. "Preparation method of gamma-acetyl n-propanol". Paragraph 0036; 0037. . Retrieved 2017/12/09.
• 2、 Sawden, J,Turner, N J. "Stereospecific carbon-carbon bond formation using rabbit muscle aldolase". . p. 90 - 93. Retrieved 2007/10/02.