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Good factory supply good D-Arabinitol 488-82-4

  • Molecular Formula: C5H12O3
  • Molecular Weight: 152.147
  • Appearance/Colour: white to off-white fine crystalline powder 
  • Vapor Pressure: 7.47E-12mmHg at 25°C 
  • Melting Point: 101-104 °C 
  • Refractive Index: 1.57 
  • Boiling Point: 494.5 °C at 760 mmHg 
  • PKA: 13.24±0.20(Predicted) 
  • Flash Point: 261.9 °C 
  • PSA: 101.15000 
  • Density: 1.525 g/cm3 
  • LogP: -2.94630 

D-Arabinitol(Cas 488-82-4) Usage

Purification Methods

This pentol, which occurs in lichens and fungi, is purified by recrystallisation from 90% EtOH or MeOH. [Ashina & Yamagita Chem Ber 67 801 1934, derivarives: Nakagawa et al. Bull Chem Soc Jpn 40 2150 1967, Prince & Reichstein Helv Chim Acta 20 101 1937, Hough & Theobald Methods in Carbohydrate Chemistry I 94 1962, Academic Press, Beilstein 1 IV 2832.]

Definition

ChEBI: D-arabinitol is the D-enantiomer of arabinitol. It is an enantiomer of a L-arabinitol. It is a metabolite found in the aging mouse brain.

Biotechnological Applications

D-arabinitol detectionAnother approach to the diagnosis of invasive candidosis involves the detection in serum or urine of a metabolite, D-arabinitol, which is produced by most of the medically important Candida species with the exception of C. krusei and perhaps C. glabrata. Various methods have been developed to measure D-arabinitol concentrations in human serum and urine, including enzymatic-fluorometric and enzymatic-colorimetric procedures. Because increased levels of arabinitol are also found in human body fluids when renal function is impaired, the results are reported as the D-arabinitol- creatinine ratio. Although several large studies have demonstrated that patients with candidaemia have ele- vated serum D-arabinitol- creatinine ratios, this approach has still to achieve widespread clinical use.

InChI:InChI=1/C5H12O5/c6-1-3(8)5(10)4(9)2-7/h3-10H,1-2H2/t3-,4-/m1/s1

488-82-4 Relevant articles

Continuous transfer hydrogenation of sugars to alditols with bioderived donors over Cu-Ni-Al catalysts

Scholz, David,Aellig, Christof,Mondelli, Cecilia,Pérez-Ramírez, Javier

, p. 1551 - 1558 (2015)

The transfer hydrogenation of sugars to ...

Efficient Synthesis of Sugar Alcohols over a Synergistic and Sustainable Catalyst

Lin, Lu,Qiu, Jiarong,Sun, Yong,Tang, Xing,Zeng, Xianhai,Zhang, Liangqing

, p. 2467 - 2476 (2021)

A series of catalysts were prepared for ...

Room temperature versatile conversion of biomass-derived compounds by means of supported TiO2 photocatalysts

Colmenares, Juan C.,Magdziarz, Agnieszka

, p. 156 - 162 (2013)

The selective oxidation of glucose and d...

Ruthenium nanoparticles supported on zeolite y as an efficient catalyst for selective hydrogenation of xylose to xylitol

Mishra, Dinesh Kumar,Dabbawala, Aasif Asharaf,Hwang, Jin-Soo

, p. 63 - 70 (2013)

Zeolite Y (HYZ) supported ruthenium (Ru)...

Elucidating the effect of solid base on the hydrogenation of C5 and C6 sugars over Pt–Sn bimetallic catalyst at room temperature

Tathod, Anup P.,Dhepe, Paresh L.

, (2021)

Conversion of sugars into sugar alcohols...

Unexpected reactivity related to support effects during xylose hydrogenation over ruthenium catalysts

Fongarland, Pascal,Freitas, Victoria D. S.,Paez, Ana,Philippe, Régis,Veyre, Laurent,Vilcocq, Léa

, p. 39387 - 39398 (2021/12/27)

Xylose is a major component of hemicellu...

Hydrogenolysis of sorbitol into valuable C3-C2 alcohols at low H2 pressure promoted by the heterogeneous Pd/Fe3O4 catalyst

Gumina, Bianca,Mauriello, Francesco,Pietropaolo, Rosario,Galvagno, Signorino,Espro, Claudia

, p. 152 - 160 (2018/02/17)

The hydrogenolysis of sorbitol and vario...

488-82-4 Process route

α-cellulose

α-cellulose

1,4-sorbitan
20662-31-1

1,4-sorbitan

β-D-glucose
492-61-5

β-D-glucose

1,2,3,4,5-pentahydroxy-pentane
87-99-0,488-81-3,488-82-4,2152-56-9,6917-36-8,7643-75-6

1,2,3,4,5-pentahydroxy-pentane

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

sorbitol

Conditions
Conditions Yield
With sulfuric acid; 5% active carbon-supported ruthenium; water; hydrogen; tungsten; at 159.84 ℃; for 1h; under 37503.8 Torr; Autoclave;
D-xylose
58-86-6

D-xylose

D-Arabitol
488-82-4

D-Arabitol

XYLITOL
87-99-0

XYLITOL

Conditions
Conditions Yield
With hydrogen; Ni6.66Fe1Al1.55; In water; at 180 ℃; for 0.5h; under 22502.3 Torr; Temperature; High pressure;
76.97%
20.73%
With Butane-1,4-diol; Cu3Ni3Al2; In water; at 149.84 ℃; pH=9 - 10;
60%
10%
With hydrogen; In water; at 60 ℃; for 4h; under 12001.2 Torr; Time; Catalytic behavior; Green chemistry;
50%
6%
With hydrogen; In water; at 120 ℃; for 1h; under 41254.1 Torr; Reagent/catalyst; Temperature; Concentration; Pressure; Catalytic behavior; Autoclave; Inert atmosphere; Green chemistry;
With hydrogen; In water; at 130 ℃; for 2h; under 12001.2 Torr; Autoclave;
66 %Chromat.
13 %Chromat.

488-82-4 Upstream products

  • 10323-20-3
    10323-20-3

    D-Arabinose

  • 1114-34-7
    1114-34-7

    D-lyxose

  • 2280-44-6
    2280-44-6

    D-Glucose

  • 154-17-6
    154-17-6

    D-2-deoxyglucose

488-82-4 Downstream products

  • 107-92-6
    107-92-6

    butyric acid

  • 119248-59-8
    119248-59-8

    pentakis-O -(2,4-dinitro-phenyl)-D-arabitol

  • 5329-57-7
    5329-57-7

    1.5-dibenzoyloxy-D-arabino -pentanetriol-(2.3.4)

  • 26293-27-6
    26293-27-6

    trifluoroacetylated arabinitol

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