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A3381

Sigma-Aldrich

D-(+)-Arabitol

≥99% (GC)

Synonyme(s) :

D-arabino-Pentitol, D-lyxo-Pentitol

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About This Item

Formule empirique (notation de Hill):
C5H12O5
Numéro CAS:
488-82-4
Poids moléculaire :
152.15
Numéro Beilstein :
1720520
Numéro CE :
207-686-2
Numéro MDL:
MFCD00004709
Code UNSPSC :
12352201
ID de substance PubChem :
24890762
Nomenclature NACRES :
NA.25

Pureté

≥99% (GC)

Forme

powder

Sucrosité

0.7 × sucrose

Couleur

white

Solubilité

water: 50 mg/mL, clear, colorless to faintly yellow

Température de stockage

room temp

Chaîne SMILES 

OC[C@@H](O)C(O)[C@H](O)CO

InChI

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

Clé InChI

HEBKCHPVOIAQTA-QWWZWVQMSA-N

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Application

D-Arabitol, a rare sugar alcohol, is a substrate used to identify, differentiate and characterize enzyme such as the gluconobacter oxydans dehydrogenase(s), Gox2181, hyperthermophilic D-arabitol dehydrogenase from Thermotoga maritime and NAD-dependent D-arabitoldehydrogenase from acetic acid bacterium, Acetobacter suboxydans.

Actions biochimiques/physiologiques

Used to produce xylitol via biotransformation.

Autres remarques

To gain a comprehensive understanding of our extensive range of Sugar alcohols for your research, we encourage you to visit our Carbohydrates Category page.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)

Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Verena Kallnik et al.
Applied microbiology and biotechnology, 90(4), 1285-1293 (2011-02-25)
The first hyperthermophilic D-arabitol dehydrogenase from Thermotoga maritima was heterologously purified from Escherichia coli. The protein was purified with and without a Strep-tag. The enzyme exclusively catalyzed the NAD(H)-dependent oxidoreduction of D-arabitol, D-xylitol, D-ribulose, or D-xylulose. A twofold increase of
Vivien Krell et al.
World journal of microbiology & biotechnology, 34(8), 108-108 (2018-07-05)
Successful commercialization of microbial biocontrol agents, such as Metarhizium spp., is often constrained by poor drying survival and shelf life. Here, we hypothesized that culture age would influence endogenous arabitol, erythritol, mannitol and trehalose contents in M. brunneum mycelium and
Xu Liu et al.
Biochemical and biophysical research communications, 415(2), 410-415 (2011-11-02)
Gluconobacter oxydans enable to oxidize sugars and polyols incompletely to corresponding materials with potential industrial applications, containing around 75 putative dehydrogenases. One of these putative dehydrogenases, Gox2181, was cloned and expressed in Escherichia coli BL21 (DE3), and its X-ray crystal
L Schakenraad et al.
Placenta, 104, 220-231 (2021-01-12)
An increasing number of women becomes pregnant while suffering from chronic kidney disease (CKD). As a result of decreased renal function, uremic solutes circulate at high levels in the maternal circulation. This study aimed to acquire more knowledge about the
Zhiguo Zhang et al.
International journal of molecular sciences, 15(9), 17130-17147 (2014-09-27)
The aim of this study was to evaluate effect of diosgenin (DG) on rats that had osteoporosis-like features induced by ovariectomy (OVX). Seventy-two six-month-old female Wistar rats were subjected to either ovariectomy (n = 60) or Sham operation (SHAM group
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