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A3381

Sigma-Aldrich

D-(+)-Arabitol

≥99% (GC)

Synonym(s):

D-arabino-Pentitol, D-lyxo-Pentitol

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About This Item

Empirical Formula (Hill Notation):
C5H12O5
CAS Number:
488-82-4
Molecular Weight:
152.15
Beilstein:
1720520
EC Number:
207-686-2
MDL number:
MFCD00004709
UNSPSC Code:
12352201
PubChem Substance ID:
24890762
NACRES:
NA.25

Quality Level

200

Assay

≥99% (GC)

form

powder

sweetness

0.7 × sucrose

color

white

solubility

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

storage temp.

room temp

SMILES string

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

InChI key

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.

Biochem/physiol Actions

Used to produce xylitol via biotransformation.

Other Notes

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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
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
Gregory D Tredwell et al.
PloS one, 6(1), e16286-e16286 (2011-02-02)
Metabolic profiling is increasingly being used to investigate a diverse range of biological questions. Due to the rapid turnover of intracellular metabolites it is important to have reliable, reproducible techniques for sampling and sample treatment. Through the use of non-targeted
Monika Kordowska-Wiater et al.
Polish journal of microbiology, 61(4), 291-297 (2012-01-01)
L-arabitol is used in the food and pharmaceutical industries. It can be secreted by genetically modified Saccharomyces cerevisiae carrying the genes responsible for pentose metabolism in yeast cells. The process of the biotransformation of L-arabinose to arabitol is highly dependent
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