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A3506

Sigma-Aldrich

L-(−)-Arabit

≥98% (GC)

Synonym(e):

L-Arabinitol

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About This Item

Empirische Formel (Hill-System):
C5H12O5
CAS-Nummer:
7643-75-6
Molekulargewicht:
152.15
Beilstein:
1720521
EG-Nummer:
231-582-6
MDL-Nummer:
MFCD00064290
UNSPSC-Code:
12352201
PubChem Substanz-ID:
24890777
NACRES:
NA.25

Qualitätsniveau

300

Assay

≥98% (GC)

Form

powder

Farbe

white

mp (Schmelzpunkt)

101-104 °C (lit.)

Löslichkeit

water: 50 mg/mL, clear, colorless

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-/m0/s1

InChIKey

HEBKCHPVOIAQTA-IMJSIDKUSA-N

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Anwendung

L-Arabitol, a rare sugar alcohol, is being studied as a food additive that reduces fat deposits in the intestines. L-Arabitol is used as an inducer of xylanase expression in Hypocrea jecorina (Trichoderma reesei). L-Arabitol is used to identify, differentiate and characterize L-arabitol dehydrogenase(s).

Sonstige Hinweise

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

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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W Onkenhout et al.
Molecular genetics and metabolism, 77(1-2), 80-85 (2002-10-03)
A female patient, the first child of healthy non-consanguineous parents, presented at the age of 16 months with delayed motor development and facial dysmorphism. In addition she displayed a palatoschizis and multiple skeletal abnormalities as hypoplastic scapulae, hypoplastic os ilea
Dominik Mojzita et al.
The Journal of biological chemistry, 285(31), 23622-23628 (2010-06-01)
The first enzyme in the pathway for l-arabinose catabolism in eukaryotic microorganisms is a reductase, reducing l-arabinose to l-arabitol. The enzymes catalyzing this reduction are in general nonspecific and would also reduce d-xylose to xylitol, the first step in eukaryotic
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
Yihong Yang et al.
The Science of the total environment, 431, 68-77 (2012-06-06)
Fungal material (i.e., spores and fragments) is an important component of atmospheric aerosols. In order to examine the variability of fungal abundance in fine particles (PM(2.5)) during a biomass burning season, an intensive measurement campaign was conducted in the Sichuan
Astrid R Mach-Aigner et al.
Applied and environmental microbiology, 77(17), 5988-5994 (2011-07-12)
The saprophytic fungus Hypocrea jecorina (anamorph, Trichoderma reesei) is an important native producer of hydrolytic enzymes, including xylanases. Regarding principles of sustainability, cheap and renewable raw materials, such as d-xylose (the backbone monomer of xylan), have been receiving increasing attention
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