A3506
L-(−)-Arabitol
≥98% (GC)
Sinônimo(s):
L-Arabinitol
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About This Item
Fórmula empírica (Notação de Hill):
C5H12O5
Número CAS:
Peso molecular:
152.15
Beilstein:
1720521
Número CE:
Número MDL:
Código UNSPSC:
12352201
ID de substância PubChem:
NACRES:
NA.25
Preço e disponibilidade não estão disponíveis no momento.
Produtos recomendados
Ensaio
≥98% (GC)
Formulário
powder
cor
white
pf
101-104 °C (lit.)
solubilidade
water: 50 mg/mL, clear, colorless
cadeia de caracteres 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-/m0/s1
chave InChI
HEBKCHPVOIAQTA-IMJSIDKUSA-N
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Aplicação
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).
Outras notas
To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
Eyeshields, Gloves, type N95 (US)
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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
Quan Wang et al.
Journal of bacteriology, 194(8), 1868-1874 (2012-02-14)
Streptococcus pneumoniae is a major human pathogen associated with many diseases worldwide. Capsular polysaccharides (CPSs) are the major virulence factor. The biosynthetic pathway of D-arabinitol, which is present in the CPSs of several S. pneumoniae serotypes, has never been identified.
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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